Three-dimensional structure of the large cytoplasmic H4-H5 loop of Na+/K+-ATPase deduced by restraint-based comparative modeling shows only one ATP binding site

Journal of Molecular Modeling

Volumn 7, Issue 6, 2001, Pages 184-192

  Ettrich, Rüdiger ^a,b   Melichercik, Milan ^c   Teisinger, Jan ^b   Ettrichova, Olga ^b   Krumscheid, Rita ^d   Hofbauerova, Katherina ^a,b   Kvasnicka, Peter ^c   Schoner, Wilhelm ^d   Amler, Evzen ^b  

^a CHARLES UNIVERSITY   (Czech Republic)

^b INSTITUTE OF PHYSIOLOGY   (Czech Republic)

^c Physics and Informatics   (Slovakia)

^d JUSTUS LIEBIG UNIVERSITY   (Germany)

Author keywords

Adenosine triphosphate binding site; Restraint based homology modeling; Sodium potassium adenosine triphosphatase; Tertiary structure

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); CYSTEINE; GLUTAMIC ACID; GLUTAMINE; HYDROGEN; LYSINE; PHENYLALANINE; SERINE;

ALGORITHM; AMINO ACID SEQUENCE; ARTICLE; BINDING SITE; CHEMICAL STRUCTURE; COMPLEX FORMATION; COMPUTER PROGRAM; CONTROLLED STUDY; CYTOPLASM; INTERMETHOD COMPARISON; MOLECULAR MECHANICS; MOLECULAR MODEL; PRIORITY JOURNAL; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY; SURFACE CHARGE; X RAY CRYSTALLOGRAPHY;

EID: 0345831226     PISSN: 16102940     EISSN: None     Source Type: Journal    
DOI: 10.1007/s008940100031     Document Type: Article

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