Structure-based substrate screening for an enzyme

Abstract Background Nowadays, more and more novel enzymes can be easily found in the whole enzyme pool with the rapid development of genetic operation. However, experimental work for substrate screening of a new enzyme is laborious, time consuming and costly. On the other hand, many computational me...

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Published in:BMC Bioinformatics
Main Authors: Wei Dongzhi, Wang Xuedong, Zhang Lujia, Xu Tao, Li Tianbi
Format: Article in Journal/Newspaper
Language:English
Published: BMC 2009
Subjects:
Online Access:https://doi.org/10.1186/1471-2105-10-257
https://doaj.org/article/cd095463007545d38f36e624bf8d5c79
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spelling ftdoajarticles:oai:doaj.org/article:cd095463007545d38f36e624bf8d5c79 2023-05-15T13:40:41+02:00 Structure-based substrate screening for an enzyme Wei Dongzhi Wang Xuedong Zhang Lujia Xu Tao Li Tianbi 2009-08-01T00:00:00Z https://doi.org/10.1186/1471-2105-10-257 https://doaj.org/article/cd095463007545d38f36e624bf8d5c79 EN eng BMC http://www.biomedcentral.com/1471-2105/10/257 https://doaj.org/toc/1471-2105 doi:10.1186/1471-2105-10-257 1471-2105 https://doaj.org/article/cd095463007545d38f36e624bf8d5c79 BMC Bioinformatics, Vol 10, Iss 1, p 257 (2009) Computer applications to medicine. Medical informatics R858-859.7 Biology (General) QH301-705.5 article 2009 ftdoajarticles https://doi.org/10.1186/1471-2105-10-257 2022-12-31T04:39:21Z Abstract Background Nowadays, more and more novel enzymes can be easily found in the whole enzyme pool with the rapid development of genetic operation. However, experimental work for substrate screening of a new enzyme is laborious, time consuming and costly. On the other hand, many computational methods have been widely used in lead screening of drug design. Seeing that the ligand-target protein system in drug design and the substrate-enzyme system in enzyme applications share the similar molecular recognition mechanism, we aim to fulfill the goal of substrate screening by in silico means in the present study. Results A computer-aided substrate screening (CASS) system which was based on the enzyme structure was designed and employed successfully to help screen substrates of Candida antarctica lipase B (CALB). In this system, restricted molecular docking which was derived from the mechanism of the enzyme was applied to predict the energetically favorable poses of substrate-enzyme complexes. Thereafter, substrate conformation, distance between the oxygen atom of the alcohol part of the ester (in some compounds, this oxygen atom was replaced by nitrogen atom of the amine part of acid amine or sulfur atom of the thioester) and the hydrogen atom of imidazole of His224, distance between the carbon atom of the carbonyl group of the compound and the oxygen atom of hydroxyl group of Ser105 were used sequentially as the criteria to screen the binding poses. 223 out of 233 compounds were identified correctly for the enzyme by this screening system. Such high accuracy guaranteed the feasibility and reliability of the CASS system. Conclusion The idea of computer-aided substrate screening is a creative combination of computational skills and enzymology. Although the case studied in this paper is tentative, high accuracy of the CASS system sheds light on the field of computer-aided substrate screening. Article in Journal/Newspaper Antarc* Antarctica Directory of Open Access Journals: DOAJ Articles BMC Bioinformatics 10 1 257
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Computer applications to medicine. Medical informatics
R858-859.7
Biology (General)
QH301-705.5
spellingShingle Computer applications to medicine. Medical informatics
R858-859.7
Biology (General)
QH301-705.5
Wei Dongzhi
Wang Xuedong
Zhang Lujia
Xu Tao
Li Tianbi
Structure-based substrate screening for an enzyme
topic_facet Computer applications to medicine. Medical informatics
R858-859.7
Biology (General)
QH301-705.5
description Abstract Background Nowadays, more and more novel enzymes can be easily found in the whole enzyme pool with the rapid development of genetic operation. However, experimental work for substrate screening of a new enzyme is laborious, time consuming and costly. On the other hand, many computational methods have been widely used in lead screening of drug design. Seeing that the ligand-target protein system in drug design and the substrate-enzyme system in enzyme applications share the similar molecular recognition mechanism, we aim to fulfill the goal of substrate screening by in silico means in the present study. Results A computer-aided substrate screening (CASS) system which was based on the enzyme structure was designed and employed successfully to help screen substrates of Candida antarctica lipase B (CALB). In this system, restricted molecular docking which was derived from the mechanism of the enzyme was applied to predict the energetically favorable poses of substrate-enzyme complexes. Thereafter, substrate conformation, distance between the oxygen atom of the alcohol part of the ester (in some compounds, this oxygen atom was replaced by nitrogen atom of the amine part of acid amine or sulfur atom of the thioester) and the hydrogen atom of imidazole of His224, distance between the carbon atom of the carbonyl group of the compound and the oxygen atom of hydroxyl group of Ser105 were used sequentially as the criteria to screen the binding poses. 223 out of 233 compounds were identified correctly for the enzyme by this screening system. Such high accuracy guaranteed the feasibility and reliability of the CASS system. Conclusion The idea of computer-aided substrate screening is a creative combination of computational skills and enzymology. Although the case studied in this paper is tentative, high accuracy of the CASS system sheds light on the field of computer-aided substrate screening.
format Article in Journal/Newspaper
author Wei Dongzhi
Wang Xuedong
Zhang Lujia
Xu Tao
Li Tianbi
author_facet Wei Dongzhi
Wang Xuedong
Zhang Lujia
Xu Tao
Li Tianbi
author_sort Wei Dongzhi
title Structure-based substrate screening for an enzyme
title_short Structure-based substrate screening for an enzyme
title_full Structure-based substrate screening for an enzyme
title_fullStr Structure-based substrate screening for an enzyme
title_full_unstemmed Structure-based substrate screening for an enzyme
title_sort structure-based substrate screening for an enzyme
publisher BMC
publishDate 2009
url https://doi.org/10.1186/1471-2105-10-257
https://doaj.org/article/cd095463007545d38f36e624bf8d5c79
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source BMC Bioinformatics, Vol 10, Iss 1, p 257 (2009)
op_relation http://www.biomedcentral.com/1471-2105/10/257
https://doaj.org/toc/1471-2105
doi:10.1186/1471-2105-10-257
1471-2105
https://doaj.org/article/cd095463007545d38f36e624bf8d5c79
op_doi https://doi.org/10.1186/1471-2105-10-257
container_title BMC Bioinformatics
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