GSTM4
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesGSTM4, GSTM4-4, GTM4, glutathione S-transferase mu 4
External IDsOMIM: 138333 MGI: 95862 HomoloGene: 37357 GeneCards: GSTM4
Orthologs
SpeciesHumanMouse
Entrez

2948

14865

Ensembl

ENSG00000168765

ENSMUSG00000027890

UniProt

Q03013

Q8R5I6

RefSeq (mRNA)

NM_000850
NM_147148
NM_147149

NM_001160411
NM_026764

RefSeq (protein)

NP_000841
NP_671489

NP_001153883
NP_081040

Location (UCSC)Chr 1: 109.66 – 109.67 MbChr 3: 107.95 – 107.95 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Glutathione S-transferase Mu 4 is an enzyme that in humans is encoded by the GSTM4 gene.[5][6]

Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Diversification of these genes has occurred in regions encoding substrate-binding domains, as well as in tissue expression patterns, to accommodate an increasing number of foreign compounds. Multiple transcript variants, each encoding a distinct protein isoform, have been identified.[6]

In the August 2009 issue of Oncogene journal, researchers at Huntsman Cancer Institute (HCI) at the University of Utah demonstrated that expression levels of GSTM4 could predict response to chemotherapy in patients with Ewing sarcoma. The study found that patients who did not respond to chemotherapy had high levels of GSTM4.[7]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000168765 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000027890 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Ross VL, Board PG, Webb GC (Feb 1994). "Chromosomal mapping of the human Mu class glutathione S-transferases to 1p13". Genomics. 18 (1): 87–91. doi:10.1006/geno.1993.1429. PMID 8276420.
  6. 1 2 "Entrez Gene: GSTM4 glutathione S-transferase M4".
  7. OncoGenetics.Org (August 2009). "New hope for deadly childhood bone cancer". OncoGenetics.Org. Archived from the original on 2015-09-24. Retrieved 2009-08-31.

Further reading

  • Overview of all the structural information available in the PDB for UniProt: Q03013 (Glutathione S-transferase Mu 4) at the PDBe-KB.


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