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Details on Person UniProt:Q8N2Z9 CENPS
| Class:Id | ReferenceGeneProduct:222868 |
|---|---|
| _chainChangeLog | chain:1-138 added on Sat February 7 2015 |
| _displayName | UniProt:Q8N2Z9 CENPS |
| _timestamp | 2025-08-15 22:17:21 |
| chain | chain:1-138 |
| checksum | CBCD22CDDE213D87 |
| comment | FUNCTION DNA-binding component of the Fanconi anemia (FA) core complex. Required for the normal activation of the FA pathway, leading to monoubiquitination of the FANCI-FANCD2 complex in response to DNA damage, cellular resistance to DNA cross-linking drugs, and prevention of chromosomal breakage (PubMed:20347428, PubMed:20347429). In complex with CENPX (MHF heterodimer), crucial cofactor for FANCM in both binding and ATP-dependent remodeling of DNA. Stabilizes FANCM (PubMed:20347428, PubMed:20347429). In complex with CENPX and FANCM (but not other FANC proteins), rapidly recruited to blocked forks and promotes gene conversion at blocked replication forks (PubMed:20347428). In complex with CENPT, CENPW and CENPX (CENP-T-W-S-X heterotetramer), involved in the formation of a functional kinetochore outer plate, which is essential for kinetochore-microtubule attachment and faithful mitotic progression (PubMed:19620631). As a component of MHF and CENP-T-W-S-X complexes, binds DNA and bends it to form a nucleosome-like structure (PubMed:20347428, PubMed:22304917). DNA-binding function is fulfilled in the presence of CENPX, with the following preference for DNA substates: Holliday junction > double-stranded > splay arm > single-stranded. Does not bind DNA on its own (PubMed:20347428, PubMed:20347429).SUBUNIT Heterodimer with CENPX, sometimes called MHF; this interaction stabilizes both partners (PubMed:19620631, PubMed:20347428, PubMed:20347429, PubMed:24522885). MHF heterodimers can assemble to form tetrameric structures (PubMed:22304917). MHF also coassemble with CENPT-CENPW heterodimers at centromeres to form the tetrameric CENP-T-W-S-X complex (PubMed:22304917, PubMed:24522885). Forms a discrete complex with FANCM and CENPX, called FANCM-MHF; this interaction, probably mediated by direct binding between CENPS and FANCM, leads to synergistic activation of double-stranded DNA binding and strongly stimulates FANCM-mediated DNA remodeling (PubMed:20347428, PubMed:20347429). Recruited by FANCM to the Fanconi anemia (FA) core complex, which consists of CENPS, CENPX, FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL, FANCM, FAAP24 and FAAP100. The FA core complex associates with Bloom syndrome (BLM) complex, which consists of at least BLM, DNA topoisomerase 3-alpha (TOP3A), RMI1/BLAP75, RPA1/RPA70 and RPA2/RPA32. The super complex between FA and BLM is called BRAFT (PubMed:20347428, PubMed:20347429). Component of the CENPA-CAD complex, composed of CENPI, CENPK, CENPL, CENPO, CENPP, CENPQ, CENPR and CENPS. The CENPA-CAD complex is probably recruited on centromeres by the CENPA-NAC complex, composed of at least CENPA, CENPC, CENPH, CENPM, CENPN, CENPT and CENPU (PubMed:16622419).INTERACTION Assembly of CENPS and CENPX and its partner subunits CENPT and CENPW at centromeres occurs through a dynamic exchange mechanism. Although exchange is continuous in the cell cycle, de novo assembly starts principally during mid-late S phase and is complete by G2. CENPS is more stably bound at the kinetochore than CENPX (PubMed:19620631, PubMed:24522885). During S phase, rapidly recruited to DNA interstrand cross-links that block replication (PubMed:20347428). Recruited to DNA damage sites about 20 minutes following UV irradiation, reaching a plateau after approximately 40 minutes (PubMed:24522885).ALTERNATIVE PRODUCTS Ubiquitously expressed.DEVELOPMENTAL STAGE Expression varies across the cell cycle, with highest levels in G2 phase (at protein level). No statistically significant changes at the transcript level.SIMILARITY Belongs to the TAF9 family. CENP-S/MHF1 subfamily. |
| created | [InstanceEdit:217385] Schmidt, EE, 2008-03-27 06:23:53 |
| description | recommendedName: Centromere protein S shortName: CENP-S alternativeName: Apoptosis-inducing TAF9-like domain-containing protein 1 alternativeName: fullName evidence="9"FANCM-associated histone fold protein 1 alternativeName: fullName evidence="10"FANCM-interacting histone fold protein 1 alternativeName: Fanconi anemia-associated polypeptide of 16 kDa |
| geneName | CENPS APITD1 FAAP16 MHF1 |
| identifier | Q8N2Z9 |
| isSequenceChanged | FALSE |
| keyword | 3D-structure Acetylation Alternative splicing Cell cycle Cell division Centromere Chromosome DNA damage DNA repair DNA-binding Kinetochore Mitosis Nucleus Proteomics identification Reference proteome |
| modified | [InstanceEdit:9836292] Weiser, Joel, 2023-05-25 [InstanceEdit:9852000] Weiser, Joel, 2023-11-03 [InstanceEdit:9926675] Weiser, Joel, 2024-11-03 [InstanceEdit:9963647] Weiser, Joel, 2025-08-15 |
| name | CENPS |
| referenceDatabase | [ReferenceDatabase:2] UniProt |
| referenceGene | [ReferenceDNASequence:8988313] ENSEMBL:ENSG00000175279 CENPS [Homo sapiens] |
| secondaryIdentifier | CENPS_HUMAN Q8NFE5 Q8NFG5 |
| sequenceLength | 138 |
| species | [Species:48887] Homo sapiens |
| (isoformParent) | [ReferenceIsoform:222869] UniProt:Q8N2Z9-2 CENPS [Homo sapiens] [ReferenceIsoform:222870] UniProt:Q8N2Z9-3 CENPS [Homo sapiens] [ReferenceIsoform:411220] UniProt:Q8N2Z9-1 CENPS [Homo sapiens] |
| (referenceEntity) | [EntityWithAccessionedSequence:375310] APITD1 [cytosol] [Homo sapiens] [EntityWithAccessionedSequence:5633510] APITD1 [nucleoplasm] [Homo sapiens] |
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No pathways have been reviewed or authored by UniProt:Q8N2Z9 CENPS (222868)
