DOBES, Petr, Jan KMUNÍČEK, Vladimír MIKEŠ and Jiří DAMBORSKÝ. Binding of Fatty Acids to b-Cryptogein: Quantitative Structure-Activity Relationships and Design of Selective Protein Mutants. Journal of Chemical Information and Modeling. USA, 2004, 44-6, No 44, p. 2126-2132. ISSN 1549-960X.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Binding of Fatty Acids to b-Cryptogein: Quantitative Structure-Activity Relationships and Design of Selective Protein Mutants.
Name in Czech Vazba mastných kyselin k b-Cryptogenu:Vztah mezi strukturou a aktivitou a vytvoření selektivních bílkovinných mutantů.
Authors DOBES, Petr (203 Czech Republic), Jan KMUNÍČEK (203 Czech Republic), Vladimír MIKEŠ (203 Czech Republic) and Jiří DAMBORSKÝ (203 Czech Republic, guarantor).
Edition Journal of Chemical Information and Modeling, USA, 2004, 1549-960X.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10600 1.6 Biological sciences
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
RIV identification code RIV/00216224:14310/04:00010577
Organization unit Faculty of Science
UT WoS 000225411300027
Keywords in English QSAR; Protein; Mutants
Tags mutants, PROTEIN, QSAR
Changed by Changed by: prof. Mgr. Jiří Damborský, Dr., učo 1441. Changed: 19/3/2010 12:17.
Abstract
Binding of fatty acids to cryptogein, the proteinaceous elicitor from Phytophthora, was studied by using molecular docking and quantitative structure-activity relationships analysis. Fatty acids bind to the groove located inside the cavity of cryptogein. The structure-activity model was constructed for the set of 27 different saturated and unsaturated fatty acids explaining 87% (81% cross-validated) of the quantitative variance in their binding affinity. The difference in binding between saturated and unsaturated fatty acids was described in the model by three electronic descriptors: the energy of the lowest unoccupied molecular orbital, the energy of the highest occupied molecular orbital and the heat of formation. The presence of double bonds in the ligand generally resulted in stronger binding. The difference in binding within the group of saturated fatty acids was explained by two steric descriptors, i.e. ellipsoidal volume and inertia moment of length, and one hydrophobicity descriptor, i.e. lipophility. Developed model predicted strong binding for two biologically important molecules, geranylgeranyol and farnesol playing an important role in plant signalling as lipid anchors of some membrane proteins. Elicitin mutants selectively binding only one type of ligands were designed for future experimental studies.
Abstract (in Czech)
Vazba mastných kyselin a cryptogenu- bílkovinné obrany Phytophthora, byla studována použitím molekulového dockingu a analýzou QSAR.
Links
MSM 143100005, plan (intention)Name: Strukturně-funkční vztahy biomolekul a jejich role v metabolismu
Investor: Ministry of Education, Youth and Sports of the CR, Biomolecular Structure-function Relationships and their role in the Metabolism
PrintDisplayed: 8/6/2024 11:34