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IID00428
UniprotO15379
ProteinHistone deacetylase 3
GeneHDAC3
OrganismHomo sapiens
Sequence LLPS PhaSepDB
PhaSePro
LLPSDB
DrLLPS
Network xml rdf
Structure
Experiment
  :order   disorder   conflict   PDB cluster   ProS   Pfam Domain   SEG
428
 order/disorder by at least rule
     disorder by at least rule
     order by at least rule
 order/disorder by majority rule
Seq 1-376 Hetero dimer : IID00109Complex
 Evidence X-RAY 4a69 A Reference
       Region 4a69 A 1-1 disorder
       Region 4a69 A 2-370 order
       Region 4a69 A 371-376 disorder
 Evidence X-RAY 4a69 B Reference
       Region 4a69 B 1-1 disorder
       Region 4a69 B 2-370 order
       Region 4a69 B 371-376 disorder
Seqphosphorylation
    424-424 Phosphoserine
 
Prediction
NeProc
Disorder 384-428
Order 1-383
ProS 384-387,395-428
AlphaFold
Disorder 1-1,384-384,386-404,406-428
Order 2-383,385-385,405-405
Pfam Hmmer
PF00850 4-316 4.8e-187
Function
Function in SwissProt
Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4), and some other non-histone substrates. Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Participates in the BCL6 transcriptional repressor activity by deacetylating the H3 'Lys-27' (H3K27) on enhancer elements, antagonizing EP300 acetyltransferase activity and repressing proximal gene expression. Probably participates in the regulation of transcription through its binding to the zinc-finger transcription factor YY1; increases YY1 repression activity. Required to repress transcription of the POU1F1 transcription factor. Acts as a molecular chaperone for shuttling phosphorylated NR2C1 to PML bodies for sumoylation (PubMed:21444723, PubMed:23911289). Contributes, together with XBP1 isoform 1, to the activation of NFE2L2-mediated HMOX1 transcription factor gene expression in a PI(3)K/mTORC2/Akt-dependent signaling pathway leading to endothelial cell (EC) survival under disturbed flow/oxidative stress (PubMed:25190803).