Article
Crystal structure of aminomethyltransferase in complex with dihydrolipoyl-H-protein of the glycine cleavage system: implications for recognition of lipoyl protein substrate, disease-related mutations, and reaction mechanism.
The Journal of biological chemistry - 11 Jun 2010
Okamura-Ikeda Kazuko, Hosaka Harumi, Maita Nobuo, Fujiwara Kazuko, Yoshizawa Akiyasu C, Nakagawa Atsushi, Taniguchi Hisaaki
Abstract excerpt
Aminomethyltransferase, a component of the glycine cleavage system termed T-protein, reversibly catalyzes the degradation of the aminomethyl moiety of glycine attached to the lipoate cofactor of H-protein, resulting in the production of ammonia, 5,10-methylenetetrahydrofolate, and dihydrolipoate-bearing H-protein in the presence of tetrahydrofolate. Several mutations in the human T-protein gene are known to cause...
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