Pyranose ring transition state is derived from cellobiohydrolase i induced conformational stability and glycosidic bond polarization

Journal of the American Chemical Society

Volumn 132, Issue 37, 2010, Pages 12800-12803

  Barnett, Christopher B ^a   Wilkinson, Karl A ^a   Naidoo, Kevin J ^a  

^a UNIVERSITY OF CAPE TOWN   (South Africa)

Author keywords

[No Author keywords available]

Indexed keywords

ADAPTIVE REACTION; BIASING METHODS; BINDING DOMAIN; BOLTZMANN SIMULATIONS; CELLOBIOHYDROLASE I; CONFORMATIONAL STABILITIES; GLUCOPYRANOSE RING; GLYCOSIDIC BOND; GLYCOSYLATION REACTIONS; IN-VACUUM; PYRANOSE; RATIONAL DESIGN; REACTION COORDINATES; RING TRANSITION STATE; RING-PUCKERING; TRANSITION STATE; TRICHODERMA REESEI;

CONFORMATIONS; FREE ENERGY; SUGARS;

CRYSTAL STRUCTURE;

CELLOOCTAOSE; CELLULOSE 1,4 BETA CELLOBIOSIDASE; FUNGAL ENZYME; OLIGOSACCHARIDE; UNCLASSIFIED DRUG;

ARTICLE; CRYSTAL STRUCTURE; ENERGY; ENZYME ACTIVE SITE; ENZYME STABILITY; ENZYME STRUCTURE; GLYCOSYLATION; HYPOCREA JECORINA; NONHUMAN; POLARIZATION; PROTEIN CONFORMATION; SIMULATION; VACUUM;

CARBOHYDRATE CONFORMATION; CELLOBIOSE; CELLULOSE 1,4-BETA-CELLOBIOSIDASE; GLUCOSE; GLYCOSIDES; GLYCOSYLATION; THERMODYNAMICS; TRICHODERMA;

EID: 77956642470     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja103766w     Document Type: Article

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