Homo sapiens Protein: VPS37D
Summary
InnateDB Protein IDBP-20243.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol VPS37D
Protein Name vacuolar protein sorting 37 homolog D (S. cerevisiae)
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000320416
InnateDB Gene IDBG-20241 (VPS37D)
Protein Structure
UniProt Annotation
Function Component of the ESCRT-I complex, a regulator of vesicular trafficking process. Required for the sorting of endocytic ubiquitinated cargos into multivesicular bodies. May be involved in cell growth and differentiation.
Subcellular Localization Late endosome membrane {ECO:0000305}; Peripheral membrane protein {ECO:0000305}.
Disease Associations Note=VPS37D is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0015031 protein transport
GO:0016032 viral process
GO:0016197 endosomal transport
GO:0019058 viral life cycle
GO:0019068 virion assembly
GO:0019082 viral protein processing
GO:0061024 membrane organization
GO:0075733 intracellular transport of virus
Cellular Component
GO:0000813 ESCRT I complex
GO:0010008 endosome membrane
GO:0031902 late endosome membrane
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR009851 Modifier of rudimentary, Modr
PFAM PF07200
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q86XT2
PhosphoSite PhosphoSite-Q86XT2
TrEMBL
UniProt Splice Variant
Entrez Gene 155382
UniGene Hs.650315
RefSeq NP_001071089
HUGO HGNC:18287
OMIM 610039
CCDS CCDS43596
HPRD
IMGT
EMBL AC073846 AY081952 BC064621
GenPept AAH64621 AAL91075