Title of article :
Molecular insights of SAH enzyme catalysis and implication for inhibitor design
Author/Authors :
Wei، نويسنده , , Huachun and Zhang، نويسنده , , Rui and Wang، نويسنده , , Chunfang and Zheng، نويسنده , , Huiqin and Li، نويسنده , , Aixiu and Chou، نويسنده , , Kuo-Chen and Wei، نويسنده , , Dong-Qing، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
11
From page :
692
To page :
702
Abstract :
Abstracts ical 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.
Keywords :
S-adenosylhomocysteine hydrolase (SAH) , enzyme catalysis , inhibitor design , Docking
Journal title :
Journal of Theoretical Biology
Serial Year :
2007
Journal title :
Journal of Theoretical Biology
Record number :
1538320
Link To Document :
بازگشت