Disease:Antibodies against CENPA are present in sera from patients with autoimmune diseases that developed autoantibodies against centrosomal proteins. ,Domain:The CATD (CENPA targeting domain) region is responsible for the more compact structure of nucleosomes containing CENPA and is necessary and sufficient to mediate the localization into centromeres. ,Function:Histone H3-like variant which exclusively replaces conventional H3 in the nucleosome core of centromeric chromatin at the inner plate of the kinetochore. Required for recruitment and assembly of kinetochore proteins , mitotic progression and chromosome segregation. May serve as an epigenetic mark that propagates centromere identity through replication and cell division. ,PTM:Phosphorylation of Ser-7 by Aurora-A/STK6 and Aurora-B/STK12 during prophase is required for localization of Aurora-A/STK6 and Aurora-B/STK12 at inner centromere and is essential for kinetochore function. Initial phosphorylation during prophase is mediated by Aurora-A/STK6 and is maintained by Aurora-B/STK12. ,PTM:Ubiquitinated (Probable) . Interaction with herpes virus HSV-1 ICP0 protein , leads to its degradation by the proteasome pathway. ,similarity:Belongs to the histone H3 family. ,subcellular location:Localizes exclusively in the kinetochore domain of centromeres. ,subunit:Forms a nucleosome-like histone octamer containing two molecules each of H2A , H2B , CENPA and H4 assembled in one CENPA-H4 heterotetramer and two H2A-H2B heterodimers. Nucleosomes containing CENPA also contain histone H2A variants such as macroH2A H2AFY and H2A.Z/H2AFZ. The CENPA-H4 heterotetramer is more compact and structurally more rigid than corresponding H3-H4 heterotetramers. Component of the CENPA-NAC complex , at least composed of CENPA , CENPC , CENPH , CENPM , CENPN , CENPT and MLF1IP/CENPU. Interacts (via CATD domain) with HJURP; the interaction is direct and is required for its localization to centromeres. Interacts directly with herpes virus HSV-1 ICP0 protein. ,
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