A Clinically Relevant Variant of the Human Hydrogen Sulfide-Synthesizing Enzyme Cystathionine β -Synthase

The human disease classical homocystinuria results from mutations in the gene encoding the pyridoxal 5′-phosphate- (PLP-) dependent cystathionine β-synthase (CBS), a key enzyme in the transsulfuration pathway that controls homocysteine levels, and is a major source of the signaling molecule hydrogen...

Full description

Bibliographic Details
Main Author: Vicente, João B. (author)
Other Authors: Colaço, Henrique G. (author), Malagrinò, Francesca (author), Santo, Paulo E. (author), Gutierres, André (author), Bandeiras, Tiago M. (author), Leandro, Paula (author), Brito, José A. (author), Giuffrè, Alessandro (author)
Format: article
Language:eng
Published: 2019
Subjects:
Online Access:http://hdl.handle.net/10362/85146
Country:Portugal
Oai:oai:run.unl.pt:10362/85146