Structural models of CFTR-AMPK and CFTR-PKA interactions: R-domain flexibility is a key factor in CFTR regulation

Journal of Molecular Modeling

Volumn 18, Issue 1, 2012, Pages 83-90

  Siwiak, Marian ^a   Edelman, Aleksander ^b   Zielenkiewicz, Piotr ^a,c  

^a INSTITUTE OF BIOCHEMISTRY AND BIOPHYSICS   (Poland)

^b INSERM   (France)

^c UNIVERSITY OF WARSAW   (Poland)

Author keywords

AMPK; CFTR; Docking; Interaction; Molecular modeling; PKA

Indexed keywords

ADENYLATE KINASE; CYCLIC AMP DEPENDENT PROTEIN KINASE; SERINE; TRANSMEMBRANE CONDUCTANCE REGULATOR;

AMINO ACID SEQUENCE; ARTICLE; ENZYME ACTIVITY; ENZYME STRUCTURE; HUMAN; MOLECULAR MODEL; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; STRUCTURE ANALYSIS;

AMINO ACID SEQUENCE; AMP-ACTIVATED PROTEIN KINASES; CYCLIC AMP-DEPENDENT PROTEIN KINASES; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; HUMANS; MODELS, MOLECULAR; PHOSPHORYLATION; PROTEIN INTERACTION DOMAINS AND MOTIFS; PROTEIN STRUCTURE, TERTIARY; SEQUENCE ANALYSIS, PROTEIN;

EID: 84856298335     PISSN: 16102940     EISSN: 09485023     Source Type: Journal    
DOI: 10.1007/s00894-011-1029-0     Document Type: Article

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