The myristoylation of guanylate cyclase-activating protein-2 causes an increase in thermodynamic stability in the presence but not in the absence of Ca2+

Protein Science

Volumn 20, Issue 7, 2011, Pages 1155-1165

  Schröder, Thomas ^a   Lilie, Hauke ^a   Lange, Christian ^a  

^a MARTIN LUTHER UNIVERSITY HALLE WITTENBERG   (Germany)

Author keywords

Ca2+ binding protein; Conformational switch; Guanylate cyclase activating protein 2; Myristoylation; Protein stability

Indexed keywords

CALCIUM ION; GUANYLATE CYCLASE ACTIVATING PROTEIN 2; GUANYLATE CYCLASE ACTIVATOR; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; CONFORMATION; CONTROLLED STUDY; DATA ANALYSIS; HYDROPHOBICITY; MEDICAL RECORD; MYRISTYLATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN STRUCTURE; THERMODYNAMICS;

ANIMALS; CALCIUM; CATTLE; CELL LINE; GUANYLATE CYCLASE-ACTIVATING PROTEINS; HUMANS; MYRISTIC ACID; PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN FOLDING; PROTEIN MULTIMERIZATION; PROTEIN STABILITY; TEMPERATURE; THERMODYNAMICS;

EID: 79959334004     PISSN: 09618368     EISSN: 1469896X     Source Type: Journal    
DOI: 10.1002/pro.643     Document Type: Article

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