USP20
Ubiquitin carboxyl-terminal hydrolase 20
Also known as: KIAA1003, UBP20_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y2K6
- Gene
- USP20
- Ensembl
- ENSG00000136878
- Chromosome
- 9
- Canonical length
- 914 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane,Cytosol
OverviewNCBI Gene
This gene encodes a ubiquitin specific processing protease that was first identified as a substrate of the VHL (von Hippel-Lindau disease) protein E3 ubiquitin ligase complex. In addition to being ubiquitinated by the VHL-E3 ligase complex, this enzyme deubiquitinates hypoxia-inducible factor (HIF)-1 alpha and thereby causes increased expression of HIF-1alpha targeted genes which play a role in angiogenesis, glucose metabolism, cell proliferation and metastasis. The enzyme encoded by this gene also regulates G-protein coupled receptor signaling by mediating the deubiquitination of beta-2 adrenergic receptor (ADRB2). This enzyme is a ubiquitously expressed thiolester hydrolase. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jan 2013]
Canonical amino-acid sequenceUniProt
914 residues, UniProt reviewed canonical sequence.
>Q9Y2K6|USP20
1 MGDSRDLCPH LDSIGEVTKE DLLLKSKGTC QSCGVTGPNL WACLQVACPY VGCGESFADH
61 STIHAQAKKH NLTVNLTTFR LWCYACEKEV FLEQRLAAPL LGSSSKFSEQ DSPPPSHPLK
121 AVPIAVADEG ESESEDDDLK PRGLTGMKNL GNSCYMNAAL QALSNCPPLT QFFLECGGLV
181 RTDKKPALCK SYQKLVSEVW HKKRPSYVVP TSLSHGIKLV NPMFRGYAQQ DTQEFLRCLM
241 DQLHEELKEP VVATVALTEA RDSDSSDTDE KREGDRSPSE DEFLSCDSSS DRGEGDGQGR
301 GGGSSQAETE LLIPDEAGRA ISEKERMKDR KFSWGQQRTN SEQVDEDADV DTAMAALDDQ
361 PAEAQPPSPR SSSPCRTPEP DNDAHLRSSS RPCSPVHHHE GHAKLSSSPP RASPVRMAPS
421 YVLKKAQVLS AGSRRRKEQR YRSVISDIFD GSILSLVQCL TCDRVSTTVE TFQDLSLPIP
481 GKEDLAKLHS AIYQNVPAKP GACGDSYAAQ GWLAFIVEYI RRFVVSCTPS WFWGPVVTLE
541 DCLAAFFAAD ELKGDNMYSC ERCKKLRNGV KYCKVLRLPE ILCIHLKRFR HEVMYSFKIN
601 SHVSFPLEGL DLRPFLAKEC TSQITTYDLL SVICHHGTAG SGHYIAYCQN VINGQWYEFD
661 DQYVTEVHET VVQNAEGYVL FYRKSSEEAM RERQQVVSLA AMREPSLLRF YVSREWLNKF
721 NTFAEPGPIT NQTFLCSHGG IPPHKYHYID DLVVILPQNV WEHLYNRFGG GPAVNHLYVC
781 SICQVEIEAL AKRRRIEIDT FIKLNKAFQA EESPGVIYCI SMQWFREWEA FVKGKDNEPP
841 GPIDNSRIAQ VKGSGHVQLK QGADYGQISE ETWTYLNSLY GGGPEIAIRQ SVAQPLGPEN
901 LHGEQKIEAE TRAVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against USP20 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)
- 0.4
- Highest tissue expression
- 30 nTPM
Expression across tissuesHPA
Tissue
- thymus: 30 nTPM
- bone marrow: 21 nTPM
- cerebellum: 20 nTPM
- blood vessel: 18 nTPM
- thyroid gland: 18 nTPM
- lymph node: 17 nTPM
Single-cell type
- platelets: 94 nCPM
- thymocytes: 81 nCPM
- t-cells: 67 nCPM
- megakaryocytes: 62 nCPM
- neutrophil progenitors: 55 nCPM
- nk-cells: 52 nCPM
Immune cell
- T-reg: 12 nTPM
- NK-cell: 10 nTPM
- naive CD4 T-cell: 9.8 nTPM
- MAIT T-cell: 9.1 nTPM
- naive CD8 T-cell: 8.9 nTPM
- memory CD4 T-cell: 8.7 nTPM
Brain region
- hypothalamus: 36 nTPM
- pons: 35 nTPM
- medulla oblongata: 35 nTPM
- midbrain: 33 nTPM
- basal ganglia: 32 nTPM
- cerebral cortex: 31 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)
- 0.48
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.43
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
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
- antiviral innate immune response
- endocytosis
- negative regulation of canonical NF-kappaB signal transduction
- nervous system development
- positive regulation of autophagy
- protein deubiquitination
- protein K48-linked deubiquitination
- protein K63-linked deubiquitination
- proteolysis
- regulation of G protein-coupled receptor signaling pathway
Molecular functions
- cysteine-type deubiquitinase activity
- cysteine-type endopeptidase activity
- G protein-coupled receptor binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Peptidase C19, ubiquitin carboxyl-terminal hydrolase
- Zinc finger, UBP-type
- Peptidase C19, ubiquitin-specific peptidase, DUSP domain
- Zinc finger, RING/FYVE/PHD-type
- Ubiquitin specific protease, conserved site
- Ubiquitin specific protease UPS, catalytic domain
- DUSP-like superfamily
- Papain-like cysteine peptidase superfamily
- Ubiquitin carboxyl-terminal hydrolase
- Ubiquitin carboxyl-terminal hydrolase
- Zn-finger in ubiquitin-hydrolases and other protein
- DUSP domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of USP20 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 USP20 as an antibody target. Whether an autoantibody or antibody against USP20 could matter depends on whether native USP20 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
USP20 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 USP20 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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