UBA7
Ubiquitin-like modifier-activating enzyme 7
Also known as: D8, UBA1B, UBA7_HUMAN, UBE1L, UBE2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P41226
- Gene
- UBA7
- Ensembl
- ENSG00000182179
- Chromosome
- 3
- Canonical length
- 1012 aa
- Protein class
- Metabolic proteins, Plasma proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Vesicles,Cytosol
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 E1 ubiquitin-activating enzyme family. The encoded enzyme is a retinoid target that triggers promyelocytic leukemia (PML)/retinoic acid receptor alpha (RARalpha) degradation and apoptosis in acute promyelocytic leukemia, where it is involved in the conjugation of the ubiquitin-like interferon-stimulated gene 15 protein. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
1012 residues, UniProt reviewed canonical sequence.
>P41226|UBA7
1 MDALDASKLL DEELYSRQLY VLGSPAMQRI QGARVLVSGL QGLGAEVAKN LVLMGVGSLT
61 LHDPHPTCWS DLAAQFLLSE QDLERSRAEA SQELLAQLNR AVQVVVHTGD ITEDLLLDFQ
121 VVVLTAAKLE EQLKVGTLCH KHGVCFLAAD TRGLVGQLFC DFGEDFTVQD PTEAEPLTAA
181 IQHISQGSPG ILTLRKGANT HYFRDGDLVT FSGIEGMVEL NDCDPRSIHV REDGSLEIGD
241 TTTFSRYLRG GAITEVKRPK TVRHKSLDTA LLQPHVVAQS SQEVHHAHCL HQAFCALHKF
301 QHLHGRPPQP WDPVDAETVV GLARDLEPLK RTEEEPLEEP LDEALVRTVA LSSAGVLSPM
361 VAMLGAVAAQ EVLKAISRKF MPLDQWLYFD ALDCLPEDGE LLPSPEDCAL RGSRYDGQIA
421 VFGAGFQEKL RRQHYLLVGA GAIGCELLKV FALVGLGAGN SGGLTVVDMD HIERSNLSRQ
481 FLFRSQDVGR PKAEVAAAAA RGLNPDLQVI PLTYPLDPTT EHIYGDNFFS RVDGVAAALD
541 SFQARRYVAA RCTHYLKPLL EAGTSGTWGS ATVFMPHVTE AYRAPASAAA SEDAPYPVCT
601 VRYFPSTAEH TLQWARHEFE ELFRLSAETI NHHQQAHTSL ADMDEPQTLT LLKPVLGVLR
661 VRPQNWQDCV AWALGHWKLC FHYGIKQLLR HFPPNKVLED GTPFWSGPKQ CPQPLEFDTN
721 QDTHLLYVLA AANLYAQMHG LPGSQDWTAL RELLKLLPQP DPQQMAPIFA SNLELASASA
781 EFGPEQQKEL NKALEVWSVG PPLKPLMFEK DDDSNFHVDF VVAAASLRCQ NYGIPPVNRA
841 QSKRIVGQII PAIATTTAAV AGLLGLELYK VVSGPRPRSA FRHSYLHLAE NYLIRYMPFA
901 PAIQTFHHLK WTSWDRLKVP AGQPERTLES LLAHLQEQHG LRVRILLHGS ALLYAAGWSP
961 EKQAQHLPLR VTELVQQLTG QAPAPGQRVL VLELSCEGDD EDTAFPPLHY ELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against UBA7 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)
- 0.24
- Highest tissue expression
- 63 nTPM
Expression across tissuesHPA
Tissue
- spleen: 63 nTPM
- lymph node: 48 nTPM
- small intestine: 46 nTPM
- duodenum: 41 nTPM
- salivary gland: 40 nTPM
- bone marrow: 38 nTPM
Single-cell type
- platelets: 338 nCPM
- megakaryocytes: 105 nCPM
- foveolar cells: 55 nCPM
- late spermatids: 54 nCPM
- mast cells: 48 nCPM
- enterocytes: 48 nCPM
Immune cell
- eosinophil: 39 nTPM
- intermediate monocyte: 33 nTPM
- non-classical monocyte: 28 nTPM
- classical monocyte: 23 nTPM
- total PBMC: 22 nTPM
- myeloid DC: 21 nTPM
Brain region
- white matter: 16 nTPM
- medulla oblongata: 15 nTPM
- thalamus: 12 nTPM
- pons: 12 nTPM
- spinal cord: 12 nTPM
- cerebral cortex: 9.5 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)
- 0.89
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.99
- DepMap mean gene effect
- -0.12
- 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
- DNA damage response
- innate immune response
- ISG15-protein conjugation
- modification-dependent protein catabolic process
- protein ubiquitination
Molecular functions
- ATP binding
- ubiquitin-protein transferase activity
- ISG15 activating enzyme activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Ubiquitin/SUMO-activating enzyme E1-like
- THIF-type NAD/FAD binding fold
- Ubiquitin-activating enzyme E1
- Ubiquitin-activating enzyme E1, C-terminal
- Ubiquitin-activating enzyme, SCCH domain
- Ubiquitin-activating enzyme E1, Cys active site
- Ubiquitin-activating enzyme-like
- Ubiquitin-activating enzyme E1, C-terminal domain superfamily
- Ubiquitin-activating enzyme E1, SCCH domain
- Ubiquitin-activating enzyme E1, FCCH domain superfamily
- Ubiquitin-activating enzyme E1, inactive adenylation domain, subdomain 1
- ThiF/MoeB/HesA family
- ThiF family
- Ubiquitin fold domain
- Ubiquitin-activating enzyme, SCCH domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of UBA7 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
- UL26
- ISG15
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads UBA7 as an antibody target. Whether an autoantibody or antibody against UBA7 could matter depends on whether native UBA7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
UBA7 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 UBA7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...