KCMF1
E3 ubiquitin-protein ligase KCMF1
Also known as: DEBT91, DKFZP434L1021, KCMF1_HUMAN, PCMF, ZZZ1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P0J7
- Gene
- KCMF1
- Ensembl
- ENSG00000176407
- Chromosome
- 2
- Canonical length
- 381 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Enables ubiquitin protein ligase activity. Involved in several processes, including negative regulation of HRI-mediated signaling; proteasome-mediated ubiquitin-dependent protein catabolic process; and protein polyubiquitination. Located in cytosol. Is active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
381 residues, UniProt reviewed canonical sequence.
>Q9P0J7|KCMF1
1 MSRHEGVSCD ACLKGNFRGR RYKCLICYDY DLCASCYESG ATTTRHTTDH PMQCILTRVD
61 FDLYYGGEAF SVEQPQSFTC PYCGKMGYTE TSLQEHVTSE HAETSTEVIC PICAALPGGD
121 PNHVTDDFAA HLTLEHRAPR DLDESSGVRH VRRMFHPGRG LGGPRARRSN MHFTSSSTGG
181 LSSSQSSYSP SNREAMDPIA ELLSQLSGVR RSAGGQLNSS GPSASQLQQL QMQLQLERQH
241 AQAARQQLET ARNATRRTNT SSVTTTITQS TATTNIANTE SSQQTLQNSQ FLLTRLNDPK
301 MSETERQSME SERADRSLFV QELLLSTLVR EESSSSDEDD RGEMADFGAM GCVDIMPLDV
361 ALENLNLKES NKGNEPPPPP LLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KCMF1 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)
- 0.53
- Highest tissue expression
- 130 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 130 nTPM
- pancreas: 75 nTPM
- tongue: 67 nTPM
- testis: 64 nTPM
- bone marrow: 57 nTPM
- esophagus: 55 nTPM
Single-cell type
- neutrophils: 426 nCPM
- esophageal apical cells: 391 nCPM
- endometrial glandular cells: 347 nCPM
- ocular epithelial cells: 300 nCPM
- endometrial luminal cells: 267 nCPM
- urothelial cells: 247 nCPM
Immune cell
- T-reg: 6 nTPM
- eosinophil: 5.4 nTPM
- neutrophil: 4.5 nTPM
- basophil: 3.1 nTPM
- naive B-cell: 3.1 nTPM
- gdT-cell: 2.7 nTPM
Brain region
- cerebral cortex: 72 nTPM
- thalamus: 69 nTPM
- midbrain: 67 nTPM
- medulla oblongata: 63 nTPM
- hippocampal formation: 63 nTPM
- pons: 63 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)
- 0.3
- gnomAD pLI
- 0.98
- gnomAD missense Z
- 2.68
- DepMap mean gene effect
- -0.97
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of HRI-mediated signaling
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein K48-linked ubiquitination
- protein K63-linked ubiquitination
- response to oxidative stress
- synaptic signaling
- ubiquitin-dependent protein catabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KCMF1 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 KCMF1 as an antibody target. Whether an autoantibody or antibody against KCMF1 could matter depends on whether native KCMF1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KCMF1 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 KCMF1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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