Parameter | Value |
---|---|
Gene | H3F3A; H3F3B |
Protein Name | H33_HUMAN |
Organism | Homo sapiens (Human) |
Alternative name(s) | Histone H3.3 |
Protein Family | Histone H3 family |
NCBI Gene ID | 30203021 |
UniProt ID | P84243 |
Enzyme Class | - |
Molecular Weight | 15328 |
Protein Length | 136 |
Protein Domain | InterPro | Pfam |
3D Structure |
PDBe |
PDBj |
RCSB PDB |
DrugPort
ModBase | SwissModel |
Gene Expression | Gene Expression Atlas |
Function and Disease | OMIM |
Protein-protein Interaction Database | STRING | IntAct | MINT |
Kinase Database | Phospho.ELM | PhosphoSite | NetworKIN |
Catalytic Activity (UniProt annotation) | - |
Localization | Nucleus. Chromosome. |
Function (UniProt annotation) | Variant histone H3 which replaces conventional H3 in a wide range of nucleosomes in active genes. Constitutes the predominant form of histone H3 in non-dividing cells and is incorporated into chromatin independently of DNA synthesis. Deposited at sites of nucleosomal displacement throughout transcribed genes, suggesting that it represents an epigenetic imprint of transcriptionally active chromatin. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. |
Gene Ontology | GO:0000183; GO:0000228; GO:0000784; GO:0000786; GO:0000788; GO:0000979; GO:0000980; GO:0001649; GO:0001740; GO:0005576; GO:0005634; GO:0005654; GO:0006334; GO:0006336; GO:0006997; GO:0007286; GO:0007338; GO:0007420; GO:0007566; GO:0007596; GO:0008283; GO:0008584; GO:0009725; GO:0030307; GO:0031492; GO:0031508; GO:0031509; GO:0032200; GO:0032991; GO:0035264; GO:0042692; GO:0044267; GO:0045652; GO:0045814; GO:0046982; GO:0048477; GO:0060964; GO:0070062; GO:0090230; GO:1902340 |
Gene Name | Organism | P-Site | Sequence(+/-7) | Conservation | Disorder | Curator Assessment | Reliability | Evidence Class | Evidence Logic | PubMed | Phospho-ELM | PhosphoSite-Plus |
---|---|---|---|---|---|---|---|---|---|---|---|---|
RPS6KA5 (O75582) | Homo sapiens | S11 | TKQTARKSTGGKAPR | 0.568 | 0.7718 | - | - | - | - | - | - |
|
RPS6KA5 (O75582) | Homo sapiens | S29 | ATKAARKSAPSTGGV | 0.558 | 0.6948 | - | - | - | - | - | - |
|
RPS6KA3 (P51812) | Homo sapiens | S11 | TKQTARKSTGGKAPR | 0.568 | 0.7718 | - | - | - | - | - | - |
|
CHEK1 (O14757) | Homo sapiens | S32 | AARKSAPSTGGVKKP | 0 | 0.7036 | - | - | - | - | - | - |
|
Reactome Pathways
KEGG Pathways
Pathway ID | Pathway Name |
---|---|
hsa05322 | Systemic lupus erythematosus |
hsa05322 | Systemic lupus erythematosus |
No NCI Nature pathways found