| Literature DB >> 29275181 |
Paula Giménez-Mascarell1, Tomas Majtan2, Iker Oyenarte1, June Ereño-Orbea1, Juraj Majtan3, Jaroslav Klaudiny4, Jan P Kraus2, Luis Alfonso Martínez-Cruz5.
Abstract
Cystathionine β-synthase (CBS), the key enzyme in the transsulfuration pathway, links methionine metabolism to the biosynthesis of cellular redox controlling molecules. CBS catalyzes the pyridoxal-5'-phosphate-dependent condensation of serine and homocysteine to form cystathionine, which is subsequently converted into cysteine. Besides maintaining cellular sulfur amino acid homeostasis, CBS also catalyzes multiple hydrogen sulfide-generating reactions using cysteine and homocysteine as substrates. In mammals, CBS is activated by S-adenosylmethionine (AdoMet), where it can adopt two different conformations (basal and activated), but exists as a unique highly active species in fruit fly Drosophila melanogaster. Here we present the crystal structure of CBS from honeybey Apis mellifera, which shows a constitutively active dimeric species and let explain why the enzyme is not allosterically regulated by AdoMet. In addition, comparison of available CBS structures unveils a substrate-induced closure of the catalytic cavity, which in humans is affected by the AdoMet-dependent regulation and likely impaired by the homocystinuria causing mutation T191M.Entities:
Keywords: CBS; Homocystinuria; Hydrogen sulfide; S-adenosylmethionine; Transsulfuration
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Year: 2017 PMID: 29275181 DOI: 10.1016/j.jsb.2017.12.008
Source DB: PubMed Journal: J Struct Biol ISSN: 1047-8477 Impact factor: 2.867