Database of Intermediates of Enzyme-Catalyzed Chemical Reactions ENIAD
- Authors: Moskovsky A.A.1, Firsov D.A.1, Khrenova M.G.1,2, Mironov V.A.1, Mulashkina T.I.1, Kulakova A.M.1, Nemukhin A.V.1,3
- 
							Affiliations: 
							- Moscow State University
- Federal Research Center of Biotechnology, Russian Academy of Sciences
- Institute of Biochemical Physics, Russian Academy of Sciences
 
- Issue: Vol 97, No 9 (2023)
- Pages: 1324-1328
- Section: ХЕМОИНФОРМАТИКА И КОМПЬЮТЕРНОЕ МОДЕЛИРОВАНИЕ
- Submitted: 26.02.2025
- Published: 01.09.2023
- URL: https://ruspoj.com/0044-4537/article/view/668669
- DOI: https://doi.org/10.31857/S0044453723090133
- EDN: https://elibrary.ru/XKQAYW
- ID: 668669
Cite item
Abstract
Enzymatic catalysis is characterized by multistage chemical reactions from enzyme-substrate complexes to products. In a number of cases, in the course of experimental studies, it is possible to characterize the structures and properties of intermediates of complex chemical reactions in proteins. The use of modern computer simulation methods makes it possible to significantly supplement the knowledge of the mechanisms of enzymatic catalysis reactions and provide detailed data on reaction intermediates, including structures with atomic resolution. The materials accumulated to date make it possible to create a unique dat-abase called ENIAD (ENzyme-In-Action-Databank). The article describes the principles of building the ENIAD database, as well as a multiplatform web interface for accessing data (https://lcc.chem.msu.ru/eniad/).
About the authors
A. A. Moskovsky
Moscow State University
														Email: anem@lcc.chem.msu.ru
				                					                																			                												                								Moscow, Russia						
D. A. Firsov
Moscow State University
														Email: anem@lcc.chem.msu.ru
				                					                																			                												                								Moscow, Russia						
M. G. Khrenova
Moscow State University; Federal Research Center of Biotechnology, Russian Academy of Sciences
														Email: anem@lcc.chem.msu.ru
				                					                																			                												                								Moscow, Russia; Moscow, Russia						
V. A. Mironov
Moscow State University
														Email: anem@lcc.chem.msu.ru
				                					                																			                												                								Moscow, Russia						
T. I. Mulashkina
Moscow State University
														Email: anem@lcc.chem.msu.ru
				                					                																			                												                								Moscow, Russia						
A. M. Kulakova
Moscow State University
														Email: anem@lcc.chem.msu.ru
				                					                																			                												                								Moscow, Russia						
A. V. Nemukhin
Moscow State University; Institute of Biochemical Physics, Russian Academy of Sciences
							Author for correspondence.
							Email: anem@lcc.chem.msu.ru
				                					                																			                												                								Moscow, Russia; Moscow, Russia						
References
- Варфоломеев С.Д. Химическая энзимология. М.: Научный мир, 2019. С. 543.
- Berman H.M., Henrick K., Nakamura H. // Nature Structural Biology. 2003. V. 10. № 12. P. 980. https://doi.org/10.1038/nsb1203-980
- Holliday G.L., Andreini C., Fischer J.D. et al. // Nucleic Acids Res. 2012. V. 40. P. D783.https://doi.org/10.1093/nar/gkr799
- Nagano N., Nakayama N., Ikeda K. et al. // Ibid. 2015. V. 43. P. D453.https://doi.org/10.1093/nar/gku946
- Ribeiro A.J.M., Holliday J.L., Furnham N. et al. // Ibid. 2018. V. 46. P. D618.https://doi.org/10.1093/nar/gkx1012
- Furnham N., Holliday G.L., de Beer T.A.P. et al. // Ibid. 2014. V. 42. P. D485.https://doi.org/10.1093/nar/gkt1243
- Warshel A., Levitt M. // J. Mol. Biol. 1976. V. 103. P. 227. https://doi.org/10.1016/0022-2836(76)90311-9
- Senn H.M., Thiel W. // Angew. Chemie Int. Ed. 2009. V. 48. P. 1198. https://doi.org/10.1002/anie.200802019
- Grigorenko B.L., Kots E.D., Nemukhin A.V. // Org. Biomol. Chem. 2019. V. 17. P. 4879.https://doi.org/10.1039/C9OB00463G
- Khrenova M.G., Grigorenko B.L., Kolomeisky A.B. et al. // J. Phys. Chem. B. 2015. V. 119. № 40. P. 12838.https://doi.org/10.1021/acs.jpcb.5b07238
- Khrenova M.G., Kots E.D., Nemukhin A.V. // Ibid. 2016. V. 120. № 16. P. 3873.https://doi.org/10.1021/acs.jpcb.6b03363
- Docker, Inc. https://www.docker.com, 2019.
- The Linux Foundation. https://kubernetes.io, 2019.
- Brekhov A.T., Mironov V.A., Moskovsky A.A. et al. // J. Phys.: Conf. Ser. 2019. V. 1392. P. 012049.https://doi.org/10.1088/1742-6596/1392/1/012049
- PostgreSQL Global Development Group. https://www.postgresql.org, 2019.
- Latino D.A.R.S., Aires-de-Sousa J. // Chemoinf. and Comput. Chem. Biol. 2011. V. 672. P. 325.https://doi.org/10.1007/978-1-60761-839-3_13
- O’Boyle N.M., Holliday G.L., Almonacid D.E. et al. // J. Mol. Biol. 2007. V. 368. P. 1484.https://doi.org/10.1016/j.jmb.2007.02.065
- Almonacid D.E., Babbitt P.C. // Curr. Opin. Chem. Biol. 2011. V. 15. P. 435.https://doi.org/10.1016/j.cbpa.2011.03.008
 
				
			 
					 
						 
						 
						 
						 
									

 
  
  
  Email this article
			Email this article 
 Open Access
		                                Open Access Access granted
						Access granted Subscription or Fee Access
		                                							Subscription or Fee Access
		                                					

