Title of article :
Computational studies for the structure and function of mRPE65
Author/Authors :
Guo، نويسنده , , Hao and Zheng، نويسنده , , Chong and Gaillard، نويسنده , , Elizabeth R.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
7
From page :
312
To page :
318
Abstract :
The mRPE65 protein is one form of the RPE65 protein and plays a very important role in the visual cycle. However, its 3D structure and detailed mechanism of function are still unclear because of difficulties with isolation and crystallization. This computational study reports a model for the mRPE65 protein structure derived from a model for sRPE65. The natural substrate for RPE65 has been shown to be a retinyl ester and, by utilizing the Autodock and the Ligplot programs, the interactions between the ester and the protein as well as the effects of several mutations on these interactions are studied. Finally, the position of the binding site is proposed based on an iterative process and the effects of the mutations on the binding site are also discussed.
Keywords :
mRPE65 , Protein structure and function
Journal title :
Journal of Theoretical Biology
Serial Year :
2007
Journal title :
Journal of Theoretical Biology
Record number :
1538395
Link To Document :
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