CENPU
Centromere protein U
Also known as: CENP-50, CENP-U, CENPU_HUMAN, KLIP1, MLF1IP, PBIP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q71F23
- Gene
- CENPU
- Ensembl
- ENSG00000151725
- Chromosome
- 4
- Canonical length
- 418 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Centriolar satellite
OverviewNCBI Gene
The centromere is a specialized chromatin domain, present throughout the cell cycle, that acts as a platform on which the transient assembly of the kinetochore occurs during mitosis. All active centromeres are characterized by the presence of long arrays of nucleosomes in which CENPA (MIM 117139) replaces histone H3 (see MIM 601128). MLF1IP, or CENPU, is an additional factor required for centromere assembly (Foltz et al., 2006 [PubMed 16622419]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
418 residues, UniProt reviewed canonical sequence.
>Q71F23|CENPU
1 MAPRGRRRPR PHRSEGARRS KNTLERTHSM KDKAGQKCKP IDVFDFPDNS DVSSIGRLGE
61 NEKDEETYET FDPPLHSTAI YADEEEFSKH CGLSLSSTPP GKEAKRSSDT SGNEASEIES
121 VKISAKKPGR KLRPISDDSE SIEESDTRRK VKSAEKISTQ RHEVIRTTAS SELSEKPAES
181 VTSKKTGPLS AQPSVEKENL AIESQSKTQK KGKISHDKRK KSRSKAIGSD TSDIVHIWCP
241 EGMKTSDIKE LNIVLPEFEK THLEHQQRIE SKVCKAAIAT FYVNVKEQFI KMLKESQMLT
301 NLKRKNAKMI SDIEKKRQRM IEVQDELLRL EPQLKQLQTK YDELKERKSS LRNAAYFLSN
361 LKQLYQDYSD VQAQEPNVKE TYDSSSLPAL LFKARTLLGA ESHLRNINHQ LEKLLDQGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CENPU can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.62
- Highest tissue expression
- 59 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 59 nTPM
- testis: 28 nTPM
- lymph node: 15 nTPM
- skin: 14 nTPM
- tonsil: 13 nTPM
- thymus: 12 nTPM
Single-cell type
- late spermatids: 1,614 nCPM
- late primary spermatocytes: 809 nCPM
- early primary spermatocytes: 469 nCPM
- early spermatids: 417 nCPM
- oocytes: 240 nCPM
- erythrocyte progenitors: 230 nCPM
Immune cell
- basophil: 21 nTPM
- eosinophil: 14 nTPM
- NK-cell: 3.6 nTPM
- non-classical monocyte: 2.8 nTPM
- T-reg: 2.5 nTPM
- intermediate monocyte: 2 nTPM
Brain region
- cerebellum: 1.8 nTPM
- pons: 1.8 nTPM
- white matter: 1.6 nTPM
- thalamus: 1.4 nTPM
- cerebral cortex: 1.3 nTPM
- basal ganglia: 1.2 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.98
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.46
- DepMap mean gene effect
- -0.14
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Centromere protein U
- CENP-A nucleosome associated complex (NAC) subunit
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CENPU in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CENPU as an antibody target. Whether an autoantibody or antibody against CENPU could matter depends on whether native CENPU is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CENPU is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CENPU as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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