CDC34
Ubiquitin-conjugating enzyme E2 R1
Also known as: E2-CDC34, UB2R1_HUMAN, UBC3, UBE2R1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P49427
- Gene
- CDC34
- Ensembl
- ENSG00000099804
- Chromosome
- 19
- Canonical length
- 236 aa
- Protein class
- Cancer-related genes, Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear speckles,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a member of the ubiquitin-conjugating enzyme family. Ubiquitin-conjugating enzyme catalyzes the covalent attachment of ubiquitin to other proteins. This protein is a part of the large multiprotein complex, which is required for ubiquitin-mediated degradation of cell cycle G1 regulators, and for the initiation of DNA replication. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
236 residues, UniProt reviewed canonical sequence.
>P49427|CDC34
1 MARPLVPSSQ KALLLELKGL QEEPVEGFRV TLVDEGDLYN WEVAIFGPPN TYYEGGYFKA
61 RLKFPIDYPY SPPAFRFLTK MWHPNIYETG DVCISILHPP VDDPQSGELP SERWNPTQNV
121 RTILLSVISL LNEPNTFSPA NVDASVMYRK WKESKGKDRE YTDIIRKQVL GTKVDAERDG
181 VKVPTTLAEY CVKTKAPAPD EGSDLFYDDY YEDGEVEEEA DSCFGDDEDD SGTEESLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CDC34 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)
- 0.38
- Highest tissue expression
- 108 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 108 nTPM
- testis: 101 nTPM
- liver: 92 nTPM
- heart muscle: 81 nTPM
- cerebellum: 67 nTPM
- colon: 64 nTPM
Single-cell type
- late spermatids: 385 nCPM
- erythrocytes: 109 nCPM
- esophageal apical cells: 90 nCPM
- early spermatids: 88 nCPM
- breast lactating cells: 70 nCPM
- extravillous trophoblasts: 69 nCPM
Immune cell
- neutrophil: 8.2 nTPM
- eosinophil: 4.7 nTPM
- non-classical monocyte: 3.5 nTPM
- basophil: 3.2 nTPM
- memory CD8 T-cell: 2.9 nTPM
- intermediate monocyte: 2.7 nTPM
Brain region
- cerebral cortex: 58 nTPM
- thalamus: 50 nTPM
- white matter: 50 nTPM
- hippocampal formation: 49 nTPM
- amygdala: 49 nTPM
- cerebellum: 47 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)
- 0.31
- gnomAD pLI
- 0.96
- gnomAD missense Z
- 1.83
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to interferon-beta
- DNA replication initiation
- G1/S transition of mitotic cell cycle
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein K48-linked ubiquitination
- protein modification process
- protein polyubiquitination
- protein ubiquitination
- ubiquitin-dependent protein catabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CDC34 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 CDC34 as an antibody target. Whether an autoantibody or antibody against CDC34 could matter depends on whether native CDC34 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CDC34 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 CDC34 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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