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dc.contributor.authorRicha, Tambi
dc.date.accessioned2022-03-15T10:03:02Z
dc.date.available2022-03-15T10:03:02Z
dc.date.issued2021
dc.identifier.other204-2021.168
dc.identifier.urihttps://repository.mbru.ac.ae/handle/1/907
dc.description.abstractAbstract: Understanding structural excursions of proteins under folding conditions is crucial to map energy landscapes of proteins. In the present study, OneG computational tool has been used for analyzing possible existence of cryptic intermediates and metastable states of 26 proteins for which three prerequisite inputs of the OneG such as atomic coordinates of proteins, free energy of unfolding (DGU) and free energy of exchange (DGHX) determined in the absence of denaturant were available during the course of the study. The veraciousness of the tool on predicting the partially folded states of the proteins has been comprehensively described using experimental data available for 15 of the 26 proteins. Meanwhile, possible existence of partially structured states in the folding pathways of 11 other proteins has also been delineated as predicted by the OneG. In addition to mapping the folding pathways of proteins, the salient merits of the tool on systematically addressing the discrepancy between the DGU and the DGHX of the proteins have also been dealt.en_US
dc.language.isoenen_US
dc.subjectCryptic intermediatesen_US
dc.subjectFree energyen_US
dc.subjectMetastable statesen_US
dc.subjectNative foldingen_US
dc.subjectOneGen_US
dc.titleCryptic intermediates and metastable states of proteins as predicted by OneG computational methoden_US
dc.typeArticleen_US


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