LOCUS NP_777579 263 aa linear PRI 29-DEC-2022
DEFINITION rho GTPase-activating protein 27 isoform c [Homo sapiens].
ACCESSION NP_777579 XP_371057
VERSION NP_777579.2
DBSOURCE REFSEQ: accession NM_174919.4
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (residues 1 to 263)
AUTHORS Katoh Y and Katoh M.
TITLE Identification and characterization of ARHGAP27 gene in silico
JOURNAL Int J Mol Med 14 (5), 943-947 (2004)
PUBMED 15492870
REFERENCE 2 (residues 1 to 263)
AUTHORS Sakakibara T, Nemoto Y, Nukiwa T and Takeshima H.
TITLE Identification and characterization of a novel Rho GTPase
activating protein implicated in receptor-mediated endocytosis
JOURNAL FEBS Lett 566 (1-3), 294-300 (2004)
PUBMED 15147912
REFERENCE 3 (residues 1 to 263)
AUTHORS Peck J, Douglas G 4th, Wu CH and Burbelo PD.
TITLE Human RhoGAP domain-containing proteins: structure, function and
evolutionary relationships
JOURNAL FEBS Lett 528 (1-3), 27-34 (2002)
PUBMED 12297274
REMARK Review article
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AC091132.16.
On Apr 15, 2009 this sequence version replaced NP_777579.1.
Summary: This gene encodes a member of a large family of proteins
that activate Rho-type guanosine triphosphate (GTP) metabolizing
enzymes. The encoded protein may pay a role in clathrin-mediated
endocytosis. Alternatively spliced transcript variants encoding
multiple isoforms have been observed for this gene. [provided by
RefSeq, Aug 2013].
Transcript Variant: This variant (3) is a short variant at the 5'
end of a much longer ARHGAP27 gene, and differs in the UTRs and CDS
compared to variant 4. The encoded isoform (c) is shorter than
isoform d.
CCDS Note: This CCDS represents a short variant at the 5' end of a
much longer ARHGAP27 gene. The protein includes an SH3 domain.
##Evidence-Data-START##
Transcript exon combination :: BC067345.1, AK290650.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1968540, SAMEA2142348
[ECO:0000348]
##Evidence-Data-END##
FEATURES Location/Qualifiers
source 1..263
/organism="Homo sapiens"
/db_xref="taxon:9606"
/chromosome="17"
/map="17q21.31"
Protein 1..263
/product="rho GTPase-activating protein 27 isoform c"
/note="SH3 domain containing 20; rho GTPase-activating
protein 27; CIN85-associated multi-domain-containing Rho
GTPase-activating protein 1; rho-type GTPase-activating
protein 27; SH3 domain-containing protein 20"
/calculated_mol_wt=28061
Region 10..66
/region_name="SH3_ARHGAP27"
/note="Src Homology 3 domain of Rho GTPase-activating
protein 27; cd12069"
/db_xref="CDD:213002"
Site order(15,17,20,26,44..45,60,62..63)
/site_type="other"
/note="peptide ligand binding site [polypeptide binding]"
/db_xref="CDD:213002"
Region 104..132
/region_name="Disordered.
/evidence=ECO:0000256|SAM:MobiDB-lite"
/note="propagated from UniProtKB/Swiss-Prot (Q6ZUM4.3)"
Site 156
/site_type="phosphorylation"
/note="Phosphoserine.
/evidence=ECO:0000250|UniProtKB:Q6TLK4; propagated from
UniProtKB/Swiss-Prot (Q6ZUM4.3)"
Site 216
/site_type="phosphorylation"
/note="Phosphoserine.
/evidence=ECO:0000250|UniProtKB:A2AB59; propagated from
UniProtKB/Swiss-Prot (Q6ZUM4.3)"
CDS 1..263
/gene="ARHGAP27"
/gene_synonym="CAMGAP1; PP905; SH3D20; SH3P20"
/coded_by="NM_174919.4:404..1195"
/note="isoform c is encoded by transcript variant 3"
/db_xref="CCDS:CCDS32670.1"
/db_xref="GeneID:201176"
/db_xref="HGNC:HGNC:31813"
/db_xref="MIM:610591"
ORIGIN
1 maadvvgdvy vlvehpfeyt gkdgrrvair pneryrllrr stehwwhvrr epggrpfylp
61 aqyvrelpal gnpaaaappg phpspaapep laydyrfvsa aatagpdgap eesggrassl
121 cgpaqrgaat qrsslapglp aclylrpaap vrpaqslndl acaavsppag llgssgsfka
181 csvagswvcp rplarsdsen vyeviqdlhv pppeesaeqv ppralgrggg wrardrarte
241 pgrketrsaq rrarrpplse dfg
//