Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references
Cystathionine is an intermediate in the synthesis of cysteine. IUPAC nomenclature is a system of naming chemical compounds and of describing the science of chemistry in general. ... CAS registry numbers are unique numerical identifiers for chemical compounds, polymers, biological sequences, mixtures and alloys. ... PubChem is a database of chemical molecules. ... Medical Subject Headings (MeSH) is a huge controlled vocabulary (or metadata system) for the purpose of indexing journal articles and books in the life sciences. ... The simplified molecular input line entry specification or SMILES is a specification for unambiguously describing the structure of chemical molecules using short ASCII strings. ... This article does not cite its references or sources. ... Molar mass is the mass of one mole of a chemical element or chemical compound. ... In chemistry, the standard state of a material is its state at 1 bar (100 kilopascals) and 25 degrees Celsius (298. ... Cysteine is a naturally occurring, sulfur-containing amino acid that is found in most proteins, although only in small quantities. ...
Bukovska G, Kery V, Kraus JP (1994) Expression of human cystathionine ß-synthase in Escherichia coli: purification and characterization.
Kraus JP, Rosenberg LE (1983) Cystathionine ß-synthase from human liver: Improved purification scheme and additional characterization of the enzyme in crude and pure form.
Skovby F, Kraus JP, Rosenberg LE (1984b) Biosynthesis and proteolytic activation of cystathionine ß-synthase in rat liver.
Homocystinuria is an inherited autosomal recessive defect in methionine metabolism that is caused by a deficiency in cystathionine synthase.
Cystathionine beta-synthase is encoded on chromosome 21, and deficiency in its activity causes homocystinuria.
Cystathionine beta-synthase plays a key role in the intracellular disposal of homocysteine and is the single most common locus of mutations associated with homocystinuria.
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