GZMM
Granzyme M
Also known as: GRAM_HUMAN, LMET1, MET1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P51124
- Gene
- GZMM
- Ensembl
- ENSG00000197540
- Chromosome
- 19
- Canonical length
- 257 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
Human natural killer (NK) cells and activated lymphocytes express and store a distinct subset of neutral serine proteases together with proteoglycans and other immune effector molecules in large cytoplasmic granules. These serine proteases are collectively termed granzymes and include 4 distinct gene products: granzyme A, granzyme B, granzyme H, and the protein encoded by this gene, granzyme M. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
Canonical amino-acid sequenceUniProt
257 residues, UniProt reviewed canonical sequence.
>P51124|GZMM
1 MEACVSSLLV LALGALSVGS SFGTQIIGGR EVIPHSRPYM ASLQRNGSHL CGGVLVHPKW
61 VLTAAHCLAQ RMAQLRLVLG LHTLDSPGLT FHIKAAIQHP RYKPVPALEN DLALLQLDGK
121 VKPSRTIRPL ALPSKRQVVA AGTRCSMAGW GLTHQGGRLS RVLRELDLQV LDTRMCNNSR
181 FWNGSLSPSM VCLAADSKDQ APCKGDSGGP LVCGKGRVLA RVLSFSSRVC TDIFKPPVAT
241 AVAPYVSWIR KVTGRSALocalizationUniProt · AlphaFold · HPA
Whether an antibody against GZMM 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)
- 0.3
- Highest tissue expression
- 22 nTPM
Expression across tissuesHPA
Tissue
- spleen: 22 nTPM
- bone marrow: 20 nTPM
- lymph node: 18 nTPM
- appendix: 9.4 nTPM
- thymus: 8.1 nTPM
- small intestine: 5.9 nTPM
Single-cell type
- nk-cells: 210 nCPM
- t-cells: 137 nCPM
- respiratory ionocytes: 5.1 nCPM
- innate lymphoid cells: 5 nCPM
- oocytes: 4.6 nCPM
- pdcs: 4.5 nCPM
Immune cell
- gdT-cell: 585 nTPM
- memory CD8 T-cell: 471 nTPM
- naive CD8 T-cell: 380 nTPM
- MAIT T-cell: 367 nTPM
- total PBMC: 227 nTPM
- NK-cell: 195 nTPM
Brain region
- cerebellum: 7 nTPM
- cerebral cortex: 2.5 nTPM
- medulla oblongata: 1.9 nTPM
- pons: 1.9 nTPM
- white matter: 1.9 nTPM
- thalamus: 1.8 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)
- 1.2
- gnomAD pLI
- 0.01
- gnomAD missense Z
- -0.07
- DepMap mean gene effect
- -0.05
- 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
- apoptotic process
- innate immune response
- killing of cells of another organism
- protein maturation
- proteolysis
- T cell mediated cytotoxicity
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GZMM as an antibody target. Whether an autoantibody or antibody against GZMM could matter depends on whether native GZMM is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GZMM is annotated as secreted, so native GZMM 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 GZMM as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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