Homo sapiens Protein: ZNF431
Summary
InnateDB Protein IDBP-40777.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ZNF431
Protein Name zinc finger protein 431
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000308578
InnateDB Gene IDBG-40775 (ZNF431)
Protein Structure
UniProt Annotation
Function Sequence-specific DNA binding transcriptional repressor. Represses target gene transcription by recruiting HDAC1 and HDAC2 histone deacetylases. Acts as a specific transcriptional repressor for PTCH1 during embryonic development. Required for osteoblast differentiation and sonic hedgehog/SHH signaling response. Binds to the consensus site 5'-GCGCCC-3' in the promoter of PTCH1 (By similarity). {ECO:0000250}.
Subcellular Localization Nucleus {ECO:0000250}.
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 11 experimentally validated interaction(s) in this database.
Experimentally validated
Total 11 [view]
Protein-Protein 11 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0001046 core promoter sequence-specific DNA binding
GO:0003676 nucleic acid binding
GO:0003682 chromatin binding
GO:0046872 metal ion binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0030154 cell differentiation
GO:0043433 negative regulation of sequence-specific DNA binding transcription factor activity
Cellular Component
GO:0005622 intracellular
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro IPR001909 Krueppel-associated box
IPR007087 Zinc finger, C2H2
IPR015880 Zinc finger, C2H2-like
PFAM PF01352
PF00096
PRINTS
PIRSF
SMART SM00349
SM00355
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8TF32
PhosphoSite PhosphoSite-Q8TF32
TrEMBL A0A024R7Q8
UniProt Splice Variant
Entrez Gene 170959
UniGene Hs.687547
RefSeq NP_597730
HUGO HGNC:20809
OMIM
CCDS CCDS32979
HPRD 15789
IMGT
EMBL AB075849 AK293072 BC040506 CH471106
GenPept AAH40506 BAB85555 BAF85761 EAW84889 EAW84890