Ca2+-induced linker transformation leads to a compact and rigid collagen-binding domain of Clostridium histolyticum collagenase

FEBS Journal

Volumn 276, Issue 13, 2009, Pages 3589-3601

  Philominathan, Sagaya T L ^a   Matsushita, Osamu ^b   Gensure, Robert ^c   Sakon, Joshua ^a  

^a UNIVERSITY OF ARKANSAS   (United States)

^b KITASATO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c CHILDREN S HOSPITAL   (United States)

Author keywords

Ca2+; Collagen binding domain; Linker; Stability; Structural transformation

Indexed keywords

CALCIUM ION; CHLORIDE; CLOSTRIDIOPEPTIDASE A; COLLAGEN; GUANIDINE; UREA; CALCIUM;

ALPHA HELIX; ARTICLE; BETA SHEET; CHELATION; COLLAGEN DEGRADATION; DENATURATION; ENZYME STRUCTURE; HYDROGEN BOND; ISOMERIZATION; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN FUNCTION; BINDING SITE; CHEMICAL STRUCTURE; CHEMISTRY; GENETICS; METABOLISM; MOLECULAR GENETICS; PROTEIN DENATURATION; PROTEIN SECONDARY STRUCTURE; PROTEIN TERTIARY STRUCTURE; STATIC ELECTRICITY;

CLOSTRIDIUM HISTOLYTICUM;

BINDING SITES; CALCIUM; COLLAGEN; HYDROGEN BONDING; MICROBIAL COLLAGENASE; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; PROTEIN DENATURATION; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; STATIC ELECTRICITY; UREA;

EID: 67650482810     PISSN: 1742464X     EISSN: 17424658     Source Type: Journal    
DOI: 10.1111/j.1742-4658.2009.07078.x     Document Type: Article

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