UBE2E1
Ubiquitin-conjugating enzyme E2 E1
Also known as: UB2E1_HUMAN, UbcH6
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P51965
- Gene
- UBE2E1
- Ensembl
- ENSG00000170142
- Chromosome
- 3
- Canonical length
- 193 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conjugating enzymes, or E2s, and ubiquitin-protein ligases, or E3s. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. Three alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jan 2011]
Canonical amino-acid sequenceUniProt
193 residues, UniProt reviewed canonical sequence.
>P51965|UBE2E1
1 MSDDDSRAST SSSSSSSSNQ QTEKETNTPK KKESKVSMSK NSKLLSTSAK RIQKELADIT
61 LDPPPNCSAG PKGDNIYEWR STILGPPGSV YEGGVFFLDI TFTPEYPFKP PKVTFRTRIY
121 HCNINSQGVI CLDILKDNWS PALTISKVLL SICSLLTDCN PADPLVGSIA TQYMTNRAEH
181 DRMARQWTKR YATLocalizationUniProt · AlphaFold · HPA
Whether an antibody against UBE2E1 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)
- 0.37
- Highest tissue expression
- 116 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 116 nTPM
- spinal cord: 105 nTPM
- tonsil: 101 nTPM
- parathyroid gland: 97 nTPM
- midbrain: 96 nTPM
- lymph node: 96 nTPM
Single-cell type
- esophageal apical cells: 377 nCPM
- monocytes: 334 nCPM
- microglia: 326 nCPM
- neutrophil progenitors: 279 nCPM
- sertoli cells: 273 nCPM
- neutrophils: 268 nCPM
Immune cell
- intermediate monocyte: 4.7 nTPM
- NK-cell: 4.3 nTPM
- classical monocyte: 4.2 nTPM
- plasmacytoid DC: 4 nTPM
- myeloid DC: 3.8 nTPM
- eosinophil: 3.7 nTPM
Brain region
- white matter: 92 nTPM
- hypothalamus: 81 nTPM
- medulla oblongata: 78 nTPM
- spinal cord: 77 nTPM
- cerebellum: 74 nTPM
- pons: 71 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)
- 0.57
- gnomAD pLI
- 0.71
- gnomAD missense Z
- 1.99
- DepMap mean gene effect
- 0.02
- 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
- ISG15-protein conjugation
- positive regulation of transcription by RNA polymerase II
- protein K48-linked ubiquitination
- protein monoubiquitination
- protein polyubiquitination
- protein ubiquitination
- ubiquitin-dependent protein catabolic process
Molecular functions
- ATP binding
- ISG15 transferase activity
- ubiquitin conjugating enzyme activity
- ubiquitin-protein transferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of UBE2E1 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 UBE2E1 as an antibody target. Whether an autoantibody or antibody against UBE2E1 could matter depends on whether native UBE2E1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
UBE2E1 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 UBE2E1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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