GSTT2B
Glutathione S-transferase theta-2B
Also known as: GSTT2_HUMAN, GSTT2P
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P0CG30
- Gene
- GSTT2B
- Ensembl
- ENSG00000133433
- Chromosome
- 22
- Canonical length
- 244 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
The protein encoded by this gene, glutathione S-transferase (GST) theta 2B (GSTT2B), is a member of a superfamily of proteins that catalyze the conjugation of reduced glutathione to a variety of electrophilic and hydrophobic compounds. Human GSTs can be divided into five main classes: alpha, mu, pi, theta, and zeta. The theta class includes GSTT1, GSTT2, and GSTT2B. GSTT2 and GSTT2B are nearly identical to each other, and share 55% amino acid identity with GSTT1. All three genes may play a role in human carcinogenesis. The GSTT2B gene is a pseudogene in some populations. [provided by RefSeq, Sep 2015]
Canonical amino-acid sequenceUniProt
244 residues, UniProt reviewed canonical sequence.
>P0CG30|GSTT2B
1 MGLELFLDLV SQPSRAVYIF AKKNGIPLEL RTVDLVKGQH KSKEFLQINS LGKLPTLKDG
61 DFILTESSAI LIYLSCKYQT PDHWYPSDLQ ARARVHEYLG WHADCIRGTF GIPLWVQVLG
121 PLIGVQVPEE KVERNRTAMD QALQWLEDKF LGDRPFLAGQ QVTLADLMAL EELMQPVALG
181 YELFEGRPRL AAWRGRVEAF LGAELCQEAH SIILSILEQA AKKTLPTPSP EAYQAMLLRI
241 ARIPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GSTT2B 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.25
- Highest tissue expression
- 290 nTPM
Expression across tissuesHPA
Tissue
- breast: 290 nTPM
- adrenal gland: 79 nTPM
- skin: 45 nTPM
- tongue: 38 nTPM
- prostate: 38 nTPM
- liver: 38 nTPM
Single-cell type
- loop of henle epithelial cells: 6.8 nCPM
- renal collecting duct principal cells: 5.6 nCPM
- papillary tip epithelial cells: 5.1 nCPM
- renal connecting tubule cells: 5 nCPM
- distal convoluted tubule cells: 4.4 nCPM
- proximal tubule cells: 3.8 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- thalamus: 17 nTPM
- hypothalamus: 17 nTPM
- midbrain: 13 nTPM
- medulla oblongata: 13 nTPM
- amygdala: 11 nTPM
- cerebral cortex: 11 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)
- 0.71
- gnomAD pLI
- 0.72
- gnomAD missense Z
- 0.72
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Glutathione S-transferase, N-terminal
- Glutathione S-transferase, C-terminal
- Glutathione S-transferase, C-terminal-like
- Thioredoxin-like superfamily
- Glutathione S-transferase, C-terminal domain superfamily
- Glutathione S-transferase Theta, N-terminal
- Glutathione S-transferase Theta, C-terminal
- Glutathione transferase family
- Glutathione S-transferase Theta
- Glutathione S-transferase, C-terminal domain
- Glutathione S-transferase, N-terminal domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GSTT2B as an antibody target. Whether an autoantibody or antibody against GSTT2B could matter depends on whether native GSTT2B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GSTT2B 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 GSTT2B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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