Molecular insights of SAH enzyme catalysis and implication for inhibitor design |
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Authors: | Wei Huachun Zhang Rui Wang Chunfang Zheng Huiqin Li Aixiu Chou Kuo-Chen Wei Dong-Qing |
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Affiliation: | College of Life Sciences and Biotechnology, Shanghai Jiaotong University, 800 Dongchuan Road, Minhang District, Shanghai 200240, China. |
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Abstract: | Biological transmethylation reaction is a key step in the duplication of virus life cycle, in which S-adenosylmethionine plays as the methyl donor. The product of this reactions, S-adenosylhomocysteine (AdoHcy) inhibits the transmethylation process. AdoHcy is hydrolysed to adenosine and L-homocysteine by the action of S-adenosylhomocysteine hydrolase (SAH). Thus the virus life cycle should be cut off once the action of SAH is inhibited. Our study was focussed on the discovery of potential inhibitor against SAH. We performed a similarity search in Traditional Chinese Medicine Database and retrieved 17 hits with high similarity. After that we virtually docked the 17 compounds as well as the natural substrates to the hydrolase using Autodock 3.0.1 software. Then we discussed about the mechanism of the inhibition reaction, followed by proposing the potential inhibitors by comparing best docked solutions and possible modification for the best inhibitors. |
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Keywords: | S-adenosylhomocysteine hydrolase (SAH) Docking Enzyme catalysis Inhibitor design |
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