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Computational studies for the structure and function of mRPE65
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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094118/ https://www.ncbi.nlm.nih.gov/pubmed/17123547 http://dx.doi.org/10.1016/j.jtbi.2006.10.002 |
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author | Guo, Hao Zheng, Chong Gaillard, Elizabeth R. |
author_facet | Guo, Hao Zheng, Chong Gaillard, Elizabeth R. |
author_sort | Guo, Hao |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7094118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70941182020-03-25 Computational studies for the structure and function of mRPE65 Guo, Hao Zheng, Chong Gaillard, Elizabeth R. J Theor Biol Article 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. Elsevier Ltd. 2007-03-21 2006-10-07 /pmc/articles/PMC7094118/ /pubmed/17123547 http://dx.doi.org/10.1016/j.jtbi.2006.10.002 Text en Copyright © 2006 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Guo, Hao Zheng, Chong Gaillard, Elizabeth R. Computational studies for the structure and function of mRPE65 |
title | Computational studies for the structure and function of mRPE65 |
title_full | Computational studies for the structure and function of mRPE65 |
title_fullStr | Computational studies for the structure and function of mRPE65 |
title_full_unstemmed | Computational studies for the structure and function of mRPE65 |
title_short | Computational studies for the structure and function of mRPE65 |
title_sort | computational studies for the structure and function of mrpe65 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094118/ https://www.ncbi.nlm.nih.gov/pubmed/17123547 http://dx.doi.org/10.1016/j.jtbi.2006.10.002 |
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