ADAMTS5
A disintegrin and metalloproteinase with thrombospondin motifs 5
Also known as: ADAMTS11, ADMP-2, ATS5_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UNA0
- Gene
- ADAMTS5
- Ensembl
- ENSG00000154736
- Chromosome
- 21
- Canonical length
- 930 aa
- Protein class
- Cancer-related genes, Predicted secreted proteins
- Subcellular location
- Nucleoplasm
- Secretome location
- Secreted to extracellular matrix
OverviewNCBI Gene
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature enzyme. This enzyme contains two C-terminal TS motifs and functions as an aggrecanase that cleaves aggrecan, a major proteoglycan of cartilage, and may mediate cartilage destruction in osteoarthritis. [provided by RefSeq, Feb 2016]
Canonical amino-acid sequenceUniProt
930 residues, UniProt reviewed canonical sequence.
>Q9UNA0|ADAMTS5
1 MLLGWASLLL CAFRLPLAAV GPAATPAQDK AGQPPTAAAA AQPRRRQGEE VQERAEPPGH
61 PHPLAQRRRS KGLVQNIDQL YSGGGKVGYL VYAGGRRFLL DLERDGSVGI AGFVPAGGGT
121 SAPWRHRSHC FYRGTVDGSP RSLAVFDLCG GLDGFFAVKH ARYTLKPLLR GPWAEEEKGR
181 VYGDGSARIL HVYTREGFSF EALPPRASCE TPASTPEAHE HAPAHSNPSG RAALASQLLD
241 QSALSPAGGS GPQTWWRRRR RSISRARQVE LLLVADASMA RLYGRGLQHY LLTLASIANR
301 LYSHASIENH IRLAVVKVVV LGDKDKSLEV SKNAATTLKN FCKWQHQHNQ LGDDHEEHYD
361 AAILFTREDL CGHHSCDTLG MADVGTICSP ERSCAVIEDD GLHAAFTVAH EIGHLLGLSH
421 DDSKFCEETF GSTEDKRLMS SILTSIDASK PWSKCTSATI TEFLDDGHGN CLLDLPRKQI
481 LGPEELPGQT YDATQQCNLT FGPEYSVCPG MDVCARLWCA VVRQGQMVCL TKKLPAVEGT
541 PCGKGRICLQ GKCVDKTKKK YYSTSSHGNW GSWGSWGQCS RSCGGGVQFA YRHCNNPAPR
601 NNGRYCTGKR AIYRSCSLMP CPPNGKSFRH EQCEAKNGYQ SDAKGVKTFV EWVPKYAGVL
661 PADVCKLTCR AKGTGYYVVF SPKVTDGTEC RLYSNSVCVR GKCVRTGCDG IIGSKLQYDK
721 CGVCGGDNSS CTKIVGTFNK KSKGYTDVVR IPEGATHIKV RQFKAKDQTR FTAYLALKKK
781 NGEYLINGKY MISTSETIID INGTVMNYSG WSHRDDFLHG MGYSATKEIL IVQILATDPT
841 KPLDVRYSFF VPKKSTPKVN SVTSHGSNKV GSHTSQPQWV TGPWLACSRT CDTGWHTRTV
901 QCQDGNRKLA KGCPLSQRPS AFKQCLLKKCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ADAMTS5 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.35
- Highest tissue expression
- 25 nTPM
Expression across tissuesHPA
Tissue
- placenta: 25 nTPM
- ovary: 24 nTPM
- adipose tissue: 16 nTPM
- endometrium: 12 nTPM
- breast: 9.9 nTPM
- spleen: 7.3 nTPM
Single-cell type
- fibro-adipogenic progenitors: 224 nCPM
- breast myoepithelial cells: 165 nCPM
- fibroblasts: 162 nCPM
- endometrial stromal cells: 119 nCPM
- adipocytes: 115 nCPM
- myosatellite cells: 111 nCPM
Immune cell
- classical monocyte: 0.1 nTPM
- basophil: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 7.3 nTPM
- choroid plexus: 5.9 nTPM
- spinal cord: 3.5 nTPM
- medulla oblongata: 3.2 nTPM
- white matter: 2.9 nTPM
- midbrain: 2.2 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)
- 0.7
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.77
- DepMap mean gene effect
- 0.03
- 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
- aortic valve morphogenesis
- defense response to bacterium
- endocardial cushion morphogenesis
- extracellular matrix disassembly
- extracellular matrix organization
- myoblast fusion
- negative regulation of cold-induced thermogenesis
- proteolysis
- pulmonary valve morphogenesis
Molecular functions
- endopeptidase activity
- extracellular matrix binding
- heparin binding
- identical protein binding
- integrin binding
- metalloendopeptidase activity
- metallopeptidase activity
- peptidase activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Thrombospondin type-1 (TSP1) repeat
- Peptidase M12B, ADAM/reprolysin
- ADAM, cysteine-rich domain
- ADAMTS/ADAMTS-like, Spacer 1
- ADAMTS/ADAMTS-like
- Metallopeptidase, catalytic domain superfamily
- Thrombospondin type-1 repeat superfamily
- ADAMTS, cysteine-rich domain 2
- ADAMTS/ADAMTS-like, cysteine-rich domain 3
- ADAMTS and ADAMTS-like
- Thrombospondin type 1 domain
- Reprolysin (M12B) family zinc metalloprotease
- ADAM-TS Spacer 1
- ADAMTS cysteine-rich domain 2
- Thrombospondin type 1 domain
- ADAMTS cysteine-rich domain
- Peptidase M12B, ADAM-TS5
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ADAMTS5 as an antibody target. Whether an autoantibody or antibody against ADAMTS5 could matter depends on whether native ADAMTS5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ADAMTS5 is annotated as secreted, so native ADAMTS5 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label ADAMTS5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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