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Journal articles
Thumb-loops up for catalysis: a structure/function investigation of a functional loop movement in a GH11 xylanase
Abstract : Dynamics is a key feature of enzyme catalysis. Unfortunately, current experimental and computational techniques do not yet provide a comprehensive understanding and description of functional macromolecular motions. In this work, we have extended a novel computational technique, which combines molecular modeling methods and robotics algorithms, to investigate functional motions of protein loops. This new approach has been applied to study the functional importance of the so-called thumb-loop in the glycoside hydrolase family 11 xylanase from Thermobacillus xylanilyticus (Tx-xyl). The results obtained provide new insight into the role of the loop in the glycosylation/deglycosylation catalytic cycle, and underline the key importance of the nature of the residue located at the tip of the thumb-loop. The effect of mutations predicted in silico has been validated by in vitro site-directed mutagenesis experiments. Overall, we propose a comprehensive model of Tx-xyl catalysis in terms of substrate and product dynamics by identifying the action of the thumb-loop motion during catalysis.
Cited literature [55 references]
https://hal.archives-ouvertes.fr/hal-01267831
Contributor : Archive Ouverte Prodinra <>
Submitted on : Wednesday, June 26, 2019 - 10:43:36 AM
Last modification on : Friday, December 18, 2020 - 3:46:02 PM
Contributor : Archive Ouverte Prodinra <>
Submitted on : Wednesday, June 26, 2019 - 10:43:36 AM
Last modification on : Friday, December 18, 2020 - 3:46:02 PM
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