General Information:

Id: 3,387 (click here to show other Interactions for entry)
Diseases: Carnitine deficiency, systemic primary - [OMIM]
Diabetes mellitus, type II - [OMIM]
Insulin resistance
Mammalia
review
Reference: Vaz FM and Wanders RJ(2002) Carnitine biosynthesis in mammals Biochem. J. Pt: 3 417-429 [PMID: 11802770]

Interaction Information:

Comment HTMLA might be identical to serine hydroxymethyltransferase (SHMT; EC 2.1.2.1), since it has been shown that SHMT purified from rabbit liver acts upon HTML, yielding TMABA and glycine. SHMT catalyses the tetrahydrofolate-dependent interconversion of serine and glycine, a reaction that generates one-carbon units for methionine, thymidylate and purine biosynthesis. SHMT also catalyses the aldol cleavage of other beta-hydroxyamino acids in the absence of tetrahydrofolate, including HTML. Two isoforms of SHMT are present in eukaryotic cells: one localized in the cytoplasm and one localized in mitochondria. In humans, the gene encoding the cytosolic SHMT is located on chromosome 17p11.2, and the gene encoding the mitochondrial isoenzyme is on chromosome 12q13.2.
Formal Description
Interaction-ID: 46099

gene/protein

SHMT1

affects_quantity of

drug/chemical compound

Glycine

Drugbank entries Show/Hide entries for SHMT1 or Glycine