Search Results
Overview
| Uniprot ID | Q9UIG0 |
|---|---|
| Protein Name | Tyrosine-protein kinase BAZ1B |
| Gene Name | BAZ1B |
| Organism | Homo sapiens |
Kla Sites from experimental identification
| Position | Flanking peptide |
|---|---|
| 1121 | APKQKRRKLQSEDSA |
| 1335 | DELVLQTKRSSRRQS |
| 200 | RARRSPRKLPTSLKK |
| 206 | RKLPTSLKKGERKWA |
| 322 | RKPSKKSKTDNSSLS |
| 352 | SLSGSPLKVKNSKNS |
| 354 | SGSPLKVKNSKNSKS |
| 386 | HTNFHIPKKGPPAKK |
| 387 | TNFHIPKKGPPAKKP |
| 416 | KGILNGQKSTGNSKS |
| 843 | EDMISAVKSRRLLAI |
| 942 | YRFNHHCKDHTVSGD |
Function
Atypical tyrosine-protein kinase that plays a central role in chromatin remodeling and acts as a transcription regulator (PubMed:19092802). Involved in DNA damage response by phosphorylating 'Tyr-142' of histone H2AX (H2AXY142ph) (PubMed:19092802, PubMed:19234442). H2AXY142ph plays a central role in DNA repair and acts as a mark that distinguishes between apoptotic and repair responses to genotoxic stress (PubMed:19092802, PubMed:19234442). Regulatory subunit of the ATP-dependent WICH-1 and WICH-5 ISWI chromatin remodeling complexes, which form ordered nucleosome arrays on chromatin and facilitate access to DNA during DNA-templated processes such as DNA replication, transcription, and repair (PubMed:11980720, PubMed:28801535). Both complexes regulate the spacing of nucleosomes along the chromatin and have the ability to slide mononucleosomes to the center of a DNA template (PubMed:28801535). The WICH-1 ISWI chromatin remodeling complex has a lower ATP hydrolysis rate than the WICH-5 ISWI chromatin remodeling complex (PubMed:28801535). The WICH-5 ISWI chromatin-remodeling complex regulates the transcription of various genes, has a role in RNA polymerase I transcription (By similarity). Within the B-WICH complex has a role in RNA polymerase III transcription (PubMed:16603771). Mediates the recruitment of the WICH-5 ISWI chromatin remodeling complex to replication foci during DNA replication (PubMed:15543136)
Protein Sequence
Gene Ontology
| Classification | GO ID | Description |
|---|---|---|
| Cellular Component | GO:0000793 | condensed chromosome |
| Cellular Component | GO:0005730 | nucleolus |
| Cellular Component | GO:0005654 | nucleoplasm |
| Cellular Component | GO:0005634 | nucleus |
| Cellular Component | GO:0005721 | pericentric heterochromatin |
| Cellular Component | GO:0090535 | WICH complex |
| Molecular Function | GO:0005524 | ATP binding |
| Molecular Function | GO:0042393 | histone binding |
| Molecular Function | GO:0140801 | histone H2AXY142 kinase activity |
| Molecular Function | GO:0035173 | histone kinase activity |
| Molecular Function | GO:0004715 | non-membrane spanning protein tyrosine kinase activity |
| Molecular Function | GO:0008270 | zinc ion binding |
| Biological Process | GO:0006338 | chromatin remodeling |
| Biological Process | GO:0006974 | DNA damage response |
| Biological Process | GO:0006351 | DNA-templated transcription |
| Biological Process | GO:1905213 | negative regulation of mitotic chromosome condensation |
| Biological Process | GO:0045943 | positive regulation of transcription by RNA polymerase I |
| Biological Process | GO:0045944 | positive regulation of transcription by RNA polymerase II |
| Biological Process | GO:0045945 | positive regulation of transcription by RNA polymerase III |
| Biological Process | GO:0043687 | post-translational protein modification |
| Biological Process | GO:0006357 | regulation of transcription by RNA polymerase II |
Reference
[1] He C, Zhang J, Bai X, Lu C, Zhang K. Lysine lactylation-based insight to understanding the characterization of cervical cancer.. Biochim Biophys Acta Mol Basis Dis 1870(7):167356. 2024 Oct. PMID: 39025375.
[2] He J, Lai T, Zhou Z, Yang H, Lei Z et al.. Multiomics profiling reveals the involvement of protein lactylation in nonhomologous end joining pathway conferring radioresistance in lung adenocarcinoma cell.. Sci Rep 15(1):24651. 2025 Jul 9. PMID: 40634431.
[3] Wu Q, Li Z, Gong T, Zheng X, Zhou X et al.. Porphyromonas gingivalis infection induces lysine lactylation reprogramming in human umbilical vein endothelial cells.. Front Cell Infect Microbiol 16:1706727. 2026. PMID: 41696360.