A rational approach to the regioselective deacetylation of 2′,3′,5′-tri-O-acetyluridine by Novozym 435 catalysed alcoholysis

Biochimica et Biophysica Acta - Proteins and Proteomics

Volumn 1824, Issue 4, 2012, Pages 627-636

  Gudino E D ^a   Iglesias, L E ^a   Ferreira, M L ^b  

^a UNIVERSIDAD NACIONAL DE QUILMES   (Argentina)

^b PLAPIQUI UNS CONICET   (Argentina)

Author keywords

Candida antarctica lipase B; Molecular modeling; Nucleoside; Regioselectivity; Transesterification

Indexed keywords

2',3',5' TRI O ACETYLURIDINE; CANDIDA ANTARCTICA LIPASE B; CHOLINE; FUNGAL ENZYME; HISTIDINE; LIPASE B; NOVOZYME 435; PROTEIN INTERACTING WITH PROTEIN KINASE C; SERINE; UNCLASSIFIED DRUG;

ALCOHOLYSIS; ARTICLE; DEACETYLATION; HYDROLYSIS; METHANOLYSIS; PRIORITY JOURNAL;

ACETYLATION; AMINO ACID MOTIFS; BIOCATALYSIS; CANDIDA; CATALYTIC DOMAIN; COMPUTER SIMULATION; ETHANOL; FUNGAL PROTEINS; HYDROGEN BONDING; HYDROLYSIS; KINETICS; LIPASE; MODELS, MOLECULAR; PROTEIN BINDING; URIDINE; WATER;

CANDIDA ANTARCTICA;

EID: 84857272140     PISSN: 15709639     EISSN: 18781454     Source Type: Journal    
DOI: 10.1016/j.bbapap.2012.01.009     Document Type: Article

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