MMP23B
Matrix metalloproteinase-23
Also known as: MIFR, MIFR-1, MMP22, MMP23_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75900
- Gene
- MMP23B
- Ensembl
- ENSG00000189409
- Chromosome
- 1
- Canonical length
- 390 aa
- Protein class
- Enzymes, Predicted intracellular proteins, Transporters
OverviewNCBI Gene
This gene (MMP23B) encodes a member of the matrix metalloproteinase (MMP) family, and it is part of a duplicated region of chromosome 1p36.3. 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. This gene belongs to the more telomeric copy of the duplicated region. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
390 residues, UniProt reviewed canonical sequence.
>O75900|MMP23B
1 MGRGARVPSE APGAGVERRW LGAALVALCL LPALVLLARL GAPAVPAWSA AQGDVAALGL
61 SAVPPTRVPG PLAPRRRRYT LTPARLRWDH FNLTYRILSF PRNLLSPRET RRALAAAFRM
121 WSDVSPFSFR EVAPEQPSDL RIGFYPINHT DCLVSALHHC FDGPTGELAH AFFPPHGGIH
181 FDDSEYWVLG PTRYSWKKGV WLTDLVHVAA HEIGHALGLM HSQHGRALMH LNATLRGWKA
241 LSQDELWGLH RLYGCLDRLF VCASWARRGF CDARRRLMKR LCPSSCDFCY EFPFPTVATT
301 PPPPRTKTRL VPEGRNVTFR CGQKILHKKG KVYWYKDQEP LEFSYPGYLA LGEAHLSIIA
361 NAVNEGTYTC VVRRQQRVLT TYSWRVRVRGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MMP23B 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- ovary: 26 nTPM
- blood vessel: 21 nTPM
- heart muscle: 14 nTPM
- endometrium: 13 nTPM
- lung: 13 nTPM
- prostate: 11 nTPM
Single-cell type
- peritubular myoid cells: 15 nCPM
- leydig cells: 15 nCPM
- ovarian stromal cells: 9.5 nCPM
- corticotrophs: 7.6 nCPM
- hepatic stellate cells: 6.5 nCPM
- oocytes: 4.6 nCPM
Immune cell
- plasmacytoid DC: 11 nTPM
- NK-cell: 2.2 nTPM
- total PBMC: 1.7 nTPM
- gdT-cell: 1.5 nTPM
- memory CD8 T-cell: 1 nTPM
- MAIT T-cell: 0.9 nTPM
Brain region
- cerebral cortex: 3.4 nTPM
- basal ganglia: 3.3 nTPM
- amygdala: 3.2 nTPM
- medulla oblongata: 3 nTPM
- cerebellum: 2.6 nTPM
- hippocampal formation: 2.5 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)
- 1.83
- gnomAD pLI
- 0.12
- gnomAD missense Z
- 0.54
- DepMap mean gene effect
- -0.13
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Peptidase M10, metallopeptidase
- ShKT domain
- Immunoglobulin domain subtype
- Peptidase, metallopeptidase
- Immunoglobulin-like domain
- Immunoglobulin-like fold
- Peptidase M10A
- Metallopeptidase, catalytic domain superfamily
- Peptidase M10A, catalytic domain
- Immunoglobulin-like domain superfamily
- Matrixin
- ShK domain-like
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MMP23B as an antibody target. Whether an autoantibody or antibody against MMP23B could matter depends on whether native MMP23B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MMP23B 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 MMP23B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...