Target intelligence / Profile preview

Thiol methyltransferase 1B (TMT1B)

Target
TMT1B
Molecular classification
Enzyme, Methyltransferase, Small molecule methyltransferase
01

Overview

Thiol methyltransferase 1B (TMT1B), more commonly known as METTL7B or methyltransferase-like protein 7B, is an enzyme of the methyltransferase family that catalyzes S-methylation of alkyl thiols using S-adenosyl-L-methionine as a methyl donor[1][2][4]. It is membrane-associated, localizing mainly to the endoplasmic reticulum and lipid droplets, and displays broad substrate specificity for exogenous thiol-containing small molecules but not for endogenous thiols such as cysteine or glutathione[1][2]. TMT1B is increasingly recognized for its upregulation in several cancers, where its expression correlates with tumor progression, migration, invasion, and poor prognosis, making it a potential oncogenic biomarker and target[4][5]. The enzyme also appears to play a role in hydrogen sulfide metabolism, cellular redox balance, and possibly inflammation, though its full physiological role remains incompletely understood[2][3][4]. No specific inhibitors are currently used clinically, but altered TMT1B levels may influence the metabolism and effects of certain thiol-containing drugs[1].

Other names
METTL7BMethyltransferase-like protein 7BThiol S-methyltransferase METTL7BAssociated with lipid droplets 1ALDIUNQ594/PRO1180MGC17301
02

Mechanism of action

SAM-dependent methyl transfer (using S-adenosyl-L-methionine as methyl donor) to alkyl thiols, including drug metabolites and potentially hydrogen sulfide (H₂S)[1][2][4]

03

Biological functions

S-methylation of alkyl thiolsMethylation of small molecule thiol-containing substratesRegulation of hydrogen sulfide metabolismRoles in cell proliferation, migration, and invasionInvolvement in redox state regulation and ROS scavenging
04

Disease associations

Cancer (noted in gliomas, non-small cell lung cancer, acute myeloid leukemia, thyroid cancer, breast cancer)Inflammation (implicated in sepsis, lipopolysaccharide-induced inflammatory response)Potential role in rheumatoid arthritis, preeclampsia, and non-alcoholic steatohepatitis
05

Safety considerations

Altered thiol drug metabolism may impact drug toxicity or pharmacological activity if TMT1B is inhibited or overexpressed[1]Potential impact on hydrogen sulfide homeostasis and cellular redox status, which could affect multiple cellular pathways[4]No specific clinical safety concerns identified for direct targeting due to lack of TMT1B inhibitors in clinical use
06

Interacting drugs

Exogenous thiol-containing drugs such as mertansine and captopril are substrates (but not specific inhibitors)

2 more in the full profile.

07

Biomarkers

METTL7B/TMT1B expression as a biomarker for advanced tumor stage and poor prognosis in various cancers (gliomas, NSCLC, AML)[4]Increased METTL7B expression correlates with tumor aggressiveness and drug resistance[4]

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