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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
IPR061179 | 61,179 | WIAG-tail domain | WIAG-tail_dom | Domain | 414 | false | false | This 80-amino acid domain occurs in proteins from bacilli in a single copy at the C terminus. In most proteins, the domain immediately follows a long, variable run of tandem 10-amino acid repeats. The domain is named for its C-terminal motif, WIAxGx, hence the name WIAG-tail. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF012201"
] | [
"WIAG-tail"
] | [
414
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacillales"
] | [
414
] | 1 | [] | [] | 0 | true | Domain | WIAG-tail domain | WIAG-tail domain | WIAG-tail_dom | 5 |
IPR061180 | 61,180 | Spike base protein Rcc01079-like | Rcc01079-like | Family | 864 | false | false | Proteins of this family are found in tailed bacteriophages and proteobacterial prophages, including Spike base proteinRcc01079 from Rhodobacter capsulatus ( ). Some members form the base of the spike on the capsids of phage and phage-related gene transfer agents [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF048002"
] | [
"spike_base"
] | [
864
] | 1 | [] | [] | [] | 0 | [
"6tb9",
"6tba",
"6tsu",
"6tui",
"8cjz"
] | 5 | [
"PUB00153971"
] | [
"32541663"
] | [
"Structure and mechanism of DNA delivery of a gene transfer agent."
] | [
2020
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Viruses",
"metagenomes"
] | [
802,
44,
18
] | 3 | [] | [] | 0 | true | Family | Spike base protein Rcc01079-like | Spike base protein Rcc01079-like | Rcc01079-like | 6 |
IPR061181 | 61,181 | Arginine synthesis PII-interacting regulator PirA | PirA | Family | 283 | false | false | This entry represents a group of cyanobacterial proteins, including PirA from Synechocystis sp. ( ). It has been shown that the small protein PirA regulates flux into the ornithine-ammonia cycle (OAC), the key hub of cyanobacterial nitrogen stockpiling and remobilisation. PirA interacts with the central carbon/nitrogen... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF050139"
] | [
"PirA_Argsyn"
] | [
283
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162602"
] | [
"33758091"
] | [
"The Novel P<sub>II</sub>-Interacting Protein PirA Controls Flux into the Cyanobacterial Ornithine-Ammonia Cycle."
] | [
2021
] | 1 | [] | [] | 0 | 0 | null | [
"Cyanobacteriota"
] | [
283
] | 1 | [] | [] | 0 | true | Family | Arginine synthesis PII-interacting regulator PirA | Arginine synthesis PII-interacting regulator PirA | PirA | 4 |
IPR061182 | 61,182 | Bacteriocin fulvocin C-related | Fulvocin-rel | Family | 274 | false | false | This protein family represents a group of uncharacterised proteins from bacteria and fungi, including putative precursors of Bacteriocin fulvocin-C ( ). Fulvocin C was described as a bacteriocin from Myxococcus fulvus, 45 amino acids long with 8 cysteines [ ]. The precursor form was not described. However, the most clo... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033852"
] | [
"fulvocin_rel"
] | [
274
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105374"
] | [
"6783114"
] | [
"The primary structure of fulvocin C from Myxococcus fulvus."
] | [
1981
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Pezizomycotina"
] | [
236,
38
] | 2 | [] | [] | 0 | true | Family | Bacteriocin fulvocin C-related | Bacteriocin fulvocin C-related | Fulvocin-rel | 7 |
IPR061183 | 61,183 | PLxRFG domain | Tail-700 | Domain | 242 | false | false | This domain, nearly 700 residues long, begins with a nearly invariant motif YxPLxRFGx[YF]. It occurs as the extreme C-terminal domain of large size proteins mainly found in tailed bacteriophages and bacterial prophages, some over 5000 amino acids long with an average of nearly 3000. The function is unknown. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF032893"
] | [
"tail-700"
] | [
242
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Caudoviricetes",
"Fusarium",
"Pseudomonadati",
"metagenomes"
] | [
29,
2,
195,
16
] | 4 | [] | [] | 0 | true | Domain | PLxRFG domain | PLxRFG domain | Tail-700 | 3 |
IPR061186 | 61,186 | P110/LppT-like adhesin, N-terminal domain | P110_N | Domain | 182 | false | false | This entry represents a domain found at the N-terminal end of the multifunctional adhesin P110 from Mycoplasma hyopneumoniae and homologues presumed also to be adhesins, including LppT (lipoprotein T), which despite its name seems to lack the signal peptide region Cys residue required for conversion into a lipoprotein,... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038058"
] | [
"adhes_P110_Nter"
] | [
182
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105542",
"PUB00105543"
] | [
"12576592",
"9695283"
] | [
"Characterization of LppS, an adhesin of Mycoplasma conjunctivae.",
"Identification of a novel adhesin-like glycoprotein from Mycoplasma hyopneumoniae."
] | [
2003,
1998
] | 2 | [] | [] | 0 | 0 | null | [
"Mesomycoplasma"
] | [
182
] | 1 | [] | [] | 0 | true | Domain | P110/LppT-like adhesin, N-terminal domain | P110/LppT-like adhesin, N-terminal domain | P110_N | 5 |
IPR061187 | 61,187 | SCO2400-like | SCO2400-like | Family | 864 | false | false | SCO2400 from Streptomyces coelicolor ( ), and its apparent orthologues from other Streptomyces species, have small regions of strong sequence conservation, separated by long regions of low-complexity sequence that is rather poorly conserved. These proteins include the N-terminal region of 30 amino acids that includes a... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF049861"
] | [
"SCO2400_fam"
] | [
864
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Actinomycetes"
] | [
864
] | 1 | [] | [] | 0 | true | Family | SCO2400-like | SCO2400-like | SCO2400-like | 6 |
IPR061188 | 61,188 | RDAC-containing | RDAC-containing | Family | 153 | false | false | Members of this uncharacterised protein family average about 80 amino acids in length, and do not seem to belong to any well-conserved gene neighbourhoods. The family is named for a motif rather well conserved in some members. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047998"
] | [
"RDAC_fam"
] | [
153
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"metagenomes"
] | [
151,
2
] | 2 | [] | [] | 0 | true | Family | RDAC-containing | RDAC-containing | RDAC-containing | 6 |
IPR061189 | 61,189 | Histone-like protein Rv3852 | Rv3852 | Family | 154 | false | false | Proteins of this family were initially annotated as histone-like nucleoid-structuring protein. However, a recent study has shown that protein Rv3852 is not a typical nucleoid-associated protein (NAP) and is not Involved in nucleoid compaction and virulence regulation [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF050153"
] | [
"Rv3852_fam"
] | [
154
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162825"
] | [
"28559300"
] | [
"Rv3852 (H-NS) of Mycobacterium tuberculosis Is Not Involved in Nucleoid Compaction and Virulence Regulation."
] | [
2017
] | 1 | [] | [] | 0 | 0 | null | [
"Mycobacteriaceae"
] | [
154
] | 1 | [] | [] | 0 | true | Family | Histone-like protein Rv3852 | Histone-like protein Rv3852 | Rv3852 | 2 |
IPR061190 | 61,190 | Bdr, N-terminal domain | Bdr_N | Domain | 187 | false | false | Bdr (Borrelia direct repeat) proteins have an N-terminal domain, a variable length region of repeats, typically 11 amino acids long with a KID repeat, and a non-repetitive C-terminal domain. This entry represents the conserved N-terminal domain of families other than BdrA, BdrB, and BdrC, which are described by the rel... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040500"
] | [
"Bdr_N_group2"
] | [
187
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Borreliaceae"
] | [
187
] | 1 | [] | [] | 0 | true | Domain | Bdr, N-terminal domain | Bdr, N-terminal domain | Bdr_N | 1 |
IPR061192 | 61,192 | NMCC_0638 family (lipo)protein | Lipo_NMCC_0638 | Family | 275 | false | false | Members of this protein, including NMCC_0638 from Neisseria meningitidis, have two mostly invariant Cys residues. In about a quarter of family members, an additional Cys residue is present in what appears to be a lipoprotein signal peptide. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047650"
] | [
"lipo_NMCC_0638"
] | [
275
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Eukaryota",
"Pseudomonadati"
] | [
2,
273
] | 2 | [] | [] | 0 | true | Family | NMCC_0638 family (lipo)protein | NMCC_0638 family (lipo)protein | Lipo_NMCC_0638 | 9 |
IPR061193 | 61,193 | LIC10280-like | LIC10280-like | Family | 210 | false | false | This entry represents a group of uncharacterised bacterial proteins, including LIC10280 from Leptospira interrogans ( ). The lfb1 gene is widely used for Leptospira identification. A short signal peptide is found in the N-terminal of Lfb1 proteins. It has been reported that Lfb1 was associated with Leptospira interroga... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF050085"
] | [
"LIC10280_fam"
] | [
210
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00163040",
"PUB00163041"
] | [
"36112204",
"21176235"
] | [
"Identifying Leptospira interrogans putative virulence factors with a yeast protein expression screen.",
"Rapid Leptospira identification by direct sequencing of the diagnostic PCR products in New Caledonia."
] | [
2022,
2010
] | 2 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
210
] | 1 | [] | [] | 0 | true | Family | LIC10280-like | LIC10280-like | LIC10280-like | 4 |
IPR061194 | 61,194 | Multiple cyclophane triceptide AmcA, group 1 | AmcA_1 | Family | 136 | false | false | Members of this family belong to one of several classes of peptide natural product synthesised on the ribosome and then post-translationally modified (RiPP), where the modification begins with the actinobacterial multiple cyclophane-forming radical SAM peptide maturase AmcB ( ) [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041721"
] | [
"phane_AmcA_1"
] | [
136
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00152924"
] | [
"36454686"
] | [
"A Prevalent Group of Actinobacterial Radical SAM/SPASM Maturases Involved in Triceptide Biosynthesis."
] | [
2022
] | 1 | [] | [] | 0 | 0 | null | [
"Actinomycetes"
] | [
136
] | 1 | [] | [] | 0 | true | Family | Multiple cyclophane triceptide AmcA, group 1 | Multiple cyclophane triceptide AmcA, group 1 | AmcA_1 | 8 |
IPR061196 | 61,196 | Type VI secretion system protein IglI-like | IglI-like | Family | 133 | false | false | IglI (intracellular growth locus I), from Francisella tularensis, occurs within the type VI secretion system (T6SS) locus, and is important to virulence [ ]. This entry represents a broad family of related proteins, the majority of which are likewise encoded in the vicinity of other T6SS proteins such as baseplate subu... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041244"
] | [
"IglI_fam"
] | [
133
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00106258"
] | [
"21690239"
] | [
"IglG and IglI of the Francisella pathogenicity island are important virulence determinants of Francisella tularensis LVS."
] | [
2011
] | 1 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
133
] | 1 | [] | [] | 0 | true | Family | Type VI secretion system protein IglI-like | Type VI secretion system protein IglI-like | IglI-like | 2 |
IPR061200 | 61,200 | IlvX | IlvX | Family | 125 | false | false | The very short peptide IlvX, 16 amino acids long, is found in Escherchia coli and related species as the apparent first encoded peptide from the ilvXGEDA operon, for which ilvL, further upstream, is the classical attentuator system leader peptide controlling expression. IlvX is preceded by a ribosome binding site, term... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038286"
] | [
"peptide_16_IlvX"
] | [
125
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00104040"
] | [
"19734316"
] | [
"Small stress response proteins in Escherichia coli: proteins missed by classical proteomic studies."
] | [
2010
] | 1 | [] | [] | 0 | 0 | null | [
"Enterobacteriaceae"
] | [
125
] | 1 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Family | IlvX | IlvX | IlvX | 9 |
IPR061201 | 61,201 | Adhesin RatA-like | RatA-like | Family | 698 | false | false | This entry represents a group of uncharacterised proteins from enterobacterales, including RatA ( ). RatA, encoded in a Salmonella pathogenicity island next to its homologue RatB, is a long protein consisting almost entirely of repeats of a Bacterial Immunoglobulin-like 21/Adhesion domain pair (see and , respectively) ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF011843"
] | [
"PRK15315.1"
] | [
698
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00016646"
] | [
"12540539"
] | [
"Molecular and phenotypic analysis of the CS54 island of Salmonella enterica serotype typhimurium: identification of intestinal colonization and persistence determinants."
] | [
2003
] | 1 | [] | [] | 0 | 0 | null | [
"Salmonella"
] | [
698
] | 1 | [] | [] | 0 | true | Family | Adhesin RatA-like | Adhesin RatA-like | RatA-like | 8 |
IPR061202 | 61,202 | Membrane protein Msa | Msa | Family | 124 | false | false | Msa (SA1233) was first described in Staphylococcus aureus as Modulator of SarA, but later reports suggested the locus was actually a non-coding gene, msaC, in the 3'-untranslated region of cold shock protein CspA (msaB) [ , , ]. This protein family includes Msa and its homologues across a broad taxonomic range within f... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038270"
] | [
"membran_MsaC"
] | [
124
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105686",
"PUB00105687",
"PUB00105688"
] | [
"16946251",
"18047728",
"25155591"
] | [
"Identification and characterization of msa (SA1233), a gene involved in expression of SarA and several virulence factors in Staphylococcus aureus.",
"Structure and function predictions of the Msa protein in Staphylococcus aureus.",
"The msaABCR operon regulates resistance in vancomycin-intermediate Staphylococ... | [
2006,
2007,
2014
] | 3 | [] | [] | 0 | 0 | null | [
"Bacillati",
"human gut metagenome"
] | [
123,
1
] | 2 | [] | [] | 0 | true | Family | Membrane protein Msa | Membrane protein Msa | Msa | 9 |
IPR061204 | 61,204 | Colistin stress protein ABZJ_00068-like | ABZJ_00068-like | Family | 108 | false | false | This entry represents ABZJ_00068 from Acinetobacter baumannii ( ) and similar proteins from Acinetobacter species. Members of this protein family were shown to be the second most differentially up-regulated protein during colistin challenge in one study, and in a colistin-dependent mutant strain in another study [ , ].... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF051864"
] | [
"ABZJ_00068_fam"
] | [
108
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105620",
"PUB00163065"
] | [
"28275586",
"29079752"
] | [
"Colistin Resistance in <i>Acinetobacter baumannii</i> MDR-ZJ06 Revealed by a Multiomics Approach.",
"Transition of colistin dependence into colistin resistance in Acinetobacter baumannii."
] | [
2017,
2017
] | 2 | [] | [] | 0 | 0 | null | [
"Acinetobacter"
] | [
108
] | 1 | [] | [] | 0 | true | Family | Colistin stress protein ABZJ_00068-like | Colistin stress protein ABZJ_00068-like | ABZJ_00068-like | 4 |
IPR061209 | 61,209 | LIC_11139-like | LIC_11139-like | Family | 160 | false | false | Members of this family are mainly found in Leptospira, including LIC_11139 from Leptospira interrogans. They are putative lipoproteins with only a single Cys residue, invariant at the proposed lipoprotein signal cleavage site. Residues in the -1 position are unusual for lipoproteins in general, but consistent with obse... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033171"
] | [
"lipo_LIC11139"
] | [
160
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105015"
] | [
"26890609"
] | [
"What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira."
] | [
2016
] | 1 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
160
] | 1 | [] | [] | 0 | true | Family | LIC_11139-like | LIC_11139-like | LIC_11139-like | 1 |
IPR061210 | 61,210 | Npun_F0296-like domain | Npun_F0296-like_dom | Domain | 463 | false | false | This domain is found in Npun_F0296 from the filamentous cyanobacterium Nostoc punctiforme and similar bacterial sequences. This protein has a PEP-CTERM-like C-terminal protein-sorting domain that is induced specifically during the formation of hormogonia, which are filamentous colonies with a cooperative, pilus-driven,... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF050191"
] | [
"Npun_F0296_dom"
] | [
463
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162603"
] | [
"40358234"
] | [
"Cyanoexosortase B is essential for motility, biofilm formation, and scytonemin production in a filamentous cyanobacterium."
] | [
2025
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"unclassified sequences"
] | [
451,
12
] | 2 | [] | [] | 0 | true | Domain | Npun_F0296-like domain | Npun_F0296-like domain | Npun_F0296-like_dom | 3 |
IPR061211 | 61,211 | Choice-of-anchor R domain | Choice_anch_R | Domain | 415 | false | false | This GC-type dockerin domain occurs, so far, primarily in metagenome-assembled genomes from the taxonomic class Phycisphaerae, within the Planctomycetota, where it seems to anchor a number of otherwise unrelated proteins. The most frequent C-terminal anchoring domain for members of this group is PEP-CTERM (see ) or a P... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041539"
] | [
"choice_anch_R"
] | [
415
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Bacteriophage sp.",
"Eukaryota",
"metagenomes"
] | [
5,
331,
1,
5,
73
] | 5 | [] | [] | 0 | true | Domain | Choice-of-anchor R domain | Choice-of-anchor R domain | Choice_anch_R | 8 |
IPR061212 | 61,212 | SdrH-like, C-terminal domain | SdrH-like_C | Domain | 155 | false | false | This domain is found at the C-terminal end of SdrH from Staphylococcus epidermidis ( ) and similar staphylococcal proteins, SdrH is one of three MSCRAMM family proteins, but is atypical in lacking a recognisable LPXTG-like C-terminal recognition sequence for cell wall anchoring. This domain is C-terminal to the repetit... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF039170"
] | [
"SdrH_fam_CTERM"
] | [
155
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00081255",
"PUB00105777"
] | [
"10878118",
"31198057"
] | [
"The serine-aspartate repeat (Sdr) protein family in Staphylococcus epidermidis.",
"Time-variable expression levels of <i>mazF</i>, <i>atlE</i>, <i>sdrH</i>, and <i>bap</i> genes during biofilm formation in <i>Staphylococcus epidermidis</i>."
] | [
2000,
2019
] | 2 | [] | [] | 0 | 0 | null | [
"Staphylococcaceae",
"human gut metagenome"
] | [
154,
1
] | 2 | [] | [] | 0 | true | Domain | SdrH-like, C-terminal domain | SdrH-like, C-terminal domain | SdrH-like_C | 5 |
IPR061214 | 61,214 | LIC_13076-like | LIC_13076-like | Family | 141 | false | false | This family occurs in the genus Leptospira, including LIC_13076. Members are predicted to be surface-exposed proteins and are possible lipoproteins [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047624"
] | [
"LIC_13076_fam"
] | [
141
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159320"
] | [
"28352257"
] | [
"A Novel Pan-Genome Reverse Vaccinology Approach Employing a Negative-Selection Strategy for Screening Surface-Exposed Antigens against <i>leptospirosis</i>."
] | [
2017
] | 1 | [] | [] | 0 | 0 | null | [
"Leptospiraceae"
] | [
141
] | 1 | [] | [] | 0 | true | Family | LIC_13076-like | LIC_13076-like | LIC_13076-like | 8 |
IPR061215 | 61,215 | Membrane protein MAGa3780-like | MAGa3780-like | Family | 133 | false | false | Members of this entry, such as MAGa3780 from Mycoplasmopsis agalactiae, are membrane proteins. This family appears to be a related to the Pr6Pr family membrane proteins described by model . | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF046009"
] | [
"MAGa3780_fam"
] | [
133
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Mycoplasmatota"
] | [
133
] | 1 | [] | [] | 0 | true | Family | Membrane protein MAGa3780-like | Membrane protein MAGa3780-like | MAGa3780-like | 6 |
IPR061217 | 61,217 | Putative cell division protein FtsL, alphaproteobacteria | FtsL_put_alphaproteobact | Family | 2,418 | false | false | Members of this family appear to include the cell division protein FtsL from alphaproteobacteria, which lies outside the scope of model [ , , ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF049847"
] | [
"FtsL_COG5462"
] | [
2418
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162897",
"PUB00162898",
"PUB00162899"
] | [
"24975755",
"24155949",
"24532768"
] | [
"Identification of essential alphaproteobacterial genes reveals operational variability in conserved developmental and cell cycle systems.",
"Natural blood feeding and temperature shift modulate the global transcriptional profile of Rickettsia rickettsii infecting its tick vector.",
"Function and localization d... | [
2014,
2013,
2014
] | 3 | [] | [] | 0 | 0 | null | [
"Eukaryota",
"Pseudomonadati",
"metagenomes"
] | [
4,
2392,
22
] | 3 | [] | [] | 0 | true | Family | Putative cell division protein FtsL, alphaproteobacteria | Putative cell division protein FtsL, alphaproteobacteria | FtsL_put_alphaproteobact | 7 |
IPR061221 | 61,221 | MAG0920-like | MAG0920-like | Family | 59 | false | false | Members of this family include Mbov_0101 and Mbov_0775 from Mycoplasmopsis bovis, two paralogs also from Mycoplasmopsis agalactiae and MAG0920 from M. agalactiae ( ). | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045996"
] | [
"MAG0920_fam"
] | [
59
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Mycoplasmatota"
] | [
59
] | 1 | [] | [] | 0 | true | Family | MAG0920-like | MAG0920-like | MAG0920-like | 2 |
IPR061223 | 61,223 | Post-COAP-1 domain | Post_COAP_1_dom | Domain | 63 | false | false | Post-COAP-1 is a C-terminal domain, about 115 amino acids in length, found in a subset of proteins with the choice-of-anchor P (COAP) domain (see ). This domain is seen primarily in non-cultured prokaryotes. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041523"
] | [
"post_COAP_1"
] | [
63
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Fistulifera solaris",
"marine sediment metagenome"
] | [
8,
50,
1,
4
] | 4 | [] | [] | 0 | true | Domain | Post-COAP-1 domain | Post-COAP-1 domain | Post_COAP_1_dom | 5 |
IPR061225 | 61,225 | LDCC motif small metal-binding domain | CC_mini_metal | Domain | 158 | false | false | This small and previously undescribed domain, just over 30 amino acids in length, occurs primarily in small proteins of unknown function. It is identified as a probable heavy metal-binding domain by its CysCys pair (seen often in mercury resistance proteins), by the presence of metal-binding or transport domains such a... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040898"
] | [
"CC_mini_metal"
] | [
158
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"ecological metagenomes"
] | [
152,
6
] | 2 | [] | [] | 0 | true | Domain | LDCC motif small metal-binding domain | LDCC motif small metal-binding domain | CC_mini_metal | 2 |
IPR061228 | 61,228 | PA0050-like | PA0050-like | Family | 49 | false | false | Members of this family of small proteins include PA0050 in Pseudomonas aeruginosa ( ), average about 46 amino acids in length, starting with an apparent N-terminal signal peptide and containing four invariant Cys residues, and including a CxC motif near the C terminus. While the function remains unknown, expression was... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047882"
] | [
"PA0050_fam"
] | [
49
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00163019",
"PUB00163020"
] | [
"17581126",
"12644476"
] | [
"Responses of Pseudomonas aeruginosa to low oxygen indicate that growth in the cystic fibrosis lung is by aerobic respiration.",
"Identification, timing, and signal specificity of Pseudomonas aeruginosa quorum-controlled genes: a transcriptome analysis."
] | [
2007,
2003
] | 2 | [] | [] | 0 | 0 | null | [
"Diploscapter pachys",
"Pseudomonas"
] | [
2,
47
] | 2 | [] | [] | 0 | true | Family | PA0050-like | PA0050-like | PA0050-like | 3 |
IPR061230 | 61,230 | PDxFFG domain | PDxFFG_dom | Domain | 143 | false | false | This model represents the conserved N-terminal domain of family of large proteins with signal peptides, found in Mycoplasmatota. A short conserved N-terminal domain and a large conserved C-terminal domain are separated by poorly conserved regions of variable length in members of this group. This domain is named for its... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF012210"
] | [
"PDxFFG"
] | [
143
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Mycoplasmatota"
] | [
143
] | 1 | [] | [] | 0 | true | Domain | PDxFFG domain | PDxFFG domain | PDxFFG_dom | 6 |
IPR061234 | 61,234 | Type I-G CRISPR-associated protein | Cas3-like_IG | Family | 176 | false | false | This protein occurs in Cas (CRISPR-associated) protein regions of type I-G CRISPR/Cas systems, occasionally as an extra C-terminal domain of a long Cas3 protein. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF049934"
] | [
"adjac_Cas3_IG"
] | [
176
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"mine drainage metagenome"
] | [
173,
3
] | 2 | [] | [] | 0 | true | Family | Type I-G CRISPR-associated protein | Type I-G CRISPR-associated protein | Cas3-like_IG | 3 |
IPR061235 | 61,235 | SCO6881-like | SCO6881-like | Family | 306 | false | false | This family is named for SCO6881 from Streptomyces coelicolor ( ), a protein of length 462, largely hydrophobic through most of its length, although the C-terminal 140 amino acid region is low-complexity sequence, rich in Gly, Pro, Ser, Thr, and Asp. One article calls it homologous to CmdD ( ), which resembles it in ov... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047967"
] | [
"SCO6881_fam"
] | [
306
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162978"
] | [
"19650935"
] | [
"cmdABCDEF, a cluster of genes encoding membrane proteins for differentiation and antibiotic production in Streptomyces coelicolor A3(2)."
] | [
2009
] | 1 | [] | [] | 0 | 0 | null | [
"Streptomycetaceae"
] | [
306
] | 1 | [] | [] | 0 | true | Family | SCO6881-like | SCO6881-like | SCO6881-like | 5 |
IPR061237 | 61,237 | After-VIT domain | After_VWA_1 | Domain | 130 | false | false | The after-VIT domain is a bacterial surface protein C-terminal domain found on some proteins that have both the Vault protein Inter-alpha-Trypsin (VIT) domain and a von Willebrand factor type A domain. Some of after-VIT domain-containing proteins may have a known C-terminal sorting signal, such as LPXTG or PEP-CTERM, i... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033769"
] | [
"after_VWA_1"
] | [
130
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Cyanobacteriota"
] | [
130
] | 1 | [] | [] | 0 | true | Domain | After-VIT domain | After-VIT domain | After_VWA_1 | 5 |
IPR061238 | 61,238 | AAA family ATPase, Pro-rich N-terminal domain | Pro-rich_N | Domain | 387 | false | false | This entry represents an extremely rich N-terminal domain that is well-conserved for a family of AAA family ATPases seen in Streptomyces. It is an unusual, low-complexity domain. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040555"
] | [
"Pro-rich_NTERM"
] | [
387
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Streptomyces"
] | [
387
] | 1 | [] | [] | 0 | true | Domain | AAA family ATPase, Pro-rich N-terminal domain | AAA family ATPase, Pro-rich N-terminal domain | Pro-rich_N | 8 |
IPR061240 | 61,240 | PTPA-CTERM protein sorting domain | PTPA-CTERM | Domain | 74 | false | false | This C-terminal sorting and processing signal, called PTPA-CTERM, is a variant of the widespread PEP-CTERM domain. It is restricted a subset of Cyanobacteria that encode cognate sorting enzyme, named cyanoexosortase C (CrtC), and frequently is encoded near its sorting enzyme. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033465"
] | [
"PTPA-CTERM"
] | [
74
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Cyanobacteriota"
] | [
74
] | 1 | [] | [] | 0 | true | Domain | PTPA-CTERM protein sorting domain | PTPA-CTERM protein sorting domain | PTPA-CTERM | 6 |
IPR061241 | 61,241 | Biofilm-regulating peptide BriC-like | BriC-like | Family | 37 | false | false | BriC (Biofilm-Regulating peptide Induced by Competence), as characterised in Streptococcus pneumoniae, is a cell-cell communication peptide, or peptide pheromone, that is induced by expression of ComE (a master regulator of competence). BriC contributes to biofilm formation, and to colonisation in a mouse mole. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033771"
] | [
"colonize_BriC"
] | [
37
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105308"
] | [
"30308062"
] | [
"Function of BriC peptide in the pneumococcal competence and virulence portfolio."
] | [
2018
] | 1 | [] | [] | 0 | 0 | null | [
"Streptococcus"
] | [
37
] | 1 | [] | [] | 0 | true | Family | Biofilm-regulating peptide BriC-like | Biofilm-regulating peptide BriC-like | BriC-like | 4 |
IPR061242 | 61,242 | Cpg-like | Cpg-like | Family | 38 | false | false | Cpg1 (Cowdria polymorphic gene 1) was described in Ehrlichia (previously Cowdria) ruminantium and investigated as a possible vaccine antigen. E. ruminantium, an obligate intracellular pathogen, causes the disease heartwater. Members of this family are found in additional species of Ehrlichia, as well as in Anaplasma an... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047987"
] | [
"cpg1_fam"
] | [
38
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00163161",
"PUB00163162"
] | [
"12381580",
"37042556"
] | [
"Sequencing of a 15-kb Ehrlichia ruminantium clone and evaluation of the cpg1 open reading frame for protection against heartwater.",
"Th1 and Th2 epitopes of Cowdria polymorphic gene 1 of Ehrlichia ruminantium."
] | [
2002,
2023
] | 2 | [] | [] | 0 | 0 | null | [
"Anaplasmataceae",
"Hevea brasiliensis"
] | [
37,
1
] | 2 | [] | [] | 0 | true | Family | Cpg-like | Cpg-like | Cpg-like | 8 |
IPR061244 | 61,244 | EYxxD motif small membrane protein | Small_EYxxD | Family | 111 | false | false | This family includes small proteins with an EYxxD-like motif (for which it is named) near its N terminus, a 20-residue highly hydrophobic stretch, and a short, positively charged region rich in Lys and Arg residues, for an average length in one clade of 36 residues. Strong upstream RBS motifs, ATG start codons, appropr... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045534"
] | [
"small_EYxxD"
] | [
111
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
111
] | 1 | [] | [] | 0 | true | Family | EYxxD motif small membrane protein | EYxxD motif small membrane protein | Small_EYxxD | 6 |
IPR061245 | 61,245 | ICE element protein Mbov_0400-like | ICE_Mbov_0400-like | Family | 139 | false | false | Members of this family that have been identified as belonging to Integrating Conjugative Elements (ICE) include Mbov_0400 from Mycoplasmopsis bovis, MLC_3590 and MLC_3600 from Mycoplasma mycoides subsp. capri, and MAGa3690 from Mycoplasma agalactiae. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045891"
] | [
"ICE_Mbov_0400"
] | [
139
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159433",
"PUB00159434",
"PUB00159791"
] | [
"21324191",
"22693604",
"25527550"
] | [
"Mycoplasma mycoides, from \"mycoides Small Colony\" to \"capri\". A microevolutionary perspective.",
"Comparative geno-plasticity analysis of Mycoplasma bovis HB0801 (Chinese isolate).",
"Integrative conjugative elements are widespread in field isolates of Mycoplasma species pathogenic for ruminants."
] | [
2011,
2012,
2015
] | 3 | [] | [] | 0 | 0 | null | [
"Mycoplasmatota"
] | [
139
] | 1 | [] | [] | 0 | true | Family | ICE element protein Mbov_0400-like | ICE element protein Mbov_0400-like | ICE_Mbov_0400-like | 5 |
IPR061246 | 61,246 | DxFTY motif-containing membrane protein | DxFTY_mem_plasm | Family | 66 | false | false | This protein family includes a number membrane proteins of Spiroplasmas and Mycoplasmas, and is named for its best-conserved motif, D-X-F-T-[YF], including MAG3450 from Mycoplasmopsis agalactiae PG2, and its homologues (see ). | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF046003"
] | [
"DxFTY_mem_plasm"
] | [
66
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Mollicutes"
] | [
66
] | 1 | [] | [] | 0 | true | Family | DxFTY motif-containing membrane protein | DxFTY motif-containing membrane protein | DxFTY_mem_plasm | 2 |
IPR061247 | 61,247 | AAWKG-containing, N-terminal domain | AAWKG-cont_N | Domain | 237 | false | false | This domain is found in a group of proteins primarily from Streptomyces. A region outside of this domain contains 9-residue repeats that resemble the 18-residue repeats found by in the C-terminal region of eukaryotic T-complex protein 10. This group of proteins is named for the family's most prominent motif, AAWKG, to ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038047"
] | [
"not_Tcp10"
] | [
237
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Actinomycetes"
] | [
237
] | 1 | [] | [] | 0 | true | Domain | AAWKG-containing, N-terminal domain | AAWKG-containing, N-terminal domain | AAWKG-cont_N | 2 |
IPR061251 | 61,251 | Type VI secretion system tip protein TssI/VgrG, short form | T6SS_TssI_Fran | Family | 31 | false | false | Members of this family are TssI/VgrG proteins of type VI secretion systems of a variant short form found in Francisella tularensis and related species. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041249"
] | [
"T6SS_TssI_Fran"
] | [
31
] | 1 | [] | [] | [] | 0 | [
"6u9e",
"6u9f",
"6u9g"
] | 3 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Gammaproteobacteria"
] | [
31
] | 1 | [] | [] | 0 | true | Family | Type VI secretion system tip protein TssI/VgrG, short form | Type VI secretion system tip protein TssI/VgrG, short form | T6SS_TssI_Fran | 3 |
IPR061253 | 61,253 | Garvicin Q family class II bacteriocin, core domain | GarQ_core | Domain | 95 | false | false | This entry represents the core (mature) peptide region of GarQ, the class II bacteriocin garvicin (garvieacin) Q, and homologous peptides with similar core regions. Some members, such as GarQ itself, have a classical GlyGly-containing ComC/BlpC-like leader peptide, but others have N-terminal regions (probable leader pe... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033837"
] | [
"GarQ_core"
] | [
95
] | 1 | [] | [] | [] | 0 | [
"9oil",
"9wju",
"9wjw"
] | 3 | [
"PUB00105364",
"PUB00105365",
"PUB00105366"
] | [
"22210221",
"28827688",
"30361679"
] | [
"Garvieacin Q, a novel class II bacteriocin from Lactococcus garvieae BCC 43578.",
"The Non-Lantibiotic Bacteriocin Garvicin Q Targets Man-PTS in a Broad Spectrum of Sensitive Bacterial Genera.",
"The extracellular loop of Man-PTS subunit IID is responsible for the sensitivity of Lactococcus garvieae to garvici... | [
2012,
2017,
2018
] | 3 | [] | [] | 0 | 0 | null | [
"Bacillati"
] | [
95
] | 1 | [] | [] | 0 | true | Domain | Garvicin Q family class II bacteriocin, core domain | Garvicin Q family class II bacteriocin, core domain | GarQ_core | 7 |
IPR061254 | 61,254 | Putative surface protein MAG1430-like, central domain | MAG1430-like_central | Domain | 58 | false | false | This entry represents a well-conserved central region of putative proteins from the Mycoplasmatota. Member proteins have apparent N-terminal signal-anchor sequences but are not lipoproteins. The family is highly divergent, but the motif S[FY]ANDxxGxL[FY]L is extremely well conserved. The function is unknown. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045954"
] | [
"MAG1430_dom"
] | [
58
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Mycoplasmatota"
] | [
58
] | 1 | [] | [] | 0 | true | Domain | Putative surface protein MAG1430-like, central domain | Putative surface protein MAG1430-like, central domain | MAG1430-like_central | 4 |
IPR061255 | 61,255 | Sigma factor SigX-regulated lipoprotein | SrpBC | Family | 113 | false | false | It has been reported that the expression of three genes, including srpA (LIMLP_06130), srpB (LIMLP_15890), and srpC, (LIMLP_03790), was regulated by the sigma factor SigX (LIMLP_03680) and anti-sigma factor Rsx (LIMLP_03685) in pathogenic species of Leptospira. This entry represents a group of proteins from Leptospira ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047530"
] | [
"SrpBC"
] | [
113
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159362"
] | [
"33301041"
] | [
"4-Methylcytosine DNA modification is critical for global epigenetic regulation and virulence in the human pathogen Leptospira interrogans."
] | [
2020
] | 1 | [] | [] | 0 | 0 | null | [
"Leptospira"
] | [
113
] | 1 | [] | [] | 0 | true | Family | Sigma factor SigX-regulated lipoprotein | Sigma factor SigX-regulated lipoprotein | SrpBC | 4 |
IPR061263 | 61,263 | TomO, hydrophobic C-terminal domain | C_TomO | Domain | 77 | false | false | This domain is found in Wolbachia-like bacteria and some lower eukaryotes. It occurs near the C terminus of distantly related paralogues such as WD_1278 and WD_0630. WD_1278 has been named TomO (toxic manipulator of oogenesis) for its effects on cultured Drosophila cells. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047986"
] | [
"C_WD1278_WD0630"
] | [
77
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162895",
"PUB00162896"
] | [
"27498563",
"29076641"
] | [
"Wolbachia Protein TomO Targets nanos mRNA and Restores Germ Stem Cells in Drosophila Sex-lethal Mutants.",
"Mi Casa es Su Casa: how an intracellular symbiont manipulates host biology."
] | [
2016,
2017
] | 2 | [] | [] | 0 | 0 | null | [
"Arthropoda",
"Bacteria"
] | [
32,
45
] | 2 | [] | [] | 0 | true | Domain | TomO, hydrophobic C-terminal domain | TomO, hydrophobic C-terminal domain | C_TomO | 6 |
IPR061264 | 61,264 | Loki-CTERM protein-sorting domain | Loki-CTERM | Domain | 93 | false | false | This C-terminal protein-sorting signal is mainly found in the Asgard archaea, including the Lokiarchaeota, but resembles the PGF-CTERM sorting signal found on the S-layer-forming major cell surface glycoprotein of halophilic archaea. The most likely sorting enzyme is archaeosortase H (ArtH, ), which is most closely rel... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033507"
] | [
"Loki-CTERM"
] | [
93
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00060405"
] | [
"22037399"
] | [
"Archaeosortases and exosortases are widely distributed systems linking membrane transit with posttranslational modification."
] | [
2012
] | 1 | [] | [] | 0 | 0 | null | [
"Bacillati",
"Promethearchaeaceae",
"marine sediment metagenome"
] | [
3,
10,
80
] | 3 | [] | [] | 0 | true | Domain | Loki-CTERM protein-sorting domain | Loki-CTERM protein-sorting domain | Loki-CTERM | 2 |
IPR061266 | 61,266 | VenA family class IV lanthipeptide | Lanti_IV_VenA | Family | 87 | false | false | Members of this family include VenA, precursor of the class IV lanthipeptide venezuelin, and all detectable homologues. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038147"
] | [
"lanti_IV_venA"
] | [
87
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105577"
] | [
"20351769"
] | [
"Discovery of unique lanthionine synthetases reveals new mechanistic and evolutionary insights."
] | [
2010
] | 1 | [] | [] | 0 | 0 | null | [
"Actinomycetes"
] | [
87
] | 1 | [] | [] | 0 | true | Family | VenA family class IV lanthipeptide | VenA family class IV lanthipeptide | Lanti_IV_VenA | 4 |
IPR061267 | 61,267 | MG406-like | MG406-like | Family | 66 | false | false | This protein family includes homologues to MG406 from Mycoplasma genitalium and MPN605 from Mycoplasma pneumoniae, which are about 150 amino acids long on average, highly hydrophobic, widespread in but restricted to the Mollicutes, and highly divergent there. MG406 itself appears to be essential. ATP synthase protein I... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033688"
] | [
"MG406_fam"
] | [
66
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105244"
] | [
"16407165"
] | [
"Essential genes of a minimal bacterium."
] | [
2006
] | 1 | [] | [] | 0 | 0 | null | [
"Bacillati"
] | [
66
] | 1 | [] | [] | 0 | true | Family | MG406-like | MG406-like | MG406-like | 2 |
IPR061269 | 61,269 | Selenite/tellurite reduction operon protein ExtJ-like | ExtJ-like | Family | 62 | false | false | ExtJ ( ), encoded within a selenite/tellurite reduction operon, has an N-terminal signal peptide, and an unusual Gly-Cys dipeptide at the C-terminal end. The length is variable, with the longer form averaging about 105 amino acids, and the shorter form averaging about 75. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040942"
] | [
"hypo_ExtJ"
] | [
62
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00106046"
] | [
"29534491"
] | [
"Characterization of a Novel Porin-Like Protein, ExtI, from Geobacter sulfurreducens and Its Implication in the Reduction of Selenite and Tellurite."
] | [
2018
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"ecological metagenomes"
] | [
60,
2
] | 2 | [] | [] | 0 | true | Family | Selenite/tellurite reduction operon protein ExtJ-like | Selenite/tellurite reduction operon protein ExtJ-like | ExtJ-like | 9 |
IPR061271 | 61,271 | Metal transporter CNNM-like, C-terminal CNBH domain | CNBH_CNNM2_C | Domain | 5,747 | false | false | This CNBH domain (cyclic nucleotide-binding homology domain) is found towards the C-terminal of human Metal transporter CNNM2 and similar proteins predominantly found in animals. CNNM2 is a divalent metal cation transporter. This domain does not bind cyclic nucleotides; instead, it mediates a flat-shaped dimerisation i... | [] | [] | [] | 0 | [
"PFAM"
] | [
"PF25562"
] | [
"CNBH_CNNM2_C"
] | [
5747
] | 1 | [] | [] | [] | 0 | [
"6dfd",
"6dj3",
"6g52",
"6mn6",
"6n7e"
] | 5 | [
"PUB00098025",
"PUB00111936",
"PUB00160601"
] | [
"31864811",
"30341174",
"31842432"
] | [
"Mg<sup>2+</sup>-ATP Sensing in CNNM, a Putative Magnesium Transporter.",
"The cyclic nucleotide-binding homology domain of the integral membrane protein CNNM mediates dimerization and is required for Mg<sup>2+</sup> efflux activity.",
"Structural Insights into the Intracellular Region of the Human Magnesium Tr... | [
2020,
2018,
2019
] | 3 | [] | [] | 0 | 0 | null | [
"Eukaryota",
"Spirosoma aureum"
] | [
5746,
1
] | 2 | [
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
4,
18,
1,
10,
9,
14
] | 6 | true | Domain | Metal transporter CNNM-like, C-terminal CNBH domain | Metal transporter CNNM-like, C-terminal CNBH domain | CNBH_CNNM2_C | 2 |
IPR061272 | 61,272 | Inhibitor of vertebrate lysozyme (Ivy)-like domain | Ivy | Domain | 2,314 | false | false | C-type lysozyme enzymes, such as hen egg white lysozyme (HEWL), provide anti-bacterial activity by cleaving peptidoglycan in Gram-positive bacterial cell walls. In humans, C-type lysozyme is found in all secretions, including tears and saliva. Certain Gram-positive bacteria can produce proteins with anti-lysozyme activ... | [] | [] | [] | 0 | [
"PFAM"
] | [
"PF08816"
] | [
"Ivy"
] | [
2314
] | 1 | [] | [] | [] | 0 | [
"1gpq",
"1uuz",
"1xs0",
"4ps6"
] | 4 | [
"PUB00027883",
"PUB00027919",
"PUB00042565"
] | [
"11278658",
"15141308",
"17405861"
] | [
"Escherichia coli ykfE ORFan gene encodes a potent inhibitor of C-type lysozyme.",
"Periplasmic lysozyme inhibitor contributes to lysozyme resistance in Escherichia coli.",
"Structure and evolution of the Ivy protein family, unexpected lysozyme inhibitors in Gram-negative bacteria."
] | [
2001,
2004,
2007
] | 3 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Halorubrum tibetense",
"Opisthokonta",
"ecological metagenomes"
] | [
2305,
1,
4,
4
] | 4 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Domain | Inhibitor of vertebrate lysozyme (Ivy)-like domain | Inhibitor of vertebrate lysozyme (Ivy)-like domain | Ivy | 3 |
IPR061274 | 61,274 | Afadin, Ras-associating domain 2 | RA2_Afadin | Domain | 3,244 | false | false | Afadin, also termed ALL1-fused gene from chromosome 6 protein (AF-6), is involved in many fundamental signalling cascades in cells. In addition, it is involved in oncogenesis and metastasis. AFDN belongs to the adhesion system, probably together with the E-cadherin-catenin system, that plays a role in the organisation ... | [] | [] | [] | 0 | [
"CDD"
] | [
"cd01781"
] | [
"RA2_Afadin"
] | [
3244
] | 1 | [
"REACTOME",
"REACTOME",
"REACTOME"
] | [
"R-HSA-418990",
"R-MMU-418990",
"R-RNO-418990"
] | [
"REACTOME:R-HSA-418990",
"REACTOME:R-MMU-418990",
"REACTOME:R-RNO-418990"
] | 3 | [
"1wxa"
] | 1 | [
"PUB00018559",
"PUB00031294",
"PUB00040466",
"PUB00069444",
"PUB00108730"
] | [
"12456712",
"15684424",
"16671149",
"23481206",
"20395419"
] | [
"Nectin and afadin: novel organizers of intercellular junctions.",
"Solution structure of AF-6 PDZ domain and its interaction with the C-terminal peptides from Neurexin and Bcr.",
"Discovery of low-molecular-weight ligands for the AF6 PDZ domain.",
"Afadin/AF-6 and canoe: roles in cell adhesion and beyond.",
... | [
2003,
2005,
2006,
2013,
2010
] | 5 | [
"IPR000159"
] | [] | 1 | 0 | 1 | [
"Eumetazoa"
] | [
3244
] | 1 | [
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
48,
8,
8,
4,
8
] | 5 | true | Domain | Afadin, Ras-associating domain 2 | Afadin, Ras-associating domain 2 | RA2_Afadin | 4 |
IPR061275 | 61,275 | Afadin, Ras-associating domain 1 | RA1_Afadin | Domain | 3,165 | false | false | This entry represents the first RA domain of afadin, which mediates its self-association [ , , , , ]. Afadin, also termed ALL1-fused gene from chromosome 6 protein (AF-6), is involved in many fundamental signalling cascades in cells. In addition, it is involved in oncogenesis and metastasis. AFDN belongs to the adhesio... | [] | [] | [] | 0 | [
"CDD"
] | [
"cd01782"
] | [
"RA1_Afadin"
] | [
3165
] | 1 | [
"REACTOME",
"REACTOME",
"REACTOME"
] | [
"R-HSA-418990",
"R-MMU-418990",
"R-RNO-418990"
] | [
"REACTOME:R-HSA-418990",
"REACTOME:R-MMU-418990",
"REACTOME:R-RNO-418990"
] | 3 | [] | 0 | [
"PUB00018559",
"PUB00031294",
"PUB00040466",
"PUB00069444",
"PUB00108730",
"PUB00108731"
] | [
"12456712",
"15684424",
"16671149",
"23481206",
"20395419",
"11024295"
] | [
"Nectin and afadin: novel organizers of intercellular junctions.",
"Solution structure of AF-6 PDZ domain and its interaction with the C-terminal peptides from Neurexin and Bcr.",
"Discovery of low-molecular-weight ligands for the AF6 PDZ domain.",
"Afadin/AF-6 and canoe: roles in cell adhesion and beyond.",
... | [
2003,
2005,
2006,
2013,
2010,
2000
] | 6 | [
"IPR000159"
] | [] | 1 | 0 | 1 | [
"Eumetazoa"
] | [
3165
] | 1 | [
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
5,
48,
8,
8,
7,
5
] | 6 | true | Domain | Afadin, Ras-associating domain 1 | Afadin, Ras-associating domain 1 | RA1_Afadin | 9 |
IPR061276 | 61,276 | Afadin, PDZ domain | PDZ_AFDN | Domain | 3,450 | false | false | This entry represents the PDZ (PSD-95 (Postsynaptic density protein 95), Dlg (Discs large protein), and ZO-1 (Zonula occludens-1)) domain of afadin (AFDN, also known as ALL1-fused gene from chromosome 6 protein (AF6) and MLLT4), and related animal proteins. The AFDN PDZ domain interaction partners include poliovirus re... | [] | [] | [] | 0 | [
"CDD"
] | [
"cd06789"
] | [
"PDZ_AFDN-like"
] | [
3450
] | 1 | [
"REACTOME",
"REACTOME",
"REACTOME"
] | [
"R-HSA-418990",
"R-MMU-418990",
"R-RNO-418990"
] | [
"REACTOME:R-HSA-418990",
"REACTOME:R-MMU-418990",
"REACTOME:R-RNO-418990"
] | 3 | [
"1t2m",
"1xz9",
"2ain",
"2exg",
"3axa",
"7mfw",
"7qcr"
] | 7 | [
"PUB00018559",
"PUB00031294",
"PUB00040466",
"PUB00069444",
"PUB00078424",
"PUB00108730",
"PUB00156108",
"PUB00156650",
"PUB00156652",
"PUB00156653"
] | [
"12456712",
"15684424",
"16671149",
"23481206",
"25534554",
"20395419",
"30712672",
"30473688",
"18173749",
"18052198"
] | [
"Nectin and afadin: novel organizers of intercellular junctions.",
"Solution structure of AF-6 PDZ domain and its interaction with the C-terminal peptides from Neurexin and Bcr.",
"Discovery of low-molecular-weight ligands for the AF6 PDZ domain.",
"Afadin/AF-6 and canoe: roles in cell adhesion and beyond.",
... | [
2003,
2005,
2006,
2013,
2015,
2010,
2019,
2018,
2008,
2007
] | 10 | [
"IPR001478"
] | [] | 1 | 0 | 1 | [
"Eumetazoa"
] | [
3450
] | 1 | [
"Caenorhabditis elegans",
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
15,
50,
9,
9,
4,
8
] | 6 | true | Domain | Afadin, PDZ domain | Afadin, PDZ domain | PDZ_AFDN | 7 |
IPR061277 | 61,277 | Rha78A-like, N-terminal immunoglobulin domain | Ig_Rha78A_N | Domain | 11,957 | false | false | This domain is found at the N-terminal of Alpha-L-rhamnosidase from Streptomyces avermitilis (Rha78A) and similar proteins. This domain adopts an immunoglobulin-like (Ig-like) fold. This domain is also found in the middle region of Bifunctional sulfatase/alpha-L-rhamnosidase. Rha78A is able to degrade p-nitrophenyl-alp... | [] | [] | [] | 0 | [
"PFAM"
] | [
"PF25788"
] | [
"Ig_Rha78A_N"
] | [
11957
] | 1 | [
"EC",
"METACYC"
] | [
"3.2.1.40",
"PWY-7134"
] | [
"EC:3.2.1.40",
"METACYC:PWY-7134"
] | 2 | [
"3w5m",
"3w5n",
"6dg5",
"6gsz",
"6i60"
] | 5 | [
"PUB00011520",
"PUB00021302",
"PUB00023642",
"PUB00024541",
"PUB00039525",
"PUB00040414",
"PUB00065054",
"PUB00160632"
] | [
"10632887",
"10736232",
"10210178",
"10753826",
"16293754",
"16477002",
"23291751",
"30387766"
] | [
"The thermostable alpha-L-rhamnosidase RamA of Clostridium stercorarium: biochemical characterization and primary structure of a bacterial alpha-L-rhamnoside hydrolase, a new type of inverting glycoside hydrolase.",
"The solution structure of the cytokine-binding domain of the common beta-chain of the receptors f... | [
2000,
2000,
1999,
2000,
2005,
2006,
2013,
2018
] | 8 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Caudoviricetes",
"Eukaryota",
"unclassified sequences"
] | [
92,
9289,
31,
2421,
124
] | 5 | [
"Homo sapiens",
"Mus musculus"
] | [
2,
1
] | 2 | true | Domain | Rha78A-like, N-terminal immunoglobulin domain | Rha78A-like, N-terminal immunoglobulin domain | Ig_Rha78A_N | 1 |
IPR061279 | 61,279 | Afadin, forkhead associated domain | FHA_AFDN | Domain | 3,242 | false | false | This is the FHA domain of afardin. FHA domain is a small phosphopeptide recognition module, but this group may lack the conserved residues that are required for binding phosphothreonine [ , , , , ]. Afadin, also termed ALL1-fused gene from chromosome 6 protein (AF-6), is involved in many fundamental signalling cascades... | [] | [] | [] | 0 | [
"CDD"
] | [
"cd22711"
] | [
"FHA_AFDN"
] | [
3242
] | 1 | [
"REACTOME",
"REACTOME",
"REACTOME"
] | [
"R-HSA-418990",
"R-MMU-418990",
"R-RNO-418990"
] | [
"REACTOME:R-HSA-418990",
"REACTOME:R-MMU-418990",
"REACTOME:R-RNO-418990"
] | 3 | [
"1wln"
] | 1 | [
"PUB00018559",
"PUB00031294",
"PUB00040466",
"PUB00069444",
"PUB00108730",
"PUB00108732",
"PUB00108733"
] | [
"12456712",
"15684424",
"16671149",
"23481206",
"20395419",
"9679199",
"8242616"
] | [
"Nectin and afadin: novel organizers of intercellular junctions.",
"Solution structure of AF-6 PDZ domain and its interaction with the C-terminal peptides from Neurexin and Bcr.",
"Discovery of low-molecular-weight ligands for the AF6 PDZ domain.",
"Afadin/AF-6 and canoe: roles in cell adhesion and beyond.",
... | [
2003,
2005,
2006,
2013,
2010,
1998,
1993
] | 7 | [
"IPR000253"
] | [] | 1 | 0 | 1 | [
"Eumetazoa"
] | [
3242
] | 1 | [
"Danio rerio",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
48,
10,
4,
8
] | 4 | true | Domain | Afadin, forkhead associated domain | Afadin, forkhead associated domain | FHA_AFDN | 6 |
IPR061281 | 61,281 | Protein of unknown function DUF272 | DUF272 | Family | 135 | false | false | This protein family represents a group of proteins from Caenorhabditis species that have no known function. | [] | [] | [] | 0 | [
"PANTHER"
] | [
"PTHR21516"
] | [
""
] | [
135
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Rhabditomorpha"
] | [
135
] | 1 | [
"Caenorhabditis elegans"
] | [
37
] | 1 | true | Family | Protein of unknown function DUF272 | Protein of unknown function DUF272 | DUF272 | 1 |
IPR061283 | 61,283 | Ephrin, cysteine rich domain | EPH_CRD | Domain | 20,982 | false | false | This entry represents the cysteine-rich domain found in ephrin proteins. Ephrins are important cell surface proteins that act as ligands for Eph receptor tyrosine kinases There are 10 EphA receptors and six EphB receptors, distinguished on sequence difference and binding preferences. They interact with the six glycosyl... | [] | [] | [] | 0 | [
"PFAM"
] | [
"PF25599"
] | [
"Ephrin_CRD"
] | [
20982
] | 1 | [
"EC",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
... | [
"2.7.10.1",
"R-DRE-2682334",
"R-DRE-3928662",
"R-DRE-3928663",
"R-DRE-3928664",
"R-DRE-3928665",
"R-GGA-2682334",
"R-GGA-3928663",
"R-GGA-3928665",
"R-HSA-2682334",
"R-HSA-2892247",
"R-HSA-373760",
"R-HSA-3928662",
"R-HSA-3928663",
"R-HSA-3928664",
"R-HSA-3928665",
"R-HSA-9013149",
... | [
"EC:2.7.10.1",
"REACTOME:R-DRE-2682334",
"REACTOME:R-DRE-3928662",
"REACTOME:R-DRE-3928663",
"REACTOME:R-DRE-3928664",
"REACTOME:R-DRE-3928665",
"REACTOME:R-GGA-2682334",
"REACTOME:R-GGA-3928663",
"REACTOME:R-GGA-3928665",
"REACTOME:R-HSA-2682334",
"REACTOME:R-HSA-2892247",
"REACTOME:R-HSA-373... | 45 | [
"2x10",
"2x11",
"3fl7",
"3mbw",
"3mx0",
"4bk4",
"4bk5",
"4bka",
"4bkf",
"4m4p",
"4m4r",
"7k7j",
"7s7k",
"8trs",
"8trt",
"8trv",
"8tv1",
"8tv5"
] | 18 | [
"PUB00004289",
"PUB00010665",
"PUB00052266",
"PUB00059869",
"PUB00065391",
"PUB00073291",
"PUB00160614",
"PUB00160615",
"PUB00160616"
] | [
"9853759",
"11780069",
"19525919",
"20228801",
"20505120",
"23021982",
"23812375",
"23959867",
"33770085"
] | [
"Crystal structure of the ligand-binding domain of the receptor tyrosine kinase EphB2.",
"Crystal structure of an Eph receptor-ephrin complex.",
"Ligand recognition by A-class Eph receptors: crystal structures of the EphA2 ligand-binding domain and the EphA2/ephrin-A1 complex.",
"An extracellular steric seedi... | [
1998,
2001,
2009,
2010,
2010,
2012,
2013,
2013,
2021
] | 9 | [] | [] | 0 | 0 | null | [
"Eukaryota"
] | [
20982
] | 1 | [
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
91,
11,
53,
47,
57
] | 5 | true | Domain | Ephrin, cysteine rich domain | Ephrin, cysteine rich domain | EPH_CRD | 1 |
IPR061284 | 61,284 | DDX60, middle domain | TPR_DDX60 | Domain | 893 | false | false | This entry represents a middle domain in DDX60 and similar proteins. This domain contains a helical fold. DDX60 binds ssRNA, dsRNA and dsDNA and can promote the binding of RIGI to dsRNA. DDX60 is non-essential in mammals [ ] but it is required for the cell fitness in kinetoplastids and trypanosomatids and plays a speci... | [] | [] | [] | 0 | [
"PFAM"
] | [
"PF26167"
] | [
"TPR_DDX60"
] | [
893
] | 1 | [
"EC",
"METACYC"
] | [
"3.6.4.-",
"PWY-7250"
] | [
"EC:3.6.4.-",
"METACYC:PWY-7250"
] | 2 | [] | 0 | [
"PUB00056836",
"PUB00140287",
"PUB00154169"
] | [
"21478870",
"21791617",
"33357443"
] | [
"A diverse range of gene products are effectors of the type I interferon antiviral response.",
"DDX60, a DEXD/H box helicase, is a novel antiviral factor promoting RIG-I-like receptor-mediated signaling.",
"Structural Differences in Translation Initiation between Pathogenic Trypanosomatids and Their Mammalian H... | [
2011,
2011,
2020
] | 3 | [] | [] | 0 | 0 | null | [
"Eukaryota"
] | [
893
] | 1 | [
"Caenorhabditis elegans",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus",
"Schizosaccharomyces pombe (strain 972 / ATCC 24843)"
] | [
1,
7,
2,
7,
1
] | 5 | true | Domain | DDX60, middle domain | DDX60, middle domain | TPR_DDX60 | 8 |
IPR061285 | 61,285 | Rho GTPase-activating protein 18-like, RhoGAP domain | RhoGAP_ARHGAP18-like | Domain | 2,729 | false | false | This entry represents the RhoGAP (GTPase-activator protein [GAP] for Rho-like small GTPases) domain of Rho GTPase-activating protein 18/28 (ARHGAP18/28) and similar animal proteins. ARHGAP18 suppresses F-actin polymerisation by inhibiting Rho [ ]. It plays a key role in tissue tension and 3D tissue shape by regulating ... | [] | [] | [] | 0 | [
"CDD"
] | [
"cd04391"
] | [
"RhoGAP_ARHGAP18"
] | [
2729
] | 1 | [
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME",
"REACTOME"
] | [
"R-DME-8980692",
"R-DME-9013148",
"R-HSA-8980692",
"R-HSA-9013106",
"R-MMU-8980692",
"R-MMU-9013106"
] | [
"REACTOME:R-DME-8980692",
"REACTOME:R-DME-9013148",
"REACTOME:R-HSA-8980692",
"REACTOME:R-HSA-9013106",
"REACTOME:R-MMU-8980692",
"REACTOME:R-MMU-9013106"
] | 6 | [] | 0 | [
"PUB00160465",
"PUB00160466"
] | [
"21865595",
"25778702"
] | [
"ARHGAP18, a GTPase-activating protein for RhoA, controls cell shape, spreading, and motility.",
"YAP is essential for tissue tension to ensure vertebrate 3D body shape."
] | [
2011,
2015
] | 2 | [
"IPR000198"
] | [] | 1 | 0 | 1 | [
"Bilateria"
] | [
2729
] | 1 | [
"Danio rerio",
"Drosophila melanogaster",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
7,
2,
6,
5,
7
] | 5 | true | Domain | Rho GTPase-activating protein 18-like, RhoGAP domain | Rho GTPase-activating protein 18-like, RhoGAP domain | RhoGAP_ARHGAP18-like | 3 |
IPR061286 | 61,286 | SepQ/SsaQ | SepQ/SsaQ | Family | 668 | false | false | This entry represents Secretion system apparatus protein SsaQ from Salmonella typhimurium and similar proteins from enterobacterales. SsaQ is part of a type III secretion system [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF005956"
] | [
"PRK08035.1"
] | [
668
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00097916"
] | [
"24722491"
] | [
"Functional characterization of the type III secretion ATPase SsaN encoded by Salmonella pathogenicity island 2."
] | [
2014
] | 1 | [
"IPR013385"
] | [] | 1 | 0 | 1 | [
"Enterobacterales"
] | [
668
] | 1 | [] | [] | 0 | true | Family | SepQ/SsaQ | SepQ/SsaQ | SepQ/SsaQ | 7 |
IPR061287 | 61,287 | Synaptosomal-associated protein 47, N-terminal SNARE domain | SNARE_SNAP47N | Domain | 950 | false | false | This entry represents the N-terminal SNARE domain of SNAP47 (Synaptosomal-associated protein 47), a member of the Qb/Qc subfamily of SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) proteins. SNAP47 is a SNARE protein that may play a role in intracellular membrane fusion and is involved in ... | [] | [] | [] | 0 | [
"CDD"
] | [
"cd15888"
] | [
"SNARE_SNAP47N"
] | [
950
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00018360",
"PUB00020397",
"PUB00032793",
"PUB00113733",
"PUB00113734",
"PUB00134575",
"PUB00134576"
] | [
"9861047",
"11737951",
"9731768",
"11252968",
"11066058",
"16621800",
"25247712"
] | [
"Conserved structural features of the synaptic fusion complex: SNARE proteins reclassified as Q- and R-SNAREs.",
"The syntaxins.",
"The synaptic SNARE complex is a parallel four-stranded helical bundle.",
"SNARE-mediated membrane fusion.",
"Fusion of membranes during the acrosome reaction: a tale of two SNA... | [
1998,
2001,
1998,
2001,
2000,
2006,
2014
] | 7 | [
"IPR000727"
] | [] | 1 | 0 | 1 | [
"Deuterostomia"
] | [
950
] | 1 | [
"Danio rerio",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
2,
10,
4,
2
] | 4 | true | Domain | Synaptosomal-associated protein 47, N-terminal SNARE domain | Synaptosomal-associated protein 47, N-terminal SNARE domain | SNARE_SNAP47N | 3 |
IPR061288 | 61,288 | Synaptosomal-associated protein 47, C-terminal SNARE domain | SNARE_SNAP47C | Domain | 236 | false | false | This entry represents the C-terminal SNARE domain of SNAP47 (Synaptosomal-associated protein 47), a member of the Qb/Qc subfamily of SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) proteins. SNAP47 is a SNARE protein that may play a role in intracellular membrane fusion and is involved in ... | [] | [] | [] | 0 | [
"CDD"
] | [
"cd15854"
] | [
"SNARE_SNAP47C"
] | [
236
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00018360",
"PUB00020397",
"PUB00032793",
"PUB00113725",
"PUB00113733",
"PUB00113734",
"PUB00113735",
"PUB00134575",
"PUB00134576"
] | [
"9861047",
"11737951",
"9731768",
"9635186",
"11252968",
"11066058",
"11718851",
"16621800",
"25247712"
] | [
"Conserved structural features of the synaptic fusion complex: SNARE proteins reclassified as Q- and R-SNAREs.",
"The syntaxins.",
"The synaptic SNARE complex is a parallel four-stranded helical bundle.",
"Membrane fusion: all done with SNAREpins?",
"SNARE-mediated membrane fusion.",
"Fusion of membranes ... | [
1998,
2001,
1998,
1998,
2001,
2000,
2001,
2006,
2014
] | 9 | [
"IPR000727"
] | [] | 1 | 0 | 1 | [
"Deuterostomia"
] | [
236
] | 1 | [
"Danio rerio",
"Homo sapiens",
"Rattus norvegicus"
] | [
2,
3,
1
] | 3 | true | Domain | Synaptosomal-associated protein 47, C-terminal SNARE domain | Synaptosomal-associated protein 47, C-terminal SNARE domain | SNARE_SNAP47C | 3 |
IPR061289 | 61,289 | Minor curlin subunit | CsgB | Family | 648 | false | false | This protein family includes Minor curlin subunit from Escherichia coli (CsgB) and similar proteins from enterobacteriales. CsgB is the structural subunit of the curli fimbriae and functions as a nucleator in the assembly of curlin monomers. Curli, which can bind to fibronectin, are coiled surface structures that assem... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF007506"
] | [
"PRK10101.1"
] | [
648
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00086869",
"PUB00104551",
"PUB00163224"
] | [
"24097954",
"31932609",
"22493266"
] | [
"Cellulose as an architectural element in spatially structured Escherichia coli biofilms.",
"Assembly and substrate recognition of curli biogenesis system.",
"The E. coli CsgB nucleator of curli assembles to β-sheet oligomers that alter the CsgA fibrillization mechanism."
] | [
2013,
2020,
2012
] | 3 | [] | [] | 0 | 0 | null | [
"Gammaproteobacteria",
"Tylenchina"
] | [
646,
2
] | 2 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Family | Minor curlin subunit | Minor curlin subunit | CsgB | 5 |
IPR061290 | 61,290 | Carotenoid hydratase CrtC | CrtC | Family | 749 | false | false | This entry represents the acyclic carotenoid 1,2-hydratase (CrtC) from photosynthetic bacteria including Rhodobacter and Cereibacter species. CrtC functions as a lycopene hydratase ( ) in the biosynthesis of carotenoids spheroidene and spirilloxanthin. It catalyses the hydration of neurosporene to hydroxyneurosporene a... | [] | [] | [] | 0 | [
"PFAM",
"CDD"
] | [
"PF27123",
"cd21471"
] | [
"CrtC_C",
"CrtC-like"
] | [
747,
745
] | 2 | [
"EC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC",
"METACYC"
] | [
"4.2.1.131",
"PWY-6279",
"PWY-6286",
"PWY-6581",
"PWY-7591",
"PWY-7940",
"PWY-7947"
] | [
"EC:4.2.1.131",
"METACYC:PWY-6279",
"METACYC:PWY-6286",
"METACYC:PWY-6581",
"METACYC:PWY-7591",
"METACYC:PWY-7940",
"METACYC:PWY-7947"
] | 7 | [] | 0 | [
"PUB00013014",
"PUB00141387",
"PUB00145344",
"PUB00145345",
"PUB00145346",
"PUB00145347",
"PUB00145348",
"PUB00145349",
"PUB00145350",
"PUB00145351",
"PUB00145352"
] | [
"12745254",
"12788703",
"26481619",
"21590288",
"1612412",
"19136077",
"11114184",
"7721699",
"21921032",
"2747617",
"14734565"
] | [
"Heterologous expression, purification, and enzymatic characterization of the acyclic carotenoid 1,2-hydratase from Rubrivivax gelatinosus.",
"Genes involved in the biosynthesis of photosynthetic pigments in the purple sulfur photosynthetic bacterium Thiocapsa roseopersicina.",
"Identification of catalytically ... | [
2003,
2003,
2016,
2011,
1992,
2009,
2000,
1995,
2011,
1989,
2004
] | 11 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Chiloscyllium punctatum",
"freshwater sediment metagenome"
] | [
747,
1,
1
] | 3 | [] | [] | 0 | true | Family | Carotenoid hydratase CrtC | Carotenoid hydratase CrtC | CrtC | 6 |
IPR061293 | 61,293 | Type IV secretion system protein VirB5 | VirB5 | Family | 659 | false | false | This entry contains VirB5, a protein that is involved in the type IV DNA secretion systems typified by the Agrobacterium Ti plasmid vir system where it interacts with several other proteins essential for proper pilus formation [ ]. VirB5 is homologous to the IncN (N-type) conjugation system protein TraC [ ] as well as ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"TIGR02791"
] | [
"VirB5"
] | [
659
] | 1 | [] | [] | [] | 0 | [
"7o3v",
"8rt9",
"8rtd"
] | 3 | [
"PUB00020399",
"PUB00034402",
"PUB00034409"
] | [
"14673074",
"12855161",
"15901731"
] | [
"Structural and functional characterization of the VirB5 protein from the type IV secretion system encoded by the conjugative plasmid pKM101.",
"F factor conjugation is a true type IV secretion system.",
"Identification of the VirB4-VirB8-VirB5-VirB2 pilus assembly sequence of type IV secretion systems."
] | [
2003,
2003,
2005
] | 3 | [
"IPR014158"
] | [] | 1 | 0 | 1 | [
"Bacteria",
"Opisthokonta",
"metagenomes"
] | [
652,
2,
5
] | 3 | [] | [] | 0 | true | Family | Type IV secretion system protein VirB5 | Type IV secretion system protein VirB5 | VirB5 | 2 |
IPR061299 | 61,299 | Transcriptional regulator HrcA | HrcA_epsilonbact | Family | 264 | false | false | This entry is restricted to HrcA proteins from epsilonbacteria. HrcA proteins are heat-inducible transcription repressors that negatively regulate class I heat shock genes including grpE-dnaK- dnaJ and groELS operons [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF003033"
] | [
"PRK03911.1"
] | [
264
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162492"
] | [
"31765672"
] | [
"Mechanism of HrcA function in heat shock regulation in Mycobacterium tuberculosis."
] | [
2020
] | 1 | [
"IPR002571"
] | [] | 1 | 0 | 1 | [
"Campylobacterales"
] | [
264
] | 1 | [] | [] | 0 | true | Family | Transcriptional regulator HrcA | Transcriptional regulator HrcA | HrcA_epsilonbact | 9 |
IPR061300 | 61,300 | AzlC-like, N-terminal domain | AzlC-like_N | Domain | 22,000 | false | false | This entry represents a domain found at the N-terminal of some uncharacterised bacterial proteins and the branched-chain amino acid transport protein AzlC encoded by azlC gene, which is part of the azl operon, involved in branched-chain amino acid transport [ ]. AzlCD is a bipartite histidine exporter consisting of Azl... | [] | [] | [] | 0 | [
"PFAM"
] | [
"PF03591"
] | [
"AzlC"
] | [
22000
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00011254",
"PUB00152867"
] | [
"9287000",
"36377869"
] | [
"An lrp-like gene of Bacillus subtilis involved in branched-chain amino acid transport.",
"How To Deal with Toxic Amino Acids: the Bipartite AzlCD Complex Exports Histidine in <i>Bacillus subtilis</i>."
] | [
1997,
2022
] | 2 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"unclassified sequences"
] | [
436,
21288,
13,
263
] | 4 | [
"Escherichia coli (strain K12)"
] | [
1
] | 1 | true | Domain | AzlC-like, N-terminal domain | AzlC-like, N-terminal domain | AzlC-like_N | 3 |
IPR061301 | 61,301 | Oxamate carbamoyltransferase subunit AllF | AllF | Family | 2,341 | false | false | This protein family includes Oxamate carbamoyltransferase subunit AllF from Escherichia coli and similar bacterial proteins. AllF is a component of a carbamoyltransferase involved in the anaerobic nitrogen utilisation via the assimilation of allantoin that catalyses the conversion of oxalurate (N-carbamoyl-2-oxoglycine... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF004760"
] | [
"PRK06091.1"
] | [
2341
] | 1 | [] | [] | [] | 0 | [
"3dmy"
] | 1 | [
"PUB00155434",
"PUB00162022"
] | [
"38888336",
"34494882"
] | [
"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>).",
"An Escherichia coli FdrA Variant Derived from Syntrophic Coculture with a Methanogen Increases Succinate Production Due to Changes in Allantoin Degradation."
] | [
2024,
2021
] | 2 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"ecological metagenomes"
] | [
4,
2320,
2,
15
] | 4 | [
"Escherichia coli (strain K12)"
] | [
2
] | 1 | true | Family | Oxamate carbamoyltransferase subunit AllF | Oxamate carbamoyltransferase subunit AllF | AllF | 2 |
IPR061302 | 61,302 | SPI-1 type III secretion system effector SipA | SipA | Family | 703 | false | false | Salmonella invasion protein A (SipA) is a virulence factor that is translocated into host cells by a type III secretion system. In the host cell it binds to actin, stimulates actin polymerisation and counteracts F-actin destabilising proteins. This contributes towards cytoskeletal rearrangements that allow the entry of... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF011903"
] | [
"PRK15376.1"
] | [
703
] | 1 | [] | [] | [] | 0 | [
"8vfm"
] | 1 | [
"PUB00054077",
"PUB00163366"
] | [
"11331579",
"25486861"
] | [
"Cooperation between actin-binding proteins of invasive Salmonella: SipA potentiates SipC nucleation and bundling of actin.",
"PERP, a host tetraspanning membrane protein, is required for Salmonella-induced inflammation."
] | [
2001,
2015
] | 2 | [] | [] | 0 | 0 | null | [
"Pseudomonadota"
] | [
703
] | 1 | [] | [] | 0 | true | Family | SPI-1 type III secretion system effector SipA | SPI-1 type III secretion system effector SipA | SipA | 3 |
IPR061303 | 61,303 | Channel accessory protein ArfC, N-terminal domain | Rv0901_ArfC_N | Domain | 154 | false | false | The three-gene arf (Ammonia Release Facilitator) operon in Mycobacterium tuberculosis encodes proteins called ArfA (or OmpATb), ArfB, and ArfC. Most versions of ArfC, including Rv0901 from M. tuberculosis, contain a spacer region and then a C-terminal 'sunset' domain, but some ArfC lack the spacer region and sunset dom... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF051455"
] | [
"Rv0901_ArfC_N"
] | [
154
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00101374",
"PUB00161803",
"PUB00161804"
] | [
"22206986",
"19168955",
"21410778"
] | [
"Molecular structure and peptidoglycan recognition of Mycobacterium tuberculosis ArfA (Rv0899).",
"Rv0901 from Mycobacterium tuberculosis, a possible novel virulent gene proved through the recombinant Mycobacterium smegmatis.",
"Expression of the ompATb operon accelerates ammonia secretion and adaptation of Myc... | [
2012,
2009,
2011
] | 3 | [] | [] | 0 | 0 | null | [
"Actinomycetes"
] | [
154
] | 1 | [] | [] | 0 | true | Domain | Channel accessory protein ArfC, N-terminal domain | Channel accessory protein ArfC, N-terminal domain | Rv0901_ArfC_N | 5 |
IPR061304 | 61,304 | M protein serotype 5/6, C-terminal domain | M_group_A_cterm | Domain | 65 | false | false | M protein (emm) is an important virulence protein and serology-defining surface antigen of Streptococcus pyogenes (group A Streptococcus). M protein has an amino-terminal YSIRK-type signal sequence (associated with cross-wall targeting in dividing cells), and a C-terminal LPXTG domain for processing by sortase and cova... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033777"
] | [
"M_group_A_cterm"
] | [
65
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105313"
] | [
"2670192"
] | [
"Streptococcal M protein: molecular design and biological behavior."
] | [
1989
] | 1 | [] | [] | 0 | 0 | null | [
"Streptococcus"
] | [
65
] | 1 | [] | [] | 0 | true | Domain | M protein serotype 5/6, C-terminal domain | M protein serotype 5/6, C-terminal domain | M_group_A_cterm | 2 |
IPR061305 | 61,305 | MARTX multifunctional-autoprocessing repeats-in-toxin, N-terminal | MARTX_Nterm | Domain | 291 | false | false | This entry describes the N-terminal 1900 amino acids of MARTX family multifunctional-autoprocessing repeats-in-toxin holotoxins, which contain both repeat regions that facilitate their entry into eukaryotic target cells, and multiple effector domains [ , , ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF012221"
] | [
"MARTX_Nterm"
] | [
291
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00053274",
"PUB00105003",
"PUB00105004"
] | [
"17464284",
"18591243",
"19620709"
] | [
"Autoprocessing of the Vibrio cholerae RTX toxin by the cysteine protease domain.",
"Structure-function analysis of inositol hexakisphosphate-induced autoprocessing of the Vibrio cholerae multifunctional autoprocessing RTX toxin.",
"Structural and molecular mechanism for autoprocessing of MARTX toxin of Vibrio ... | [
2007,
2008,
2009
] | 3 | [] | [] | 0 | 0 | null | [
"Pseudomonadota"
] | [
291
] | 1 | [] | [] | 0 | true | Domain | MARTX multifunctional-autoprocessing repeats-in-toxin, N-terminal | MARTX multifunctional-autoprocessing repeats-in-toxin, N-terminal | MARTX_Nterm | 7 |
IPR061306 | 61,306 | Spiralin lipoprotein | Spiralin_LP | Family | 41 | false | false | This entry represents Spiralin from Spiroplasma citri and similar proteins from Tenericutes. The surface of spiroplasma bacteria is crowded with the membrane-anchored lipoprotein spiralin, whose structure and function are unknown, although its cellular function is thought to be a structural and mechanical one rather th... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038030"
] | [
"spiralin_LP"
] | [
41
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00010230",
"PUB00105527",
"PUB00105528"
] | [
"11988221",
"16250340",
"2211527"
] | [
"Secondary structure of spiralin in solution, at the air/water interface, and in interaction with lipid monolayers.",
"Purification and characterization of spiralin, the main protein of the Spiroplasma citri membrane.",
"Spiralins of Spiroplasma citri and Spiroplasma melliferum: amino acid sequences and putativ... | [
2002,
1977,
1990
] | 3 | [] | [] | 0 | 0 | null | [
"Spiroplasma"
] | [
41
] | 1 | [] | [] | 0 | true | Family | Spiralin lipoprotein | Spiralin lipoprotein | Spiralin_LP | 6 |
IPR061307 | 61,307 | Magnetosome protein MamO | MamO | Family | 24 | false | false | Magnetosomes are special lipid-bound organelles that comprise magnetic mineral crystals in magnetotactic bacteria (MTB). Magnetosomes are important for MTB to search for preferred microaerophilic environment. Proteins of this family are essential in the formation of bacterial magnetosomes. MamO promotes crystal nucleat... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040961"
] | [
"MamO"
] | [
24
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00093597",
"PUB00106095",
"PUB00106096"
] | [
"26981620",
"35110403",
"20674739"
] | [
"MamO Is a Repurposed Serine Protease that Promotes Magnetite Biomineralization through Direct Transition Metal Binding in Magnetotactic Bacteria.",
"A protease-mediated switch regulates the growth of magnetosome organelles in Magnetospirillum magneticum.",
"mamO and mamE genes are essential for magnetosome cry... | [
2016,
2022,
2010
] | 3 | [] | [] | 0 | 0 | null | [
"Pseudomonadota"
] | [
24
] | 1 | [] | [] | 0 | true | Family | Magnetosome protein MamO | Magnetosome protein MamO | MamO | 4 |
IPR061308 | 61,308 | Magnetosome protein MamX | MamX | Family | 10 | false | false | Magnetosomes are special lipid-bound organelles that comprise magnetic mineral crystals in magnetotactic bacteria (MTB). Magnetosomes are important for MTB to search for preferred microaerophilic environment. Proteins of this family are involved in biomineralization through redox control [ , ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040996"
] | [
"MamX"
] | [
10
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00093603",
"PUB00106121"
] | [
"23889511",
"24020498"
] | [
"The magnetosome proteins MamX, MamZ and MamH are involved in redox control of magnetite biomineralization in Magnetospirillum gryphiswaldense.",
"MamX encoded by the mamXY operon is involved in control of magnetosome maturation in Magnetospirillum gryphiswaldense MSR-1."
] | [
2013,
2013
] | 2 | [] | [] | 0 | 0 | null | [
"Rhodospirillales"
] | [
10
] | 1 | [] | [] | 0 | true | Family | Magnetosome protein MamX | Magnetosome protein MamX | MamX | 8 |
IPR061309 | 61,309 | Liposome tubulation protein MamY | MamY | Family | 7 | false | false | Magnetosomes are special lipid-bound organelles that comprise magnetic mineral crystals in magnetotactic bacteria (MTB). Magnetosomes are important for MTB to search for preferred microaerophilic environment. Proteins of this family are involved in liposome tubulation during the formation of magnetosomes [ , ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040997"
] | [
"MamY"
] | [
7
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00106122",
"PUB00106123"
] | [
"20345667",
"30039923"
] | [
"Identification and functional characterization of liposome tubulation protein from magnetotactic bacteria.",
"Enhanced Tubulation of Liposome Containing Cardiolipin by MamY Protein from Magnetotactic Bacteria."
] | [
2010,
2018
] | 2 | [] | [] | 0 | 0 | null | [
"Rhodospirillales"
] | [
7
] | 1 | [] | [] | 0 | true | Family | Liposome tubulation protein MamY | Liposome tubulation protein MamY | MamY | 3 |
IPR061310 | 61,310 | Cytochrome b559 subunit beta, long form | PSBFL | Family | 6 | false | false | Long forms of cytochrome b559 subunit beta (PsbF) are found in Prochlorococcus. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF002717"
] | [
"PRK02561.1-1"
] | [
6
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [
"IPR006241"
] | [] | 1 | 0 | 1 | [
"Prochlorococcus marinus"
] | [
6
] | 1 | [] | [] | 0 | true | Family | Cytochrome b559 subunit beta, long form | Cytochrome b559 subunit beta, long form | PSBFL | 6 |
IPR061312 | 61,312 | DISARM system helicase DrmA, short form | DISARM_DrmAS | Family | 751 | false | false | Members of this family are DrmA helicases from representative DISARM anti-phage gene clusters, mostly from class I systems, but a few from class II systems. This entry excludes those members of class II systems that both are divergent in sequence from this set and have a characteristic long insert [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038325"
] | [
"DISARM_DrmAS"
] | [
751
] | 1 | [] | [] | [] | 0 | [
"7s9v",
"7s9w"
] | 2 | [
"PUB00105719"
] | [
"29085076"
] | [
"DISARM is a widespread bacterial defence system with broad anti-phage activities."
] | [
2018
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Phage sp. ctrsQ3",
"metagenomes"
] | [
747,
1,
3
] | 3 | [] | [] | 0 | true | Family | DISARM system helicase DrmA, short form | DISARM system helicase DrmA, short form | DISARM_DrmAS | 3 |
IPR061313 | 61,313 | DNA relaxase MbeA | Relax_MbeA_E1 | Family | 421 | false | false | MbeA, as described in the mobilization region of the ColE1 plasmid, fully overlaps two tandem mobilization proteins on the same strand, MbeB and MbeD [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047848"
] | [
"relax_MbeA_E1"
] | [
421
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159609"
] | [
"12675806"
] | [
"Genetic and biochemical characterization of MbeA, the relaxase involved in plasmid ColE1 conjugative mobilization."
] | [
2003
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"plasmids",
"uncultured prokaryote"
] | [
414,
2,
2,
3
] | 4 | [] | [] | 0 | true | Family | DNA relaxase MbeA | DNA relaxase MbeA | Relax_MbeA_E1 | 7 |
IPR061316 | 61,316 | Opacity-associated protein OapA | Opacity_OapA | Family | 84 | false | false | This family consists of full-length homologues to OapA, opacity-associated protein A as described in Haemophilus influenzae. OapA shares a C-terminal homology domain, called the OapA domain, with the Escherichia coli protein YtfB, which is now known to bind peptidoglycan through its OapA domain and to act as a cell div... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033909"
] | [
"opacity_OapA"
] | [
84
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00094178",
"PUB00105421"
] | [
"29686141",
"10417187"
] | [
"YtfB, an OapA Domain-Containing Protein, Is a New Cell Division Protein in Escherichia coli.",
"Opacity-associated protein A contributes to the binding of Haemophilus influenzae to chang epithelial cells."
] | [
2018,
1999
] | 2 | [] | [] | 0 | 0 | null | [
"Pasteurellaceae"
] | [
84
] | 1 | [] | [] | 0 | true | Family | Opacity-associated protein OapA | Opacity-associated protein OapA | Opacity_OapA | 3 |
IPR061317 | 61,317 | WxPxxD membrane protein | WxPxxD_TM | Family | 76 | false | false | This uncommon, extremely hydrophobic protein of about 240 amino acids occurs sporadically in members of the Firmicutes, including the Listeria, Bacillus, Anoxybacillus, and Terribacillus genera. The protein is named for its most distinctive motif. The function is unknown, but the size and hydrophobicity suggests a tran... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF035952"
] | [
"WxPxxD_TM"
] | [
76
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacillota"
] | [
76
] | 1 | [] | [] | 0 | true | Family | WxPxxD membrane protein | WxPxxD membrane protein | WxPxxD_TM | 5 |
IPR061318 | 61,318 | TUL4 lipoprotein | OM_lipo_TUL4 | Family | 139 | false | false | TUL4 family lipoproteins, including paralogues designated LpnA and LpnB, are highly expressed on the outer membrane in the genus Francisella [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038367"
] | [
"OM_lipo_TUL4"
] | [
139
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105749"
] | [
"1612751"
] | [
"Humoral and cell-mediated immunity in mice to a 17-kilodalton lipoprotein of Francisella tularensis expressed by Salmonella typhimurium."
] | [
1992
] | 1 | [] | [] | 0 | 0 | null | [
"Thiotrichales"
] | [
139
] | 1 | [] | [] | 0 | true | Family | TUL4 lipoprotein | TUL4 lipoprotein | OM_lipo_TUL4 | 9 |
IPR061319 | 61,319 | DNA metabolism protein TP0183 | TP0183_fam | Family | 49 | false | false | TP_0183 is a protein of approximately 281 amino acids that is processed from a precursor containing an N-terminal signal peptide. Protein-protein interactions of TP0183 of Treponema pallidum with DnaA, with the DNA repair helicase TP0380, and with SbcD, a protein involved in replication restart after DNA repair, sugges... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF049867"
] | [
"TP0183_fam"
] | [
49
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162494"
] | [
"18509523"
] | [
"The binary protein interactome of Treponema pallidum--the syphilis spirochete."
] | [
2008
] | 1 | [] | [] | 0 | 0 | null | [
"Spirochaetales"
] | [
49
] | 1 | [] | [] | 0 | true | Family | DNA metabolism protein TP0183 | DNA metabolism protein TP0183 | TP0183_fam | 2 |
IPR061320 | 61,320 | Spore coat protein CotG | Spore_coat_G | Family | 49 | false | false | CotG is a lysine-rich repetitive endospore coat protein that is among the most highly charged proteins known. It is reported to mediate spore surface permeability [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047411"
] | [
"spore_coat_G"
] | [
49
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159445"
] | [
"36354330"
] | [
"CotG Mediates Spore Surface Permeability in Bacillus subtilis."
] | [
2022
] | 1 | [] | [] | 0 | 0 | null | [
"Bacillus"
] | [
49
] | 1 | [] | [] | 0 | true | Family | Spore coat protein CotG | Spore coat protein CotG | Spore_coat_G | 3 |
IPR061321 | 61,321 | Calmodulin-dependent glutamylase SidJ | SidJ_poly_Glu | Family | 47 | false | false | SidJ, called a pseudokinase because its polyglutamylation activity differs from what might be expected from its kinase-like fold, is the founding member of a family of such pseudokinases. SidJ itself, as described in Legionella pneumophila, is exported by a type IV secretion system (T4SS), and modifies and modulates th... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033873"
] | [
"SidJ_poly_Glu"
] | [
47
] | 1 | [] | [] | [] | 0 | [
"6k4k",
"6k4l",
"6k4r",
"6oqq",
"6plm",
"6s5t",
"7mir",
"7mis",
"7ppo",
"7pqe"
] | 10 | [
"PUB00105393"
] | [
"31123136"
] | [
"Bacterial pseudokinase catalyzes protein polyglutamylation to inhibit the SidE-family ubiquitin ligases."
] | [
2019
] | 1 | [] | [] | 0 | 0 | null | [
"Legionella"
] | [
47
] | 1 | [] | [] | 0 | true | Family | Calmodulin-dependent glutamylase SidJ | Calmodulin-dependent glutamylase SidJ | SidJ_poly_Glu | 8 |
IPR061322 | 61,322 | ArtA-dependent S-layer glycoprotein, Haloferax gibbonsii-type | Surf_glcprot_Halo | Family | 15 | false | false | S-layer (surface layer) proteins form a paracrystalline surface layer in most archaea and some bacteria. A number of different, unrelated families exist. Members of these families typically are glycoproteins, often with extensive post-translational modification. This entry includes the cell surface glycoprotein from Ha... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041335"
] | [
"surf_glcprot_Halo"
] | [
15
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00060405",
"PUB00106339"
] | [
"22037399",
"29558455"
] | [
"Archaeosortases and exosortases are widely distributed systems linking membrane transit with posttranslational modification.",
"Comparative Analysis of Surface Layer Glycoproteins and Genes Involved in Protein Glycosylation in the Genus Haloferax."
] | [
2012,
2018
] | 2 | [] | [] | 0 | 0 | null | [
"Haloferax"
] | [
15
] | 1 | [] | [] | 0 | true | Family | ArtA-dependent S-layer glycoprotein, Haloferax gibbonsii-type | ArtA-dependent S-layer glycoprotein, Haloferax gibbonsii-type | Surf_glcprot_Halo | 1 |
IPR061323 | 61,323 | IgA Fc-binding protein BAC | GBS_IgA_bnd_BAC | Family | 11 | false | false | The IgA Fc-region binding protein of Streptococcus agalactiae (group B streptococcus) is a surface-anchored virulence factor with a YSIRK-type signal sequence at the N-terminal and an LPXTG sorting signal near the C-terminal. It is also called beta-antigen [ , ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038253"
] | [
"GBS_IgA_bnd_BAC"
] | [
11
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105667",
"PUB00105668"
] | [
"17004655",
"26047354"
] | [
"Adjacent location of the bac gene and two-component regulatory system genes within the putative Streptococcus agalactiae pathogenicity island.",
"Natural Mutations in Streptococcus agalactiae Resulting in Abrogation of β Antigen Production."
] | [
2006,
2015
] | 2 | [] | [] | 0 | 0 | null | [
"Streptococcus"
] | [
11
] | 1 | [] | [] | 0 | true | Family | IgA Fc-binding protein BAC | IgA Fc-binding protein BAC | GBS_IgA_bnd_BAC | 3 |
IPR061324 | 61,324 | Type V CRISPR-associated effector Cas12f2 | CRISPR_Cas12f2 | Family | 2 | false | false | Members of this family belong to the Cas12f2 subfamily of the type V CRISPR-associated effector Cas12. Note that members of this family at one time called Cas14 (see ), but based on recent reviews, the term Cas14 now belongs to the unrelated family found in type VII CRISPR systems. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF049972"
] | [
"CRISPR_Cas12f2"
] | [
2
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162584"
] | [
"30337455"
] | [
"Programmed DNA destruction by miniature CRISPR-Cas14 enzymes."
] | [
2018
] | 1 | [] | [] | 0 | 0 | null | [
"Micrarchaeota archaeon (strain CG1_02_47_40)",
"Thermodesulfobacterium geofontis"
] | [
1,
1
] | 2 | [] | [] | 0 | true | Family | Type V CRISPR-associated effector Cas12f2 | Type V CRISPR-associated effector Cas12f2 | CRISPR_Cas12f2 | 5 |
IPR061325 | 61,325 | LETM1-related biofilm-associated protein | LETM1-rel_film | Family | 677 | false | false | This bacterial protein family is related to the mitochondrial protein LETM1. The founding member from the fish pathogen Flavobacterium columnare, called a calcium-binding EF hand protein, was found highly up-regulated in expression during biofilm formation [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040639"
] | [
"LETM1_rel_film"
] | [
677
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105865"
] | [
"31272369"
] | [
"Transcriptome analysis of the fish pathogen Flavobacterium columnare in biofilm suggests calcium role in pathogenesis."
] | [
2019
] | 1 | [] | [] | 0 | 0 | null | [
"Flavobacteriales",
"ecological metagenomes"
] | [
674,
3
] | 2 | [] | [] | 0 | true | Family | LETM1-related biofilm-associated protein | LETM1-related biofilm-associated protein | LETM1-rel_film | 6 |
IPR061326 | 61,326 | CLCA_X | CLCA_X | Family | 615 | false | false | CLCAs, named for calcium-activated chloride channel bCLCA1, are proteins that resemble certain zinc-dependent metalloproteases in fold by lacking the signature HEXXH motifs. The CLCA_X family, described by this entry, was identified based on weak similarities [ ] as a notable CLCA-like family with a consistent architec... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041907"
] | [
"CLCA_X"
] | [
615
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00075429",
"PUB00091133"
] | [
"23671590",
"28559295"
] | [
"CLCAs - a family of metalloproteases of intriguing phylogenetic distribution and with cases of substituted catalytic sites.",
"Polyvalent Proteins, a Pervasive Theme in the Intergenomic Biological Conflicts of Bacteriophages and Conjugative Elements."
] | [
2013,
2017
] | 2 | [] | [] | 0 | 0 | null | [
"Bacteria",
"ecological metagenomes"
] | [
610,
5
] | 2 | [] | [] | 0 | true | Family | CLCA_X | CLCA_X | CLCA_X | 7 |
IPR061327 | 61,327 | Adhesin RatB | RatB | Family | 640 | false | false | RatB, encoded in a Salmonella pathogenicity island next to its homologue RatA, is a long protein consisting almost entirely of repeats of a and [ ]. The domain is also found in the inverse autotransporter adhesin/invasin, where it is called an adhesion domain. The domain is a Bacterial Immunoglobulin-like domain, BIg21... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF011842"
] | [
"PRK15314.1"
] | [
640
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00016646"
] | [
"12540539"
] | [
"Molecular and phenotypic analysis of the CS54 island of Salmonella enterica serotype typhimurium: identification of intestinal colonization and persistence determinants."
] | [
2003
] | 1 | [] | [] | 0 | 0 | null | [
"Enterobacteriaceae"
] | [
640
] | 1 | [] | [] | 0 | true | Family | Adhesin RatB | Adhesin RatB | RatB | 8 |
IPR061328 | 61,328 | Bdr-like, N-terminal domain | Bdr_N_group1 | Domain | 514 | false | false | Bdr (Borrelia direct repeat) proteins have an N-terminal domain, a variable length region of repeats, typically 11 amino acids long with a KID repeat, and a non-repetitive C-terminal domain. This entry describes the conserved N-terminal domain of families designated BdrA, BdrB, and BdrC [ ]. A related but non-overlappi... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040499"
] | [
"Bdr_N_group1"
] | [
514
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105795"
] | [
"10644495"
] | [
"Evolutionary and molecular analyses of the Borrelia bdr super gene family: delineation of distinct sub-families and demonstration of the genus wide conservation of putative functional domains, structural properties and repeat motifs."
] | [
2000
] | 1 | [] | [] | 0 | 0 | null | [
"Borreliaceae"
] | [
514
] | 1 | [] | [] | 0 | true | Domain | Bdr-like, N-terminal domain | Bdr-like, N-terminal domain | Bdr_N_group1 | 8 |
IPR061329 | 61,329 | CBS-HotDog domain-containing transcription factor SpxR | TF_CBS_SpxR | Family | 389 | false | false | SpxR from Streptococcus pneumoniae, like its full-length homologue YtoI from Listeria monocytogenes, is a transcriptional regulator with an N-terminal DNA-binding domain, and with CBS and HotDog domains. SpxR regulates the pyruvate oxidase SpxB [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038279"
] | [
"TF_CBS_SpxR"
] | [
389
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105694"
] | [
"18179423"
] | [
"Polymorphism and regulation of the spxB (pyruvate oxidase) virulence factor gene by a CBS-HotDog domain protein (SpxR) in serotype 2 Streptococcus pneumoniae."
] | [
2008
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Trichuris trichiura"
] | [
388,
1
] | 2 | [] | [] | 0 | true | Family | CBS-HotDog domain-containing transcription factor SpxR | CBS-HotDog domain-containing transcription factor SpxR | TF_CBS_SpxR | 6 |
IPR061330 | 61,330 | Exc2 lipoprotein-like | Exc2_fam | Family | 380 | false | false | Exc2, a plasmid-encoded predicted lipoprotein of small size, was once described as a plasmid entry exclusion protein [ ]. However, [ ], says entry exclusion activity should instead be ascribed to MbeD. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033828"
] | [
"entry_exc2_fam"
] | [
380
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105356",
"PUB00105357"
] | [
"2991225",
"7592368"
] | [
"Nucleotide sequence and gene organization of ColE1 DNA.",
"A ColE1-encoded gene directs entry exclusion of the plasmid."
] | [
1985,
1995
] | 2 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
380
] | 1 | [] | [] | 0 | true | Family | Exc2 lipoprotein-like | Exc2 lipoprotein-like | Exc2_fam | 4 |
IPR061334 | 61,334 | Putative pilus system protein FilA | Pilus_FilA | Family | 218 | false | false | FilA is found almost exclusively in the genus Acinetobacter and is assigned as a putative pilus assembly protein from local genomic contexts that include several additional putative pilus system proteins [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF050077"
] | [
"pilus_FilA"
] | [
218
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162658"
] | [
"29939498"
] | [
"Transcriptome analysis of Porphyromonas gingivalis and Acinetobacter baumannii in polymicrobial communities."
] | [
2018
] | 1 | [] | [] | 0 | 0 | null | [
"Gammaproteobacteria"
] | [
218
] | 1 | [] | [] | 0 | true | Family | Putative pilus system protein FilA | Putative pilus system protein FilA | Pilus_FilA | 8 |
IPR061335 | 61,335 | BREX-1 system phosphatase PglZ, type B | BREX_PglZ_1_B | Family | 217 | false | false | BREX (bacteriophage exclusion) is a phage resistance resistance, in which two protein families are core but other proteins are variable. BREX subtypes are based on PglZ domain protein, a putative phosphatase. This family is one of two major subtypes of PglZ as seen in type 1 BREX systems [ ]. describes the alternative ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033450"
] | [
"BREX_PglZ_1_B"
] | [
217
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00093365"
] | [
"25452498"
] | [
"BREX is a novel phage resistance system widespread in microbial genomes."
] | [
2015
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Methanomicrobia",
"ecological metagenomes"
] | [
203,
9,
5
] | 3 | [] | [] | 0 | true | Family | BREX-1 system phosphatase PglZ, type B | BREX-1 system phosphatase PglZ, type B | BREX_PglZ_1_B | 6 |
IPR061336 | 61,336 | Hormogonium tapered terminus morphoprotein TftA | Horm_taper_TftA | Family | 204 | false | false | TftA, an amidase that can act on peptidoglycan, is found strictly in a subset of the Cyanobacteria, where it is required for the proper morphology of hormogonia (mobile colony filaments), which normally are tapered at both ends [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF050040"
] | [
"horm_taper_TftA"
] | [
204
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162599"
] | [
"37971486"
] | [
"Identification of a morphogene required for tapered filament termini in filamentous cyanobacteria."
] | [
2023
] | 1 | [] | [] | 0 | 0 | null | [
"Cyanobacteriota"
] | [
204
] | 1 | [] | [] | 0 | true | Family | Hormogonium tapered terminus morphoprotein TftA | Hormogonium tapered terminus morphoprotein TftA | Horm_taper_TftA | 2 |
IPR061337 | 61,337 | Phage exclusion lipoprotein Cor-like | Lamb_exclu_cor | Family | 201 | false | false | The lipoprotein Cor, as found in temperate lambdoid phage that depend on FhuA as a phage receptor, functions in phage exclusion through its interaction with FhuA [ , ]. This entry also includes uncharacterised bacterial sequences. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047972"
] | [
"lamb_exclu_cor"
] | [
201
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162644",
"PUB00162645",
"PUB00162646"
] | [
"30043202",
"15518820",
"8631731"
] | [
"Cor interacts with outer membrane proteins to exclude FhuA-dependent phages.",
"An orthologue of the cor gene is involved in the exclusion of temperate lambdoid phages. Evidence that Cor inactivates FhuA receptor functions.",
"Proteins responsible for lysogenic conversion caused by coliphages N15 and phi80 are... | [
2018,
2004,
1996
] | 3 | [] | [] | 0 | 0 | null | [
"Caudoviricetes",
"Enterobacterales"
] | [
88,
113
] | 2 | [] | [] | 0 | true | Family | Phage exclusion lipoprotein Cor-like | Phage exclusion lipoprotein Cor-like | Lamb_exclu_cor | 6 |
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