Physical nature of interactions Within the active site of cytosine-5-methyltransferase

Journal of Physical Chemistry A

Volumn 110, Issue 6, 2006, Pages 2308-2313

  Forde, Gareth K ^a   Kedzierski, Pawel ^b   Sokalski, W Andrzej ^b   Forde, Aviane E ^a   Hill, Glake A ^a   Leszczynski, Jerzy ^a  

^a JACKSON STATE UNIVERSITY   (United States)

^b WROCLAW UNIVERSITY OF TECHNOLOGY   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSINE-5-METHYLTRANSFERASE (CMT); DELOCALIZATION; INTERACTION ENERGY;

ELECTROSTATICS; ENZYME INHIBITION; MATHEMATICAL MODELS; PERTURBATION TECHNIQUES;

ENZYME KINETICS;

ARGININE; CYTOSOL AMINOPEPTIDASE; DNA (CYTOSINE 5) METHYLTRANSFERASE; ENZYME INHIBITOR; GLUTAMIC ACID; PROTON;

ARTICLE; BINDING SITE; CHEMICAL MODEL; CHEMISTRY; DRUG ANTAGONISM; ELECTRICITY; ENZYME ACTIVE SITE; ENZYME STABILITY; METABOLISM; THERMODYNAMICS;

ARGININE; BINDING SITES; CATALYTIC DOMAIN; DNA (CYTOSINE-5-)-METHYLTRANSFERASE; ELECTROSTATICS; ENZYME INHIBITORS; ENZYME STABILITY; GLUTAMIC ACID; LEUCYL AMINOPEPTIDASE; MODELS, CHEMICAL; PROTONS; THERMODYNAMICS;

EID: 33644747695     PISSN: 10895639     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp056415u     Document Type: Article

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