51st Vietnam Conference on Theoretical Physics (VCTP-51)
Hội nghị Vật lý lý thuyết Việt Nam lần thứ 51
Nha Trang, 3-6 August, 2026

Programme

P.87 -- Posters, VCTP-51

Date: Thursday, 6 August 2026

Time: 09:30 - 10:30

The structural stability of monomeric Glucose-6-phosphate dehydrogenase and its relationship to G6PD deficiency

Nhung T. T. Nguyen (1), Le Hoang Phong (1), Nguyen Thi Hai Yen (1), Phuong Thuy Bui (2,3), Mai Thi Lan (4), and Trinh Xuan Hoang (1)

(1) Institute of Physics, Vietnam Academy of Science and Technology, 10 Dao Tan, Giang Vo, Hanoi 11108, Vietnam; (2) Institute of Theoretical and Applied Research, Duy Tan University, Hanoi, 100000, Vietnam; (3) Faculty of Pharmacy, Duy Tan University, Da Nang, 550000, Vietnam; (4) Faculty of Engineering Physics, Hanoi University of Science and Technology, 1 Dai Co Viet Road, Hanoi, Vietnam

G6PD deficiency, an enzymopathy associated with glucose-6-phosphate dehydrogenase (G6PD), is caused by genetic mutations that reduce the enzyme activity, resulting in hemolytic anemia. Biochemical studies have shown that G6PD deficiency in various variants is associated with reduced thermal stability, reduced catalytic activity, or both. In this study, we investigate the structural stability of the wild-type G6PD monomer at a physiological temperature using molecular dynamics simulations, in the absence and in the presence of its G6P and NADP+ ligands. We find that the G6P ligand has a low affinity for the G6PD monomer, which may result from fluctuations in the size of its binding pocket. This finding helps explain the catalytic inactivity of monomeric G6PD. The binding of NADP+ ligands is found to enhance the structural stability of the protein and the G6P-binding pocket. Our analysis also shows that, with a statistically significant confidence, class I mutations occur preferentially at residues that are more flexible than randomly selected residues, whereas class II mutations tend to occur at residues that are less flexible than randomly selected ones. This result reflects the distinct structural roles of the G6PD mutation sites and further supports the relationship between enzyme activity and thermal stability.

Presenter: Nguyen Thi Thuy Nhung


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