GSTM3

Gene Information
 
Gene Symbol
GSTM3
 
Aliases
GST5, GSTB, GSTM3-3, GTM3
 
Entrez Gene ID
 
Gene Name
Glutathione S-transferase mu 3
 
Chromosomal Location
1p13.3
 
HGNC ID
 
Summary
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. Mutations of this class mu gene have been linked with a slight increase in a number of cancers, likely due to exposure with environmental toxins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0006749 Biological process Glutathione metabolic process IBA 21873635
GO:0006749 Biological process Glutathione metabolic process IDA 8373352, 10587441
GO:0008065 Biological process Establishment of blood-nerve barrier TAS 2345169
GO:0018916 Biological process Nitrobenzene metabolic process IDA 8373352
GO:0042178 Biological process Xenobiotic catabolic process IBA 21873635
Protein Information
 
Protein Name
Glutathione S-transferase Mu 3, GST class-mu 3, S-(hydroxyalkyl)glutathione lyase M3, brain GST, brain type mu-glutathione S-transferase, epididymis secretory sperm binding protein, glutathione S-alkyltransferase M3, glutathione S-aralkyltransferase M3, glutathione S-aryltransferase M3, glutathione S-transferase M3 (brain), glutathione S-transferase mu 3 (brain), glutathione S-transferase, Mu-3, hGSTM3-3
 
Function
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. May govern uptake and detoxification of both endogenous compounds and xenobiotics at the testis and brain blood barriers.
 
UniProt
 
PDB
 
Pfam
Pfam Accession Pfam ID
PF00043 GST_C
PF02798 GST_N
Pathways
 
KEGG
 
Reactome
 

Glutathione metabolism
Metabolism of xenobiotics by cytochrome P450
Drug metabolism - cytochrome P450
Drug metabolism - other enzymes
Metabolic pathways
Platinum drug resistance
Pathways in cancer
Chemical carcinogenesis
Hepatocellular carcinoma
Fluid shear stress and atherosclerosis

 

Glutathione conjugation

Interactions
 
STRING MINT IntAct
ENSP00000405330 P03372 P03372
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Digestive System Diseases
Hepatitis
Liver Diseases
Endocrine System Diseases
PCOS
Neoplasms
Colorectal Cancer
Prostate cancer
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
Proapolipoprotein Apo-A1, annexin V,PRDX2,triosephosphate isomerase, peroxiredoxin 2 isoform a, actin and adipocyte plasma membrane-associated protein 
Visceral adiposity 
 
Presence of oligo-ovulation, clinical and/or biochemical hyperandrogenism, and exclusion of hyperprolactinemia, non-classic congenital adrenal hyperplasia and androgen-secreting tumors 
Related 
 
This preliminary study revealed differences in expression of proteins that may be involved in lipid and glucose metabolism, oxidative stress processes and adipocyte differentiation; they include proapolipoprotein Apo-A1, annexin V, glutathione S-transferase M3 (GSTM3), triosephosphate isomerase, peroxiredoxin 2 isoform a, actin and adipocyte plasma membrane-associated protein. 
DHEAS, SHBG, 2-h plasma glucose,malondialdehyde (MDA), protein carbonyl (PC), reduced glutathione (GSH), carotene, vitamin A, C, E and the enzyme activities of catalase 
Oxidative stress,Insulin resistance and Hyperglycemia 
 
 
Related 
 
Oxidative stress characterized by increased oxidants and decreased antioxidant levels which are independent of IR may be involved in the pathogenesis of PCOS in young non-obese women. 

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