Homo sapiens Protein: VHLL
Summary
InnateDB Protein IDBP-721894.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol VHLL
Protein Name
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000464258
InnateDB Gene IDBG-103466 (VHLL)
Protein Structure
UniProt Annotation
Function Functions as a dominant-negative VHL to serve as a protector of HIFalpha. {ECO:0000269PubMed:14757845}.
Subcellular Localization
Disease Associations
Tissue Specificity Abundantly expressed in the placenta. {ECO:0000269PubMed:14757845}.
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
GO:0005515 protein binding
GO:0032403 protein complex binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0001525 angiogenesis
GO:0001666 response to hypoxia
GO:0006355 regulation of transcription, DNA-templated
GO:0010498 proteasomal protein catabolic process
GO:0016567 protein ubiquitination
GO:0030163 protein catabolic process
GO:0030182 neuron differentiation
GO:0030198 extracellular matrix organization
GO:0042069 regulation of catecholamine metabolic process
GO:0043534 blood vessel endothelial cell migration
GO:0045471 response to ethanol
GO:0051291 protein heterooligomerization
GO:0070243 regulation of thymocyte apoptotic process
GO:0070244 negative regulation of thymocyte apoptotic process
GO:2001233 regulation of apoptotic signaling pathway
Cellular Component
GO:0005634 nucleus
GO:0005739 mitochondrion
GO:0005829 cytosol
GO:0005929 cilium
GO:0030891 VCB complex
Protein Structure and Domains
PDB ID
InterPro IPR022772 von Hippel-Lindau disease tumour suppressor, beta/alpha domain
PFAM PF01847
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q6RSH7
PhosphoSite PhosphoSite-Q6RSH7
TrEMBL
UniProt Splice Variant
Entrez Gene 391104
UniGene Hs.532378
RefSeq NP_001004319
HUGO HGNC:30666
OMIM
CCDS
HPRD 15648
IMGT
EMBL AY494836 BC130596 BC130598
GenPept AAI30597 AAI30599 AAS48916