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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
IPR061338 | 61,338 | Putative pilus system protein FilF | Pilus_FilF | Family | 196 | false | false | FilF 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"
] | [
"NF050081"
] | [
"pilus_FilF"
] | [
196
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162658"
] | [
"29939498"
] | [
"Transcriptome analysis of Porphyromonas gingivalis and Acinetobacter baumannii in polymicrobial communities."
] | [
2018
] | 1 | [] | [] | 0 | 0 | null | [
"Moraxellaceae"
] | [
196
] | 1 | [] | [] | 0 | true | Family | Putative pilus system protein FilF | Putative pilus system protein FilF | Pilus_FilF | 6 |
IPR061339 | 61,339 | LA_3696-like, N-terminal | LA_3696_Nterm | Domain | 186 | false | false | Members of this entry, found primarily but not exclusively in the genus Leptospira, share this homology region at the N-terminal, typically share a shorter C-terminal domain as well, and are variable in length and sequence between the two well-conserved regions. The function is unknown. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047472"
] | [
"LA_3696_Nterm"
] | [
186
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"hot springs metagenome"
] | [
184,
2
] | 2 | [] | [] | 0 | true | Domain | LA_3696-like, N-terminal | LA_3696-like, N-terminal | LA_3696_Nterm | 4 |
IPR061340 | 61,340 | LIC_13355-like lipoprotein | Lipo_LIC13355 | Family | 163 | false | false | Members of this family are lipoproteins found broadly in the genus Leptospira. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033170"
] | [
"lipo_LIC13355"
] | [
163
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
163
] | 1 | [] | [] | 0 | true | Family | LIC_13355-like lipoprotein | LIC_13355-like lipoprotein | Lipo_LIC13355 | 8 |
IPR061341 | 61,341 | LA_3334-like | LA_3334_fam | Family | 160 | false | false | This uncharacterised protein family is restricted to the genus Leptospira, and is named for LA_3334 ( ) from Leptospira interrogans serovar Lai str. 56601 | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047432"
] | [
"LA_3334_fam"
] | [
160
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Leptospira"
] | [
160
] | 1 | [] | [] | 0 | true | Family | LA_3334-like | LA_3334-like | LA_3334_fam | 7 |
IPR061342 | 61,342 | NF038215-like lipoprotein | Acineto_lipo_PV | Family | 153 | false | false | This small lipoprotein, about 60 amino acids long on average in precursor form, is widespread in the genus Acinetobacter. The motif PVxxxDY is conserved in most members. The function is unknown. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038215"
] | [
"acineto_lipo_PV"
] | [
153
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Acinetobacter"
] | [
153
] | 1 | [] | [] | 0 | true | Family | NF038215-like lipoprotein | NF038215-like lipoprotein | Acineto_lipo_PV | 7 |
IPR061343 | 61,343 | Oligosaccharide repeat unit polymerase | Wzy_O6_O28 | Family | 154 | false | false | Members of this family are oligosaccharide repeat unit polymerases in a subfamily that includes the Wzy proteins for polymerization of the O-antigens O6, O28, O39, O59, and several others [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033860"
] | [
"Wzy_O6_O28"
] | [
154
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105376"
] | [
"17244797"
] | [
"Relationship between O-antigen subtypes, bacterial surface structures and O-antigen gene clusters in Escherichia coli O123 strains carrying genes for Shiga toxins and intimin."
] | [
2007
] | 1 | [] | [] | 0 | 0 | null | [
"Pseudomonadati",
"human gut metagenome"
] | [
153,
1
] | 2 | [] | [] | 0 | true | Family | Oligosaccharide repeat unit polymerase | Oligosaccharide repeat unit polymerase | Wzy_O6_O28 | 3 |
IPR061345 | 61,345 | PhiSA1p31 domain | PhiSA1p31 | Domain | 140 | false | false | This domain occurs in Streptomyces and related lineages, in proteins with highly variable architectures, typically at or near the C-terminal. Member proteins include at least two from known temperate phage of Streptomyces, including phiSA1p31, for which it is named, from Streptomyces phage phiSASD1. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038082"
] | [
"phiSA1p31"
] | [
140
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Actinomycetes",
"Caudoviricetes",
"Zophobas morio"
] | [
131,
8,
1
] | 3 | [] | [] | 0 | true | Domain | PhiSA1p31 domain | PhiSA1p31 domain | PhiSA1p31 | 2 |
IPR061346 | 61,346 | NF038120 family PEP-CTERM protein | PEP_CTERM_QFxxD | Family | 136 | false | false | This family of PEP-CTERM proteins has a notable motif, QFxxD, near the PEP-CTERM region, for which it is named. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038120"
] | [
"PEP_CTERM_QFxxD"
] | [
136
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
136
] | 1 | [] | [] | 0 | true | Family | NF038120 family PEP-CTERM protein | NF038120 family PEP-CTERM protein | PEP_CTERM_QFxxD | 7 |
IPR061347 | 61,347 | Mbov_0399 family ICE element protein | ICE_Mbov_0399 | Family | 139 | false | false | Members of this family, such as Mbov_0399 from Mycoplasmopsis bovis, MAG3890 from Mycoplasma agalactiae, and SFLOR_RS04885 from Spiroplasma floricola, are large proteins from Integrating Conjugative Elements (ICE) of a type related to VirB-like type IV secretion systems and prevalent in the Mycoplasmatota [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045892"
] | [
"ICE_Mbov_0399"
] | [
139
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159434"
] | [
"22693604"
] | [
"Comparative geno-plasticity analysis of Mycoplasma bovis HB0801 (Chinese isolate)."
] | [
2012
] | 1 | [] | [] | 0 | 0 | null | [
"Mycoplasmatota"
] | [
139
] | 1 | [] | [] | 0 | true | Family | Mbov_0399 family ICE element protein | Mbov_0399 family ICE element protein | ICE_Mbov_0399 | 9 |
IPR061348 | 61,348 | NF038130 family PEP-CTERM protein | PEP_NF038130 | Family | 132 | false | false | This family of PEP-CTERM proteins occurs in Cyanobacteria such as Nostoc, but also in floc-forming bacteria such as Zoogloea ramigera and Candidatus Accumulibacter phosphatis [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038130"
] | [
"PEP_NF038130"
] | [
132
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00060405"
] | [
"22037399"
] | [
"Archaeosortases and exosortases are widely distributed systems linking membrane transit with posttranslational modification."
] | [
2012
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
132
] | 1 | [] | [] | 0 | true | Family | NF038130 family PEP-CTERM protein | NF038130 family PEP-CTERM protein | PEP_NF038130 | 6 |
IPR061349 | 61,349 | Cistern family PEP-CTERM protein | PEP-cistern | Family | 133 | false | false | Members of this family are PEP-CTERM proteins, that is, surface proteins of Gram-negative organisms that carry a short C-terminal region used to help target proteins to their proper cellular location, hold them in position for post-translational modifications that might need to occur (such as glycosylation), and which ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033947"
] | [
"PEP-cistern"
] | [
133
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00060405"
] | [
"22037399"
] | [
"Archaeosortases and exosortases are widely distributed systems linking membrane transit with posttranslational modification."
] | [
2012
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
133
] | 1 | [] | [] | 0 | true | Family | Cistern family PEP-CTERM protein | Cistern family PEP-CTERM protein | PEP-cistern | 8 |
IPR061350 | 61,350 | GapS4b-like | Antiphage_GapS4b | Family | 130 | false | false | Proteins of this family are homologues of the anti-phage protein GapS4b in Vibrio parahaemolyticus [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047934"
] | [
"antiphage_GapS4b"
] | [
130
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00161243"
] | [
"39443754"
] | [
"Gamma-Mobile-Trio systems are mobile elements rich in bacterial defensive and offensive tools."
] | [
2024
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
130
] | 1 | [] | [] | 0 | true | Family | GapS4b-like | GapS4b-like | Antiphage_GapS4b | 4 |
IPR061351 | 61,351 | LIC_10494-like lipoprotein | Lipo_LIC10494 | Family | 128 | false | false | Members of this family are lipoproteins found broadly in the genus Leptospira. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033169"
] | [
"lipo_LIC10494"
] | [
128
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Leptospira"
] | [
128
] | 1 | [] | [] | 0 | true | Family | LIC_10494-like lipoprotein | LIC_10494-like lipoprotein | Lipo_LIC10494 | 8 |
IPR061353 | 61,353 | MHFG family PEP-CTERM protein | PEP_CTERM_MHFG | Family | 126 | false | false | This PEP-CTERM protein, dependent on exosortase for processing and export, is named for a distinctive MHFG motif. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038119"
] | [
"PEP_CTERM_MHFG"
] | [
126
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Burkholderiales",
"Tanacetum cinerariifolium"
] | [
125,
1
] | 2 | [] | [] | 0 | true | Family | MHFG family PEP-CTERM protein | MHFG family PEP-CTERM protein | PEP_CTERM_MHFG | 4 |
IPR061354 | 61,354 | Lipoprotein LipL21 | Lipo_LipL21 | Family | 132 | false | false | Members of this family are lipoprotein LipL21, as described in Leptospira interrogans serovar Copenhageni str. Fiocruz L1-130 but found broadly in the genus Leptospira. Close homologs that are not lipoproteins by sequence are likely defective in their reported coding region. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033162"
] | [
"lipo_LipL21"
] | [
132
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Leptospiraceae"
] | [
132
] | 1 | [] | [] | 0 | true | Family | Lipoprotein LipL21 | Lipoprotein LipL21 | Lipo_LipL21 | 3 |
IPR061355 | 61,355 | Lipoprotein LipL46 | Lipo_LipL46 | Family | 120 | false | false | Members of this family are lipoprotein LipL46, as described in Leptospira interrogans serovar Copenhageni str. Fiocruz L1-130 but found broadly in the genus Leptospira. Close homologs that are not lipoproteins by sequence are likely defective in their reported coding region. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033164"
] | [
"lipo_LipL46"
] | [
120
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Leptospira"
] | [
120
] | 1 | [] | [] | 0 | true | Family | Lipoprotein LipL46 | Lipoprotein LipL46 | Lipo_LipL46 | 4 |
IPR061356 | 61,356 | LIC11755 lipoprotein | Lipo_LIC11755 | Family | 121 | false | false | LIC11755 proteins are predicted to be surface-exposed outer membrane lipoproteins of the genus Leptospira. Shorter members of this family average about 700 amino acids, while longer versions have an additional C-terminal region of 250 to 300 amino acids. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047473"
] | [
"lipo_LIC11755"
] | [
121
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105762"
] | [
"28496441"
] | [
"Discovery of Novel Leptospirosis Vaccine Candidates Using Reverse and Structural Vaccinology."
] | [
2017
] | 1 | [] | [] | 0 | 0 | null | [
"Leptospira"
] | [
121
] | 1 | [] | [] | 0 | true | Family | LIC11755 lipoprotein | LIC11755 lipoprotein | Lipo_LIC11755 | 4 |
IPR061357 | 61,357 | Flagellar basal body rod modification protein | PRK12812.1 | Family | 119 | false | false | This entry represents a family of Flagellar basal body rod modification proteins. They act as a scaffold for the assembly of hook proteins onto the flagellar basal body rod. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF009452"
] | [
"PRK12812.1"
] | [
119
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00104831",
"PUB00104832"
] | [
"11298288",
"14617189"
] | [
"Transposon mutagenesis of Campylobacter jejuni identifies a bipartite energy taxis system required for motility.",
"Transcription of sigma54-dependent but not sigma28-dependent flagellar genes in Campylobacter jejuni is associated with formation of the flagellar secretory apparatus."
] | [
2001,
2003
] | 2 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
119
] | 1 | [] | [] | 0 | true | Family | Flagellar basal body rod modification protein | Flagellar basal body rod modification protein | PRK12812.1 | 9 |
IPR061358 | 61,358 | LIC11469 lipoprotein adhesin Lsa20 | LIC11469_Lsa20 | Family | 112 | false | false | It has been reported that the Lsa20 protein from L. interrogans serovar Copenhageni strain M20 bound to laminin and human plasminogen [ ]. It is predicted to be a lipoprotein. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047614"
] | [
"LIC11469_fam"
] | [
112
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159370"
] | [
"21844229"
] | [
"The novel leptospiral surface adhesin Lsa20 binds laminin and human plasminogen and is probably expressed during infection."
] | [
2011
] | 1 | [] | [] | 0 | 0 | null | [
"Leptospiraceae"
] | [
112
] | 1 | [] | [] | 0 | true | Family | LIC11469 lipoprotein adhesin Lsa20 | LIC11469 lipoprotein adhesin Lsa20 | LIC11469_Lsa20 | 2 |
IPR061359 | 61,359 | LIC_10705 lipoprotein | Lipo_LIC_10705 | Family | 102 | false | false | The LIC_10705 family of lipoproteins, found in the genus Leptospira, includes tandem-encoded paralogs such as LIC_10705 and LIC_10706 in L. interrogans serovar Copenhageni str. Fiocruz L1-130. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038393"
] | [
"lipo_LIC_10705"
] | [
102
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Leptospira"
] | [
102
] | 1 | [] | [] | 0 | true | Family | LIC_10705 lipoprotein | LIC_10705 lipoprotein | Lipo_LIC_10705 | 7 |
IPR061361 | 61,361 | Exosortase Y-associated Wzy-like protein | XrtY_assoc_Wzy | Family | 93 | false | false | Members of this family are encoded in a surface polysaccharide biosynthesis locus that also includes the putative protein-sorting endopeptidase exosortase Y (NF046083). Members show distant relatedness to oligosaccharide repeat unit polymerases such as Wzy proteins of O-antigen biosynthesis. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF046084"
] | [
"XrtY_assoc_Wzy"
] | [
93
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteroidota"
] | [
93
] | 1 | [] | [] | 0 | true | Family | Exosortase Y-associated Wzy-like protein | Exosortase Y-associated Wzy-like protein | XrtY_assoc_Wzy | 3 |
IPR061362 | 61,362 | Ecr-like regulatory small membrane protein | Ecr-like_memb | Family | 90 | false | false | Ecr, as described in the genus Enterobacter, is a small membrane protein predicted to span the inner membrane. It was found to modulate expression of PhoP, part of the PhoP-PhoQ two component system, which in turn induces the arnBCADTEF operon, leading to modification of LPS and conferring elevated resistance to colist... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033861"
] | [
"sm_mem_Ecr"
] | [
90
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105377"
] | [
"31169899"
] | [
"Heterogeneous resistance to colistin in Enterobacter cloacae complex due to a new small transmembrane protein."
] | [
2019
] | 1 | [] | [] | 0 | 0 | null | [
"Gammaproteobacteria"
] | [
90
] | 1 | [] | [] | 0 | true | Family | Ecr-like regulatory small membrane protein | Ecr-like regulatory small membrane protein | Ecr-like_memb | 9 |
IPR061363 | 61,363 | Myxosortase-dependent M36 metallopeptidase | Myxo_dep_M36 | Family | 86 | false | false | Members of this bacterial protein family have an M36 family metallopeptidase domain, like fungalysin ( ), and a C-terminal MYXO-CTERM domain ( ), suggesting processing and surface-anchoring by a type II CAAX prenyl protease-related sorting enzyme, myxosortase. Members of this family include MXAN_3564 (mepA), part of th... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038112"
] | [
"myxo_dep_M36"
] | [
86
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00103726",
"PUB00105566"
] | [
"31975447",
"25250022"
] | [
"MYXO-CTERM sorting tag directs proteins to the cell surface via the type II secretion system.",
"The lethal cargo of Myxococcus xanthus outer membrane vesicles."
] | [
2020,
2014
] | 2 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
86
] | 1 | [] | [] | 0 | true | Family | Myxosortase-dependent M36 metallopeptidase | Myxosortase-dependent M36 metallopeptidase | Myxo_dep_M36 | 2 |
IPR061364 | 61,364 | Antiviral RADAR system adenosine triphosphatase RdrA | RdrA | Family | 84 | false | false | Proteins of this family are the essential components of the anti-phage system RADAR (restriction by an adenosine deaminase acting on RNA). RADAR mediates RNA editing in response to phage infections. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041743"
] | [
"RdrA"
] | [
84
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00152882"
] | [
"32855333"
] | [
"Diverse enzymatic activities mediate antiviral immunity in prokaryotes."
] | [
2020
] | 1 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
84
] | 1 | [] | [] | 0 | true | Family | Antiviral RADAR system adenosine triphosphatase RdrA | Antiviral RADAR system adenosine triphosphatase RdrA | RdrA | 3 |
IPR061365 | 61,365 | Chryseobasin-related MNIO class RiPP peptide | ChrA-rel_RiPP | Family | 78 | false | false | Members of this family closely resemble the chryseobasin RiPP precursor ChrA, especially in having the seven C-terminal residues as CP[GA]CG[LM]G. However, the central region differs greatly, is substantially shorter, and contains an invariant Cys residue whose significance is not yet clear. Members are found in multip... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF050125"
] | [
"ChrA_rel_RiPP"
] | [
78
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00153338"
] | [
"37252350"
] | [
"Macrocyclization and Backbone Rearrangement During RiPP Biosynthesis by a SAM-Dependent Domain-of-Unknown-Function 692."
] | [
2023
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteroidota"
] | [
78
] | 1 | [] | [] | 0 | true | Family | Chryseobasin-related MNIO class RiPP peptide | Chryseobasin-related MNIO class RiPP peptide | ChrA-rel_RiPP | 9 |
IPR061368 | 61,368 | Scytonemin biosynthesis cyclase/decarboxylase ScyC | Scytonem_ScyC | Family | 69 | false | false | Of the various markers of scytonemin biosynthesis, ScyC appears to be the clearest, as there are few or no close homologs from outside of the set of confidently predicted scytonemin producer bacteria. ScyC, an enzyme in the biosynthesis pathway for the cyanobacterial natural sunscreen scytonemin, performs a cyclization... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF035924"
] | [
"scytonem_ScyC"
] | [
69
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105457"
] | [
"18954141"
] | [
"Investigating the initial steps in the biosynthesis of cyanobacterial sunscreen scytonemin."
] | [
2008
] | 1 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
69
] | 1 | [] | [] | 0 | true | Family | Scytonemin biosynthesis cyclase/decarboxylase ScyC | Scytonemin biosynthesis cyclase/decarboxylase ScyC | Scytonem_ScyC | 9 |
IPR061369 | 61,369 | BN159_2729 protein | BN159_2729-like | Family | 67 | false | false | This uncharacterised protein family occurs in Streptomyces and related species. Some members have insertions of long stretches of low-complexity sequences. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038081"
] | [
"BN159_2729_fam"
] | [
67
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Streptomycetaceae"
] | [
67
] | 1 | [] | [] | 0 | true | Family | BN159_2729 protein | BN159_2729 protein | BN159_2729-like | 5 |
IPR061371 | 61,371 | MEMAR_RS02690 S-layer glycoprotein | S_layer_MEMAR | Family | 69 | false | false | Members of this family are archaeal S-layer glycoproteins in the family of MEMAR_RS02690. Most members of this family have the PGF-CTERM domain, recognized and processed by the archaeosortase A (ArtA). Surprisingly, while MEMAR_RS02690 itself, from Methanoculleus marisnigri, a methanogen from the Order Methanomicrobial... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041431"
] | [
"S_layer_MEMAR"
] | [
69
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00106393"
] | [
"35481895"
] | [
"Characterizing the N- and O-linked glycans of the PGF-CTERM sorting domain-containing S-layer protein of Methanoculleus marisnigri."
] | [
2022
] | 1 | [] | [] | 0 | 0 | null | [
"Methanomicrobiales",
"hydrocarbon metagenome"
] | [
67,
2
] | 2 | [] | [] | 0 | true | Family | MEMAR_RS02690 S-layer glycoprotein | MEMAR_RS02690 S-layer glycoprotein | S_layer_MEMAR | 7 |
IPR061374 | 61,374 | LEVG PEP-CTERM protein | PEP_CTERM_LEVG | Family | 61 | false | false | This well-conserved family of PEP-CTERM proteins occurs in Cyanobacteria. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038121"
] | [
"PEP_CTERM_LEVG"
] | [
61
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Cyanophyceae"
] | [
61
] | 1 | [] | [] | 0 | true | Family | LEVG PEP-CTERM protein | LEVG PEP-CTERM protein | PEP_CTERM_LEVG | 1 |
IPR061375 | 61,375 | Bgr_08870 protein, N-terminal | Bgr08870_N | Domain | 61 | false | false | This entry describes the N-terminal region of Bgr_08870 from Bartonella grahamii. Homologs appear restricted to other species of the same genus. The C-terminal region includes extensive low-complexity sequence, but also regions of homology with other at least one other family of Bartonella proteins. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041327"
] | [
"Bgr08870_fam"
] | [
61
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bartonella"
] | [
61
] | 1 | [] | [] | 0 | true | Domain | Bgr_08870 protein, N-terminal | Bgr_08870 protein, N-terminal | Bgr08870_N | 7 |
IPR061376 | 61,376 | GapS6b protein | GapS6b-like | Family | 60 | false | false | Proteins of this family are homologs of the anti-phage protein GapS6b in Vibrio parahaemolyticus. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047936"
] | [
"antiphage_GapS6b"
] | [
60
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00161243"
] | [
"39443754"
] | [
"Gamma-Mobile-Trio systems are mobile elements rich in bacterial defensive and offensive tools."
] | [
2024
] | 1 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
60
] | 1 | [] | [] | 0 | true | Family | GapS6b protein | GapS6b protein | GapS6b-like | 6 |
IPR061377 | 61,377 | Lipoprotein LipL36 | LipL36 | Family | 60 | false | false | Members of this family are lipoprotein LipL36, as described in Leptospira interrogans serovar Copenhageni str. Fiocruz L1-130 but found broadly in the genus Leptospira. Close homologs that are not lipoproteins by sequence are likely defective in their reported coding region. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033160"
] | [
"lipo_LipL36"
] | [
60
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Leptospira"
] | [
60
] | 1 | [] | [] | 0 | true | Family | Lipoprotein LipL36 | Lipoprotein LipL36 | LipL36 | 2 |
IPR061378 | 61,378 | LA_3150 lipoprotein | LA_3150-like | Family | 56 | false | false | Members of this lipoprotein family average 150 amino acids in length, and occur only in the genus Leptospira. In addition to the conserved Cys residue of the lipoprotein signal peptide, four additional invariant Cys residues are found. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047459"
] | [
"LA_3150_fam_lipo"
] | [
56
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Leptospira"
] | [
56
] | 1 | [] | [] | 0 | true | Family | LA_3150 lipoprotein | LA_3150 lipoprotein | LA_3150-like | 1 |
IPR061379 | 61,379 | Adventurous gliding motility lipoprotein CglC | CglC | Family | 52 | false | false | CglC (cell contact-dependent gliding (or conditional gliding) motility protein C, also called adventurous gliding motility protein AgmO, is found in delta-proteobacterial species that exhibit a taxonomically restricted form of gliding motility. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033754"
] | [
"gliding_CglC"
] | [
52
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105302",
"PUB00105303"
] | [
"22343295",
"26132848"
] | [
"Identification of the cglC, cglD, cglE, and cglF genes and their role in cell contact-dependent gliding motility in Myxococcus xanthus.",
"Contact- and Protein Transfer-Dependent Stimulation of Assembly of the Gliding Motility Machinery in Myxococcus xanthus."
] | [
2012,
2015
] | 2 | [] | [] | 0 | 0 | null | [
"Cystobacterineae"
] | [
52
] | 1 | [] | [] | 0 | true | Family | Adventurous gliding motility lipoprotein CglC | Adventurous gliding motility lipoprotein CglC | CglC | 5 |
IPR061380 | 61,380 | TRP75-like N-terminal | TRP75_N | Domain | 53 | false | false | This N-terminal domain is found in TRP75 (tandem repeat protein, 75 kDa) of Ehrlichia chaffeensis and TRP95 of Ehrlichia canis, preceding the region of 24 amino acid long direct repeats. It appears also in non-repetitive proteins from Anaplasma and Wolbachia, which likewise are members of the alphaproteobacteria. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038243"
] | [
"TRP75_fam_Nterm"
] | [
53
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105646",
"PUB00105647"
] | [
"21606187",
"29643078"
] | [
"Tyrosine-phosphorylated Ehrlichia chaffeensis and Ehrlichia canis tandem repeat orthologs contain a major continuous cross-reactive antibody epitope in lysine-rich repeats.",
"Ehrlichia chaffeensis TRP75 Interacts with Host Cell Targets Involved in Homeostasis, Cytoskeleton Organization, and Apoptosis Regulation... | [
2011,
2018
] | 2 | [] | [] | 0 | 0 | null | [
"Anaplasmataceae",
"Eukaryota"
] | [
43,
10
] | 2 | [] | [] | 0 | true | Domain | TRP75-like N-terminal | TRP75-like N-terminal | TRP75_N | 3 |
IPR061381 | 61,381 | Adventurous gliding motility protein GltG | GltG | Family | 52 | false | false | GltG proteins, including the founding member MXAN_4867 from Myxococcus xanthus, occur in certain delta-proteobacteria and are involved in adventurous gliding (A-)motility. GltG has an N-terminal forkhead-associated (FHA) domain domain, often associated with signal transduction. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033760"
] | [
"gliding_GltG"
] | [
52
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105303"
] | [
"26132848"
] | [
"Contact- and Protein Transfer-Dependent Stimulation of Assembly of the Gliding Motility Machinery in Myxococcus xanthus."
] | [
2015
] | 1 | [] | [] | 0 | 0 | null | [
"Cystobacterineae"
] | [
52
] | 1 | [] | [] | 0 | true | Family | Adventurous gliding motility protein GltG | Adventurous gliding motility protein GltG | GltG | 7 |
IPR061382 | 61,382 | Adventurous gliding motility protein GltJ | GltJ | Family | 50 | false | false | Adventurous gliding motility protein GltJ, also known as AgmX, occurs in delta-proteobacteria such as Myxococcus xanthus. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033761"
] | [
"gliding_GltJ"
] | [
50
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105303"
] | [
"26132848"
] | [
"Contact- and Protein Transfer-Dependent Stimulation of Assembly of the Gliding Motility Machinery in Myxococcus xanthus."
] | [
2015
] | 1 | [] | [] | 0 | 0 | null | [
"Cystobacterineae"
] | [
50
] | 1 | [] | [] | 0 | true | Family | Adventurous gliding motility protein GltJ | Adventurous gliding motility protein GltJ | GltJ | 8 |
IPR061383 | 61,383 | BAR domain-like protein A BdpA | BdpA | Family | 47 | false | false | BdpA is required for uniform size distribution of membrane vesicles and influences scaffolding of (outer membrane extensions) OMEs into a consistent diameter and curvature. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF049843"
] | [
"BdpA"
] | [
47
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162648"
] | [
"34643180"
] | [
"A bacterial membrane sculpting protein with BAR domain-like activity."
] | [
2021
] | 1 | [] | [] | 0 | 0 | null | [
"Gammaproteobacteria",
"uncultured organism"
] | [
46,
1
] | 2 | [] | [] | 0 | true | Family | BAR domain-like protein A BdpA | BAR domain-like protein A BdpA | BdpA | 4 |
IPR061384 | 61,384 | RadB lipoprotein | RadB | Family | 47 | false | false | The small lipoprotein RadB, as found in Fusobacterium nucleatum, is encoded between the genes for the lipoprotein FAD-I and the large adhesin RadD. The name RapB (RadD-Associated Proteins B) was also suggested for RadB. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041844"
] | [
"lipo_RadB_fam"
] | [
47
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00152951",
"PUB00152979"
] | [
"31906541",
"34074747"
] | [
"Role of FAD-I in Fusobacterial Interspecies Interaction and Biofilm Formation.",
"Genetic and molecular determinants of polymicrobial interactions in Fusobacterium nucleatum."
] | [
2020,
2021
] | 2 | [] | [] | 0 | 0 | null | [
"Fusobacterium"
] | [
47
] | 1 | [] | [] | 0 | true | Family | RadB lipoprotein | RadB lipoprotein | RadB | 8 |
IPR061385 | 61,385 | Rhombosortase-dependent M36 metallopeptidase | Rhom_dep_M36 | Family | 47 | false | false | Members of this bacterial protein family have an M36 family metallopeptidase domain, like fungalysin (see PF02128), and a C-terminal GlyGly-CTERM domain, recognized and cleaved by rhombosortase. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038111"
] | [
"rhom_dep_M36"
] | [
47
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00060404",
"PUB00105565"
] | [
"22194940",
"30352106"
] | [
"GlyGly-CTERM and rhombosortase: a C-terminal protein processing signal in a many-to-one pairing with a rhomboid family intramembrane serine protease.",
"C-terminal processing of GlyGly-CTERM containing proteins by rhombosortase in Vibrio cholerae."
] | [
2011,
2018
] | 2 | [] | [] | 0 | 0 | null | [
"Gammaproteobacteria"
] | [
47
] | 1 | [] | [] | 0 | true | Family | Rhombosortase-dependent M36 metallopeptidase | Rhombosortase-dependent M36 metallopeptidase | Rhom_dep_M36 | 9 |
IPR061386 | 61,386 | Outer membrane exchange protein TraB | TraB_OM | Family | 50 | false | false | TraB, as described originally in the delta-proteobacterium, is a protein with a C-terminal OmpA-like domain, and is encoded in an operon with TraA. Together TraAB make it possible for bacterial cells with close enough kinship to exchange outer membrane lipoproteins, such that certain motility defects in mutant cells ca... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033763"
] | [
"exchanger_TraB"
] | [
50
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00074074"
] | [
"22511878"
] | [
"Cell contact-dependent outer membrane exchange in myxobacteria: genetic determinants and mechanism."
] | [
2012
] | 1 | [] | [] | 0 | 0 | null | [
"Cystobacterineae"
] | [
50
] | 1 | [] | [] | 0 | true | Family | Outer membrane exchange protein TraB | Outer membrane exchange protein TraB | TraB_OM | 6 |
IPR061388 | 61,388 | NGK_0946 protein | NGK_0946-like | Family | 41 | false | false | Members of this family including the apparent lipoprotein NGK_0946, found to be one of the most highly expressed proteins in the gonorrhea-causing pathogen Neisseria gonorrhoeae in the female genital tract. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF046038"
] | [
"NGK_0946_fam"
] | [
41
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159667"
] | [
"26244506"
] | [
"The Gonococcal Transcriptome during Infection of the Lower Genital Tract in Women."
] | [
2015
] | 1 | [] | [] | 0 | 0 | null | [
"Pseudomonadati",
"hydrothermal vent metagenome"
] | [
40,
1
] | 2 | [] | [] | 0 | true | Family | NGK_0946 protein | NGK_0946 protein | NGK_0946-like | 7 |
IPR061389 | 61,389 | Collagen-binding adhesin Cnm | Cnm | Family | 40 | false | false | This entry describes the non-repetitive region of the collagen-binding adhesin Cnm from the N terminus to just before the start of the glycosylated Thr-rich repeat region. The length of the repeat region is highly variable. Cnm is found in about 20 percent of strains of the dental caries-causing oral pathogen Streptoco... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF050822"
] | [
"collag_bnd_Cnm"
] | [
40
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162710",
"PUB00162711",
"PUB00162712",
"PUB00162713"
] | [
"36862654",
"34406827",
"15218042",
"36708081"
] | [
"cnm-positive Streptococcus mutans is associated with galactose-deficient IgA in patients with IgA nephropathy.",
"Amyloid Aggregation of Streptococcus mutans Cnm Influences Its Collagen-Binding Activity.",
"Streptococcus mutans strains harboring collagen-binding adhesin.",
"Harboring Cnm-expressing Streptoco... | [
2023,
2021,
2004,
2023
] | 4 | [] | [] | 0 | 0 | null | [
"Streptococcus mutans"
] | [
40
] | 1 | [] | [] | 0 | true | Family | Collagen-binding adhesin Cnm | Collagen-binding adhesin Cnm | Cnm | 2 |
IPR061390 | 61,390 | von Willebrand factor binding protein Vwb | Vwb | Family | 43 | false | false | The von Willebrand factor binding protein Vwb, like its paralog staphylocoagulase, is a coagulase and a virulence factor. It induces clotting, not by being an enzyme, but by activating prothrombin to generate fibrin. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033750"
] | [
"vWF_bind_Staph"
] | [
43
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105297",
"PUB00105298"
] | [
"12101292",
"28182324"
] | [
"A novel von Willebrand factor binding protein expressed by Staphylococcus aureus.",
"Clumping factor A, von Willebrand factor-binding protein and von Willebrand factor anchor Staphylococcus aureus to the vessel wall."
] | [
2002,
2017
] | 2 | [] | [] | 0 | 0 | null | [
"Staphylococcus"
] | [
43
] | 1 | [] | [] | 0 | true | Family | von Willebrand factor binding protein Vwb | von Willebrand factor binding protein Vwb | Vwb | 4 |
IPR061391 | 61,391 | FTN_0109 protein | FTN_0109-like | Family | 39 | false | false | It has been shown that proteins of this family were involved in F. tularensis virulence in Drosophila. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF049881"
] | [
"FTN_0109_fam"
] | [
39
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162993",
"PUB00162994"
] | [
"22368770",
"20479082"
] | [
"The Drosophila melanogaster host model.",
"Directed screen of Francisella novicida virulence determinants using Drosophila melanogaster."
] | [
2012,
2010
] | 2 | [] | [] | 0 | 0 | null | [
"Francisellaceae"
] | [
39
] | 1 | [] | [] | 0 | true | Family | FTN_0109 protein | FTN_0109 protein | FTN_0109-like | 9 |
IPR061392 | 61,392 | Pilin subunit UpsA | UpsA | Family | 39 | false | false | Proteins of this family are encoded by the archaeal upsA gene on the UV-inducible pili operon (ups operon), which is involved in UV-induced pili assembly, cellular aggregation, and subsequent DNA exchange between cells. UpsA and UpsB are major pilin subunits in the ups pili. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF046073"
] | [
"UpsA"
] | [
39
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159058"
] | [
"24106028"
] | [
"Molecular analysis of the UV-inducible pili operon from Sulfolobus acidocaldarius."
] | [
2013
] | 1 | [] | [] | 0 | 0 | null | [
"Archaea"
] | [
39
] | 1 | [] | [] | 0 | true | Family | Pilin subunit UpsA | Pilin subunit UpsA | UpsA | 7 |
IPR061393 | 61,393 | Outer membrane exchange accessory lipoprotein TraC | TraC_OM | Family | 45 | false | false | This lipoprotein family, found Myxococcus xanthus and other members of the Myxococcocales branch of the Deltaproteobacteria, is involved in a kinship recognition-dependent system for exchange of outer membrane lipoproteins. TraC is described as an accessory protein to the TraAB pair that was shown to be critical to out... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040658"
] | [
"Myxo_OME_TraC"
] | [
45
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105882"
] | [
"34517761"
] | [
"Modular Lipoprotein Toxins Transferred by Outer Membrane Exchange Target Discrete Cell Entry Pathways."
] | [
2021
] | 1 | [] | [] | 0 | 0 | null | [
"Cystobacterineae"
] | [
45
] | 1 | [] | [] | 0 | true | Family | Outer membrane exchange accessory lipoprotein TraC | Outer membrane exchange accessory lipoprotein TraC | TraC_OM | 5 |
IPR061394 | 61,394 | Pilin subunit UpsB | UpsB | Family | 38 | false | false | Proteins of this family are encoded by the archaeal upsB gene on the UV-inducible pili operon (ups operon), which is involved in UV-induced pili assembly, cellular aggregation, and subsequent DNA exchange between cells. UpsA and UpsB are major pilin subunits in the ups pili. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF046074"
] | [
"UpsB"
] | [
38
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159058"
] | [
"24106028"
] | [
"Molecular analysis of the UV-inducible pili operon from Sulfolobus acidocaldarius."
] | [
2013
] | 1 | [] | [] | 0 | 0 | null | [
"Sulfolobaceae"
] | [
38
] | 1 | [] | [] | 0 | true | Family | Pilin subunit UpsB | Pilin subunit UpsB | UpsB | 1 |
IPR061395 | 61,395 | DISARM system helicase DrmA, long form | DISARM_DrmAL | Family | 37 | false | false | This entry describes some DrmA helicases from class II DISARM anti-phage systems, and none from class I systems. Members distinguished from the shorter, more common form ( ) both by sequence divergence in regions that align and by an insert that makes members of this set longer. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038326"
] | [
"DISARM_DrmAL"
] | [
37
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105719"
] | [
"29085076"
] | [
"DISARM is a widespread bacterial defence system with broad anti-phage activities."
] | [
2018
] | 1 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria"
] | [
16,
21
] | 2 | [] | [] | 0 | true | Family | DISARM system helicase DrmA, long form | DISARM system helicase DrmA, long form | DISARM_DrmAL | 9 |
IPR061396 | 61,396 | S-layer protein SlpA | SlpA | Family | 37 | false | false | In Clostridiodes difficile, the S-layer protein precursor, SlpA, is one member of a large paralogous family of protein that share several cell wall-binding repeats. SlpA is cleaved into a larger and smaller protein. The S-layer protein itself is important to adhesion, and portions of it are highly variable, and then N-... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033435"
] | [
"S-layer_Clost"
] | [
37
] | 1 | [] | [] | [] | 0 | [
"7acx",
"7acy",
"7acz",
"7qgq",
"8bby",
"9f8f"
] | 6 | [
"PUB00051147",
"PUB00105102"
] | [
"19183279",
"12081960"
] | [
"Structural insights into the molecular organization of the S-layer from Clostridium difficile.",
"Patterns of sequence conservation in the S-Layer proteins and related sequences in Clostridium difficile."
] | [
2009,
2002
] | 2 | [] | [] | 0 | 0 | null | [
"Clostridioides difficile"
] | [
37
] | 1 | [] | [] | 0 | true | Family | S-layer protein SlpA | S-layer protein SlpA | SlpA | 9 |
IPR061397 | 61,397 | Francisella virulence factor A | FvfA | Family | 36 | false | false | It has been reported that members of this family play a role in protection of Francisella from osmotic shock and its survival in macrophages. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF049880"
] | [
"FvfA"
] | [
36
] | 1 | [] | [] | [] | 0 | [
"5evf",
"5evg"
] | 2 | [
"PUB00162991",
"PUB00162992"
] | [
"25987704",
"28994410"
] | [
"Identifying Francisella tularensis genes required for growth in host cells.",
"Structure of the conserved Francisella virulence protein FvfA."
] | [
2015,
2017
] | 2 | [] | [] | 0 | 0 | null | [
"Thiotrichales"
] | [
36
] | 1 | [] | [] | 0 | true | Family | Francisella virulence factor A | Francisella virulence factor A | FvfA | 6 |
IPR061398 | 61,398 | Cell-cell cohesion protein MtsD | MtsD | Family | 36 | false | false | MtsD belongs to the six gene mts (myxococcus thrombospondin D) operon, and is one of four with repeats described as thrombospondin type 3 (TSP3) repeats. Members of the locus participate in cell-cell cohesion that contributes to social motility and fruiting-body development, among other processes. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047639"
] | [
"throspo3_MtsD"
] | [
36
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159597"
] | [
"17720782"
] | [
"New locus important for Myxococcus social motility and development."
] | [
2007
] | 1 | [] | [] | 0 | 0 | null | [
"Cystobacterineae"
] | [
36
] | 1 | [] | [] | 0 | true | Family | Cell-cell cohesion protein MtsD | Cell-cell cohesion protein MtsD | MtsD | 6 |
IPR061399 | 61,399 | PTPDL protein | PTPDL-like | Family | 35 | false | false | This protein family, named for its best conserved motif, appears exclusively in the Verrucomicrobiota. Some members have C-terminal suffix region with a resemblance to sorting signals. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041881"
] | [
"PTPDL_fam"
] | [
35
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Verrucomicrobiota"
] | [
35
] | 1 | [] | [] | 0 | true | Family | PTPDL protein | PTPDL protein | PTPDL-like | 9 |
IPR061400 | 61,400 | LBF_0142 lipoprotein | LBF_0142-like | Family | 34 | false | false | This subfamily of lipoproteins, named for LBF_0142 from the saprophytic species Leptospira biflexa, is found in a subset of Leptospira species, with additional members found outside the genus. Members belong to the broader DUF6503 family described by PF20113.2. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047762"
] | [
"lipo_LBF_0142"
] | [
34
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
34
] | 1 | [] | [] | 0 | true | Family | LBF_0142 lipoprotein | LBF_0142 lipoprotein | LBF_0142-like | 1 |
IPR061401 | 61,401 | Serine-rich aggregation substance UasX | Agg_sub_LPXTH | Family | 28 | false | false | Members of this protein family are repetitive, serine-rich surface proteins of the Firmicutes, found primarily in the genus Leuconostoc. The variant form of sortase signal, LPXTH, is replaced by LPXTG in members from some lineages, such as Weissella oryzae, and therefore recognizable. Some members of this family have t... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF035936"
] | [
"agg_sub_LPXTH"
] | [
28
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105460"
] | [
"25013139"
] | [
"Draft Genome Sequence of Weissella oryzae SG25T, Isolated from Fermented Rice Grains."
] | [
2014
] | 1 | [] | [] | 0 | 0 | null | [
"Lactobacillaceae"
] | [
28
] | 1 | [] | [] | 0 | true | Family | Serine-rich aggregation substance UasX | Serine-rich aggregation substance UasX | Agg_sub_LPXTH | 9 |
IPR061402 | 61,402 | FTL_1293 small RNA FtrC-regulated protein | FTL_1293-like | Family | 27 | false | false | It has been reported that the small RNA FtrC (Francisella tularensis RNA C) binds to FTL_1293 family proteins and regulate their expression. However, FTL_1293 is not required for F. tularensis virulence in vitro or in vivo. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF049902"
] | [
"FTL_1293_fam"
] | [
27
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159254"
] | [
"22848684"
] | [
"Identification of a novel small RNA modulating Francisella tularensis pathogenicity."
] | [
2012
] | 1 | [] | [] | 0 | 0 | null | [
"Francisellaceae"
] | [
27
] | 1 | [] | [] | 0 | true | Family | FTL_1293 small RNA FtrC-regulated protein | FTL_1293 small RNA FtrC-regulated protein | FTL_1293-like | 7 |
IPR061404 | 61,404 | Motility-associated protein Scm1 | Scm1 | Family | 27 | false | false | Scm1 (Spiroplasma citri motility gene 1) was shown by loss-of-function mutation to be involved in motility. The Scm1 family is widespread in the genus Spiroplasma, members of the Mollicutes (bacteria with no cell wall) that have a spiral shape organized around a contractile ribbon fibril made of repeating subunits of t... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033571"
] | [
"motil_scm1_spiro"
] | [
27
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105182"
] | [
"9244268"
] | [
"Isolation, characterization, and complementation of a motility mutant of Spiroplasma citri."
] | [
1997
] | 1 | [] | [] | 0 | 0 | null | [
"Spiroplasma"
] | [
27
] | 1 | [] | [] | 0 | true | Family | Motility-associated protein Scm1 | Motility-associated protein Scm1 | Scm1 | 8 |
IPR061405 | 61,405 | Lp6.6 lipoprotein | Lipo_6_6 | Family | 27 | false | false | In Borrelia burgdorferi, the tiny lipoprotein Lp6.6 is plasmid-borne and was originally described as a major low-molecular-weight lipoprotein that could constitute 2% of the dry weight of defatted cells. Lp6.6 was later found to facilitate transmission from ticks to mice, and to be down-regulated after infection. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033515"
] | [
"lipo_6_6_Borrel"
] | [
27
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105149",
"PUB00105150",
"PUB00105151"
] | [
"1452330",
"19703109",
"9009290"
] | [
"Purification and immunological characterization of a major low-molecular-weight lipoprotein from Borrelia burgdorferi.",
"Borrelia burgdorferi small lipoprotein Lp6.6 is a member of multiple protein complexes in the outer membrane and facilitates pathogen transmission from ticks to mice.",
"Molecular character... | [
1992,
2009,
1997
] | 3 | [] | [] | 0 | 0 | null | [
"Borreliaceae"
] | [
27
] | 1 | [] | [] | 0 | true | Family | Lp6.6 lipoprotein | Lp6.6 lipoprotein | Lipo_6_6 | 6 |
IPR061406 | 61,406 | CotZ-related putative spore coat protein | CotZ-rel | Family | 26 | false | false | Members of this appear only in endospore-forming bacteria, and are distantly related to spore coat protein CotZ. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040827"
] | [
"CotZ_rel"
] | [
26
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacillales"
] | [
26
] | 1 | [] | [] | 0 | true | Family | CotZ-related putative spore coat protein | CotZ-related putative spore coat protein | CotZ-rel | 1 |
IPR061407 | 61,407 | CDI system lipoprotein BcpO | BcpO | Family | 25 | false | false | BcpO is a small lipoprotein, about 74 amino acids long on average, encoded in Burkholderia bcpAIOB locus systems for two-partner secretion and contact dependent growth inhibition. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF037971"
] | [
"lipo_BcpO"
] | [
25
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105492"
] | [
"22912595"
] | [
"The Burkholderia bcpAIOB genes define unique classes of two-partner secretion and contact dependent growth inhibition systems."
] | [
2012
] | 1 | [] | [] | 0 | 0 | null | [
"Burkholderiaceae"
] | [
25
] | 1 | [] | [] | 0 | true | Family | CDI system lipoprotein BcpO | CDI system lipoprotein BcpO | BcpO | 7 |
IPR061408 | 61,408 | CNF1-like cytotoxic necrotizing factor | CNF1-like | Family | 23 | false | false | The CNF1 family of cytotoxic necrotizing factors are glutamine amidases that find their way to their eukaryotic host cells' cytosol and permanently activate certain GTPases. It includes full-length homologues of CNF1, CNF2, CNF3, and CNFY, but it excludes smaller proteins such as the type 3 secretion system effector Vo... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033651"
] | [
"cyto_nec_fctrs"
] | [
23
] | 1 | [] | [] | [] | 0 | [
"6yhk",
"6yhl"
] | 2 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Gammaproteobacteria"
] | [
23
] | 1 | [] | [] | 0 | true | Family | CNF1-like cytotoxic necrotizing factor | CNF1-like cytotoxic necrotizing factor | CNF1-like | 8 |
IPR061409 | 61,409 | LifA/Efa1-related large cytotoxin | LifA/Efa1-rel_toxin | Family | 23 | false | false | Members of this family are large and almost certainly multifunctional proteins found in various pathogens from genus Chlamydia, about 3000 amino acids in size and related to lymphostatin (Efa1/LifA) from enteropathogenic Escherichia coli. Roles have been suggested for Efa1 (EHEC factor for adherence) in adhesion, so so... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033479"
] | [
"Efa1_rel_toxin"
] | [
23
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105128"
] | [
"11707582"
] | [
"Chlamydia trachomatis cytotoxicity associated with complete and partial cytotoxin genes."
] | [
2001
] | 1 | [] | [] | 0 | 0 | null | [
"Chlamydia"
] | [
23
] | 1 | [] | [] | 0 | true | Family | LifA/Efa1-related large cytotoxin | LifA/Efa1-related large cytotoxin | LifA/Efa1-rel_toxin | 8 |
IPR061410 | 61,410 | T9SS-dependent outer membrane TapA/TapC-like | TapA/TapC-like | Family | 22 | false | false | TapA (TprA-associated protein A, ) and TapC ( ), nearly tandem full-length homologues, are encoded in the oral pathogen Porphyromonas gingivalis next to the genes for TapB, and interact with the tetratricopeptide repeat protein TprA ( ). All four contribute to virulence. Full length close homologues of TapA and TapC ar... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF050177"
] | [
"TapA_OM_Porphy"
] | [
22
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162725"
] | [
"20351137"
] | [
"Tetratricopeptide repeat protein-associated proteins contribute to the virulence of Porphyromonas gingivalis."
] | [
2010
] | 1 | [] | [] | 0 | 0 | null | [
"Porphyromonas"
] | [
22
] | 1 | [] | [] | 0 | true | Family | T9SS-dependent outer membrane TapA/TapC-like | T9SS-dependent outer membrane TapA/TapC-like | TapA/TapC-like | 2 |
IPR061411 | 61,411 | NGO1622-like phage-associated putative holin | NGO1622-like | Family | 22 | false | false | Members of this family, including NGO1622 from Neisseria gonorrhoeae ( ), are phage region-encoded proteins strictly limited to Neisseria species. Members are suggested to act as holins, but the actual function has not yet been shown [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF046041"
] | [
"holin_NGO1622"
] | [
22
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00106624"
] | [
"17615066"
] | [
"Characterization of the dsDNA prophage sequences in the genome of Neisseria gonorrhoeae and visualization of productive bacteriophage."
] | [
2007
] | 1 | [] | [] | 0 | 0 | null | [
"Neisseria"
] | [
22
] | 1 | [] | [] | 0 | true | Family | NGO1622-like phage-associated putative holin | NGO1622-like phage-associated putative holin | NGO1622-like | 8 |
IPR061412 | 61,412 | MAG1680-like | MAG1680-like | Family | 22 | false | false | This protein family includes paralogous lipoproteins each in Mycoplasmopsis bovis and Mycoplasmopsis agalactiae, such as MAG1680 ( ). Members are homologous from end to end and average about 470 amino acids in length. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045878"
] | [
"Mbov_0186_LP"
] | [
22
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Mycoplasmopsis"
] | [
22
] | 1 | [] | [] | 0 | true | Family | MAG1680-like | MAG1680-like | MAG1680-like | 6 |
IPR061414 | 61,414 | Cell invasion LPXTG-type Vip | Vip_LPXTG | Family | 19 | false | false | Vip (Virulence protein), like the LPXTG-type internalins, is an LPXTG-anchored surface protein of the mammalian cell-invading pathogen Listeria monocytogenes, but absent from the related species Listeria innocua. For certain cell types, Vip is required for Listeria's ability to invade. It appears to bind the endoplasmi... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033201"
] | [
"Vip_LPXTG_Lm"
] | [
19
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105023"
] | [
"16015374"
] | [
"Gp96 is a receptor for a novel Listeria monocytogenes virulence factor, Vip, a surface protein."
] | [
2005
] | 1 | [] | [] | 0 | 0 | null | [
"Listeria monocytogenes"
] | [
19
] | 1 | [] | [] | 0 | true | Family | Cell invasion LPXTG-type Vip | Cell invasion LPXTG-type Vip | Vip_LPXTG | 6 |
IPR061415 | 61,415 | MyrrNad domain | Myrrnad_dom | Domain | 18 | false | false | This entry (MyrrNad, MYcoplasma Repeat-Rich protein C-terminal Anchor Domain) represents the N-terminal domain counterpart to MyrrCad ( ), found in a family of LRR-like repeat proteins. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF038275"
] | [
"Myrrnad"
] | [
18
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105691"
] | [
"28630471"
] | [
"Candidatus Mycoplasma girerdii replicates, diversifies, and co-occurs with Trichomonas vaginalis in the oral cavity of a premature infant."
] | [
2017
] | 1 | [] | [] | 0 | 0 | null | [
"Candidatus Malacoplasma girerdii"
] | [
18
] | 1 | [] | [] | 0 | true | Domain | MyrrNad domain | MyrrNad domain | Myrrnad_dom | 6 |
IPR061416 | 61,416 | Serine-rich glycoprotein adhesin, prefix domain | SerRich_N | Domain | 37 | false | false | This entry represents a Limosilactobacillus-restricted N-terminal non-repetitive sequence region shared by proteins with extensive serine-rich repeat regions, all likely to function as adhesins. This region contains a variant form of the KxYKxGKxW motif ( ) followed by a region related to serine-rich glycoprotein adhes... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033676"
] | [
"Lacb_SerRich_Nt"
] | [
37
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Limosilactobacillus"
] | [
37
] | 1 | [] | [] | 0 | true | Domain | Serine-rich glycoprotein adhesin, prefix domain | Serine-rich glycoprotein adhesin, prefix domain | SerRich_N | 6 |
IPR061417 | 61,417 | CDS14-like ICE transfer lipoprotein | ICE_LP_CDS14 | Family | 18 | false | false | Integrative conjugative elements (ICE) in Mycoplasma-related wall-less bacteria undergo lateral gene transfer by mechanisms that require living donor and recipient cells. Members of this highly diverse family are large lipoproteins encoded in ICE loci. This entry includes CDS14 ( ), which was shown to be required to en... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045940"
] | [
"ICE_LP_CDS14"
] | [
18
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159792",
"PUB00159793"
] | [
"29970462",
"23888872"
] | [
"The Integrative Conjugative Element (ICE) of <i>Mycoplasma agalactiae</i>: Key Elements Involved in Horizontal Dissemination and Influence of Coresident ICEs.",
"ICEA of Mycoplasma agalactiae: a new family of self-transmissible integrative elements that confers conjugative properties to the recipient strain."
] | [
2018,
2013
] | 2 | [] | [] | 0 | 0 | null | [
"Mycoplasmatota"
] | [
18
] | 1 | [] | [] | 0 | true | Family | CDS14-like ICE transfer lipoprotein | CDS14-like ICE transfer lipoprotein | ICE_LP_CDS14 | 4 |
IPR061418 | 61,418 | Type VI secretion system immunity protein TaeI-like | TaeI-like | Family | 17 | false | false | TaeI from Acinetobacter baumannii is an immunity protein for the anti-fungal type VI secretion system effector DNase TafE [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041834"
] | [
"immunity_TaeI"
] | [
17
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00152966"
] | [
"36625573"
] | [
"Acinetobacter baumannii Kills Fungi via a Type VI DNase Effector."
] | [
2023
] | 1 | [] | [] | 0 | 0 | null | [
"Acinetobacter"
] | [
17
] | 1 | [] | [] | 0 | true | Family | Type VI secretion system immunity protein TaeI-like | Type VI secretion system immunity protein TaeI-like | TaeI-like | 7 |
IPR061419 | 61,419 | MAG1890-like | MAG1890-like | Family | 16 | false | false | Members of this family are restricted to the Mycoplasmatota, and average about 325 amino acids in length, including MAG1890 from Mycoplasmopsis agalactiae ( ). An invariant Cys residue at position 32 suggests that members may be lipoproteins. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045970"
] | [
"MAG1890_fam_LP"
] | [
16
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159650"
] | [
"27765069"
] | [
"Genetic loci of Mycoplasma agalactiae involved in systemic spreading during experimental intramammary infection of sheep."
] | [
2016
] | 1 | [] | [] | 0 | 0 | null | [
"Mycoplasmopsis"
] | [
16
] | 1 | [] | [] | 0 | true | Family | MAG1890-like | MAG1890-like | MAG1890-like | 2 |
IPR061420 | 61,420 | Adhesion factor FAF | Adhesion_FAF | Family | 16 | false | false | FAF (Finegoldia adhesion factor) has firstly been characterised in the opportunistic pathogen Finegoldia magna. FAF mediate bacterial adhesion to hosts through interactions with the basement membrane protein BM-40 [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040765"
] | [
"adhesion_FAF"
] | [
16
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105947"
] | [
"18808384"
] | [
"Identification of a novel protein promoting the colonization and survival of Finegoldia magna, a bacterial commensal and opportunistic pathogen."
] | [
2008
] | 1 | [] | [] | 0 | 0 | null | [
"Finegoldia"
] | [
16
] | 1 | [] | [] | 0 | true | Family | Adhesion factor FAF | Adhesion factor FAF | Adhesion_FAF | 6 |
IPR061421 | 61,421 | CFI-box putative sorting motif | Sort_motif_CFI | Conserved_site | 18 | false | false | By several criteria, the motif represented by this entry seems likely to be a site of post-translational modification associated with protein-sorting and probably with attachment to the bacterial cell surface. Some members of have an extension with this motif while others do not. Some proteins in Desulfatibacillum alip... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041763"
] | [
"sort_motif_CFI"
] | [
18
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Eukaryota",
"marine sediment metagenome"
] | [
13,
4,
1
] | 3 | [] | [] | 0 | true | Conserved_site | CFI-box putative sorting motif | CFI-box putative sorting motif | Sort_motif_CFI | 5 |
IPR061422 | 61,422 | Collagen-binding adhesin autotransporter EmaA | EmaA | Family | 15 | false | false | This protein family includes EmaA (extracellular matrix protein adhesin) from Aggregatibacter (Actinobacillus) actinomycetemcomitans, and related proteins from gammaproteobacteria. It is an outer membrane glycoprotein, and has a C-terminal β-barrel domain that marks it as an autotransporter. It serves as an adhesin tha... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033477"
] | [
"EmaA_autotrans"
] | [
15
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105123",
"PUB00105124",
"PUB00105125"
] | [
"15289564",
"17660409",
"22689812"
] | [
"Identification of an extracellular matrix protein adhesin, EmaA, which mediates the adhesion of Actinobacillus actinomycetemcomitans to collagen.",
"Molecular heterogeneity of EmaA, an oligomeric autotransporter adhesin of Aggregatibacter (Actinobacillus) actinomycetemcomitans.",
"O-polysaccharide glycosylatio... | [
2004,
2007,
2012
] | 3 | [] | [] | 0 | 0 | null | [
"Aggregatibacter"
] | [
15
] | 1 | [] | [] | 0 | true | Family | Collagen-binding adhesin autotransporter EmaA | Collagen-binding adhesin autotransporter EmaA | EmaA | 1 |
IPR061423 | 61,423 | GEGP motif-containing diheme protein | Diheme_GEGP | Family | 14 | false | false | This uncharacterised protein family is named for a pair of heme-binding CXXCH motifs in the N-terminal region and a nearly invariant GEGP motif. All members have predicted N-terminal signal peptides. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041762"
] | [
"diheme_GEGP"
] | [
14
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
14
] | 1 | [] | [] | 0 | true | Family | GEGP motif-containing diheme protein | GEGP motif-containing diheme protein | Diheme_GEGP | 5 |
IPR061424 | 61,424 | Autotransporter adhesin RadD | RadD | Family | 15 | false | false | This protein family includes RadD from Fusobacterium nucleatum and related sequences. RadD is named as an arginine (R)-inducible adhesin, and as the fourth gene (D) of a locus in which the other genes were designated radA, radB, and radC prior to characterisation. Full-length homologues from other species of Fusobacter... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF049908"
] | [
"RadD_AT_adhesin"
] | [
15
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00163126",
"PUB00163127",
"PUB00163128",
"PUB00163129"
] | [
"19007407",
"33227279",
"39169124",
"30986689"
] | [
"The Fusobacterium nucleatum outer membrane protein RadD is an arginine-inhibitable adhesin required for inter-species adherence and the structured architecture of multispecies biofilm.",
"Fusobacteriumnucleatum Adheres to Clostridioides difficile via the RadD Adhesin to Enhance Biofilm Formation in Intestinal Mu... | [
2009,
2021,
2024,
2019
] | 4 | [] | [] | 0 | 0 | null | [
"Fusobacterium"
] | [
15
] | 1 | [] | [] | 0 | true | Family | Autotransporter adhesin RadD | Autotransporter adhesin RadD | RadD | 8 |
IPR061425 | 61,425 | AMEP412-like elicitor-associated permease-like | Elici_assc_perm | Family | 13 | false | false | Members of this family are found as part of a conserved bacterial gene neighbourhood, along with AMEP412 family proteins and an apparent ABC transporter ATP-binding protein. The hydrophobic nature of this protein suggests the protein is a transporter subunit associated with AMEP412 family protein export. Members of the... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040842"
] | [
"elici_assc_perm"
] | [
13
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacillales"
] | [
13
] | 1 | [] | [] | 0 | true | Family | AMEP412-like elicitor-associated permease-like | AMEP412-like elicitor-associated permease-like | Elici_assc_perm | 8 |
IPR061426 | 61,426 | TrhA, N-terminal extension domain | TrhA_N | Domain | 12 | false | false | This rather rare domain appears as an occasional N-terminal extension to TrhA, or as a free-standing protein. TrhA (transmembrane homeostasis protein A), a plasma membrane protein that belongs to the PAQR family, named for eukaryotic Progestin and AdipoQ Receptors, and that appears involved in the homeostasis of membra... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047868"
] | [
"TrhA_N_extend"
] | [
12
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159123",
"PUB00159124",
"PUB00159125"
] | [
"35285724",
"37345585",
"38054739"
] | [
"Bacterial Homologs of Progestin and AdipoQ Receptors (PAQRs) Affect Membrane Energetics Homeostasis but Not Fluidity.",
"PAQR proteins and the evolution of a superpower: Eating all kinds of fats: Animals rely on evolutionarily conserved membrane homeostasis proteins to compensate for dietary variation.",
"TrhA... | [
2022,
2023,
2024
] | 3 | [] | [] | 0 | 0 | null | [
"Bacteria",
"mine drainage metagenome"
] | [
11,
1
] | 2 | [] | [] | 0 | true | Domain | TrhA, N-terminal extension domain | TrhA, N-terminal extension domain | TrhA_N | 1 |
IPR061427 | 61,427 | Myxosortase MrtZ | MrtZ | Family | 10 | false | false | MrtZ is a myxosortase, that is, an intramembrane glutamic endopeptidase for the MYXO-CTERM C-terminal protein-sorting signal. Members of this protein family are found in nannocystales. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040915"
] | [
"CPBP_fam_MrtZ"
] | [
10
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00154714"
] | [
"38084967"
] | [
"<i>In silico</i> discovery of the myxosortases that process MYXO-CTERM and three novel prokaryotic C-terminal protein-sorting signals that share invariant Cys residues."
] | [
2024
] | 1 | [] | [] | 0 | 0 | null | [
"Nannocystaceae"
] | [
10
] | 1 | [] | [] | 0 | true | Family | Myxosortase MrtZ | Myxosortase MrtZ | MrtZ | 8 |
IPR061429 | 61,429 | EspK/GogB-like type III secretion system effector | EspK/GogB-like | Family | 9 | false | false | Members of this family, typically found in the genus Yersinia, are probably type III secretion system (T3SS) effectors homologous to the EspK from enterohaemorrhagic Escherichia coli (EHEC) and the anti-inflammatory effector GogB from Salmonella enterica [ , ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF011915"
] | [
"PRK15386.1-4"
] | [
9
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00104989",
"PUB00104990"
] | [
"16958848",
"15843015"
] | [
"Identification and characterization of EspK, a type III secreted effector protein of enterohaemorrhagic Escherichia coli O157:H7.",
"Genetic and molecular analysis of GogB, a phage-encoded type III-secreted substrate in Salmonella enterica serovar typhimurium with autonomous expression from its associated phage.... | [
2006,
2005
] | 2 | [] | [] | 0 | 0 | null | [
"Yersinia pseudotuberculosis complex"
] | [
9
] | 1 | [] | [] | 0 | true | Family | EspK/GogB-like type III secretion system effector | EspK/GogB-like type III secretion system effector | EspK/GogB-like | 7 |
IPR061430 | 61,430 | Collagen-binding adhesin Cbm, N-terminal domain | Cbm_N | Domain | 9 | false | false | This entry represents the non-repetitive region of the collagen-binding adhesin Cbm from the N terminus to just before the start of the glycosylated Thr-rich repeat region. The length of the repeat region is highly variable. Cbm is found in a minority of strains of the dental caries-causing oral pathogen Streptococcus ... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF050823"
] | [
"collag_bnd_Cbm"
] | [
9
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162714",
"PUB00162715",
"PUB00162716"
] | [
"22759315",
"29524318",
"32002675"
] | [
"Identification and characterization of a collagen-binding protein, Cbm, in Streptococcus mutans.",
"Whole genome sequence and phenotypic characterization of a Cbm<sup>+</sup> serotype e strain of Streptococcus mutans.",
"Association of Streptococcus mutans collagen binding genes with severe childhood caries."
... | [
2012,
2018,
2020
] | 3 | [] | [] | 0 | 0 | null | [
"Streptococcus mutans"
] | [
9
] | 1 | [] | [] | 0 | true | Domain | Collagen-binding adhesin Cbm, N-terminal domain | Collagen-binding adhesin Cbm, N-terminal domain | Cbm_N | 3 |
IPR061432 | 61,432 | Trimeric autotransporter actin-nucleating factor BimA | BimA | Family | 8 | false | false | This entry represents BimA (Burkholderia intracellular motility A, ) and similar proteins in Burkholderia mallei or B. pseudomallei. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040983"
] | [
"BimA_second"
] | [
8
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00106113",
"PUB00106114"
] | [
"16267310",
"21811486"
] | [
"Actin-binding proteins from Burkholderia mallei and Burkholderia thailandensis can functionally compensate for the actin-based motility defect of a Burkholderia pseudomallei bimA mutant.",
"Autotransporters and Their Role in the Virulence of Burkholderia pseudomallei and Burkholderia mallei."
] | [
2005,
2011
] | 2 | [] | [] | 0 | 0 | null | [
"pseudomallei group"
] | [
8
] | 1 | [] | [] | 0 | true | Family | Trimeric autotransporter actin-nucleating factor BimA | Trimeric autotransporter actin-nucleating factor BimA | BimA | 7 |
IPR061433 | 61,433 | Transglutaminase-like, putative | Transglutaminase-like_put | Family | 8 | false | false | Members of this family are thought to belong to the transglutaminase-like superfamily. The function of this family of large proteins (about 650 amino acids long) remains unknown. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045997"
] | [
"Mbov0119_fam"
] | [
8
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Mycoplasmatota"
] | [
8
] | 1 | [] | [] | 0 | true | Family | Transglutaminase-like, putative | Transglutaminase-like, putative | Transglutaminase-like_put | 4 |
IPR061434 | 61,434 | Omp28-related selenoprotein | Omp28-rel_seleno | Family | 17 | false | false | Members of this family are selenoproteins distantly related to the Porphyromonas gingivalis protein named Omp28 ( ). A selenocysteine-containing motif UPYCP aligns to CLYCP in Omp28. Members have been found, so far, primarily in Candidatus Marinimicrobia species. Some members of this family have a long C-terminal exten... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045500"
] | [
"Omp28_seleno"
] | [
17
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00053486",
"PUB00106154"
] | [
"12030966",
"35883471"
] | [
"Characterization and expression of a novel Porphyromonas gingivalis outer membrane protein, Omp28.",
"Selenium Metabolism and Selenoproteins in Prokaryotes: A Bioinformatics Perspective."
] | [
2002,
2022
] | 2 | [] | [] | 0 | 0 | null | [
"marine metagenome"
] | [
17
] | 1 | [] | [] | 0 | true | Family | Omp28-related selenoprotein | Omp28-related selenoprotein | Omp28-rel_seleno | 1 |
IPR061435 | 61,435 | Colicin Z toxin | Colicin_Z | Family | 7 | false | false | This entry represents full-length homologues of the colicin Z activity protein [ ]. The C-terminal domain is found more broadly, and is described by . | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041263"
] | [
"colicin_Z_full"
] | [
7
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00106274"
] | [
"31366939"
] | [
"Colicin Z, a structurally and functionally novel colicin type that selectively kills enteroinvasive Escherichia coli and Shigella strains."
] | [
2019
] | 1 | [] | [] | 0 | 0 | null | [
"Enterobacterales"
] | [
7
] | 1 | [] | [] | 0 | true | Family | Colicin Z toxin | Colicin Z toxin | Colicin_Z | 1 |
IPR061436 | 61,436 | PLuB system helicase-like | PLuB_helicase-like | Family | 7 | false | false | The PLuB system is found in deltaproteobacteria. Proteins in this entry, with an AAA+ domain, shows strong local homology to various helicases. The system also includes a CPBP family intramembrane glutamic endopeptidase and a PQQ-binding-like β-propeller repeat protein. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF040671"
] | [
"PLuB_AAA"
] | [
7
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bradymonadales"
] | [
7
] | 1 | [] | [] | 0 | true | Family | PLuB system helicase-like | PLuB system helicase-like | PLuB_helicase-like | 4 |
IPR061437 | 61,437 | Type III-I CRISPR-associated gRAMP effector Cas7-11i | Cas_III-I_gRAMP | Family | 6 | false | false | The giant RAMP (gRAMP) effector of type III-E CRISPR/Cas systems is named Cas7-11 because of its multiple domain structure includes a Cas7 and a Cas11-like region. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF049957"
] | [
"Cas_III-I_gRAMP"
] | [
6
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria"
] | [
6
] | 1 | [] | [] | 0 | true | Family | Type III-I CRISPR-associated gRAMP effector Cas7-11i | Type III-I CRISPR-associated gRAMP effector Cas7-11i | Cas_III-I_gRAMP | 5 |
IPR061438 | 61,438 | Type III-E CRISPR-associated protein Csx30 | CAS_csx30 | Family | 6 | false | false | Csx30, encoded in type III-E CRISPR systems, was identified as the proteolytic target of craspase (CRISPR-guided caspase), which is a complex of the gRAMP (giant RAMP) protein Cas7-11 and the TPR-CHAT protein Csx29 [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041234"
] | [
"CAS_csx30"
] | [
6
] | 1 | [] | [] | [] | 0 | [
"8eey"
] | 1 | [
"PUB00106253"
] | [
"36007061"
] | [
"Craspase is a CRISPR RNA-guided, RNA-activated protease."
] | [
2022
] | 1 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
6
] | 1 | [] | [] | 0 | true | Family | Type III-E CRISPR-associated protein Csx30 | Type III-E CRISPR-associated protein Csx30 | CAS_csx30 | 2 |
IPR061439 | 61,439 | PARCEL repeat surface lipoprotein Mbov_0838-like | Mbov_0838-like | Family | 6 | false | false | This protein family represents one of several surface lipoproteins that are paralogous in the cattle pathogen Mycoplasmopsis bovis, including Mbov_0838 ( ). Members average over 400 amino acids in length, and contain a 100 amino acid region with (mostly weak) PARCEL tandem repeats ( ). | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045896"
] | [
"Mbov_0838_LP"
] | [
6
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00159277",
"PUB00159673"
] | [
"20626840",
"21134966"
] | [
"A versatile palindromic amphipathic repeat coding sequence horizontally distributed among diverse bacterial and eucaryotic microbes.",
"Complete genome sequence of Mycoplasma bovis type strain PG45 (ATCC 25523)."
] | [
2010,
2011
] | 2 | [] | [] | 0 | 0 | null | [
"Mycoplasmopsis bovis"
] | [
6
] | 1 | [] | [] | 0 | true | Family | PARCEL repeat surface lipoprotein Mbov_0838-like | PARCEL repeat surface lipoprotein Mbov_0838-like | Mbov_0838-like | 3 |
IPR061440 | 61,440 | Type III-E CRISPR-associated TPR-CHAT protein Csx29 | CAS_csx29_CRASP | Family | 5 | false | false | Csx29, the protease subunit of the craspase complex, is a TPR-CHAP family protein of type III-E CRISPR/Cas systems. Craspase is guided by crRNA, but cleaves protein, not nucleotide, and therefore is highly interesting for potential technological applications [ , ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041237"
] | [
"CAS_csx29_CRASP"
] | [
5
] | 1 | [] | [] | [] | 0 | [
"7x8a",
"7xc7",
"7xsq",
"7xsr",
"7xss",
"7xt4",
"7y83",
"7y84",
"7y85",
"7y8t",
"7y8y",
"7y9x",
"7y9y",
"7ynd",
"7zoq",
"8d9f",
"8d9g",
"8d9h",
"8eex",
"8eey",
"8gs2",
"8gu6",
"8wmc"
] | 23 | [
"PUB00105607",
"PUB00106253"
] | [
"31857715",
"36007061"
] | [
"Evolutionary classification of CRISPR-Cas systems: a burst of class 2 and derived variants.",
"Craspase is a CRISPR RNA-guided, RNA-activated protease."
] | [
2020,
2022
] | 2 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
5
] | 1 | [] | [] | 0 | true | Family | Type III-E CRISPR-associated TPR-CHAT protein Csx29 | Type III-E CRISPR-associated TPR-CHAT protein Csx29 | CAS_csx29_CRASP | 5 |
IPR061441 | 61,441 | Type III-E CRISPR-associated gRAMP effector Cas7-11e | Cas_III-E_gRAMP | Family | 5 | false | false | The giant RAMP (gRAMP) effector of type III-E CRISPR/Cas systems, named Cas7-11 because of its multiple domains, works together with the caspase-like TPR-CHAT protease (Csx29) in a subset of type III-E systems. The complex of the Cas7-11 and the TPR-CHAT subunits is called craspase (CRISPR-guided caspase) [ , , ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041225"
] | [
"Cas_III-E_gRAMP"
] | [
5
] | 1 | [] | [] | [] | 0 | [
"7wah",
"7x7a",
"7x7r",
"7x8a",
"7xc7",
"7xso",
"7xsp",
"7xsq",
"7xsr",
"7xss",
"7xt4",
"7y80",
"7y81",
"7y82",
"7y83",
"7y84",
"7y85",
"7y8t",
"7y8y",
"7y9x",
"7y9y",
"7yn9",
"7yna",
"7ynb",
"7ync",
"7ynd",
"7zol",
"7zoq",
"8d1v",
"8d8n",
"8d97",
"8d9e"... | 45 | [
"PUB00105607",
"PUB00106252",
"PUB00106253"
] | [
"31857715",
"35643083",
"36007061"
] | [
"Evolutionary classification of CRISPR-Cas systems: a burst of class 2 and derived variants.",
"Structure and engineering of the type III-E CRISPR-Cas7-11 effector complex.",
"Craspase is a CRISPR RNA-guided, RNA-activated protease."
] | [
2020,
2022,
2022
] | 3 | [] | [] | 0 | 0 | null | [
"Pseudomonadati"
] | [
5
] | 1 | [] | [] | 0 | true | Family | Type III-E CRISPR-associated gRAMP effector Cas7-11e | Type III-E CRISPR-associated gRAMP effector Cas7-11e | Cas_III-E_gRAMP | 4 |
IPR061443 | 61,443 | Exosortase XrtG-like, N-terminal extension domain | XrtG_Nterm_ext | Domain | 3 | false | false | This domain appears as an N-terminal extension, or an accompanying protein, for a minority of exosortase XrtG family putative protein-sorting intramembrane endopeptidases. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF045489"
] | [
"XrtG_Nterm_ext"
] | [
3
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Lactobacillus"
] | [
3
] | 1 | [] | [] | 0 | true | Domain | Exosortase XrtG-like, N-terminal extension domain | Exosortase XrtG-like, N-terminal extension domain | XrtG_Nterm_ext | 3 |
IPR061445 | 61,445 | Triculamin-like lasso peptide precursor | Triculamin_precursor | Family | 3 | false | false | Triculamin and lariocidin are very similar naturally occurring peptide antibiotics derived by post-translational modification of ribosomally synthesised precursor peptides. They differ four positions in a core (mature) peptide length of 17. However, the precursor peptide architectures differ substantially, with the cor... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF050031"
] | [
"triculamin_pre"
] | [
3
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00162851",
"PUB00162852",
"PUB00162853"
] | [
"35748039",
"6072424",
"39977644"
] | [
"Triculamin: An Unusual Lasso Peptide with Potent Antimycobacterial Activity.",
"Triculamin, a new antituberculosis substance.",
"Evolution-Guided Discovery of Antimycobacterial Triculamin-Like Lasso Peptides."
] | [
2022,
1967,
2025
] | 3 | [] | [] | 0 | 0 | null | [
"Streptomyces"
] | [
3
] | 1 | [] | [] | 0 | true | Family | Triculamin-like lasso peptide precursor | Triculamin-like lasso peptide precursor | Triculamin_precursor | 3 |
IPR061446 | 61,446 | LPXTG-anchored fibronectin-binding protein FbpA | FbpA | Family | 2 | false | false | FbpA, a fibronectin-binding protein described in Streptococcus pyogenes, has a YSIRK-type (crosswall-targeting) signal peptide and a C-terminal LPXTG motif for covalent attachment to the cell wall [ ]. It is unrelated to the PavA-like protein from Streptococcus gordonii that was given the identical name, so the phase L... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033913"
] | [
"fibronec_FbpA"
] | [
2
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105423"
] | [
"28808160"
] | [
"Incremental Contributions of FbaA and Other Impetigo-Associated Surface Proteins to Fitness and Virulence of a Classical Group A Streptococcal Skin Strain."
] | [
2017
] | 1 | [] | [] | 0 | 0 | null | [
"Streptococcus pyogenes"
] | [
2
] | 1 | [] | [] | 0 | true | Family | LPXTG-anchored fibronectin-binding protein FbpA | LPXTG-anchored fibronectin-binding protein FbpA | FbpA | 9 |
IPR061447 | 61,447 | PorH-like | PorH-like | Family | 2 | false | false | Proteins of this family form major outer membrane hetero-oligomeric pores on the cell wall of Corynebacterium with PorA porins [ ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033937"
] | [
"porH_1"
] | [
2
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105442"
] | [
"19966008"
] | [
"Reconstitution experiments and gene deletions reveal the existence of two-component major cell wall channels in the genus Corynebacterium."
] | [
2010
] | 1 | [] | [] | 0 | 0 | null | [
"Corynebacterium diphtheriae"
] | [
2
] | 1 | [] | [] | 0 | true | Family | PorH-like | PorH-like | PorH-like | 5 |
IPR061450 | 61,450 | MFS transporter auxiliary subunit, OFA tail-like domain | MFS_OXA_tail_dom | Domain | 2,992 | false | false | This entry represents a domain that covers the whole length of the protein in a group of small, hydrophobic bacterial proteins that typically occur next to a much larger MFS (major facilitator superfamily) transporter. In some members of this group, this region occurs as a C-terminal extension domain to MFS transporter... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF047966"
] | [
"MFS_OXA_tail_dom"
] | [
2992
] | 1 | [] | [] | [] | 0 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Bacteria",
"Opisthokonta",
"unclassified sequences"
] | [
2972,
2,
18
] | 3 | [] | [] | 0 | true | Domain | MFS transporter auxiliary subunit, OFA tail-like domain | MFS transporter auxiliary subunit, OFA tail-like domain | MFS_OXA_tail_dom | 5 |
IPR061451 | 61,451 | Major curlin subunit, enterobacterales | CsgA_enterobact | Family | 588 | false | false | Curli is a type of pilin characterised by export of unfolded structural subunits and then amyloid-type self-assembly into fibres. This entry represents CsgA, the major subunit of the type of curli fibres found in E.coli and other enterobacterales. Translocation of CsgA is by the Sec system through the inner membrane, a... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF007470"
] | [
"PRK10051.1"
] | [
588
] | 1 | [
"REACTOME"
] | [
"R-HSA-9638630"
] | [
"REACTOME:R-HSA-9638630"
] | 1 | [
"8enq",
"8enr"
] | 2 | [
"PUB00027885",
"PUB00104532"
] | [
"9457880",
"28496159"
] | [
"Curli fibers are highly conserved between Salmonella typhimurium and Escherichia coli with respect to operon structure and regulation.",
"A comprehensive guide to pilus biogenesis in Gram-negative bacteria."
] | [
1998,
2017
] | 2 | [] | [] | 0 | 0 | null | [
"Gammaproteobacteria",
"Opisthokonta"
] | [
585,
3
] | 2 | [
"Escherichia coli (strain K12)"
] | [
2
] | 1 | true | Family | Major curlin subunit, enterobacterales | Major curlin subunit, enterobacterales | CsgA_enterobact | 8 |
IPR061452 | 61,452 | Secreted effector protein SptP | SptP | Family | 563 | false | false | This entry represents a family of proteins from Sallmonella species, including Secreted effector protein SptP, which facilitates bacterial survival in host cells and includes tyrosine phosphatase and GTPase activating protein (GAP) activities [ , , ]. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF011902"
] | [
"PRK15375.1"
] | [
563
] | 1 | [
"EC"
] | [
"3.1.3.48"
] | [
"EC:3.1.3.48"
] | 1 | [] | 0 | [
"PUB00006663",
"PUB00006683",
"PUB00021650"
] | [
"8866485",
"10499590",
"11163217"
] | [
"A secreted protein tyrosine phosphatase with modular effector domains in the bacterial pathogen Salmonella typhimurium.",
"A salmonella protein antagonizes Rac-1 and Cdc42 to mediate host-cell recovery after bacterial invasion.",
"Modulation of host signaling by a bacterial mimic: structure of the Salmonella e... | [
1996,
1999,
2000
] | 3 | [] | [] | 0 | 0 | null | [
"Salmonella"
] | [
563
] | 1 | [] | [] | 0 | true | Family | Secreted effector protein SptP | Secreted effector protein SptP | SptP | 2 |
IPR061453 | 61,453 | Choice-of-anchor X domain | Choice_anch_X_dom | Domain | 2,940 | false | false | This entry represents a domain mainly found in a group of eukaryotic Calcium-activated chloride channel regulators and prokaryotic proteins with C-terminal sorting signals for processing by rhombosortases and myxosortases and eventual surface attachment. | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF041940"
] | [
"choice_anch_X"
] | [
2940
] | 1 | [
"REACTOME",
"REACTOME"
] | [
"R-HSA-2672351",
"R-MMU-2672351"
] | [
"REACTOME:R-HSA-2672351",
"REACTOME:R-MMU-2672351"
] | 2 | [] | 0 | [] | [] | [] | [] | 0 | [] | [] | 0 | 0 | null | [
"Archaea",
"Bacteria",
"Eukaryota",
"ecological metagenomes"
] | [
43,
1070,
1777,
50
] | 4 | [
"Danio rerio",
"Homo sapiens",
"Mus musculus",
"Rattus norvegicus"
] | [
3,
5,
12,
6
] | 4 | true | Domain | Choice-of-anchor X domain | Choice-of-anchor X domain | Choice_anch_X_dom | 8 |
IPR061454 | 61,454 | Flocculation-associated PEP-CTERM protein PepA-like | PepA-like | Family | 247 | false | false | PepA was described in Zoogloea resiniphila as a PEP-CTERM protein regulated by the PrsK/PrsR two-component system. Knocking out that system blocks flocculation, after which expression of recombinant PepA can restore flocculation [ ]. This entry represents a group of PEP-CTERM-containing proteins from proteobacteria, in... | [] | [] | [] | 0 | [
"NCBIFAM"
] | [
"NF033554"
] | [
"floc_PepA"
] | [
247
] | 1 | [] | [] | [] | 0 | [] | 0 | [
"PUB00105164",
"PUB00152935"
] | [
"29473278",
"36658495"
] | [
"Both widespread PEP-CTERM proteins and exopolysaccharides are required for floc formation of Zoogloea resiniphila and other activated sludge bacteria.",
"An RpoN-dependent PEP-CTERM gene is involved in floc formation of an Aquincola tertiaricarbonis strain."
] | [
2018,
2023
] | 2 | [] | [] | 0 | 0 | null | [
"Bacteria",
"bioreactor metagenome"
] | [
246,
1
] | 2 | [] | [] | 0 | true | Family | Flocculation-associated PEP-CTERM protein PepA-like | Flocculation-associated PEP-CTERM protein PepA-like | PepA-like | 2 |
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