interpro_id string | interpro_numeric_id int64 | name string | short_name string | entry_type string | protein_count int64 | is_llm bool | is_llm_reviewed bool | abstract string | go_ids list | go_terms list | go_categories list | go_count int64 | member_databases list | member_accessions list | member_names list | member_protein_counts list | member_count int64 | external_databases list | external_accessions list | external_xrefs list | external_xref_count int64 | pdb_ids list | structure_count int64 | publication_ids list | pubmed_ids list | publication_titles list | publication_years list | publication_count int64 | parent_ids list | child_ids list | parent_count int64 | child_count int64 | tree_depth float64 | taxonomy_names list | taxonomy_protein_counts list | taxonomy_count int64 | key_species_names list | key_species_protein_counts list | key_species_count int64 | in_entry_list bool | entry_list_type string | entry_list_name string | names_dat_name string | short_names_dat_name string | split_bucket int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
IPR023961 | 23,961 | Nitric oxide reductase FlRd-NAD(+) reductase | NO_rdtase_NorW | Family | 1,149 | false | false | This entry represents an accessory proteins for anaerobicnitric oxide (NO) reductase. It is thought to reduce the rubredoxin moiety of NOreductase. | [
"GO:0016731"
] | [
"oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor"
] | [
"molecular_function"
] | 1 | [
"HAMAP"
] | [
"MF_01313"
] | [
"NorW"
] | [
1149
] | 1 | [
"EC"
] | [
"1.18.1.-"
] | [
"EC:1.18.1.-"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [
"IPR050260"
] | [] | 1 | 0 | 1 | [
"Bacteria"
] | [
1149
] | 1 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Family | Nitric oxide reductase FlRd-NAD(+) reductase | Nitric oxide reductase FlRd-NAD(+) reductase | NO_rdtase_NorW | 1 |
IPR023963 | 23,963 | Methanobactin precursor, Mb-OB3b | Methanobactin_OB3b | Family | 37 | false | false | Methanobactins are siderophore-like copper-chelating natural products with considerable variety from species to species [ , , ]. The 11-residue methanobactin of Methylosinus trichosporium OB3b is derived from a 30-residue precursor. A very similar 31-residue precursor is found in the rice endophyte Azospirillum sp. B51... | [] | [] | [] | 0 | [
"PFAM",
"NCBIFAM"
] | [
"PF25751",
"TIGR04071"
] | [
"Methanobactin",
"methanobac_OB3b"
] | [
25,
37
] | 2 | [
"GP"
] | [
"GenProp0962"
] | [
"GP:GenProp0962"
] | 1 | [
"7fc0"
] | 1 | [
"PUB00060471",
"PUB00106811",
"PUB00106856",
"PUB00160639",
"PUB00160640"
] | [
"20961038",
"26984926",
"21900235",
"15361623",
"21254756"
] | [
"A comparison of methanobactins from Methylosinus trichosporium OB3b and Methylocystis strain Sb2 predicts methanobactins are synthesized from diverse peptide precursors modified to create a common core for binding and reducing copper ions.",
"Methanobactin and the Link between Copper and Bacterial Methane Oxidat... | [
2010,
2016,
2011,
2004,
2011
] | 5 | [] | [] | 0 | 0 | null | [
"Pseudomonadota"
] | [
37
] | 1 | [] | [] | 0 | true | Family | Methanobactin precursor, Mb-OB3b | Methanobactin precursor, Mb-OB3b | Methanobactin_OB3b | 9 |
IPR023965 | 23,965 | Capreomycidine synthase | Capreomycidine_synthase | Family | 144 | false | false | Members of this family are capreomycidine synthases, which perform the second of two steps in the biosynthesis of 2S,3R-capreomycidine from arginine. The best characterised member is VioD from the biosynthetic pathway for viomycin [ ]. Capreomycidine is an unusual amino acid used by non-ribosomal peptide synthases (NRP... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03947"
] | [
"viomycin_VioD"
] | [
144
] | 1 | [
"GP"
] | [
"GenProp0909"
] | [
"GP:GenProp0909"
] | 1 | [
"4m2j",
"4m2k",
"4m2m"
] | 3 | [
"PUB00055106"
] | [
"15368581"
] | [
"Formation of the nonproteinogenic amino acid 2S,3R-capreomycidine by VioD from the viomycin biosynthesis pathway."
] | [
2004
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
144
] | 1 | [] | [] | 0 | true | Family | Capreomycidine synthase | Capreomycidine synthase | Capreomycidine_synthase | 7 |
IPR023966 | 23,966 | Arginine beta-hydroxylase, Fe2/alpha-ketoglutarate-dependent | Arginine_beta-hydroxylase | Family | 74 | false | false | Members of this protein family are L-arginine beta-hydroxylase, members of a broader family of enzymes dependent on Fe(II), alpha-ketoglutarate, and molecular oxygen. Enzymes in the broader family but excluded by this model include clavaminate synthase, taurine dioxygenase, and prolyl-4-hydroxylase [ , ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03946"
] | [
"viomycin_VioC"
] | [
74
] | 1 | [
"GP"
] | [
"GenProp0909"
] | [
"GP:GenProp0909"
] | 1 | [
"2wbo",
"2wbp",
"2wbq",
"4m23",
"4m25",
"4m26",
"4m27",
"4m2c",
"4m2e",
"4m2f",
"4m2g",
"4m2i",
"4ne0",
"6alm",
"6aln",
"6alo",
"6alp",
"6alq",
"6alr",
"6dax",
"6daz",
"6db2",
"6mp8",
"6mp9",
"6y0n",
"6y12",
"7vgl",
"7vgn",
"7y5f",
"7y5i",
"7y5p",
"7yhe"... | 34 | [
"PUB00050101",
"PUB00077127"
] | [
"19490124",
"17967013"
] | [
"Structural basis for the erythro-stereospecificity of the l-arginine oxygenase VioC in viomycin biosynthesis.",
"CD and MCD of CytC3 and taurine dioxygenase: role of the facial triad in alpha-KG-dependent oxygenases."
] | [
2009,
2007
] | 2 | [
"IPR014503"
] | [] | 1 | 0 | 1 | [
"Actinomycetes"
] | [
74
] | 1 | [] | [] | 0 | true | Family | Arginine beta-hydroxylase, Fe2/alpha-ketoglutarate-dependent | Arginine beta-hydroxylase, Fe2/alpha-ketoglutarate-dependent | Arginine_beta-hydroxylase | 8 |
IPR023967 | 23,967 | Conserved hypothetical protein CHP03996, oxidoreductase | CHP03996_oxidoreductase | Family | 207 | false | false | This protein family occurs in the vicinity of the putative mycofactocin biosynthesis operon in a number of Actinobacteria such as Frankia sp. and Rhodococcus sp. Family members contain a TIM-barrel fold commonly found in NADH:flavin oxidoreductase/NADH oxidase enzymes that use FMN/FAD as cofactor. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03996"
] | [
"mycofact_OYE_1"
] | [
207
] | 1 | [
"GP"
] | [
"GenProp0917"
] | [
"GP:GenProp0917"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"freshwater metagenome"
] | [
191,
16
] | 2 | [] | [] | 0 | true | Family | Conserved hypothetical protein CHP03996, oxidoreductase | Conserved hypothetical protein CHP03996, oxidoreductase | CHP03996_oxidoreductase | 4 |
IPR023968 | 23,968 | Bacteriocin precursor, CLI3235 family, putative | Bacteriocin_CLI3235 | Family | 126 | false | false | Members of this protein family are Cys-rich putative bacteriocin precursor peptides restricted to Clostridia but found in multiple species, with up to three per genome. They are found next to a CLI_3234 family radical SAM protein that may perform post-translational modification. This model describes approximately 35 re... | [] | [] | [] | 0 | [
"PFAM",
"NCBIFAM"
] | [
"PF27803",
"TIGR04065"
] | [
"Bacteriocin_CLI3235",
"ocin_CLI_3235"
] | [
126,
111
] | 2 | [
"GP"
] | [
"GenProp0945"
] | [
"GP:GenProp0945"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
126
] | 1 | [] | [] | 0 | true | Family | Bacteriocin precursor, CLI3235 family, putative | Bacteriocin precursor, CLI3235 family, putative | Bacteriocin_CLI3235 | 8 |
IPR023969 | 23,969 | Conserved hypothetical protein CHP04072, B12-binding/radical SAM-type | CHP04072_B12-bd/rSAM | Family | 106 | false | false | Members of this protein family occur in conserved genomic contexts highly suggestive of lipid biosynthesis, including an island shared between Kuenenia stuttgartiensis, which produces ladderanes [ ], and Desulfotalea psychrophila, which produces a different kind of unusual polyunsaturated hydrocarbon. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04072"
] | [
"rSAM_ladder_B12"
] | [
106
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00055107"
] | [
"19220888"
] | [
"A comparative genomics study of genetic products potentially encoding ladderane lipid biosynthesis."
] | [
2009
] | 1 | [
"IPR034466"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"ecological metagenomes"
] | [
102,
4
] | 2 | [] | [] | 0 | true | Family | Conserved hypothetical protein CHP04072, B12-binding/radical SAM-type | Conserved hypothetical protein CHP04072, B12-binding/radical SAM-type | CHP04072_B12-bd/rSAM | 2 |
IPR023971 | 23,971 | Selenoprotein GSU1558/SbtA-like | GSU1558/StbA-like | Family | 26 | false | false | Members of this protein family are small peptides found in the vicinity of a peptide modification-type radical SAM protein family, nearly always selenopeptides. Multiple members of this protein family occur in species with a selenocysteine incorporation systems and have a TGA stop codon at position that aligns with cys... | [] | [] | [] | 0 | [
"PFAM",
"NCBIFAM"
] | [
"PF27804",
"TIGR04081"
] | [
"GSU1558_StbA-like",
""
] | [
25,
26
] | 2 | [
"GP"
] | [
"GenProp0956"
] | [
"GP:GenProp0956"
] | 1 | [] | 0 | [
"PUB00055953",
"PUB00106225"
] | [
"21478363",
"34730336"
] | [
"Biological systems discovery in silico: radical S-adenosylmethionine protein families and their target peptides for posttranslational modification.",
"New Role for Radical SAM Enzymes in the Biosynthesis of Thio(seleno)oxazole RiPP Natural Products."
] | [
2011,
2021
] | 2 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
26
] | 1 | [] | [] | 0 | true | Family | Selenoprotein GSU1558/SbtA-like | Selenoprotein GSU1558/SbtA-like | GSU1558/StbA-like | 6 |
IPR023972 | 23,972 | Conserved hypothetical protein CHP04069, acyl carrier-related | CHP04069_acyl_carrier-rel | Family | 65 | false | false | Members of this family are often related to an acyl carrier-like domain and are found in genomic contexts associated with a small Cys-rich peptide and a radical SAM protein which probably modifies the peptide. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04069"
] | [
"ocin_ACP_rel"
] | [
65
] | 1 | [
"GP"
] | [
"GenProp0945"
] | [
"GP:GenProp0945"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacillota"
] | [
65
] | 1 | [] | [] | 0 | true | Family | Conserved hypothetical protein CHP04069, acyl carrier-related | Conserved hypothetical protein CHP04069, acyl carrier-related | CHP04069_acyl_carrier-rel | 5 |
IPR023973 | 23,973 | Methanobactin biosynthesis cassette protein MbnC-like | MbnC-like | Family | 273 | false | false | This entry represents a family of proteins from proteobacteria, including Methanobactin biosynthesis cassette protein MbnC from Methylosinus trichosporium, part of the he iron-containing heterodimeric MbnBC enzyme complex, which is central to the biosynthesis of methanobactins (Mbns), copper-binding metallophores isola... | [] | [] | [] | 0 | [
"PFAM",
"NCBIFAM"
] | [
"PF27805",
"TIGR04061"
] | [
"MbnC-like",
"AZL_007950_fam"
] | [
273,
235
] | 2 | [] | [] | [] | 0 | [
"7dz9",
"7fc0",
"7tcr",
"7tcu",
"7tcw",
"7tcx"
] | 6 | [
"PUB00106909",
"PUB00106910"
] | [
"35320042",
"29348173"
] | [
"A mixed-valent Fe(II)Fe(III) species converts cysteine to an oxazolone/thioamide pair in methanobactin biosynthesis.",
"Methanobactins: Maintaining copper homeostasis in methanotrophs and beyond."
] | [
2022,
2018
] | 2 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
273
] | 1 | [] | [] | 0 | true | Family | Methanobactin biosynthesis cassette protein MbnC-like | Methanobactin biosynthesis cassette protein MbnC-like | MbnC-like | 3 |
IPR023974 | 23,974 | His-Xaa-Ser system protein HxsD | HxsD | Family | 547 | false | false | This rare conserved hypothetical protein of small size occurs exclusively, and perhaps universally, in the context of a pair of (uncharacterised) radical SAM proteins, HxsC ( ) and HxsB ( ). Many members of this family have invariant motifs LYW and LLNDYxLRE, but PSI-BLAST starting from family members well below 20% pa... | [] | [] | [] | 0 | [
"PFAM",
"NCBIFAM"
] | [
"PF27806",
"TIGR03976"
] | [
"HxsD",
"chp_LLNDYxLRE"
] | [
547,
451
] | 2 | [
"GP"
] | [
"GenProp0921"
] | [
"GP:GenProp0921"
] | 1 | [] | 0 | [
"PUB00055953"
] | [
"21478363"
] | [
"Biological systems discovery in silico: radical S-adenosylmethionine protein families and their target peptides for posttranslational modification."
] | [
2011
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Nanobdellati",
"metagenomes"
] | [
538,
4,
5
] | 3 | [] | [] | 0 | true | Family | His-Xaa-Ser system protein HxsD | His-Xaa-Ser system protein HxsD | HxsD | 4 |
IPR023975 | 23,975 | Six-cysteine peptide SCIFF | Six-Cys_pep_SCIFF | Family | 1,363 | false | false | Members of this protein family are essentially universal in the class Clostridia and therefore highly abundant in the human gut microbiome. This short peptide is designated SCIFF, for Six Cysteines in Forty-Five residues. It is a presumed ribosomal natural product precursor, always found associated with a yet-uncharact... | [] | [] | [] | 0 | [
"PFAM",
"NCBIFAM"
] | [
"PF13165",
"TIGR03973"
] | [
"SCIFF",
"six_Cys_in_45"
] | [
1363,
1360
] | 2 | [
"GP"
] | [
"GenProp0919"
] | [
"GP:GenProp0919"
] | 1 | [] | 0 | [
"PUB00055953",
"PUB00106801",
"PUB00106802"
] | [
"21478363",
"27410522",
"32713052"
] | [
"Biological systems discovery in silico: radical S-adenosylmethionine protein families and their target peptides for posttranslational modification.",
"SkfB Abstracts a Hydrogen Atom from Cα on SkfA To Initiate Thioether Cross-Link Formation.",
"The SCIFF-Derived Ranthipeptides Participate in Quorum Sensing in ... | [
2011,
2016,
2020
] | 3 | [] | [] | 0 | 0 | null | [
"Bacteria",
"unclassified sequences"
] | [
1351,
12
] | 2 | [] | [] | 0 | true | Family | Six-cysteine peptide SCIFF | Six-cysteine peptide SCIFF | Six-Cys_pep_SCIFF | 7 |
IPR023976 | 23,976 | Conserved hypothetical protein CHP04031, Htur1727 | CHP04031_Htur1727 | Family | 216 | false | false | Members of this protein family show homology to the putative PaaH (or PaaB) subunit of the phenylacetate-CoA oxygenase complex. However, all members are found in the Halobacteriales in the vicinity of a radical SAM protein homologous to the PqqE protein of pyroquinoline quinone (PQQ) biosynthesis. Members are well-cons... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04031"
] | [
"Htur_1727_fam"
] | [
216
] | 1 | [
"GP"
] | [
"GenProp1065"
] | [
"GP:GenProp1065"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [
"IPR009359"
] | [] | 1 | 0 | 1 | [
"Halobacteriales"
] | [
216
] | 1 | [] | [] | 0 | true | Family | Conserved hypothetical protein CHP04031, Htur1727 | Conserved hypothetical protein CHP04031, Htur1727 | CHP04031_Htur1727 | 9 |
IPR023977 | 23,977 | Copper-binding protein MbnP-like | MbnP-like | Family | 579 | false | false | Members of this rare protein family regularly occur next to a member of the MXAN_0977 subfamily ( ) of the di-heme cytochrome c peroxidase/MauG family ( ). MauG itself ( ) is a protein modification enzyme responsible for the tryptophan tryptophylquinone (TTQ) modification involved in methylamine dehydrogenase activatio... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04052"
] | [
"MbnP_like_WxW"
] | [
579
] | 1 | [
"GP"
] | [
"GenProp0940"
] | [
"GP:GenProp0940"
] | 1 | [
"7l6g"
] | 1 | [
"PUB00060471",
"PUB00153588"
] | [
"20961038",
"34074779"
] | [
"A comparison of methanobactins from Methylosinus trichosporium OB3b and Methylocystis strain Sb2 predicts methanobactins are synthesized from diverse peptide precursors modified to create a common core for binding and reducing copper ions.",
"Copper binding by a unique family of metalloproteins is dependent on k... | [
2010,
2021
] | 2 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Durusdinium trenchii",
"bioreactor metagenome"
] | [
577,
1,
1
] | 3 | [] | [] | 0 | true | Family | Copper-binding protein MbnP-like | Copper-binding protein MbnP-like | MbnP-like | 4 |
IPR023978 | 23,978 | Glucose-methanol-choline oxidoreductase, bacteria | GMC_oxidoreductase_bact | Family | 784 | false | false | This entry describes a set of dehydrogenases belonging to the glucose-methanol-choline oxidoreductase (GMC oxidoreductase) family. Members of the family are found in bacterial genome contexts containing also members of families and , and are proposed to be uniform in function. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03970"
] | [
"Rv0697"
] | [
784
] | 1 | [
"GP"
] | [
"GenProp0917"
] | [
"GP:GenProp0917"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [
"IPR012132"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Geodia barretti",
"ecological metagenomes",
"uncultured marine group II/III euryarchaeote KM3_170_G02"
] | [
718,
17,
48,
1
] | 4 | [] | [] | 0 | true | Family | Glucose-methanol-choline oxidoreductase, bacteria | Glucose-methanol-choline oxidoreductase, bacteria | GMC_oxidoreductase_bact | 6 |
IPR023979 | 23,979 | Conserved hypothetical protein CHP04014, B12-binding/radical SAM-type | CHP04014_B12-bd/rSAM | Family | 113 | false | false | Members of this family, which are found in methanogenic archaea, have both a B12 binding homology domain ( ) and a radical SAM domain ( ). They occur only once per genome. Some species that express proteins of this family also express a related protein with a similar domain architecture (see ). | [] | [] | [] | 0 | [
"SFLD",
"NCBIFAM"
] | [
"SFLDG01217",
"TIGR04014"
] | [
"B12-binding_methylthiotransfer",
"B12_SAM_MJ_0865"
] | [
111,
113
] | 2 | [] | [] | [] | 0 | [
"9ccb"
] | 1 | [] | [] | [] | [] | 0 | [
"IPR034466"
] | [] | 1 | 0 | 1 | [
"Archaea",
"hydrocarbon metagenome"
] | [
111,
2
] | 2 | [] | [] | 0 | true | Family | Conserved hypothetical protein CHP04014, B12-binding/radical SAM-type | Conserved hypothetical protein CHP04014, B12-binding/radical SAM-type | CHP04014_B12-bd/rSAM | 6 |
IPR023981 | 23,981 | Pre-mycofactocin glycosyltransferase | MftF | Family | 1,295 | false | false | Pre-mycofactocin glycosyltransferase MftF is a glycosyltransferase that catalyses the oligoglycosylation of pre-mycofactocin (PMFT), adding up to nine beta-1,4-linked glucose residues [ ]. It is involved in the biosynthesis of the enzyme cofactor mycofactocin (MFT), a redox cofactor which belongs to the family of ribos... | [
"GO:0016740"
] | [
"transferase activity"
] | [
"molecular_function"
] | 1 | [
"NCBIFAM"
] | [
"TIGR03965"
] | [
"mycofact_glyco"
] | [
1295
] | 1 | [
"EC",
"GP",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"... | [
"2.4.1.-",
"GenProp0917",
"PWY-1901",
"PWY-1961",
"PWY-1981",
"PWY-2021",
"PWY-2881",
"PWY-2901",
"PWY-2902",
"PWY-4421",
"PWY-4801",
"PWY-5094",
"PWY-5105",
"PWY-5129",
"PWY-5139",
"PWY-5160",
"PWY-5161",
"PWY-5268",
"PWY-5284",
"PWY-5286",
"PWY-5310",
"PWY-5312",
"PWY-5... | [
"EC:2.4.1.-",
"GP:GenProp0917",
"METACYC:PWY-1901",
"METACYC:PWY-1961",
"METACYC:PWY-1981",
"METACYC:PWY-2021",
"METACYC:PWY-2881",
"METACYC:PWY-2901",
"METACYC:PWY-2902",
"METACYC:PWY-4421",
"METACYC:PWY-4801",
"METACYC:PWY-5094",
"METACYC:PWY-5105",
"METACYC:PWY-5129",
"METACYC:PWY-513... | 201 | [] | 0 | [
"PUB00096692",
"PUB00096693"
] | [
"31113891",
"33014324"
] | [
"Mycofactocin Is Associated with Ethanol Metabolism in Mycobacteria.",
"Structure elucidation of the redox cofactor mycofactocin reveals oligo-glycosylation by MftF."
] | [
2019,
2020
] | 2 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Halobacteriales",
"ecological metagenomes"
] | [
1241,
3,
51
] | 3 | [] | [] | 0 | true | Family | Pre-mycofactocin glycosyltransferase | Pre-mycofactocin glycosyltransferase | MftF | 6 |
IPR023982 | 23,982 | Conserved hypothetical protein CHP04029, CMD-like | CHP04029_CMD-like | Family | 764 | false | false | Sequences in this family occur as the N-terminal domain of a fusion protein with a C-terminal peroxidase-like protein, or as discrete proteins encoded next to a peroxidase-like protein. The two partners regularly are encoded near to, and in the same genomes as, a putative FMN-dependent luciferase-like monooxygenase (LL... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04029"
] | [
"CMD_Avi_7170"
] | [
764
] | 1 | [
"GP"
] | [
"GenProp0935"
] | [
"GP:GenProp0935"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
764
] | 1 | [] | [] | 0 | true | Family | Conserved hypothetical protein CHP04029, CMD-like | Conserved hypothetical protein CHP04029, CMD-like | CHP04029_CMD-like | 6 |
IPR023983 | 23,983 | DNA sulphur modification system-associated protein 4 | DNA_S_mod_dnd_assoc_4 | Family | 385 | false | false | A DNA sulphur modification system, dnd (degradation during electrophoresis), is sparsely and sporadically distributed among the bacteria. Members of this protein family are strictly limited to species with the dnd operon, and are found close to the dnd operon on the chromosomes of species such as Nostoc sp. PCC 7120, G... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04062"
] | [
"dnd_assoc_4"
] | [
385
] | 1 | [
"GP"
] | [
"GenProp0701"
] | [
"GP:GenProp0701"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [
"IPR060766"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"ecological metagenomes"
] | [
383,
2
] | 2 | [] | [] | 0 | true | Family | DNA sulphur modification system-associated protein 4 | DNA sulphur modification system-associated protein 4 | DNA_S_mod_dnd_assoc_4 | 2 |
IPR023984 | 23,984 | Ribosomal peptide maturation radical SAM protein 1 | rSAM_ocin_1 | Family | 944 | false | false | Members of this family of peptide-modifying radical SAM proteins include BstC, BstF, and BstJ, three enzymes involved in the biosynthesis of the antibiotic bottromycin D from a ribosomally translated peptide precursor that lacks a leader peptide. They appear to perform methylations of carbon atoms [ , ]. Other members ... | [] | [] | [] | 0 | [
"SFLD",
"NCBIFAM"
] | [
"SFLDF00324",
"TIGR03975"
] | [
"bacteriocin_maturation",
"rSAM_ocin_1"
] | [
938,
931
] | 2 | [
"GP"
] | [
"GenProp0861"
] | [
"GP:GenProp0861"
] | 1 | [] | 0 | [
"PUB00055015",
"PUB00074064",
"PUB00105079"
] | [
"20500830",
"22983711",
"22984777"
] | [
"Expansion of ribosomally produced natural products: a nitrile hydratase- and Nif11-related precursor family.",
"Metagenome mining reveals polytheonamides as posttranslationally modified ribosomal peptides.",
"Structure and biosynthesis of the antibiotic bottromycin D."
] | [
2010,
2012,
2012
] | 3 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"ecological metagenomes"
] | [
2,
928,
14
] | 3 | [] | [] | 0 | true | Family | Ribosomal peptide maturation radical SAM protein 1 | Ribosomal peptide maturation radical SAM protein 1 | rSAM_ocin_1 | 8 |
IPR023985 | 23,985 | Mycofactocin-dependent oxidoreductase | SDR_subfam_1 | Family | 6,952 | false | false | Members of this protein subfamily are putative oxidoreductases belonging to the larger SDR family. All members occur in genomes that encode a cassette for the biosynthesis of mycofactocin, a proposed electron carrier of a novel redox pool. Characterised members of this family are described as NDMA-dependent, meaning th... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03971"
] | [
"SDR_subfam_1"
] | [
6952
] | 1 | [
"GP"
] | [
"GenProp0917"
] | [
"GP:GenProp0917"
] | 1 | [
"3oec",
"3pgx",
"3pxx",
"3s55",
"3sx2",
"3t7c",
"3tsc",
"3uve",
"4rgb",
"5ej2"
] | 10 | [
"PUB00055045"
] | [
"21223593"
] | [
"Bioinformatic evidence for a widely distributed, ribosomally produced electron carrier precursor, its maturation proteins, and its nicotinoprotein redox partners."
] | [
2011
] | 1 | [
"IPR002347"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Didymella rabiei",
"Halobacteriales",
"metagenomes"
] | [
6853,
1,
47,
51
] | 4 | [] | [] | 0 | true | Family | Mycofactocin-dependent oxidoreductase | Mycofactocin-dependent oxidoreductase | SDR_subfam_1 | 8 |
IPR023986 | 23,986 | Glycosyltransferase, putative, MSMEG0565 family | GlycosylTfrase_MSMEG0565 | Family | 1,016 | false | false | A conserved gene cluster found sporadically from Actinobacteria to Proteobacteria to Cyanobacteria features a radical SAM protein, an N-acetyltransferase, an oxidoreductase, and two additional proteins whose functional classes are unclear. The metabolic role of the cluster is probably biosynthetic. This glycosyltransfe... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04047"
] | [
"MSMEG_0565_glyc"
] | [
1016
] | 1 | [
"GP"
] | [
"GenProp0939"
] | [
"GP:GenProp0939"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"ecological metagenomes"
] | [
1006,
10
] | 2 | [] | [] | 0 | true | Family | Glycosyltransferase, putative, MSMEG0565 family | Glycosyltransferase, putative, MSMEG0565 family | GlycosylTfrase_MSMEG0565 | 8 |
IPR023987 | 23,987 | Conserved hypothetical protein CHP03977, oxidoreductase | CHP03977_oxidoreductase | Family | 229 | false | false | This protein family occurs in the vicinity of the the putative mycofactocin biosynthesis operon in a number of Actinobacteria such as Frankia sp. and Rhodococcus sp., in Pelotomaculum thermopropionicum SI (Firmicutes), and in Geobacter uraniireducens Rf4 (Deltaproteobacteria). Family members contain a TIM-barrel fold c... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03997"
] | [
"mycofact_OYE_2"
] | [
229
] | 1 | [
"GP"
] | [
"GenProp0917"
] | [
"GP:GenProp0917"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"freshwater metagenome"
] | [
212,
17
] | 2 | [] | [] | 0 | true | Family | Conserved hypothetical protein CHP03977, oxidoreductase | Conserved hypothetical protein CHP03977, oxidoreductase | CHP03977_oxidoreductase | 7 |
IPR023988 | 23,988 | Mycofactocin precursor peptide | MftA | Family | 1,075 | false | false | Mycofactocin precursor peptide MftA is the precursor peptide that leads to mycofactocin (MFT), a redox cofactor which belongs to the family of ribosomally synthesized and post-translationally modified peptides (RiPPs) and is involved in alcohol metabolism of mycobacteria including Mycobacterium tuberculosis [ , ]. MftA... | [] | [] | [] | 0 | [
"PFAM",
"NCBIFAM"
] | [
"PF23709",
"TIGR03969"
] | [
"MftA",
"mycofactocin"
] | [
1054,
1075
] | 2 | [
"GP"
] | [
"GenProp0917"
] | [
"GP:GenProp0917"
] | 1 | [] | 0 | [
"PUB00096692",
"PUB00096693",
"PUB00096696",
"PUB00155614"
] | [
"31113891",
"33014324",
"27158836",
"36243697"
] | [
"Mycofactocin Is Associated with Ethanol Metabolism in Mycobacteria.",
"Structure elucidation of the redox cofactor mycofactocin reveals oligo-glycosylation by MftF.",
"The Radical S-Adenosyl-l-methionine Enzyme MftC Catalyzes an Oxidative Decarboxylation of the C-Terminus of the MftA Peptide.",
"Comparative ... | [
2019,
2020,
2016,
2022
] | 4 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Halobacteriales",
"ecological metagenomes"
] | [
1033,
6,
36
] | 3 | [] | [] | 0 | true | Family | Mycofactocin precursor peptide | Mycofactocin precursor peptide | MftA | 9 |
IPR023989 | 23,989 | Pre-mycofactocin synthase | MftD | Family | 1,232 | false | false | Pre-mycofactocin synthase MftD is involved in the biosynthesis of the enzyme cofactor mycofactocin (MFT), a ribosomally synthesized and post-translationally modified (RiPP) redox cofactor, and catalyses the oxidative deamination of AHDP (3-amino-5-[(4-hydroxyphenyl)methyl]-4,4-dimethyl-2-pyrrolidin-2-one), forming an a... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03966"
] | [
"actino_HemFlav"
] | [
1232
] | 1 | [
"EC",
"GP"
] | [
"1.4.3.26",
"GenProp0917"
] | [
"EC:1.4.3.26",
"GP:GenProp0917"
] | 2 | [] | 0 | [
"PUB00096693",
"PUB00096697"
] | [
"33014324",
"31381312"
] | [
"Structure elucidation of the redox cofactor mycofactocin reveals oligo-glycosylation by MftF.",
"MftD Catalyzes the Formation of a Biologically Active Redox Center in the Biosynthesis of the Ribosomally Synthesized and Post-translationally Modified Redox Cofactor Mycofactocin."
] | [
2020,
2019
] | 2 | [
"IPR012133"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"metagenomes"
] | [
1208,
24
] | 2 | [] | [] | 0 | true | Family | Pre-mycofactocin synthase | Pre-mycofactocin synthase | MftD | 6 |
IPR023990 | 23,990 | Butyryl-CoA:acetate CoA-transferase | Butryl-CoA_acetate_CoA_Tfrase | Family | 627 | false | false | This enzyme represents one of at least two mechanisms for reclaiming CoA from butyryl-CoA at the end of butyrate biosynthesis (an important process performed by some colonic bacteria), namely transfer of CoA to acetate [ ]. An alternate mechanism transfers the butyrate onto inorganic phosphate, after which butyrate kin... | [
"GO:0019605"
] | [
"butyrate metabolic process"
] | [
"biological_process"
] | 1 | [
"HAMAP",
"HAMAP",
"NCBIFAM"
] | [
"MF_03227",
"MF_03228",
"TIGR03948"
] | [
"But_acet_CoA_trans",
"But_CoA_trans",
"butyr_acet_CoA"
] | [
285,
623,
290
] | 3 | [
"EC",
"GP",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC"
] | [
"2.8.3.-",
"GenProp0911",
"PWY-5022",
"PWY-5677",
"PWY-7382",
"PWY-7401",
"PWY-8326"
] | [
"EC:2.8.3.-",
"GP:GenProp0911",
"METACYC:PWY-5022",
"METACYC:PWY-5677",
"METACYC:PWY-7382",
"METACYC:PWY-7401",
"METACYC:PWY-8326"
] | 7 | [] | 0 | [
"PUB00055058",
"PUB00094482"
] | [
"19807780",
"23468890"
] | [
"Diversity of human colonic butyrate-producing bacteria revealed by analysis of the butyryl-CoA:acetate CoA-transferase gene.",
"A proteomic view at the biochemistry of syntrophic butyrate oxidation in Syntrophomonas wolfei."
] | [
2010,
2013
] | 2 | [
"IPR046433"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"ecological metagenomes"
] | [
617,
10
] | 2 | [] | [] | 0 | true | Family | Butyryl-CoA:acetate CoA-transferase | Butyryl-CoA:acetate CoA-transferase | Butryl-CoA_acetate_CoA_Tfrase | 5 |
IPR023991 | 23,991 | Bacteriocin, class IIb, lactobin A/cerein 7B family | Bacteriocin_IIb_lactobn/cerein | Family | 906 | false | false | Members of this protein family are described variably as bacteriocins per se, one chain of a two-chain bacteriocin, or bacteriocin enhancer proteins. All members of the seed alignment occur in paired gene contexts with another member of the same protein family. This family includes bacteriocins that appear not to under... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03949"
] | [
"bact_IIb_cerein"
] | [
906
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Candidatus Nitrososphaera evergladensis SR1",
"ecological metagenomes"
] | [
899,
1,
6
] | 3 | [] | [] | 0 | true | Family | Bacteriocin, class IIb, lactobin A/cerein 7B family | Bacteriocin, class IIb, lactobin A/cerein 7B family | Bacteriocin_IIb_lactobn/cerein | 3 |
IPR023992 | 23,992 | Pre-heme d1 synthase NirJ | HemeD1_Synth_NirJ | Family | 816 | false | false | Heme D1 occurs in the cytochrome Cd1 subunit of nitrite reductase in species such as Pseudomonas stutzeri. NirJ is a radical SAM protein that contains two iron-sulfur clusters. It catalyzes the removal of two propionate side chains during heme D1 biosynthesis [ ]. In a number of species, distinct genes NirJ1 and NirJ2 ... | [
"GO:0003824",
"GO:0051539"
] | [
"catalytic activity",
"4 iron, 4 sulfur cluster binding"
] | [
"molecular_function",
"molecular_function"
] | 2 | [
"SFLD",
"NCBIFAM"
] | [
"SFLDF00393",
"TIGR04051"
] | [
"heme_D1_biosynthesis_(NirJ-lik",
"rSAM_NirJ"
] | [
812,
816
] | 2 | [] | [] | [] | 0 | [] | 0 | [
"PUB00097908"
] | [
"29076625"
] | [
"The Radical SAM enzyme NirJ catalyzes the removal of two propionate side chains during heme d1 biosynthesis."
] | [
2017
] | 1 | [
"IPR017200"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"unclassified sequences"
] | [
801,
15
] | 2 | [] | [] | 0 | true | Family | Pre-heme d1 synthase NirJ | Pre-heme d1 synthase NirJ | HemeD1_Synth_NirJ | 3 |
IPR023993 | 23,993 | S-adenosyl-L-methionine-dependent tRNA 4-demethylwyosine synthase, archaea | TYW1_archaea | Family | 780 | false | false | Members of this protein family are the archaeal protein TYW1 [ ], a radical SAM protein that catalyses the second step in creating the wye-bases, wyosine and derivatives such as wybutosine, for tRNA base modification [ ]. | [
"GO:0016829",
"GO:0051539",
"GO:0008033"
] | [
"lyase activity",
"4 iron, 4 sulfur cluster binding",
"tRNA processing"
] | [
"molecular_function",
"molecular_function",
"biological_process"
] | 3 | [
"HAMAP",
"NCBIFAM"
] | [
"MF_01921",
"TIGR03972"
] | [
"TYW1_archaea",
"rSAM_TYW1"
] | [
713,
780
] | 2 | [
"EC",
"METACYC",
"METACYC"
] | [
"4.1.3.44",
"PWY-7285",
"PWY-7286"
] | [
"EC:4.1.3.44",
"METACYC:PWY-7285",
"METACYC:PWY-7286"
] | 3 | [
"2yx0",
"2z2u",
"6djt"
] | 3 | [
"PUB00050155",
"PUB00050182"
] | [
"17881823",
"17727881"
] | [
"Structure of an archaeal TYW1, the enzyme catalyzing the second step of wye-base biosynthesis.",
"Crystal structure of the radical SAM enzyme catalyzing tricyclic modified base formation in tRNA."
] | [
2007,
2007
] | 2 | [
"IPR034556"
] | [] | 1 | 0 | 1 | [
"Archaea",
"Eukaryota",
"ecological metagenomes"
] | [
748,
22,
10
] | 3 | [] | [] | 0 | true | Family | S-adenosyl-L-methionine-dependent tRNA 4-demethylwyosine synthase, archaea | S-adenosyl-L-methionine-dependent tRNA 4-demethylwyosine synthase, archaea | TYW1_archaea | 5 |
IPR023994 | 23,994 | [NiFe]-hydrogenase assembly, chaperone, HybE | NiFe-hyd_HybE | Family | 1,720 | false | false | Members of this family are chaperones for the assembly of [NiFe] hydrogenases, in the family of HybE, which is specific for hydrogenase-2 of Escherichia coli. Members often have an additional N-terminal rubredoxin domain [ ]. | [] | [] | [] | 0 | [
"PFAM",
"NCBIFAM"
] | [
"PF11939",
"TIGR03993"
] | [
"NiFe-hyd_HybE",
"hydrog_HybE"
] | [
1720,
1540
] | 2 | [] | [] | [] | 0 | [
"2kc5"
] | 1 | [
"PUB00078075"
] | [
"19636963"
] | [
"1H, 13C and 15N resonance assignments of the chaperone HybE of hydrogenase-2 from Escherichia coli."
] | [
2009
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Durusdinium trenchii",
"metagenomes"
] | [
1698,
1,
21
] | 3 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Family | [NiFe]-hydrogenase assembly, chaperone, HybE | [NiFe]-hydrogenase assembly, chaperone, HybE | NiFe-hyd_HybE | 1 |
IPR023995 | 23,995 | Oxygen-independent coproporphyrinogen-III oxidase-like protein HemZ | HemZ | Family | 2,456 | false | false | Members of this radical SAM protein family are HemZ, a protein involved in coproporphyrinogen III decarboxylation. Alternative names for this enzyme (EC ) include coproporphyrinogen dehydrogenase and oxygen-independent coproporphyrinogen III oxidase. The family is related to, but distinct from HemN, and in Bacillus sub... | [] | [] | [] | 0 | [
"SFLD",
"NCBIFAM"
] | [
"SFLDF00310",
"TIGR03994"
] | [
"oxygen-independent_coproporphy",
"rSAM_HemZ"
] | [
2431,
2447
] | 2 | [] | [] | [] | 0 | [] | 0 | [
"PUB00055059"
] | [
"10498703"
] | [
"Transcriptional control of Bacillus subtilis hemN and hemZ."
] | [
1999
] | 1 | [
"IPR034505"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Inoviridae sp. ctDEu7",
"ecological metagenomes"
] | [
2447,
1,
8
] | 3 | [] | [] | 0 | true | Family | Oxygen-independent coproporphyrinogen-III oxidase-like protein HemZ | Oxygen-independent coproporphyrinogen-III oxidase-like protein HemZ | HemZ | 7 |
IPR023996 | 23,996 | TonB-dependent outer membrane protein, SusC/RagA | TonB-dep_OMP_SusC/RagA | Family | 91,056 | false | false | This entry describes a clade of TonB-linked outer membrane proteins (OMP). Members of the family are restricted to the Bacteriodetes lineage (except for Gemmatimonas aurantiaca T-27 from the novel phylum Gemmatimonadetes) and occur in high copy numbers, with over 100 members from Bacteroides thetaiotaomicron VPI-5482 a... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04056"
] | [
"OMP_RagA_SusC"
] | [
91056
] | 1 | [
"GP"
] | [
"GenProp0941"
] | [
"GP:GenProp0941"
] | 1 | [
"5fq6",
"5fq7",
"5fq8",
"5t3r",
"5t4y",
"6sli",
"6slj",
"6sln",
"6sm3",
"6sml",
"6smq",
"6z8i",
"6z9a",
"6zaz",
"6zlt",
"6zlu",
"6zm1",
"8a9y",
"8aa0",
"8aa1",
"8aa2",
"8aa3",
"8aa4",
"8ypt",
"8ypu"
] | 25 | [
"PUB00016547",
"PUB00055060",
"PUB00055061"
] | [
"11717282",
"15972517",
"11553542"
] | [
"Biochemical analysis of interactions between outer membrane proteins that contribute to starch utilization by Bacteroides thetaiotaomicron.",
"Sequence diversity and antigenic variation at the rag locus of Porphyromonas gingivalis.",
"Molecular cloning of a Bacteroides caccae TonB-linked outer membrane protein... | [
2001,
2005,
2001
] | 3 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"unclassified Caudoviricetes",
"unclassified sequences"
] | [
90336,
44,
9,
667
] | 4 | [] | [] | 0 | true | Family | TonB-dependent outer membrane protein, SusC/RagA | TonB-dependent outer membrane protein, SusC/RagA | TonB-dep_OMP_SusC/RagA | 5 |
IPR023997 | 23,997 | TonB-dependent outer membrane protein SusC/RagA, conserved site | TonB-dep_OMP_SusC/RagA_CS | Conserved_site | 87,685 | false | false | This entry describes a short conserved site found in the SusC/RagA family of outer membrane proteins from the Bacteriodetes. While many TonB-dependent outer membrane receptors are associated with siderophore import, this family seems to include generalized nutrient receptors that may convey fairly large oligomers of pr... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04057"
] | [
"SusC_RagA_signa"
] | [
87685
] | 1 | [] | [] | [] | 0 | [
"5fq6",
"5fq7",
"5fq8",
"5t3r",
"5t4y",
"6sli",
"6slj",
"6sln",
"6sm3",
"6sml",
"6smq",
"6z8i",
"6z9a",
"6zaz",
"6zlt",
"6zlu",
"6zm1",
"8a9y",
"8aa0",
"8aa1",
"8aa2",
"8aa3",
"8aa4",
"8ypt",
"8ypu"
] | 25 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"unclassified Caudoviricetes",
"unclassified sequences"
] | [
86876,
59,
8,
742
] | 4 | [] | [] | 0 | true | Conserved_site | TonB-dependent outer membrane protein SusC/RagA, conserved site | TonB-dependent outer membrane protein SusC/RagA, conserved site | TonB-dep_OMP_SusC/RagA_CS | 9 |
IPR023998 | 23,998 | Ferric aerobactin reductase IutB-like | FCR-like | Family | 500 | false | false | Members of this protein family are 2Fe-2S cluster binding proteins, found regularly in the context of siderophore transporters, including Ferric aerobactin reductase IutB from Vibrio vulnificus (FCR) [ , ]. Members are distantly related to FhuF from E. coli, a ferric iron reductase linked to removal of iron from hydrox... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03950"
] | [
"sidero_Fe_reduc"
] | [
500
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00055062",
"PUB00151532",
"PUB00151533"
] | [
"14756576",
"28150143",
"32681432"
] | [
"FhuF, part of a siderophore-reductase system.",
"IutB participates in the ferric-vulnibactin utilization system in Vibrio vulnificus M2799.",
"VuuB and IutB reduce ferric-vulnibactin in Vibrio vulnificus M2799."
] | [
2004,
2017,
2020
] | 3 | [] | [] | 0 | 0 | null | [
"Bacteria",
"metagenomes"
] | [
493,
7
] | 2 | [] | [] | 0 | true | Family | Ferric aerobactin reductase IutB-like | Ferric aerobactin reductase IutB-like | FCR-like | 3 |
IPR023999 | 23,999 | Formate transporter FocA | Formate_transptr_FocA | Family | 2,233 | false | false | FocA (formate channel A) forms a pentameric formate-selective channel through the plasma membrane, involved in the bidirectional transport of formate during mixed-acid fermentation [ , , , , ]. It functions to maintain relatively constant intracellular formate levels during growth, using different mechanisms for efflux... | [
"GO:0015499",
"GO:0015724",
"GO:0016020"
] | [
"formate transmembrane transporter activity",
"formate transport",
"membrane"
] | [
"molecular_function",
"biological_process",
"cellular_component"
] | 3 | [
"NCBIFAM"
] | [
"TIGR04060"
] | [
"formate_focA"
] | [
2233
] | 1 | [] | [] | [] | 0 | [
"3kcu",
"3kcv",
"3kly",
"3klz",
"3q7k",
"9g49",
"9g4d",
"9i3k"
] | 8 | [
"PUB00055063",
"PUB00060282",
"PUB00060283",
"PUB00060284",
"PUB00101342",
"PUB00101343"
] | [
"19940917",
"21493860",
"20041954",
"20010838",
"35390794",
"35377837"
] | [
"Structure of the formate transporter FocA reveals a pentameric aquaporin-like channel.",
"pH-dependent gating in a FocA formate channel.",
"Unexpected oligomeric structure of the FocA formate channel of Escherichia coli : a paradigm for the formate-nitrite transporter family of integral membrane proteins.",
... | [
2009,
2011,
2010,
2010,
2022,
2022
] | 6 | [
"IPR000292"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Beauveria bassiana D1-5",
"metagenomes"
] | [
2229,
1,
3
] | 3 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Family | Formate transporter FocA | Formate transporter FocA | Formate_transptr_FocA | 6 |
IPR024000 | 24,000 | Conserved hypothetical protein CHP04046, FMN-dependent | CHP04046_FMN-dependent | Family | 1,322 | false | false | Members of this protein family belong to a conserved seven-gene biosynthetic cluster found sparsely in Cyanobacteria, Proteobacteria, and Actinobacteria. Distant homologies to characterised proteins suggest that members are enzymes dependent on a flavinoid cofactor. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04046"
] | [
"MSMEG_0569_nitr"
] | [
1322
] | 1 | [
"GP"
] | [
"GenProp0939"
] | [
"GP:GenProp0939"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"freshwater metagenome"
] | [
1318,
4
] | 2 | [] | [] | 0 | true | Family | Conserved hypothetical protein CHP04046, FMN-dependent | Conserved hypothetical protein CHP04046, FMN-dependent | CHP04046_FMN-dependent | 6 |
IPR024001 | 24,001 | Cysteine-rich peptide, radical SAM maturase, CcpM | Cys-rich_pep_rSAM_mat_CcpM | Family | 177 | false | false | Members of this family are radical SAM enzymes that occur next to clostridial Cys-rich predicted bacteriocin (or other class of ribosomal natural product) precursors (see families and ). They include a TIGR04085 C-terminal additional 4Fe4S cluster-binding domain that is associated with peptide modification by radical S... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04068"
] | [
"rSAM_ocin_clost"
] | [
177
] | 1 | [
"GP"
] | [
"GenProp0945"
] | [
"GP:GenProp0945"
] | 1 | [] | 0 | [
"PUB00055953"
] | [
"21478363"
] | [
"Biological systems discovery in silico: radical S-adenosylmethionine protein families and their target peptides for posttranslational modification."
] | [
2011
] | 1 | [
"IPR023867"
] | [] | 1 | 0 | 1 | [
"Bacteria"
] | [
177
] | 1 | [] | [] | 0 | true | Family | Cysteine-rich peptide, radical SAM maturase, CcpM | Cysteine-rich peptide, radical SAM maturase, CcpM | Cys-rich_pep_rSAM_mat_CcpM | 9 |
IPR024003 | 24,003 | Putative luciferase-like monooxygenase, KPN01858 | Luciferase-like_KPN01858 | Family | 777 | false | false | This protein family consists of luciferase-like monooxygenases (LLM), and include KPN_01858 from Klebsiella pneumoniae as a representative member. Most are from species that lack F420 biosynthesis, so the family is likely to bind FMN as its cofactor. This family is closely associated with a binding protein-dependent AB... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04027"
] | [
"LLM_KPN_01858"
] | [
777
] | 1 | [
"GP"
] | [
"GenProp0935"
] | [
"GP:GenProp0935"
] | 1 | [
"8k74"
] | 1 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Beauveria bassiana D1-5"
] | [
776,
1
] | 2 | [] | [] | 0 | true | Family | Putative luciferase-like monooxygenase, KPN01858 | Putative luciferase-like monooxygenase, KPN01858 | Luciferase-like_KPN01858 | 5 |
IPR024005 | 24,005 | Colanic acid biosynthesis, acetyltransferase, WcaF | Colanic_acid_synth_WcaF | Family | 775 | false | false | This acetyltransferase is believed to catalyze the addition of the acetyl group that is attached through an O linkage to the first fucosyl residue of the colanic acid repetitive unit (E unit) [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04008"
] | [
"WcaF"
] | [
775
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00008202"
] | [
"8759852"
] | [
"Organization of the Escherichia coli K-12 gene cluster responsible for production of the extracellular polysaccharide colanic acid."
] | [
1996
] | 1 | [] | [] | 0 | 0 | null | [
"Gammaproteobacteria"
] | [
775
] | 1 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Family | Colanic acid biosynthesis, acetyltransferase, WcaF | Colanic acid biosynthesis, acetyltransferase, WcaF | Colanic_acid_synth_WcaF | 5 |
IPR024006 | 24,006 | Alternate signal-mediated exported protein, actinobacteria | Alt_signal_exp_actinobact | Family | 688 | false | false | Members of this Actinobacterial protein family contain the signal peptide domain , for the variant SipW form of the signal peptidase I family. The remainder of this protein, however, differs from families such as Peptidase_M73 ( ) and YqxM ( ) that share the same signal peptide domain. The two known targets for export ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04089"
] | [
"exp_by_SipW_III"
] | [
688
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Opisthokonta",
"metagenomes"
] | [
682,
3,
3
] | 3 | [] | [] | 0 | true | Family | Alternate signal-mediated exported protein, actinobacteria | Alternate signal-mediated exported protein, actinobacteria | Alt_signal_exp_actinobact | 8 |
IPR024007 | 24,007 | [FeFe]-hydrogenase maturation HydG, radical SAM | FeFe-hyd_mat_HydG | Family | 2,100 | false | false | This entry describes the radical SAM protein HydG. It is part of an enzyme metallocentre maturation system, working together with GTP-binding protein HydF and another radical SAM enzyme, HydE, in H-cluster maturation in [FeFe] hydrogenases. | [] | [] | [] | 0 | [
"SFLD",
"NCBIFAM"
] | [
"SFLDF00319",
"TIGR03955"
] | [
"Fe_hydrogenase_maturase_(HydG-",
"rSAM_HydG"
] | [
1954,
2100
] | 2 | [
"GP"
] | [
"GenProp0914"
] | [
"GP:GenProp0914"
] | 1 | [
"4rtb",
"4wcx"
] | 2 | [] | [] | [] | [] | 0 | [
"IPR034428"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Eukaryota",
"metagenomes"
] | [
2004,
75,
21
] | 3 | [] | [] | 0 | true | Family | [FeFe]-hydrogenase maturation HydG, radical SAM | [FeFe]-hydrogenase maturation HydG, radical SAM | FeFe-hyd_mat_HydG | 8 |
IPR024008 | 24,008 | BsaA-like SipW-dependent biofilm matrix protein | BsaA | Family | 331 | false | false | Members of this largely Clostridial protein family contain the signal peptide, for the variant SipW form of the signal peptidase I family. The remainder of this protein, however, differs from families such as Peptidase_M73 ( ) and YqxM that share the same signal peptide domain. The two known targets for export by the S... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04090"
] | [
"exp_by_SipW_IV"
] | [
331
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00106814"
] | [
"32737303"
] | [
"Temperature-regulated heterogeneous extracellular matrix gene expression defines biofilm morphology in Clostridium perfringens."
] | [
2020
] | 1 | [] | [] | 0 | 0 | null | [
"Bacillota"
] | [
331
] | 1 | [] | [] | 0 | true | Family | BsaA-like SipW-dependent biofilm matrix protein | BsaA-like SipW-dependent biofilm matrix protein | BsaA | 4 |
IPR024010 | 24,010 | Colanic acid biosynthesis, glycosyl transferase, WcaE | Colanic_acid_synth_WcaE | Family | 866 | false | false | This entry represents the putative glycosyl transferase gene product of wcaE, which is thought to be involved in the biosynthesis of colanic acid, an exopolysaccharide expressed in Enterobacteraceae species [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04009"
] | [
"wcaE"
] | [
866
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00008202"
] | [
"8759852"
] | [
"Organization of the Escherichia coli K-12 gene cluster responsible for production of the extracellular polysaccharide colanic acid."
] | [
1996
] | 1 | [] | [] | 0 | 0 | null | [
"Beauveria bassiana D1-5",
"Gammaproteobacteria"
] | [
1,
865
] | 2 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Family | Colanic acid biosynthesis, glycosyl transferase, WcaE | Colanic acid biosynthesis, glycosyl transferase, WcaE | Colanic_acid_synth_WcaE | 9 |
IPR024011 | 24,011 | Natural product biosynthesis luciferase-like monooxygenase domain | Biosynth_lucif-like_mOase_dom | Domain | 2,022 | false | false | This entry describes a type of bacterial luciferase-like monooxygenase (LLM) domain that regularly occurs within large non-ribosomal protein synthases/polyketide synthases, as well as smaller proteins. Luciferase-like monooxygenases include members that bind either FMN or F420. FMN is the more likely binding partner in... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04020"
] | [
"seco_metab_LLM"
] | [
2022
] | 1 | [] | [] | [] | 0 | [
"6ket"
] | 1 | [] | [] | [] | [] | 0 | [
"IPR011251"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Eukaryota",
"ecological metagenomes"
] | [
2014,
2,
6
] | 3 | [] | [] | 0 | true | Domain | Natural product biosynthesis luciferase-like monooxygenase domain | Natural product biosynthesis luciferase-like monooxygenase domain | Biosynth_lucif-like_mOase_dom | 2 |
IPR024013 | 24,013 | Putative colanic acid polymerase WcaD | WcaD | Family | 999 | false | false | This entry represents WcaD proteins involved in colanic acid biosynthesis in bacteria. WcaD is a putative colanic acid polymerase that functions in slime polysaccharide biosynthesis [ ]. These proteins are multi-pass membrane proteins localised to the inner membrane with multiple transmembrane helices. Members are foun... | [] | [] | [] | 0 | [
"PFAM",
"NCBIFAM"
] | [
"PF27321",
"TIGR04010"
] | [
"WcaD",
"WcaD"
] | [
999,
872
] | 2 | [] | [] | [] | 0 | [] | 0 | [
"PUB00008202",
"PUB00106806"
] | [
"8759852",
"34159784"
] | [
"Organization of the Escherichia coli K-12 gene cluster responsible for production of the extracellular polysaccharide colanic acid.",
"Tracking Colanic Acid Repeat Unit Formation from Stepwise Biosynthesis Inactivation in <i>Escherichia coli</i>."
] | [
1996,
2021
] | 2 | [] | [] | 0 | 0 | null | [
"Bacteria",
"metagenomes"
] | [
996,
3
] | 2 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Family | Putative colanic acid polymerase WcaD | Putative colanic acid polymerase WcaD | WcaD | 4 |
IPR024014 | 24,014 | FMNH(2)-dependent dimethylsulfone monooxygenase SfnG | DMSO2_SphG | Family | 2,743 | false | false | This family of FMNH2-dependent members of the luciferase-like monooxygenase (LLM) family includes SfnG, a monooxygenase that converts dimethylsulphone (DMSO2) to methanesulphonate [ ]. This step can be followed immediately by methanesulphonate sulphonatase (an alkanesulphonate monooxygenase - see ) for the FMNH2-depend... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04021"
] | [
"LLM_DMSO2_sfnG"
] | [
2743
] | 1 | [
"GP"
] | [
"GenProp0934"
] | [
"GP:GenProp0934"
] | 1 | [
"8t0u",
"8t0w"
] | 2 | [
"PUB00055065"
] | [
"17768252"
] | [
"Transcriptional regulation of the sulfate-starvation-induced gene sfnA by a sigma54-dependent activator of Pseudomonas putida."
] | [
2007
] | 1 | [
"IPR050172"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Eukaryota",
"Halobacteriales",
"metagenomes"
] | [
2426,
296,
12,
9
] | 4 | [
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)"
] | [
2
] | 1 | true | Family | FMNH(2)-dependent dimethylsulfone monooxygenase SfnG | FMNH(2)-dependent dimethylsulfone monooxygenase SfnG | DMSO2_SphG | 8 |
IPR024015 | 24,015 | Pyridoxamine 5'-phosphate oxidase, probable FMN-dependent, Alr4036-like | Pyridox_Oxase_FMN-dep_Alr4036 | Family | 235 | false | false | Pyridoxamine 5'-phosphate oxidase ( ) is an enzyme that is involved in the de novo synthesis of pyridoxine (vitamin B6) and pyridoxal phosphate. It oxidizes pyridoxamine-5-P (PMP) and pyridoxine-5-P (PNP) to pyridoxal-5-P. The enzyme requires the presence of flavin mononucleotide (FMN) as a cofactor, although there is ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04026"
] | [
"PPOX_FMN_cyano"
] | [
235
] | 1 | [] | [] | [] | 0 | [
"2i51"
] | 1 | [
"PUB00001735",
"PUB00002199",
"PUB00002264",
"PUB00055044",
"PUB00155385"
] | [
"8586283",
"1356963",
"7896706",
"20675471",
"23897464"
] | [
"Molecular analysis of genes encoding phenazine biosynthesis in the biological control bacterium. Pseudomonas aureofaciens 30-84.",
"Characterization of the complex pdxH-tyrS operon of Escherichia coli K-12 and pleiotropic phenotypes caused by pdxH insertion mutations.",
"Sterol uptake induced by an impairment ... | [
1995,
1992,
1995,
2010,
2013
] | 5 | [
"IPR000659"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Chlorophyta"
] | [
226,
9
] | 2 | [] | [] | 0 | true | Family | Pyridoxamine 5'-phosphate oxidase, probable FMN-dependent, Alr4036-like | Pyridoxamine 5'-phosphate oxidase, probable FMN-dependent, Alr4036-like | Pyridox_Oxase_FMN-dep_Alr4036 | 8 |
IPR024016 | 24,016 | Conserved hypothetical protein CHP04064, radical SAM | CHP04064_rSAM | Family | 17 | false | false | Members of this family are radical SAM enzymes that occur co-clustered with Nif11-related bacteriocin precursors, as described by TIGRFAMs model . They could be involved a Nif11-class bacteriocin maturation. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04064"
] | [
"rSAM_nif11"
] | [
17
] | 1 | [
"GP"
] | [
"GenProp0861"
] | [
"GP:GenProp0861"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [
"IPR023867"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"bioreactor metagenome"
] | [
16,
1
] | 2 | [] | [] | 0 | true | Family | Conserved hypothetical protein CHP04064, radical SAM | Conserved hypothetical protein CHP04064, radical SAM | CHP04064_rSAM | 8 |
IPR024017 | 24,017 | Petide cyclisation enzyme, radical SAM | Pep_cycl_rSAM | Family | 31 | false | false | Members of this family are radical SAM enzymes that appear to perform a cyclisation on an adjacent peptide from family [ ]. Genomes with the complete system include Streptococcus thermophilus LMD-9 and Lactococcus lactis subsp. cremoris MG1363, among others. | [] | [] | [] | 0 | [
"SFLD",
"NCBIFAM"
] | [
"SFLDF00347",
"TIGR04080"
] | [
"KxxxW_cyclic_peptide_maturase_",
"rSAM_pep_cyc"
] | [
12,
30
] | 2 | [
"GP"
] | [
"GenProp0954"
] | [
"GP:GenProp0954"
] | 1 | [
"5v1q",
"5v1s",
"5v1t"
] | 3 | [
"PUB00055042"
] | [
"17921293"
] | [
"Control of the transcription of a short gene encoding a cyclic peptide in Streptococcus thermophilus: a new quorum-sensing system?"
] | [
2007
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
31
] | 1 | [] | [] | 0 | true | Family | Petide cyclisation enzyme, radical SAM | Petide cyclisation enzyme, radical SAM | Pep_cycl_rSAM | 6 |
IPR024018 | 24,018 | Conserved hypothetical protein CHP04083, radical SAM | CHP04083_rSAM | Family | 157 | false | false | Members of this family are radical SAM enzymes, homologous to a variety of other peptide-modifying radical SAM, and found primarily in methanogenic archaea. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04083"
] | [
"rSAM_pep_methan"
] | [
157
] | 1 | [
"GP"
] | [
"GenProp0992"
] | [
"GP:GenProp0992"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [
"IPR023867"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Methanobacteriota",
"ecological metagenomes"
] | [
4,
148,
5
] | 3 | [] | [] | 0 | true | Family | Conserved hypothetical protein CHP04083, radical SAM | Conserved hypothetical protein CHP04083, radical SAM | CHP04083_rSAM | 8 |
IPR024019 | 24,019 | Conserved hypothetical protein CHP04096 | CHP04096 | Family | 750 | false | false | Members of this protein family show distant local sequence similarity to a number of S-adenosyl-methionine-dependent methyltransferases. The family is identified by Partial Phylogenetic Profiling as closely tied to the DNA phosphorothioation system (dnd), and members are found adjacent to dnd genes in at least 13 speci... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04096"
] | [
"dnd_rel_methyl"
] | [
750
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"ecological metagenomes"
] | [
735,
15
] | 2 | [] | [] | 0 | true | Family | Conserved hypothetical protein CHP04096 | Conserved hypothetical protein CHP04096 | CHP04096 | 5 |
IPR024020 | 24,020 | Anti sigma-R factor, mycothiol system,RsrA | Anit_sigma_mycothiol_RsrA | Family | 3,529 | false | false | Members of this family are the anti-sigma-R factor RsrA, which contains a CXXC motif as a thiol-disulphide redox switch. It interacts with sigma-R. It regulates and is regulated by the mycothiol system, which occurs in many actinomycetes [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03988"
] | [
"antisig_RsrA"
] | [
3529
] | 1 | [
"GP"
] | [
"GenProp0923"
] | [
"GP:GenProp0923"
] | 1 | [
"5frf",
"5frh"
] | 2 | [
"PUB00055066"
] | [
"18430082"
] | [
"Mycothiol regulates and is regulated by a thiol-specific antisigma factor RsrA and sigma(R) in Streptomyces coelicolor."
] | [
2008
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"metagenomes"
] | [
3497,
32
] | 2 | [] | [] | 0 | true | Family | Anti sigma-R factor, mycothiol system,RsrA | Anti sigma-R factor, mycothiol system,RsrA | Anit_sigma_mycothiol_RsrA | 4 |
IPR024021 | 24,021 | [FeFe]-hydrogenase maturation HydE, radical SAM | FeFe-hyd_HydE_rSAM | Family | 2,253 | false | false | This entry describes the radical SAM protein HydE, one of a pair of radical SAM proteins, along with GTP-binding protein HydF, for maturation of [FeFe]-hydrogenase in Chlamydomonas reinhardtii and numerous bacteria [ , ]. | [] | [] | [] | 0 | [
"SFLD",
"NCBIFAM"
] | [
"SFLDF00348",
"TIGR03956"
] | [
"FeFe_hydrogenase_maturase_(Hyd",
"rSAM_HydE"
] | [
1764,
2249
] | 2 | [
"GP"
] | [
"GenProp0914"
] | [
"GP:GenProp0914"
] | 1 | [
"3ciw",
"3cix",
"3iix",
"3iiz",
"4jxc",
"4jy8",
"4jy9",
"4jyd",
"4jye",
"4jyf",
"5fep",
"5fes",
"5few",
"5fex",
"5fez",
"5ff0",
"5ff2",
"5ff3",
"5ff4",
"7o1o",
"7o1p",
"7o1s",
"7o1t",
"7o25",
"7o26",
"8qmk",
"8qml",
"8qmm",
"8qmn"
] | 29 | [
"PUB00055029",
"PUB00055110"
] | [
"15082711",
"16513746"
] | [
"Discovery of two novel radical S-adenosylmethionine proteins required for the assembly of an active [Fe] hydrogenase.",
"Functional studies of [FeFe] hydrogenase maturation in an Escherichia coli biosynthetic system."
] | [
2004,
2006
] | 2 | [
"IPR034422"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Eukaryota",
"metagenomes"
] | [
2203,
28,
22
] | 3 | [] | [] | 0 | true | Family | [FeFe]-hydrogenase maturation HydE, radical SAM | [FeFe]-hydrogenase maturation HydE, radical SAM | FeFe-hyd_HydE_rSAM | 5 |
IPR024022 | 24,022 | Transcription regulator HTH, surface antigen | Tscrpt_reg_HTH_surface_antigen | Family | 162 | false | false | This protein is found adjacent to various classes of repetitive or low-complexity YSIRK proteins (whether unique in genome or not), in a range of species (Enterococcus faecalis X98, Ruminococcus torques, Coprobacillus sp. D7, Lysinibacillus fusiformis ZC1, Streptococcus equi subsp. equi 4047, etc). The affliated YSIRK ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04094"
] | [
"adjacent_YSIRK"
] | [
162
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00055067"
] | [
"19865839"
] | [
"Streptococcal protective antigens (Spa): a new family of type-specific proteins of group A streptococci."
] | [
2010
] | 1 | [] | [] | 0 | 0 | null | [
"Bacillati"
] | [
162
] | 1 | [] | [] | 0 | true | Family | Transcription regulator HTH, surface antigen | Transcription regulator HTH, surface antigen | Tscrpt_reg_HTH_surface_antigen | 7 |
IPR024023 | 24,023 | His-Xaa-Ser system radical SAM maturase HxsB | rSAM_paired_HxsB | Family | 689 | false | false | This entry describes HxsB, one of a pair of uncharacterised radical SAM proteins, regularly found in the context of a small protein with four or more repeats of the tripeptide His-Xaa-Ser (HXS). This enzyme may be be part of a peptide modification system. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03978"
] | [
"rSAM_paired_1"
] | [
689
] | 1 | [
"GP"
] | [
"GenProp0921"
] | [
"GP:GenProp0921"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [
"IPR023867"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Nanobdellati",
"metagenomes"
] | [
683,
2,
4
] | 3 | [] | [] | 0 | true | Family | His-Xaa-Ser system radical SAM maturase HxsB | His-Xaa-Ser system radical SAM maturase HxsB | rSAM_paired_HxsB | 5 |
IPR024024 | 24,024 | D-alanyl transfer protein DltB | DltB | Family | 2,201 | false | false | Members of this protein family are DltB, part of a four-gene operon for D-alanyl-lipoteichoic acid biosynthesis that is present in the vast majority of low-GC Gram-positive organisms [ ]. It is an O-acyltransferase that catalyzes D-alanylation of both teichoic acid and lipoteichoic acid (LTA) [ ]. D-alanylation of LTA ... | [
"GO:0016746",
"GO:0070395"
] | [
"acyltransferase activity",
"lipoteichoic acid biosynthetic process"
] | [
"molecular_function",
"biological_process"
] | 2 | [
"PIRSF",
"NCBIFAM"
] | [
"PIRSF500216",
"TIGR04091"
] | [
"DltB",
"LTA_dltB"
] | [
2068,
2185
] | 2 | [
"EC",
"GP",
"GP",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METAC... | [
"2.3.1.-",
"GenProp0958",
"GenProp1398",
"PWY-3602",
"PWY-361",
"PWY-4801",
"PWY-4922",
"PWY-5048",
"PWY-5139",
"PWY-5268",
"PWY-5284",
"PWY-5292",
"PWY-5307",
"PWY-5313",
"PWY-5317",
"PWY-5318",
"PWY-5353",
"PWY-5400",
"PWY-5473",
"PWY-5475",
"PWY-5477",
"PWY-5660",
"PWY... | [
"EC:2.3.1.-",
"GP:GenProp0958",
"GP:GenProp1398",
"METACYC:PWY-3602",
"METACYC:PWY-361",
"METACYC:PWY-4801",
"METACYC:PWY-4922",
"METACYC:PWY-5048",
"METACYC:PWY-5139",
"METACYC:PWY-5268",
"METACYC:PWY-5284",
"METACYC:PWY-5292",
"METACYC:PWY-5307",
"METACYC:PWY-5313",
"METACYC:PWY-5317",... | 221 | [
"6bug",
"6buh",
"6bui",
"8jem",
"8jes",
"8jf2"
] | 6 | [
"PUB00013853",
"PUB00068169",
"PUB00095085"
] | [
"7797557",
"9158726",
"30283133"
] | [
"Incorporation of D-alanine into lipoteichoic acid and wall teichoic acid in Bacillus subtilis. Identification of genes and regulation.",
"The dlt operon in the biosynthesis of D-alanyl-lipoteichoic acid in Lactobacillus casei.",
"Crystal structure of a membrane-bound O-acyltransferase."
] | [
1995,
1996,
2018
] | 3 | [
"IPR024194"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"metagenomes"
] | [
2198,
3
] | 2 | [] | [] | 0 | true | Family | D-alanyl transfer protein DltB | D-alanyl transfer protein DltB | DltB | 9 |
IPR024025 | 24,025 | SCIFF radical SAM maturase | SCIFF_rSAM_maturase | Family | 1,701 | false | false | Members of this protein family are predicted SPASM domain-containing radical SAM enzymes universally associated with Six Cysteines in Forty-Five protein, or SCIFF ( ), a predicted ribosomal natural product precursor that is nearly universal in the class Clostridia. Similarity of this family to radical SAM maturases (e.... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03974"
] | [
"rSAM_six_Cys"
] | [
1701
] | 1 | [
"GP"
] | [
"GenProp0919"
] | [
"GP:GenProp0919"
] | 1 | [
"5wgg",
"5why"
] | 2 | [
"PUB00055953",
"PUB00106906"
] | [
"21478363",
"28704043"
] | [
"Biological systems discovery in silico: radical S-adenosylmethionine protein families and their target peptides for posttranslational modification.",
"Structural Insights into Thioether Bond Formation in the Biosynthesis of Sactipeptides."
] | [
2011,
2017
] | 2 | [
"IPR023867"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"unclassified sequences"
] | [
1685,
16
] | 2 | [] | [] | 0 | true | Family | SCIFF radical SAM maturase | SCIFF radical SAM maturase | SCIFF_rSAM_maturase | 5 |
IPR024026 | 24,026 | 3'-RNA ribose 2'-O-methyltransferase, Hen1, bacterial | 3'-RNA_MeTfrase_Hen1_bac | Family | 2,300 | false | false | This entry represents bacterial Hen1, which is a 3' terminal RNA ribose 2'-O-methyltransferase that is involved in bacterial RNA repair [ ]. Hen1 forms a heterotetramer with Pnkp. The heterotetramer has been shown to repair transfer RNAs cleaved by ribotoxins in vitro [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04074"
] | [
"bacter_Hen1"
] | [
2300
] | 1 | [
"GP"
] | [
"GenProp0948"
] | [
"GP:GenProp0948"
] | 1 | [
"4dqz",
"4drf",
"4e6n"
] | 3 | [
"PUB00055068",
"PUB00056235"
] | [
"20007328",
"19815768"
] | [
"Bacterial Hen1 is a 3' terminal RNA ribose 2'-O-methyltransferase component of a bacterial RNA repair cassette.",
"Reconstituting bacterial RNA repair and modification in vitro."
] | [
2010,
2009
] | 2 | [
"IPR026610"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Geodia barretti",
"freshwater metagenome"
] | [
2296,
3,
1
] | 3 | [] | [] | 0 | true | Family | 3'-RNA ribose 2'-O-methyltransferase, Hen1, bacterial | 3'-RNA ribose 2'-O-methyltransferase, Hen1, bacterial | 3'-RNA_MeTfrase_Hen1_bac | 4 |
IPR024027 | 24,027 | Colanic acid biosynthesis, acetyltransferase, WcaB | Colanic_acid_synth_WcaB | Family | 687 | false | false | This protein family is one of the acetyl transferases involved in the biosynthesis of colanic acid, an exopolysaccharide expressed in Enterobacteraceae species [ ]. | [
"GO:0016747"
] | [
"acyltransferase activity, transferring groups other than amino-acyl groups"
] | [
"molecular_function"
] | 1 | [
"NCBIFAM"
] | [
"TIGR04016"
] | [
"WcaB"
] | [
687
] | 1 | [
"EC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC"... | [
"2.3.1.-",
"PWY-3602",
"PWY-361",
"PWY-4801",
"PWY-4922",
"PWY-5048",
"PWY-5139",
"PWY-5268",
"PWY-5284",
"PWY-5292",
"PWY-5307",
"PWY-5313",
"PWY-5317",
"PWY-5318",
"PWY-5353",
"PWY-5400",
"PWY-5473",
"PWY-5475",
"PWY-5477",
"PWY-5660",
"PWY-5679",
"PWY-5710",
"PWY-5794"... | [
"EC:2.3.1.-",
"METACYC:PWY-3602",
"METACYC:PWY-361",
"METACYC:PWY-4801",
"METACYC:PWY-4922",
"METACYC:PWY-5048",
"METACYC:PWY-5139",
"METACYC:PWY-5268",
"METACYC:PWY-5284",
"METACYC:PWY-5292",
"METACYC:PWY-5307",
"METACYC:PWY-5313",
"METACYC:PWY-5317",
"METACYC:PWY-5318",
"METACYC:PWY-53... | 219 | [] | 0 | [
"PUB00008202"
] | [
"8759852"
] | [
"Organization of the Escherichia coli K-12 gene cluster responsible for production of the extracellular polysaccharide colanic acid."
] | [
1996
] | 1 | [
"IPR005881"
] | [] | 1 | 0 | 1 | [
"Gammaproteobacteria",
"Oryza sativa subsp. indica"
] | [
686,
1
] | 2 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Family | Colanic acid biosynthesis, acetyltransferase, WcaB | Colanic acid biosynthesis, acetyltransferase, WcaB | Colanic_acid_synth_WcaB | 7 |
IPR024028 | 24,028 | Polynucleotide kinase-phosphatase, bacterial | PNKP_bac | Family | 2,358 | false | false | Members of this family are the bacterial polynucleotide kinase-phosphatase (Pnkp) enzymes that prepare broken RNA termini for sealing by RNA ligase [ ]. Their genes co-occur with genes for the 3' terminal RNA ribose 2'-O-methyltransferase Hen1, and the pair are thought to form a bacterial RNA repair cassette, where a c... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04075"
] | [
"bacter_Pnkp"
] | [
2358
] | 1 | [
"GP"
] | [
"GenProp0948"
] | [
"GP:GenProp0948"
] | 1 | [] | 0 | [
"PUB00055068",
"PUB00055069"
] | [
"20007328",
"17986465"
] | [
"Bacterial Hen1 is a 3' terminal RNA ribose 2'-O-methyltransferase component of a bacterial RNA repair cassette.",
"Characterization of the 2',3' cyclic phosphodiesterase activities of Clostridium thermocellum polynucleotide kinase-phosphatase and bacteriophage lambda phosphatase."
] | [
2010,
2007
] | 2 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Geodia barretti",
"freshwater metagenome"
] | [
2352,
5,
1
] | 3 | [] | [] | 0 | true | Family | Polynucleotide kinase-phosphatase, bacterial | Polynucleotide kinase-phosphatase, bacterial | PNKP_bac | 6 |
IPR024029 | 24,029 | Pyridoxamine 5-phosphate oxidase, FMN-dependent | Pyridox_Oxase_FMN-dep | Family | 6,283 | false | false | Pyridoxamine 5'-phosphate oxidase ( ) is an enzyme that is involved in the de novo synthesis of pyridoxine (vitamin B6) and pyridoxal phosphate. It oxidizes pyridoxamine-5-P (PMP) and pyridoxine-5-P (PNP) to pyridoxal-5-P. The enzyme requires the presence of flavin mononucleotide (FMN) as a cofactor, although there is ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04025"
] | [
"PPOX_FMN_DR2398"
] | [
6283
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00055044"
] | [
"20675471"
] | [
"Unexpected abundance of coenzyme F(420)-dependent enzymes in Mycobacterium tuberculosis and other actinobacteria."
] | [
2010
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"metagenomes"
] | [
6237,
6,
40
] | 3 | [] | [] | 0 | true | Family | Pyridoxamine 5-phosphate oxidase, FMN-dependent | Pyridoxamine 5-phosphate oxidase, FMN-dependent | Pyridox_Oxase_FMN-dep | 6 |
IPR024030 | 24,030 | AIR synthase-related protein, sll0787 family | AIR_synthase-rel_sll0787 | Family | 884 | false | false | This entry represents a family of uncharacterised proteins, including sll0787 from Synechocystis sp. PCC 6803. They resemble the C-terminal region of MSMEG_0567 from Mycobacterium smegmatis, where the N-terminal is a GNAT family N-acetyltransferase. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04049"
] | [
"AIR_rel_sll0787"
] | [
884
] | 1 | [
"GP"
] | [
"GenProp0939"
] | [
"GP:GenProp0939"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [
"IPR011413"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Ricinus communis",
"ecological metagenomes"
] | [
880,
1,
3
] | 3 | [] | [] | 0 | true | Family | AIR synthase-related protein, sll0787 family | AIR synthase-related protein, sll0787 family | AIR_synthase-rel_sll0787 | 5 |
IPR024031 | 24,031 | PPOX class F420-dependent enzyme, MSMEG_5819/OxyR family | MSMEG_5819/OxyR | Family | 1,555 | false | false | F420 (or 8-hydroxy-5-deazaflavin) is a coenzyme involved in redox reactions in methanogens. A Genome Properties metabolic reconstruction for F420 biosynthesis shows that slightly over 10 percent of all prokaryotes with fully sequenced genomes, including about two thirds of the Actinomycetales, make F420. This subfamily... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04023"
] | [
"PPOX_MSMEG_5819"
] | [
1555
] | 1 | [
"GP"
] | [
"GenProp0002"
] | [
"GP:GenProp0002"
] | 1 | [] | 0 | [
"PUB00055044",
"PUB00067298"
] | [
"20675471",
"23621493"
] | [
"Unexpected abundance of coenzyme F(420)-dependent enzymes in Mycobacterium tuberculosis and other actinobacteria.",
"Uncovering the Enzymes that Catalyze the Final Steps in Oxytetracycline Biosynthesis."
] | [
2010,
2013
] | 2 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacillati",
"freshwater metagenome"
] | [
6,
1524,
25
] | 3 | [] | [] | 0 | true | Family | PPOX class F420-dependent enzyme, MSMEG_5819/OxyR family | PPOX class F420-dependent enzyme, MSMEG_5819/OxyR family | MSMEG_5819/OxyR | 6 |
IPR024032 | 24,032 | His-Xaa-Ser system radical SAM maturase HxsC | rSAM_paired_HxsC | Family | 671 | false | false | This entry describes HxsC, one of a pair of uncharacterised radical SAM proteins, regularly found in the context of a small protein with four or more repeats of the tripeptide His-Xaa-Ser (HXS). This enzyme may be be part of a peptide modification system. | [] | [] | [] | 0 | [
"SFLD",
"NCBIFAM"
] | [
"SFLDG01103",
"TIGR03977"
] | [
"Uncharacterised_Radical_SAM_Su",
"rSAM_pair_HxsC"
] | [
660,
663
] | 2 | [
"GP"
] | [
"GenProp0921"
] | [
"GP:GenProp0921"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Fermentimicrarchaeum limneticum",
"metagenomes"
] | [
666,
1,
4
] | 3 | [] | [] | 0 | true | Family | His-Xaa-Ser system radical SAM maturase HxsC | His-Xaa-Ser system radical SAM maturase HxsC | rSAM_paired_HxsC | 4 |
IPR024033 | 24,033 | Oxamate carbamoyltransferase subunit AllG, helical domain | OXTCase_su_AllG_h-dom | Homologous_superfamily | 3,062 | false | false | This superfamily represents a domain found in the N-terminal region of a conserved protein (YlbE) of unknown function from Escherichia coli K12. It consists of a mainly α orthogonal bundle . This domain is associated with and immediately N-terminal to another domain of unknown function defined by (DUF1116). Tis domain ... | [] | [] | [] | 0 | [
"CATHGENE3D"
] | [
"G3DSA:1.10.10.660"
] | [
""
] | [
3062
] | 1 | [] | [] | [] | 0 | [
"3clq"
] | 1 | [
"PUB00155434"
] | [
"38888336"
] | [
"Oxamic transcarbamylase of <i>Escherichia coli</i> is encoded by the three genes <i>allFGH</i> (formerly <i>fdrA, ylbE</i>, and <i>ylbF</i>)."
] | [
2024
] | 1 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"metagenomes"
] | [
21,
2965,
5,
71
] | 4 | [
"Escherichia coli (strain K12)"
] | [
2
] | 1 | true | Homologous_superfamily | Oxamate carbamoyltransferase subunit AllG, helical domain | Oxamate carbamoyltransferase subunit AllG, helical domain | OXTCase_su_AllG_h-dom | 6 |
IPR024034 | 24,034 | ATPase, F1/V1 complex, beta/alpha subunit, C-terminal | ATPase_F1/V1_b/a_C | Homologous_superfamily | 66,049 | false | false | This entry represents a domain that is found at the C terminus of the F1 ATP synthase beta subunit and in the C terminus of the V-ATPase alpha and beta subunits. Transmembrane ATPases are membrane-bound enzyme complexes/ion transporters that use ATP hydrolysis to drive the transport of protons across a membrane. Some t... | [] | [] | [] | 0 | [
"CATHGENE3D"
] | [
"G3DSA:1.10.1140.10"
] | [
""
] | [
66049
] | 1 | [
"EC",
"METACYC",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"... | [
"7.1.2.2",
"PWY-7980",
"R-BTA-1222556",
"R-BTA-77387",
"R-BTA-917977",
"R-BTA-9639288",
"R-BTA-983712",
"R-CEL-1222556",
"R-CEL-1268020",
"R-CEL-163210",
"R-CEL-77387",
"R-CEL-8949613",
"R-CEL-917977",
"R-CEL-9639288",
"R-CEL-983712",
"R-CEL-9837999",
"R-CFA-1268020",
"R-CFA-163210... | [
"EC:7.1.2.2",
"METACYC:PWY-7980",
"REACTOME:R-BTA-1222556",
"REACTOME:R-BTA-77387",
"REACTOME:R-BTA-917977",
"REACTOME:R-BTA-9639288",
"REACTOME:R-BTA-983712",
"REACTOME:R-CEL-1222556",
"REACTOME:R-CEL-1268020",
"REACTOME:R-CEL-163210",
"REACTOME:R-CEL-77387",
"REACTOME:R-CEL-8949613",
"REAC... | 72 | [
"1bmf",
"1cow",
"1e1q",
"1e1r",
"1e79",
"1efr",
"1fx0",
"1h8e",
"1h8h",
"1kmh",
"1mab",
"1nbm",
"1ohh",
"1qo1",
"1sky",
"1vdz",
"1w0j",
"1w0k",
"2ck3",
"2f43",
"2hld",
"2jdi",
"2jiz",
"2jj1",
"2jj2",
"2qe7",
"2v7q",
"2w6e",
"2w6f",
"2w6g",
"2w6h",
"2w6i"... | 488 | [
"PUB00020603",
"PUB00020604",
"PUB00068786",
"PUB00068787",
"PUB00068788",
"PUB00068789"
] | [
"15473999",
"15078220",
"20450191",
"18937357",
"1385979",
"9741106"
] | [
"The evolution of A-, F-, and V-type ATP synthases and ATPases: reversals in function and changes in the H+/ATP coupling ratio.",
"Mechanisms of ATPases--a multi-disciplinary approach.",
"Regulation and isoform function of the V-ATPases.",
"New insights into structure-function relationships between archeal AT... | [
2004,
2004,
2010,
2008,
1992,
1998
] | 6 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"unclassified sequences"
] | [
977,
28860,
35506,
706
] | 4 | [
"Arabidopsis thaliana",
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Escherichia coli (strain K12)",
"Homo sapiens",
"Mus musculus",
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)",
"Oryza sativa subsp. japonica",
"Rattus norvegicus",... | [
23,
2,
3,
14,
1,
7,
2,
2,
24,
9,
2,
2,
39
] | 13 | true | Homologous_superfamily | ATPase, F1/V1 complex, beta/alpha subunit, C-terminal | ATPase, F1/V1 complex, beta/alpha subunit, C-terminal | ATPase_F1/V1_b/a_C | 3 |
IPR024035 | 24,035 | MSMEG_0567 GNAT N-acetyltransferase | MSMEG_0567_GNAT | Domain | 1,389 | false | false | This entry includes proteins that belong to the GNAT family ( ), in which numerous characterised examples, though not all, are shown to be N-acetyltransferases or to interact with acetyl-CoA. In some instances, this is the N-terminal GNAT domain while in other members represents the full length, such as in sll0787 from... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR04045"
] | [
"MSMEG_0567_GNAT"
] | [
1389
] | 1 | [
"GP"
] | [
"GenProp0939"
] | [
"GP:GenProp0939"
] | 1 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"ecological metagenomes"
] | [
1378,
11
] | 2 | [] | [] | 0 | true | Domain | MSMEG_0567 GNAT N-acetyltransferase | MSMEG_0567 GNAT N-acetyltransferase | MSMEG_0567_GNAT | 5 |
IPR024036 | 24,036 | tRNA-dihydrouridine synthase, putative, C-terminal | tRNA-dHydroUridine_Synthase_C | Homologous_superfamily | 25,403 | false | false | This entry represents a C-terminal four-helix bundle domain found in tRNA-dihydrouridine synthases [ ]. | [
"GO:0016491"
] | [
"oxidoreductase activity"
] | [
"molecular_function"
] | 1 | [
"CATHGENE3D"
] | [
"G3DSA:1.10.1200.80"
] | [
""
] | [
25403
] | 1 | [
"EC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC"... | [
"1.3.1.-",
"PWY-2541",
"PWY-5292",
"PWY-5301",
"PWY-5367",
"PWY-5393",
"PWY-5729",
"PWY-5818",
"PWY-5956",
"PWY-5972",
"PWY-5984",
"PWY-6088",
"PWY-6302",
"PWY-6309",
"PWY-6332",
"PWY-6786",
"PWY-6824",
"PWY-6944",
"PWY-6996",
"PWY-7096",
"PWY-7154",
"PWY-7155",
"PWY-7300... | [
"EC:1.3.1.-",
"METACYC:PWY-2541",
"METACYC:PWY-5292",
"METACYC:PWY-5301",
"METACYC:PWY-5367",
"METACYC:PWY-5393",
"METACYC:PWY-5729",
"METACYC:PWY-5818",
"METACYC:PWY-5956",
"METACYC:PWY-5972",
"METACYC:PWY-5984",
"METACYC:PWY-6088",
"METACYC:PWY-6302",
"METACYC:PWY-6309",
"METACYC:PWY-6... | 35 | [
"1vhn",
"6ei9"
] | 2 | [
"PUB00032087"
] | [
"15103641"
] | [
"The 1.59 A resolution crystal structure of TM0096, a flavin mononucleotide binding protein from Thermotoga maritima."
] | [
2004
] | 1 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"unclassified sequences"
] | [
51,
24776,
110,
466
] | 4 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Homologous_superfamily | tRNA-dihydrouridine synthase, putative, C-terminal | tRNA-dihydrouridine synthase, putative, C-terminal | tRNA-dHydroUridine_Synthase_C | 9 |
IPR024037 | 24,037 | Alternate ATP synthase, F1 complex, subunit epsilon | Alt_ATP_synth_F1_esu | Family | 845 | false | false | Transmembrane ATPases are membrane-bound enzyme complexes/ion transporters that use ATP hydrolysis to drive the transport of protons across a membrane. Some transmembrane ATPases also work in reverse, harnessing the energy from a proton gradient, using the flux of ions across the membrane via the ATPase proton channel ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03166"
] | [
"alt_F1F0_F1_eps"
] | [
845
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00015307",
"PUB00020603",
"PUB00020604",
"PUB00068786",
"PUB00068787",
"PUB00068788",
"PUB00068789"
] | [
"9425287",
"15473999",
"15078220",
"20450191",
"18937357",
"1385979",
"9741106"
] | [
"F0F1-ATPase genes from an archaebacterium, Methanosarcina barkeri.",
"The evolution of A-, F-, and V-type ATP synthases and ATPases: reversals in function and changes in the H+/ATP coupling ratio.",
"Mechanisms of ATPases--a multi-disciplinary approach.",
"Regulation and isoform function of the V-ATPases.",
... | [
1997,
2004,
2004,
2010,
2008,
1992,
1998
] | 7 | [
"IPR001469"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Methanomicrobia",
"ecological metagenomes"
] | [
795,
26,
24
] | 3 | [] | [] | 0 | true | Family | Alternate ATP synthase, F1 complex, subunit epsilon | Alternate ATP synthase, F1 complex, subunit epsilon | Alt_ATP_synth_F1_esu | 1 |
IPR024038 | 24,038 | MYXO-CTERM protein-sorting domain | MYXO-CTERM | Domain | 1,469 | false | false | This entry describes MYXO-CTERM, a C-terminal putative protein sorting domain, analogous to LPXTG ( ) and PEP-CTERM ( ). It is largely restricted to the Myxococcota, a division of the Deltaproteobacteria [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR03901"
] | [
"MYXO-CTERM"
] | [
1469
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00103726"
] | [
"31975447"
] | [
"MYXO-CTERM sorting tag directs proteins to the cell surface via the type II secretion system."
] | [
2020
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"Halobacteriales",
"ecological metagenomes"
] | [
1455,
6,
2,
6
] | 4 | [] | [] | 0 | true | Domain | MYXO-CTERM protein-sorting domain | MYXO-CTERM protein-sorting domain | MYXO-CTERM | 9 |
IPR024041 | 24,041 | Ammonium transporter AmtB-like domain | NH4_transpt_AmtB-like_dom | Domain | 57,338 | false | false | This ammonium transporter domain consists of a duplication of 2 structural repeats of five helices each plus one extra C-terminal helix. It has been described as a channel that spans the membrane 11 times [ ]. | [
"GO:0008519",
"GO:0072488",
"GO:0016020"
] | [
"ammonium channel activity",
"ammonium transmembrane transport",
"membrane"
] | [
"molecular_function",
"biological_process",
"cellular_component"
] | 3 | [
"PFAM"
] | [
"PF00909"
] | [
"Ammonium_transp"
] | [
57338
] | 1 | [
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME"
] | [
"R-BTA-444411",
"R-CFA-444411",
"R-DDI-1237044",
"R-DDI-1247673",
"R-DDI-444411",
"R-DRE-444411",
"R-HSA-1237044",
"R-HSA-1247673",
"R-HSA-444411",
"R-HSA-5619042",
"R-HSA-9037628",
"R-MMU-1237044",
"R-MMU-1247673",
"R-MMU-444411",
"R-RNO-1237044",
"R-RNO-1247673",
"R-RNO-444411",
... | [
"REACTOME:R-BTA-444411",
"REACTOME:R-CFA-444411",
"REACTOME:R-DDI-1237044",
"REACTOME:R-DDI-1247673",
"REACTOME:R-DDI-444411",
"REACTOME:R-DRE-444411",
"REACTOME:R-HSA-1237044",
"REACTOME:R-HSA-1247673",
"REACTOME:R-HSA-444411",
"REACTOME:R-HSA-5619042",
"REACTOME:R-HSA-9037628",
"REACTOME:R-M... | 19 | [
"1u77",
"1u7c",
"1u7g",
"1xqe",
"1xqf",
"2b2f",
"2b2h",
"2b2i",
"2b2j",
"2nmr",
"2nop",
"2now",
"2npc",
"2npd",
"2npe",
"2npg",
"2npj",
"2npk",
"2ns1",
"2nuu",
"3b9w",
"3b9y",
"3b9z",
"3bhs",
"3c1g",
"3c1h",
"3c1i",
"3c1j",
"3hd6",
"4nh2",
"5aex",
"5aez"... | 52 | [
"PUB00031687"
] | [
"15361618"
] | [
"Mechanism of ammonia transport by Amt/MEP/Rh: structure of AmtB at 1.35 A."
] | [
2004
] | 1 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"Megaviridae environmental sample",
"unclassified sequences"
] | [
1026,
31093,
24361,
1,
857
] | 5 | [
"Arabidopsis thaliana",
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Escherichia coli (strain K12)",
"Homo sapiens",
"Mus musculus",
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)",
"Oryza sativa subsp. japonica",
"Rattus norvegicus",... | [
22,
8,
25,
4,
1,
568,
13,
4,
23,
12,
3,
3,
22
] | 13 | true | Domain | Ammonium transporter AmtB-like domain | Ammonium transporter AmtB-like domain | NH4_transpt_AmtB-like_dom | 3 |
IPR024042 | 24,042 | TM1646-like domain superfamily | TM1646-like_dom_sf | Homologous_superfamily | 2,424 | false | false | This superfamily represents a domain consisting of a four helix bundle found in uncharacterised proteins. | [] | [] | [] | 0 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:1.20.120.490",
"SSF158397"
] | [
"",
""
] | [
2406,
2421
] | 2 | [] | [] | [] | 0 | [
"2p61",
"2qup",
"5un5",
"5un6",
"6y06"
] | 5 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"Ignicoccus islandicus DSM 13165",
"ecological metagenomes"
] | [
2397,
11,
1,
15
] | 4 | [] | [] | 0 | true | Homologous_superfamily | TM1646-like domain superfamily | TM1646-like domain superfamily | TM1646-like_dom_sf | 2 |
IPR024044 | 24,044 | NifT/FixU barrel-like domain superfamily | NifT/FixU_barrel-like_dom_sf | Homologous_superfamily | 1,181 | false | false | This superfamily represents a barrel-like domain found in bacterial proteins NifT/FixU/MosB. The function of NifT is unknown although it is thought that the protein may be involved in biosynthesis of the FeMo cofactor of nitrogenase, although perturbation of nifT expression in Klebsiella pneumoniae has only a limited e... | [] | [] | [] | 0 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:2.40.50.240",
"SSF159203"
] | [
"",
""
] | [
1181,
1181
] | 2 | [] | [] | [] | 0 | [
"2jn4"
] | 1 | [
"PUB00006373"
] | [
"9139910"
] | [
"Identification and characterization of the nifV-nifZ-nifT gene region from the filamentous cyanobacterium Anabaena sp. strain PCC 7120."
] | [
1997
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"metagenomes"
] | [
1166,
15
] | 2 | [] | [] | 0 | true | Homologous_superfamily | NifT/FixU barrel-like domain superfamily | NifT/FixU barrel-like domain superfamily | NifT/FixU_barrel-like_dom_sf | 4 |
IPR024046 | 24,046 | Flagellar assembly factor FliW domain superfamily | Flagellar_assmbl_FliW_dom_sf | Homologous_superfamily | 4,295 | false | false | This superfamily represents the structural domain of flagellar assembly factor FliW. It consists mainly of a β roll. | [] | [] | [] | 0 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:2.30.290.10",
"SSF141457"
] | [
"",
""
] | [
4293,
4295
] | 2 | [] | [] | [] | 0 | [
"2aj7",
"5dmb",
"5dmd",
"5jak"
] | 4 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Symbiodiniaceae",
"metagenomes"
] | [
4213,
2,
80
] | 3 | [] | [] | 0 | true | Homologous_superfamily | Flagellar assembly factor FliW domain superfamily | Flagellar assembly factor FliW domain superfamily | Flagellar_assmbl_FliW_dom_sf | 6 |
IPR024047 | 24,047 | MM3350-like superfamily | MM3350-like_sf | Homologous_superfamily | 9,129 | false | false | This domain superfamily is found in several uncharacterised proteins of unknown function. It consists of five α helices and a β roll. | [] | [] | [] | 0 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:3.10.290.30",
"SSF159941"
] | [
"",
""
] | [
8840,
9101
] | 2 | [] | [] | [] | 0 | [
"2i1s"
] | 1 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Cyanophage S-TIM5",
"Eukaryota",
"metagenomes"
] | [
251,
7862,
1,
870,
145
] | 5 | [] | [] | 0 | true | Homologous_superfamily | MM3350-like superfamily | MM3350-like superfamily | MM3350-like_sf | 9 |
IPR024049 | 24,049 | eRF1, domain 1 | eRF1_1_sf | Homologous_superfamily | 7,136 | false | false | The release factor eRF1 terminates protein biosynthesis by recognising stop codons at the A site of the ribosome and stimulating peptidyl-tRNA bond hydrolysis at the peptidyl transferase centre. The crystal structure of human eRF1 is known [ ]. The overall shape and dimensions of eRF1 resemble a tRNA molecule with doma... | [] | [] | [] | 0 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:3.30.960.10",
"SSF55481"
] | [
"",
""
] | [
7078,
7132
] | 2 | [
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOM... | [
"R-BTA-72764",
"R-BTA-9629569",
"R-BTA-975956",
"R-BTA-975957",
"R-CEL-72764",
"R-CEL-9629569",
"R-CEL-975956",
"R-CEL-975957",
"R-DDI-72764",
"R-DDI-975956",
"R-DDI-975957",
"R-DME-72764",
"R-DME-9629569",
"R-DME-975956",
"R-DME-975957",
"R-HSA-72764",
"R-HSA-9010553",
"R-HSA-9629... | [
"REACTOME:R-BTA-72764",
"REACTOME:R-BTA-9629569",
"REACTOME:R-BTA-975956",
"REACTOME:R-BTA-975957",
"REACTOME:R-CEL-72764",
"REACTOME:R-CEL-9629569",
"REACTOME:R-CEL-975956",
"REACTOME:R-CEL-975957",
"REACTOME:R-DDI-72764",
"REACTOME:R-DDI-975956",
"REACTOME:R-DDI-975957",
"REACTOME:R-DME-7276... | 36 | [
"1dt9",
"2lgt",
"2llx",
"2mq6",
"2mq9",
"3agk",
"3e1y",
"3e20",
"3j5y",
"3jag",
"3jah",
"3jai",
"3vmf",
"4af1",
"4crn",
"4d5n",
"4d61",
"5a8l",
"5dmq",
"5lzt",
"5lzu",
"5lzv",
"6d90",
"6hcf",
"6hcm",
"6ip8",
"6p5n",
"6xa1",
"6zme",
"7nwh",
"7o80",
"8ip8"... | 35 | [
"PUB00007747"
] | [
"10676813"
] | [
"The crystal structure of human eukaryotic release factor eRF1--mechanism of stop codon recognition and peptidyl-tRNA hydrolysis."
] | [
2000
] | 1 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria candidate phyla",
"Eukaryota",
"Megaviricetes",
"metagenomes"
] | [
1037,
2,
6025,
21,
51
] | 5 | [
"Arabidopsis thaliana",
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)",
"Oryza sativa subsp. japonica",
"Rattus norvegicus",
"Saccharomyces cerevisiae (strai... | [
8,
1,
4,
4,
5,
6,
1,
9,
2,
1,
1,
6
] | 12 | true | Homologous_superfamily | eRF1, domain 1 | eRF1, domain 1 | eRF1_1_sf | 2 |
IPR024050 | 24,050 | AICAR transformylase, insert domain superfamily | AICAR_Tfase_insert_dom_sf | Homologous_superfamily | 5,235 | false | false | This domain is found in the enzyme 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase (AICARFT). AICARFT can be part of a bifunctional enzyme catalysing the last two steps in de novo purine biosynthesis and having also an IMP (Inosine monophosphate) cyclohydrolase (IMPCHase) functional domain. The bifuncti... | [] | [] | [] | 0 | [
"CATHGENE3D"
] | [
"G3DSA:1.10.287.440"
] | [
""
] | [
5235
] | 1 | [
"EC",
"EC",
"METACYC",
"METACYC",
"METACYC",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME"
] | [
"2.1.2.3",
"3.5.4.10",
"PWY-6123",
"PWY-6124",
"PWY-7234",
"R-BTA-73817",
"R-GGA-419140",
"R-HSA-73817",
"R-HSA-9725370",
"R-MMU-73817",
"R-RNO-73817",
"R-SCE-73817",
"R-SPO-73817"
] | [
"EC:2.1.2.3",
"EC:3.5.4.10",
"METACYC:PWY-6123",
"METACYC:PWY-6124",
"METACYC:PWY-7234",
"REACTOME:R-BTA-73817",
"REACTOME:R-GGA-419140",
"REACTOME:R-HSA-73817",
"REACTOME:R-HSA-9725370",
"REACTOME:R-MMU-73817",
"REACTOME:R-RNO-73817",
"REACTOME:R-SCE-73817",
"REACTOME:R-SPO-73817"
] | 13 | [
"1g8m",
"1m9n",
"1oz0",
"1p4r",
"1pkx",
"1pl0",
"1thz",
"2b1g",
"2b1i",
"2iu0",
"2iu3",
"5uy8",
"5uz0",
"7mgq"
] | 14 | [
"PUB00025174"
] | [
"11323713"
] | [
"Crystal structure of a bifunctional transformylase and cyclohydrolase enzyme in purine biosynthesis."
] | [
2001
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"Viruses",
"metagenomes"
] | [
1472,
3743,
2,
18
] | 4 | [
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)",
"Rattus norvegicus",
"Saccharomyces cerevisiae (strain ATCC 204508 / S288c)",
"Schizosaccharomyces pombe (strai... | [
3,
2,
2,
5,
1,
1,
3,
2,
1
] | 9 | true | Homologous_superfamily | AICAR transformylase, insert domain superfamily | AICAR transformylase, insert domain superfamily | AICAR_Tfase_insert_dom_sf | 8 |
IPR024051 | 24,051 | AICAR transformylase, duplicated domain superfamily | AICAR_Tfase_dup_dom_sf | Homologous_superfamily | 32,048 | false | false | This domain is found in the enzyme 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase (AICARFT). AICARFT can be part of a bifunctional enzyme catalysing the last two steps in de novo purine biosynthesis and having also an IMP (Inosine monophosphate) cyclohydrolase (IMPCHase) functional domain. The bifuncti... | [] | [] | [] | 0 | [
"CATHGENE3D"
] | [
"G3DSA:3.40.140.20"
] | [
""
] | [
32048
] | 1 | [
"EC",
"EC",
"METACYC",
"METACYC",
"METACYC",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME"
] | [
"2.1.2.3",
"3.5.4.10",
"PWY-6123",
"PWY-6124",
"PWY-7234",
"R-BTA-73817",
"R-DDI-73817",
"R-GGA-419140",
"R-HSA-73817",
"R-HSA-9725370",
"R-MMU-73817",
"R-RNO-73817",
"R-SCE-73817",
"R-SPO-73817"
] | [
"EC:2.1.2.3",
"EC:3.5.4.10",
"METACYC:PWY-6123",
"METACYC:PWY-6124",
"METACYC:PWY-7234",
"REACTOME:R-BTA-73817",
"REACTOME:R-DDI-73817",
"REACTOME:R-GGA-419140",
"REACTOME:R-HSA-73817",
"REACTOME:R-HSA-9725370",
"REACTOME:R-MMU-73817",
"REACTOME:R-RNO-73817",
"REACTOME:R-SCE-73817",
"REACT... | 14 | [
"1g8m",
"1m9n",
"1oz0",
"1p4r",
"1pkx",
"1pl0",
"1thz",
"1zcz",
"2b1g",
"2b1i",
"2iu0",
"2iu3",
"3zzm",
"4a1o",
"4ehi",
"5uy8",
"5uz0",
"7mgq",
"9ou7"
] | 19 | [
"PUB00025174"
] | [
"11323713"
] | [
"Crystal structure of a bifunctional transformylase and cyclohydrolase enzyme in purine biosynthesis."
] | [
2001
] | 1 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"Viruses",
"unclassified sequences"
] | [
525,
25485,
5305,
16,
717
] | 5 | [
"Arabidopsis thaliana",
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Escherichia coli (strain K12)",
"Homo sapiens",
"Mus musculus",
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)",
"Oryza sativa subsp. japonica",
"Rattus norvegicus",... | [
6,
3,
2,
2,
1,
5,
1,
1,
4,
3,
2,
1,
12
] | 13 | true | Homologous_superfamily | AICAR transformylase, duplicated domain superfamily | AICAR transformylase, duplicated domain superfamily | AICAR_Tfase_dup_dom_sf | 2 |
IPR024052 | 24,052 | Phosphopentomutase DeoB cap domain superfamily | Phosphopentomutase_DeoB_cap_sf | Homologous_superfamily | 10,251 | false | false | Phosphopentomutase is involved in the purine and pyrimidine salvage pathway of nucleotide synthesis. It catalyses a phosphotransfer on ribose and deoxyribose, converting D-ribose 1-phosphate to D-ribose 5-phosphate, and 2-deoxy-D-ribose 1-phosphate to 2-deoxy-D-ribose 5-phosphate [ ]. Phosphopentomutase is composed of ... | [
"GO:0008973"
] | [
"phosphopentomutase activity"
] | [
"molecular_function"
] | 1 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:3.30.70.1250",
"SSF143856"
] | [
"",
""
] | [
10213,
9605
] | 2 | [
"EC",
"METACYC"
] | [
"5.4.2.7",
"PWY-7180"
] | [
"EC:5.4.2.7",
"METACYC:PWY-7180"
] | 2 | [
"3m7v",
"3m8w",
"3m8y",
"3m8z",
"3ot9",
"3twz",
"3tx0",
"3un2",
"3un3",
"3un5",
"3uny",
"3uo0",
"4lr7",
"4lr8",
"4lr9",
"4lra",
"4lrb",
"4lrc",
"4lrd",
"4lre",
"4lrf",
"4n7t"
] | 22 | [
"PUB00014944",
"PUB00055258"
] | [
"9692190",
"21193409"
] | [
"Phosphopentomutase of Bacillus stearothermophilus TH6-2: the enzyme and its gene ppm.",
"Bacillus cereus Phosphopentomutase Is an Alkaline Phosphatase Family Member That Exhibits an Altered Entry Point into the Catalytic Cycle."
] | [
1998,
2011
] | 2 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"metagenomes"
] | [
10162,
12,
77
] | 3 | [
"Arabidopsis thaliana",
"Escherichia coli (strain K12)"
] | [
1,
2
] | 2 | true | Homologous_superfamily | Phosphopentomutase DeoB cap domain superfamily | Phosphopentomutase DeoB cap domain superfamily | Phosphopentomutase_DeoB_cap_sf | 4 |
IPR024053 | 24,053 | von Hippel-Lindau disease tumour suppressor, beta domain | VHL_beta_dom | Domain | 2,314 | false | false | von Hippel-Landau (pVHL) protein, the gene product of VHL, is a critical regulator of the ubiquitous oxygen-sensing pathway. It is conserved throughout evolution, as its homologues are found in organisms ranging from mammals to Drosophila and Caenorhabditis. pVHL acts as the substrate recognition component of an E3 ubi... | [] | [] | [] | 0 | [
"PFAM"
] | [
"PF01847"
] | [
"VHL"
] | [
2314
] | 1 | [
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOM... | [
"R-CEL-1234176",
"R-CEL-3232142",
"R-CEL-8951664",
"R-CEL-9706019",
"R-CEL-983168",
"R-DME-1234176",
"R-DME-8951664",
"R-DME-9706019",
"R-DME-983168",
"R-HSA-1234176",
"R-HSA-3232142",
"R-HSA-8951664",
"R-HSA-9682706",
"R-HSA-9694686",
"R-HSA-9706019",
"R-HSA-983168",
"R-MMU-1234176"... | [
"REACTOME:R-CEL-1234176",
"REACTOME:R-CEL-3232142",
"REACTOME:R-CEL-8951664",
"REACTOME:R-CEL-9706019",
"REACTOME:R-CEL-983168",
"REACTOME:R-DME-1234176",
"REACTOME:R-DME-8951664",
"REACTOME:R-DME-9706019",
"REACTOME:R-DME-983168",
"REACTOME:R-HSA-1234176",
"REACTOME:R-HSA-3232142",
"REACTOME:... | 26 | [
"1lm8",
"1lqb",
"1vcb",
"3zrc",
"3zrf",
"3ztc",
"3ztd",
"3zun",
"4ajy",
"4awj",
"4b95",
"4b9k",
"4bks",
"4bkt",
"4w9c",
"4w9d",
"4w9e",
"4w9f",
"4w9g",
"4w9h",
"4w9i",
"4w9j",
"4w9k",
"4w9l",
"4wqo",
"5lli",
"5n4w",
"5nvv",
"5nvw",
"5nvx",
"5nvy",
"5nvz"... | 138 | [
"PUB00005233",
"PUB00022097",
"PUB00027102",
"PUB00079586",
"PUB00079587",
"PUB00079588",
"PUB00079589",
"PUB00079591",
"PUB00079592",
"PUB00079593",
"PUB00079594",
"PUB00079595",
"PUB00079596",
"PUB00079597",
"PUB00079598",
"PUB00079599",
"PUB00079600",
"PUB00079601",
"PUB000796... | [
"10205047",
"12004076",
"12050673",
"17998064",
"19671042",
"19657325",
"19414081",
"19402056",
"19261475",
"19243301",
"19216840",
"15611513",
"18095884",
"17932373",
"17255293",
"17245122",
"18323857",
"16728571",
"16531988",
"16869749"
] | [
"Structure of the VHL-ElonginC-ElonginB complex: implications for VHL tumor suppressor function.",
"Structure of an HIF-1alpha -pVHL complex: hydroxyproline recognition in signaling.",
"Structural basis for the recognition of hydroxyproline in HIF-1 alpha by pVHL.",
"The von hippel-lindau tumor suppressor pro... | [
1999,
2002,
2002,
2007,
2009,
2009,
2009,
2009,
2009,
2009,
2009,
2004,
2008,
2008,
2007,
2007,
2008,
2006,
2006,
2005
] | 20 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"ecological metagenomes"
] | [
313,
1988,
13
] | 3 | [
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
1,
2,
3,
12,
2,
4
] | 6 | true | Domain | von Hippel-Lindau disease tumour suppressor, beta domain | von Hippel-Lindau disease tumour suppressor, beta domain | VHL_beta_dom | 3 |
IPR024055 | 24,055 | Translation initiation factor 2, alpha subunit, C-terminal | TIF2_asu_C | Homologous_superfamily | 5,898 | false | false | This superfamily represents the C-terminal domain of the translation initiation factor 2 alpha subunit. It adopts an α-β fold, containing five β strands, two α helices, and one loosely associated C-terminal α helix [ ]. | [] | [] | [] | 0 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:3.30.70.1130",
"SSF110993"
] | [
"",
""
] | [
5868,
5889
] | 2 | [
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOM... | [
"R-BTA-156827",
"R-BTA-381042",
"R-BTA-382556",
"R-BTA-72649",
"R-BTA-72695",
"R-BTA-72702",
"R-BTA-72731",
"R-BTA-9840373",
"R-DDI-156827",
"R-DDI-382556",
"R-DDI-72695",
"R-DDI-72702",
"R-DDI-72731",
"R-DDI-9840373",
"R-DME-156827",
"R-DME-381042",
"R-DME-382556",
"R-DME-72649",
... | [
"REACTOME:R-BTA-156827",
"REACTOME:R-BTA-381042",
"REACTOME:R-BTA-382556",
"REACTOME:R-BTA-72649",
"REACTOME:R-BTA-72695",
"REACTOME:R-BTA-72702",
"REACTOME:R-BTA-72731",
"REACTOME:R-BTA-9840373",
"REACTOME:R-DDI-156827",
"REACTOME:R-DDI-382556",
"REACTOME:R-DDI-72695",
"REACTOME:R-DDI-72702",... | 83 | [
"1q8k",
"1yz6",
"1yz7",
"2aho",
"2qmu",
"2qn6",
"3aev",
"3cw2",
"3j81",
"3jap",
"3qsy",
"3v11",
"5jb3",
"5jbh",
"5k0y",
"6fec",
"6fyx",
"6fyy",
"6gsm",
"6gsn",
"6i3m",
"6i7t",
"6jly",
"6jlz",
"6k71",
"6k72",
"6o81",
"6o85",
"6o9z",
"6qg0",
"6qg1",
"6qg2"... | 75 | [
"PUB00030166"
] | [
"15341733"
] | [
"Solution structure of human initiation factor eIF2alpha reveals homology to the elongation factor eEF1B."
] | [
2004
] | 1 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"Megaviricetes",
"metagenomes"
] | [
928,
3,
4901,
19,
47
] | 5 | [
"Arabidopsis thaliana",
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)",
"Oryza sativa subsp. japonica",
"Rattus norvegicus",
"Saccharomyces cerevisiae (strai... | [
7,
1,
2,
2,
4,
2,
1,
4,
2,
1,
1,
13
] | 12 | true | Homologous_superfamily | Translation initiation factor 2, alpha subunit, C-terminal | Translation initiation factor 2, alpha subunit, C-terminal | TIF2_asu_C | 9 |
IPR024056 | 24,056 | Apical membrane antigen 1 domain superfamily | Apmem_Ag1_dom_sf | Homologous_superfamily | 2,077 | false | false | A novel antigen of Plasmodium falciparum has been cloned that contains a hydrophobic domain typical of an integral membrane protein. The antigen is designated apical membrane antigen 1 (AMA-1) by virtue of appearing to be located in the apical complex [ ]. AMA-1 appears to be transported to the merozoite surface close ... | [] | [] | [] | 0 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:4.10.1010.10",
"SSF82910"
] | [
"",
""
] | [
2077,
2077
] | 2 | [] | [] | [] | 0 | [
"1hn6",
"1w81",
"1w8k",
"2j4w",
"2j5l",
"5nqg",
"8qus",
"8rek",
"9dx6"
] | 9 | [
"PUB00008080",
"PUB00008081"
] | [
"2701947",
"2211675"
] | [
"Integral membrane protein located in the apical complex of Plasmodium falciparum.",
"A merozoite receptor protein from Plasmodium knowlesi is highly conserved and distributed throughout Plasmodium."
] | [
1989,
1990
] | 2 | [] | [] | 0 | 0 | null | [
"Plasmodium"
] | [
2077
] | 1 | [] | [] | 0 | true | Homologous_superfamily | Apical membrane antigen 1 domain superfamily | Apical membrane antigen 1 domain superfamily | Apmem_Ag1_dom_sf | 2 |
IPR024057 | 24,057 | Nucleoplasmin core domain | Nucleoplasmin_core_dom | Domain | 4,236 | false | false | This entry represents the core structural domain for the nucleoplasmin (Np) family of histone chaperone proteins. This core domain is formed by an 8-stranded β barrel [ ]. The three branches of the Np family, including nucleophosmin (NO38/B23), nucleoplasmin (Np), and nucleoplasmin-like proteins (NLP), bind core histon... | [] | [] | [] | 0 | [
"PFAM"
] | [
"PF03066"
] | [
"Nucleoplasmin"
] | [
4236
] | 1 | [
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOM... | [
"R-DME-3899300",
"R-DME-8869496",
"R-DME-9833482",
"R-HSA-180746",
"R-HSA-3899300",
"R-HSA-606279",
"R-HSA-6804115",
"R-HSA-8869496",
"R-HSA-9692914",
"R-HSA-9700645",
"R-HSA-9725370",
"R-HSA-9725371",
"R-HSA-9821993",
"R-HSA-9833482",
"R-MMU-3899300",
"R-MMU-606279",
"R-MMU-6804115"... | [
"REACTOME:R-DME-3899300",
"REACTOME:R-DME-8869496",
"REACTOME:R-DME-9833482",
"REACTOME:R-HSA-180746",
"REACTOME:R-HSA-3899300",
"REACTOME:R-HSA-606279",
"REACTOME:R-HSA-6804115",
"REACTOME:R-HSA-8869496",
"REACTOME:R-HSA-9692914",
"REACTOME:R-HSA-9700645",
"REACTOME:R-HSA-9725370",
"REACTOME:... | 24 | [
"1k5j",
"1nlq",
"1xb9",
"1xe0",
"2p1b",
"2vtx",
"3t30",
"4n8m",
"5ehd",
"8as5",
"8vhi",
"8vhj",
"8vhk"
] | 13 | [
"PUB00032376"
] | [
"15576029"
] | [
"The structure and function of Xenopus NO38-core, a histone chaperone in the nucleolus."
] | [
2004
] | 1 | [] | [] | 0 | 0 | null | [
"Opisthokonta",
"bird metagenome"
] | [
4235,
1
] | 2 | [
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
8,
3,
23,
16,
14
] | 5 | true | Domain | Nucleoplasmin core domain | Nucleoplasmin core domain | Nucleoplasmin_core_dom | 1 |
IPR024058 | 24,058 | Cytochrome f transmembrane anchor | Cyt-f_TM | Homologous_superfamily | 14,655 | false | false | The cytochrome b6f integral membrane protein complex transfers electrons between the two reaction centre complexes of oxygenic photosynthetic membranes, and participates in formation of the transmembrane electrochemical proton gradient by also transferring protons from the stromal to the internal lumen compartment. The... | [] | [] | [] | 0 | [
"SSF"
] | [
"SSF103431"
] | [
""
] | [
14655
] | 1 | [] | [] | [] | 0 | [
"1q90",
"1vf5",
"2d2c",
"2e74",
"2e75",
"2e76",
"2zt9",
"4h0l",
"4h13",
"4h44",
"4i7z",
"4ogq",
"4pv1",
"6rqf",
"7qrm",
"7r0w",
"7zxy",
"7zyv",
"9es7",
"9es8",
"9es9"
] | 21 | [
"PUB00002369",
"PUB00005037",
"PUB00005442"
] | [
"8027021",
"8762139",
"7631417"
] | [
"Structural aspects of the cytochrome b6f complex; structure of the lumen-side domain of cytochrome f.",
"The heme redox center of chloroplast cytochrome f is linked to a buried five-water chain.",
"Cytochrome f revealed."
] | [
1994,
1996,
1995
] | 3 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota"
] | [
379,
14276
] | 2 | [
"Arabidopsis thaliana",
"Oryza sativa subsp. japonica",
"Zea mays"
] | [
7,
9,
8
] | 3 | true | Homologous_superfamily | Cytochrome f transmembrane anchor | Cytochrome f transmembrane anchor | Cyt-f_TM | 8 |
IPR024059 | 24,059 | YopX-like, N-terminal | YopX-like_N | Homologous_superfamily | 14 | false | false | This superfamily represents a domain found in ORF041 from Bacteriophage 37, which forms a β sandwich structure similar to the N-terminal domain of YopX ( ). | [] | [] | [] | 0 | [
"CATHGENE3D"
] | [
"G3DSA:2.60.430.10"
] | [
""
] | [
14
] | 1 | [] | [] | [] | 0 | [
"2p84"
] | 1 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacilli",
"Staphylococcus phage 37"
] | [
13,
1
] | 2 | [] | [] | 0 | true | Homologous_superfamily | YopX-like, N-terminal | YopX-like, N-terminal | YopX-like_N | 5 |
IPR024060 | 24,060 | Ureidoglycolate lyase domain superfamily | Ureidoglycolate_lyase_dom_sf | Homologous_superfamily | 8,531 | false | false | This superfamily represents the structural domain of ureidoglycolate lyase, and consists of a β structure known as a jelly roll. | [
"GO:0004848"
] | [
"ureidoglycolate hydrolase activity"
] | [
"molecular_function"
] | 1 | [
"CATHGENE3D"
] | [
"G3DSA:2.60.120.480"
] | [
""
] | [
8531
] | 1 | [
"EC",
"METACYC",
"METACYC"
] | [
"4.3.2.3",
"PWY-5694",
"PWY-5705"
] | [
"EC:4.3.2.3",
"METACYC:PWY-5694",
"METACYC:PWY-5705"
] | 3 | [
"1xsq",
"1xsr",
"1yqc",
"2bdr"
] | 4 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"unclassified sequences"
] | [
5873,
2568,
90
] | 3 | [
"Arabidopsis thaliana",
"Escherichia coli (strain K12)",
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)",
"Oryza sativa subsp. japonica",
"Saccharomyces cerevisiae (strain ATCC 204508 / S288c)",
"Schizosaccharomyces pombe (strain 972 / ATCC 24843)",
"Zea mays"
] | [
16,
1,
1,
2,
1,
1,
4
] | 7 | true | Homologous_superfamily | Ureidoglycolate lyase domain superfamily | Ureidoglycolate lyase domain superfamily | Ureidoglycolate_lyase_dom_sf | 8 |
IPR024061 | 24,061 | NDT80, DNA-binding domain | NDT80_DNA-bd_dom | Domain | 6,280 | false | false | The NDT80 DNA-binding domain is found in the following proteins, which might all be involved in sensing nutritional status [ ]: Yeast meiosis-specific transcription factor NDT80, the key transcription factor that ultimately allows the continuation of meiosis after the successful completion of recombination. Emericella ... | [
"GO:0003677"
] | [
"DNA binding"
] | [
"molecular_function"
] | 1 | [
"PFAM",
"PROFILE"
] | [
"PF05224",
"PS51517"
] | [
"NDT80_PhoG",
"NDT80"
] | [
6233,
6241
] | 2 | [] | [] | [] | 0 | [
"1m6u",
"1m7u",
"1mn4",
"1mnn",
"2etw",
"2euv",
"2euw",
"2eux",
"2euz",
"2evf",
"2evg",
"2evh",
"2evi",
"2evj",
"5h5p",
"5yhu",
"5zhu"
] | 17 | [
"PUB00022187",
"PUB00055515",
"PUB00163233"
] | [
"12411490",
"16464624",
"28623291"
] | [
"Structure of the sporulation-specific transcription factor Ndt80 bound to DNA.",
"The Aspergillus nidulans xprG (phoG) gene encodes a putative transcriptional activator involved in the response to nutrient limitation.",
"Crystal structure of the DNA-binding domain of Myelin-gene Regulatory Factor."
] | [
2002,
2006,
2017
] | 3 | [] | [] | 0 | 0 | null | [
"Eukaryota",
"Gimesia panareensis"
] | [
6279,
1
] | 2 | [
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)",
"Rattus norvegicus",
"Saccharomyces cerevisiae (strain ATCC 204508 / S288c)"
] | [
2,
15,
3,
5,
2,
7,
8,
1
] | 8 | true | Domain | NDT80, DNA-binding domain | NDT80, DNA-binding domain | NDT80_DNA-bd_dom | 1 |
IPR024062 | 24,062 | Bacteriophage PBS2, uracil-glycosylase inhibitor | Phage_PBS2_Ugi | Homologous_superfamily | 5 | false | false | DNA glycosylases excise damaged or unconventional bases in DNA and initiate the base excision repair (BER) pathway to maintain genomic integrity. Of these, uracil-DNA glycosylase (UDG) excises uracil from DNA by cleavage of the N-glycosidic bond between uracil and deoxyribose sugar. Uracil residues in DNA arise as a re... | [] | [] | [] | 0 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:3.10.450.20",
"SSF54441"
] | [
"",
""
] | [
4,
5
] | 2 | [] | [] | [] | 0 | [
"1eui",
"1lqg",
"1lqm",
"1udi",
"1ugh",
"1ugi",
"1uug",
"2j8x",
"2ugi",
"2uug",
"2zhx",
"4lyl",
"6lyd",
"6lye",
"8aim"
] | 15 | [
"PUB00022775",
"PUB00024677",
"PUB00027104",
"PUB00055072"
] | [
"7552746",
"9776748",
"12136137",
"7479702"
] | [
"Nucleotide mimicry in the crystal structure of the uracil-DNA glycosylase-uracil glycosylase inhibitor protein complex.",
"X-ray analysis of a complex of Escherichia coli uracil DNA glycosylase (EcUDG) with a proteinaceous inhibitor. The structure elucidation of a prokaryotic UDG.",
"Domain closure and action ... | [
1995,
1998,
2002,
1995
] | 4 | [] | [] | 0 | 0 | null | [
"Ajellomyces dermatitidis (strain ER-3 / ATCC MYA-2586)",
"Caudoviricetes"
] | [
1,
4
] | 2 | [] | [] | 0 | true | Homologous_superfamily | Bacteriophage PBS2, uracil-glycosylase inhibitor | Bacteriophage PBS2, uracil-glycosylase inhibitor | Phage_PBS2_Ugi | 5 |
IPR024064 | 24,064 | FdhE-like superfamily | FdhE-like_sf | Homologous_superfamily | 5,451 | false | false | This superfamily represents a domain found in formate dehydrogenase accessory protein FdhE and homologues. It consists of an N-terminal five-helical bundle, a tandem repeat of two rubredoxin-like domains and a C-terminal helix packed together. | [] | [] | [] | 0 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:3.90.1670.10",
"SSF144020"
] | [
"",
""
] | [
4315,
5423
] | 2 | [] | [] | [] | 0 | [
"2fiy"
] | 1 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"Viruses",
"unclassified sequences"
] | [
145,
5095,
108,
21,
82
] | 5 | [
"Escherichia coli (strain K12)",
"Zea mays"
] | [
1,
1
] | 2 | true | Homologous_superfamily | FdhE-like superfamily | FdhE-like superfamily | FdhE-like_sf | 4 |
IPR024065 | 24,065 | DNA topoisomerase V, catalytic domain superfamily | TopoV_catalytic_dom_sf | Homologous_superfamily | 7 | false | false | DNA topoisomerases regulate the number of topological links between two DNA strands (i.e. change the number of superhelical turns) by catalysing transient single-or double-strand breaks, crossing the strands through one another, then resealing the breaks [ ]. These enzymes have several functions: to remove DNA supercoi... | [] | [] | [] | 0 | [
"SSF"
] | [
"SSF140979"
] | [
""
] | [
7
] | 1 | [] | [] | [] | 0 | [
"2csb",
"2csd",
"3m6k",
"3m6z",
"3m7d",
"3m7g",
"4gfj",
"5hm5",
"8df7",
"8df8",
"8df9",
"8dfb"
] | 12 | [
"PUB00005437",
"PUB00016842",
"PUB00020793",
"PUB00020794",
"PUB00040090",
"PUB00055625",
"PUB00055626"
] | [
"7770916",
"11395412",
"12596227",
"12042765",
"16395333",
"20637419",
"11353838"
] | [
"The mechanisms of DNA topoisomerases.",
"DNA topoisomerases: structure, function, and mechanism.",
"Phylogenomics of type II DNA topoisomerases.",
"Cellular roles of DNA topoisomerases: a molecular perspective.",
"Structure of the N-terminal fragment of topoisomerase V reveals a new family of topoisomerase... | [
1995,
2001,
2003,
2002,
2006,
2010,
2001
] | 7 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Methanopyrus kandleri"
] | [
5,
2
] | 2 | [] | [] | 0 | true | Homologous_superfamily | DNA topoisomerase V, catalytic domain superfamily | DNA topoisomerase V, catalytic domain superfamily | TopoV_catalytic_dom_sf | 1 |
IPR024066 | 24,066 | RGS, subdomain 1/3 | RGS_subdom1/3 | Homologous_superfamily | 18,439 | false | false | RGS (Regulator of G Protein Signalling) proteins are multi-functional, GTPase-accelerating proteins that promote GTP hydrolysis by the alpha subunit of heterotrimeric G proteins [ ]. Upon activation by GPCRs, heterotrimeric G proteins exchange GDP for GTP, are released from the receptor, and dissociate into free, activ... | [] | [] | [] | 0 | [
"CATHGENE3D"
] | [
"G3DSA:1.10.196.10"
] | [
""
] | [
18439
] | 1 | [
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOM... | [
"R-BTA-416476",
"R-BTA-418594",
"R-BTA-418597",
"R-CEL-416476",
"R-CEL-418594",
"R-CEL-418597",
"R-DME-195253",
"R-DME-196299",
"R-DME-209155",
"R-DME-209190",
"R-DME-209214",
"R-DME-209360",
"R-DME-209396",
"R-DME-209413",
"R-DME-209440",
"R-DME-209461",
"R-DME-418594",
"R-DME-432... | [
"REACTOME:R-BTA-416476",
"REACTOME:R-BTA-418594",
"REACTOME:R-BTA-418597",
"REACTOME:R-CEL-416476",
"REACTOME:R-CEL-418594",
"REACTOME:R-CEL-418597",
"REACTOME:R-DME-195253",
"REACTOME:R-DME-196299",
"REACTOME:R-DME-209155",
"REACTOME:R-DME-209190",
"REACTOME:R-DME-209214",
"REACTOME:R-DME-209... | 66 | [
"1agr",
"1cmz",
"1dk8",
"1emu",
"1ezt",
"1ezy",
"1zv4",
"2af0",
"2bt2",
"2bv1",
"2crp",
"2dlr",
"2dlv",
"2ebz",
"2gtp",
"2i59",
"2ihb",
"2ihd",
"2ik8",
"2jm5",
"2jnu",
"2ode",
"2oj4",
"2owi",
"2v4z",
"3c7k",
"3c7l",
"4ekc",
"4ekd",
"5do9",
"7y1p"
] | 31 | [
"PUB00000946",
"PUB00006536",
"PUB00015162",
"PUB00015163",
"PUB00046994",
"PUB00071325"
] | [
"9108480",
"10836135",
"15090201",
"10987813",
"18434541",
"23900842"
] | [
"Structure of RGS4 bound to AlF4--activated G(i alpha1): stabilization of the transition state for GTP hydrolysis.",
"The regulator of G protein signaling family.",
"RGS proteins: G protein-coupled receptors meet their match.",
"Regulators of G protein signaling: a bestiary of modular protein binding domains.... | [
1997,
2000,
2003,
2000,
2008,
2013
] | 6 | [] | [] | 0 | 0 | null | [
"Eukaryota",
"marine metagenome"
] | [
18438,
1
] | 2 | [
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
8,
92,
12,
56,
64,
73
] | 6 | true | Homologous_superfamily | RGS, subdomain 1/3 | RGS, subdomain 1/3 | RGS_subdom1/3 | 9 |
IPR024067 | 24,067 | Methylmalonyl-CoA mutase small subunit, N-terminal | Me-malonyl-CoA_mutase_sm_su_N | Homologous_superfamily | 957 | false | false | Methylmalonyl-CoA mutase ( ) catalyses the isomerization of succinyl-CoA to methylmalonyl-CoA during the synthesis of propionate from tricarboxylic acid-cycle intermediates in propionic acid fermentation. This entry represents the N-terminal portion of the catalytic domain found in methylmalonyl-CoA mutase small subuni... | [] | [] | [] | 0 | [
"CATHGENE3D"
] | [
"G3DSA:1.10.196.20"
] | [
""
] | [
957
] | 1 | [] | [] | [] | 0 | [
"1e1c",
"1req",
"2req",
"3req",
"4req",
"5req",
"6req",
"7req"
] | 8 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"freshwater metagenome"
] | [
952,
5
] | 2 | [] | [] | 0 | true | Homologous_superfamily | Methylmalonyl-CoA mutase small subunit, N-terminal | Methylmalonyl-CoA mutase small subunit, N-terminal | Me-malonyl-CoA_mutase_sm_su_N | 8 |
IPR024068 | 24,068 | Rotavirus NSP2, N-terminal | Rotavirus_NSP2_N | Homologous_superfamily | 2,791 | false | false | Rotavirus non-structural protein 2 (NSP2) is a basic protein which possesses RNA-binding activity and is essential for genome replication [ ]. It may also be important for viral RNA packaging. This superfamily represents the N-terminal domain of Rotavirus NSP2. | [
"GO:0016817"
] | [
"hydrolase activity, acting on acid anhydrides"
] | [
"molecular_function"
] | 1 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:3.90.1400.10",
"SSF75574"
] | [
"",
""
] | [
2791,
2791
] | 2 | [
"EC",
"METACYC"
] | [
"3.6.4.-",
"PWY-7250"
] | [
"EC:3.6.4.-",
"METACYC:PWY-7250"
] | 2 | [
"1l9v",
"2gu0",
"2r7c",
"2r7j",
"2r7p",
"2r8f",
"4g0a",
"4g0j",
"6auk",
"6cy9",
"6cya",
"7pko",
"7pkp",
"9oft",
"9ogq"
] | 15 | [
"PUB00008136"
] | [
"8380660"
] | [
"Nucleotide and amino acid sequence analysis of the rotavirus nonstructural RNA-binding protein NS35."
] | [
1993
] | 1 | [] | [] | 0 | 0 | null | [
"Rotavirus"
] | [
2791
] | 1 | [] | [] | 0 | true | Homologous_superfamily | Rotavirus NSP2, N-terminal | Rotavirus NSP2, N-terminal | Rotavirus_NSP2_N | 6 |
IPR024069 | 24,069 | AF2212-like domain superfamily | AF2212-like_dom_sf | Homologous_superfamily | 698 | false | false | This domain superfamily is found in protein AF2212 (also known as putative antitoxin VapB21) from the archaean Archaeoglobus fulgidus, and other uncharacterised proteins belonging to the UPF0165 family. The structure of AF2212 has been solved ( ) but not published. The AF2212-like domain is irregular with few secondary... | [] | [] | [] | 0 | [
"CATHGENE3D"
] | [
"G3DSA:4.10.1150.10"
] | [
""
] | [
698
] | 1 | [] | [] | [] | 0 | [
"2nwt"
] | 1 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Geodia barretti",
"ecological metagenomes"
] | [
360,
327,
1,
10
] | 4 | [] | [] | 0 | true | Homologous_superfamily | AF2212-like domain superfamily | AF2212-like domain superfamily | AF2212-like_dom_sf | 4 |
IPR024071 | 24,071 | S-Me-THD, C-terminal domain superfamily | S-Me-THD_C_sf | Homologous_superfamily | 5,939 | false | false | This β-barrel domain is found at the C-terminal of S-methyl thiohydantoin desulfurase from Variovorax sp. (S-Me-THD) and similar sequences mainly found in bacteria and fungi. S-Me-THD catalyses the hydrolysis of S-methyl-thiohydantoin-5-propanoate into hydantoin-5-propanoate and methanethiol, the third step in S-methyl... | [] | [] | [] | 0 | [
"CATHGENE3D"
] | [
"G3DSA:2.40.390.10"
] | [
""
] | [
5939
] | 1 | [] | [] | [] | 0 | [
"2o3i"
] | 1 | [
"PUB00155448"
] | [
"38389448"
] | [
"Structure and Substrate Specificity of <i>S</i>-Methyl Thiourocanate Hydratase."
] | [
2024
] | 1 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"ecological metagenomes"
] | [
194,
3505,
2168,
72
] | 4 | [
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)"
] | [
1
] | 1 | true | Homologous_superfamily | S-Me-THD, C-terminal domain superfamily | S-Me-THD, C-terminal domain superfamily | S-Me-THD_C_sf | 2 |
IPR024072 | 24,072 | Dihydrofolate reductase-like domain superfamily | DHFR-like_dom_sf | Homologous_superfamily | 109,795 | false | false | Dihydrofolate reductase (DHFR) catalyses the NADPH-dependent reduction of dihydrofolate to tetrahydrofolate, an essential step in de novo synthesis both of glycine and of purines and deoxythymidine phosphate (the precursors of DNA synthesis) [ ], and important also in the conversion of deoxyuridine monophosphate to deo... | [] | [] | [] | 0 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:3.40.430.10",
"SSF53597"
] | [
"",
""
] | [
109652,
109521
] | 2 | [
"EC",
"METACYC",
"METACYC",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME"
] | [
"1.5.1.3",
"PWY-3841",
"PWY-6614",
"R-CEL-196757",
"R-DME-196757",
"R-HSA-1474151",
"R-HSA-196757",
"R-HSA-69205",
"R-MMU-196757",
"R-RNO-196757",
"R-SCE-196757",
"R-SPO-196757"
] | [
"EC:1.5.1.3",
"METACYC:PWY-3841",
"METACYC:PWY-6614",
"REACTOME:R-CEL-196757",
"REACTOME:R-DME-196757",
"REACTOME:R-HSA-1474151",
"REACTOME:R-HSA-196757",
"REACTOME:R-HSA-69205",
"REACTOME:R-MMU-196757",
"REACTOME:R-RNO-196757",
"REACTOME:R-SCE-196757",
"REACTOME:R-SPO-196757"
] | 12 | [
"1ai9",
"1ao8",
"1aoe",
"1boz",
"1bzf",
"1cd2",
"1cz3",
"1d1g",
"1daj",
"1ddr",
"1dds",
"1df7",
"1dg5",
"1dg7",
"1dg8",
"1dhf",
"1dhi",
"1dhj",
"1dis",
"1diu",
"1dlr",
"1dls",
"1dr1",
"1dr2",
"1dr3",
"1dr4",
"1dr5",
"1dr6",
"1dr7",
"1dra",
"1drb",
"1dre"... | 715 | [
"PUB00005107"
] | [
"2830673"
] | [
"A gene for dihydrofolate reductase in a herpesvirus."
] | [
1988
] | 1 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"Plasmid R483",
"Viruses",
"unclassified sequences"
] | [
1647,
94953,
10755,
1,
1107,
1332
] | 6 | [
"Arabidopsis thaliana",
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Escherichia coli (strain K12)",
"Homo sapiens",
"Mus musculus",
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)",
"Oryza sativa subsp. japonica",
"Rattus norvegicus",... | [
28,
1,
3,
2,
2,
6,
2,
2,
18,
4,
2,
3,
35
] | 13 | true | Homologous_superfamily | Dihydrofolate reductase-like domain superfamily | Dihydrofolate reductase-like domain superfamily | DHFR-like_dom_sf | 7 |
IPR024073 | 24,073 | Argininosuccinate synthetase mutimerisation domain, C-terminal tail | AS_multimer_C_tail | Homologous_superfamily | 4,864 | false | false | The argininosuccinate synthetase (AS) monomer is composed of a nucleotide binding domain and a catalytic/multimerisation domain. The catalytic/multimerisation domain possesses a C-terminal tail, which is involved in protein dimerisation and tetramerisation [ ]. The tail contains two α helices. In a subset of bacterial ... | [
"GO:0042803"
] | [
"protein homodimerization activity"
] | [
"molecular_function"
] | 1 | [
"CATHGENE3D"
] | [
"G3DSA:1.10.287.400"
] | [
""
] | [
4864
] | 1 | [
"EC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC"
] | [
"6.3.4.5",
"PWY-4983",
"PWY-4984",
"PWY-5",
"PWY-5154",
"PWY-7400"
] | [
"EC:6.3.4.5",
"METACYC:PWY-4983",
"METACYC:PWY-4984",
"METACYC:PWY-5",
"METACYC:PWY-5154",
"METACYC:PWY-7400"
] | 6 | [
"1k92",
"1k97",
"1kp2",
"1kp3",
"5us8",
"6e5y"
] | 6 | [
"PUB00028813"
] | [
"11738042"
] | [
"The 1.6 A crystal structure of E. coli argininosuccinate synthetase suggests a conformational change during catalysis."
] | [
2001
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"metagenomes"
] | [
4690,
5,
169
] | 3 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Homologous_superfamily | Argininosuccinate synthetase mutimerisation domain, C-terminal tail | Argininosuccinate synthetase mutimerisation domain, C-terminal tail | AS_multimer_C_tail | 4 |
IPR024074 | 24,074 | Argininosuccinate synthetase, catalytic/multimerisation domain body | AS_cat/multimer_dom_body | Homologous_superfamily | 29,737 | false | false | The argininosuccinate synthetase (AS) monomer is composed of a nucleotide binding domain and a catalytic/multimerisation domain. The catalytic/multimerisation domain can be subdivided in the body of the domain and a C-terminal tail involved in multimerisation, though this tail is not present in all sequences. This entr... | [
"GO:0004055"
] | [
"argininosuccinate synthase activity"
] | [
"molecular_function"
] | 1 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:3.90.1260.10",
"SSF69864"
] | [
"",
""
] | [
29626,
29552
] | 2 | [
"EC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"REACTOME",
"REACTOME",
"REACTOME"
] | [
"6.3.4.5",
"PWY-4983",
"PWY-4984",
"PWY-5",
"PWY-5154",
"PWY-7400",
"R-BTA-70635",
"R-HSA-70635",
"R-MMU-70635"
] | [
"EC:6.3.4.5",
"METACYC:PWY-4983",
"METACYC:PWY-4984",
"METACYC:PWY-5",
"METACYC:PWY-5154",
"METACYC:PWY-7400",
"REACTOME:R-BTA-70635",
"REACTOME:R-HSA-70635",
"REACTOME:R-MMU-70635"
] | 9 | [
"1j1z",
"1j20",
"1j21",
"1k92",
"1k97",
"1kh1",
"1kh2",
"1kh3",
"1kor",
"1kp2",
"1kp3",
"1vl2",
"2nz2",
"4nzp",
"4u7j",
"4xfj",
"5us8",
"6e5y",
"6xnq",
"7k5z"
] | 20 | [
"PUB00028813"
] | [
"11738042"
] | [
"The 1.6 A crystal structure of E. coli argininosuccinate synthetase suggests a conformational change during catalysis."
] | [
2001
] | 1 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"Siphoviridae sp. ctBLh2",
"unclassified sequences"
] | [
833,
23293,
4988,
1,
622
] | 5 | [
"Arabidopsis thaliana",
"Danio rerio",
"Drosophila melanogaster",
"Escherichia coli (strain K12)",
"Homo sapiens",
"Mus musculus",
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)",
"Oryza sativa subsp. japonica",
"Rattus norvegicus",
"Saccharomyces cerevisiae... | [
4,
1,
1,
1,
10,
3,
2,
7,
3,
1,
1,
11
] | 12 | true | Homologous_superfamily | Argininosuccinate synthetase, catalytic/multimerisation domain body | Argininosuccinate synthetase, catalytic/multimerisation domain body | AS_cat/multimer_dom_body | 6 |
IPR024075 | 24,075 | DNA-directed RNA polymerase, helix hairpin domain superfamily | DNA-dir_RNA_pol_helix_hairp_sf | Homologous_superfamily | 4,070 | false | false | The single subunit DNA-directed RNA polymerase (RNAP) that is encoded by bacteriophage T7 is the prototype of a class of relatively simple RNAPs that includes the RNAPs of the related phages T3 and SP6, as well as the mitochondrial and chloroplastic RNAPs [ ]. This superfamily represents a helix hairpin structural doma... | [
"GO:0003899"
] | [
"DNA-directed RNA polymerase activity"
] | [
"molecular_function"
] | 1 | [
"CATHGENE3D"
] | [
"G3DSA:1.10.287.260"
] | [
""
] | [
4070
] | 1 | [
"EC",
"REACTOME"
] | [
"2.7.7.6",
"R-SCE-163282"
] | [
"EC:2.7.7.6",
"REACTOME:R-SCE-163282"
] | 2 | [
"1aro",
"1cez",
"1h38",
"1msw",
"1qln",
"1s0v",
"1s76",
"1s77",
"2pi4",
"2pi5",
"3e2e",
"3e3j",
"4rnp",
"6ymv",
"6ymw",
"8ap1",
"8att",
"8atv",
"8atw",
"8c5s",
"8c5u",
"8dh0",
"8dh1",
"8dh2",
"8dh3",
"8dh4",
"8dh5",
"8q63"
] | 28 | [
"PUB00003849"
] | [
"7526118"
] | [
"The phage RNA polymerases are related to DNA polymerases and reverse transcriptases."
] | [
1993
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"Viruses",
"feces metagenome"
] | [
100,
3181,
788,
1
] | 4 | [
"Arabidopsis thaliana",
"Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987)",
"Oryza sativa subsp. japonica",
"Saccharomyces cerevisiae (strain ATCC 204508 / S288c)",
"Zea mays"
] | [
17,
1,
10,
1,
28
] | 5 | true | Homologous_superfamily | DNA-directed RNA polymerase, helix hairpin domain superfamily | DNA-directed RNA polymerase, helix hairpin domain superfamily | DNA-dir_RNA_pol_helix_hairp_sf | 2 |
IPR024076 | 24,076 | Rotavirus NSP2, C-terminal | Rotavirus_NSP2_C | Homologous_superfamily | 2,797 | false | false | Rotavirus non-structural protein 2 (NSP2) is a basic protein which possesses RNA-binding activity and is essential for genome replication [ ]. It may also be important for viral RNA packaging. This superfamily represents the C-terminal domain of the Rotavirus NSP2. | [
"GO:0016817"
] | [
"hydrolase activity, acting on acid anhydrides"
] | [
"molecular_function"
] | 1 | [
"CATHGENE3D",
"SSF"
] | [
"G3DSA:3.30.428.20",
"SSF75347"
] | [
"",
""
] | [
2795,
2797
] | 2 | [
"EC",
"METACYC"
] | [
"3.6.4.-",
"PWY-7250"
] | [
"EC:3.6.4.-",
"METACYC:PWY-7250"
] | 2 | [
"1l9v",
"2gu0",
"2r7c",
"2r7j",
"2r7p",
"2r8f",
"4g0a",
"4g0j",
"6auk",
"6cy9",
"6cya",
"7pko",
"7pkp",
"9oft",
"9ogq"
] | 15 | [
"PUB00008136"
] | [
"8380660"
] | [
"Nucleotide and amino acid sequence analysis of the rotavirus nonstructural RNA-binding protein NS35."
] | [
1993
] | 1 | [] | [] | 0 | 0 | null | [
"Bacillota",
"Rotavirus"
] | [
2,
2795
] | 2 | [] | [] | 0 | true | Homologous_superfamily | Rotavirus NSP2, C-terminal | Rotavirus NSP2, C-terminal | Rotavirus_NSP2_C | 2 |
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