MMP25
Matrix metalloproteinase-25
Also known as: MMP20, MMP25_HUMAN, MMPL1, MT6-MMP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NPA2
- Gene
- MMP25
- Ensembl
- ENSG00000008516
- Chromosome
- 16
- Canonical length
- 562 aa
- Protein class
- Enzymes, Predicted secreted proteins
- Subcellular location
- Plasma membrane
- Secretome location
- Secreted to blood
OverviewNCBI Gene
Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMPs are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. However, the protein encoded by this gene is a member of the membrane-type MMP (MT-MMP) subfamily, attached to the plasma membrane via a glycosylphosphatidyl inositol anchor. In response to bacterial infection or inflammation, the encoded protein is thought to inactivate alpha-1 proteinase inhibitor, a major tissue protectant against proteolytic enzymes released by activated neutrophils, facilitating the transendothelial migration of neutrophils to inflammatory sites. The encoded protein may also play a role in tumor invasion and metastasis through activation of MMP2. The gene has previously been referred to as MMP20 but has been renamed MMP25. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
562 residues, UniProt reviewed canonical sequence.
>Q9NPA2|MMP25
1 MRLRLRLLAL LLLLLAPPAR APKPSAQDVS LGVDWLTRYG YLPPPHPAQA QLQSPEKLRD
61 AIKVMQRFAG LPETGRMDPG TVATMRKPRC SLPDVLGVAG LVRRRRRYAL SGSVWKKRTL
121 TWRVRSFPQS SQLSQETVRV LMSYALMAWG MESGLTFHEV DSPQGQEPDI LIDFARAFHQ
181 DSYPFDGLGG TLAHAFFPGE HPISGDTHFD DEETWTFGSK DGEGTDLFAV AVHEFGHALG
241 LGHSSAPNSI MRPFYQGPVG DPDKYRLSQD DRDGLQQLYG KAPQTPYDKP TRKPLAPPPQ
301 PPASPTHSPS FPIPDRCEGN FDAIANIRGE TFFFKGPWFW RLQPSGQLVS PRPARLHRFW
361 EGLPAQVRVV QAAYARHRDG RILLFSGPQF WVFQDRQLEG GARPLTELGL PPGEEVDAVF
421 SWPQNGKTYL VRGRQYWRYD EAAARPDPGY PRDLSLWEGA PPSPDDVTVS NAGDTYFFKG
481 AHYWRFPKNS IKTEPDAPQP MGPNWLDCPA PSSGPRAPRP PKATPVSETC DCQCELNQAA
541 GRWPAPIPLL LLPLLVGGVA SRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MMP25 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 75 nTPM
Expression across tissuesHPA
Tissue
- spleen: 75 nTPM
- bone marrow: 31 nTPM
- appendix: 14 nTPM
- lung: 13 nTPM
- adipose tissue: 5.2 nTPM
- tongue: 3.2 nTPM
Single-cell type
- neutrophils: 577 nCPM
- cardiomyocytes: 72 nCPM
- neutrophil progenitors: 65 nCPM
- epicardial cells: 36 nCPM
- innate lymphoid cells: 32 nCPM
- endometrial secretory cells: 29 nCPM
Immune cell
- neutrophil: 20 nTPM
- basophil: 18 nTPM
- eosinophil: 4 nTPM
- NK-cell: 0.5 nTPM
- plasmacytoid DC: 0.4 nTPM
- classical monocyte: 0.2 nTPM
Brain region
- cerebral cortex: 3.4 nTPM
- thalamus: 1.4 nTPM
- medulla oblongata: 1.2 nTPM
- pons: 1.2 nTPM
- choroid plexus: 1.1 nTPM
- amygdala: 1 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about MMP25.
Disease | ImmuneIEDB
Conditions an epitope on MMP25 was assayed in.
- multiple sclerosis B cell
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)
- 1.25
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.88
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- collagen catabolic process
- extracellular matrix organization
- hard palate development
- inflammatory response
- proteolysis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Hemopexin-like domain
- Peptidase M10, metallopeptidase
- Peptidoglycan binding-like
- Peptidase, metallopeptidase
- Hemopexin-like repeats
- Peptidase M10A
- Metallopeptidase, catalytic domain superfamily
- Peptidase M10A, catalytic domain
- Hemopexin-like domain superfamily
- Hemopexin
- Matrixin
- Putative peptidoglycan binding domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MMP25 as an antibody target. Whether an autoantibody or antibody against MMP25 could matter depends on whether native MMP25 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MMP25 is annotated at the cell surface, where native MMP25 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label MMP25 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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