Local conformational flexibility provides a basis for facile polymer formation in human neuroserpin

Biophysical Journal

Volumn 101, Issue 7, 2011, Pages 1758-1765

  Sarkar, Anindya ^a   Zhou, Crystal ^a   Meklemburg, Robert ^a   Wintrode, Patrick L ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

NEUROPEPTIDE; NEUROSERPIN; SERINE PROTEINASE INHIBITOR;

ARTICLE; CHEMISTRY; DEUTERIUM HYDROGEN EXCHANGE; ENZYME ACTIVE SITE; HUMAN; HYDROGEN BOND; MASS SPECTROMETRY; METABOLISM; MOLECULAR DYNAMICS; PRINCIPAL COMPONENT ANALYSIS; PROTEIN DEGRADATION; PROTEIN MULTIMERIZATION; PROTEIN QUATERNARY STRUCTURE; PROTEIN SECONDARY STRUCTURE; THERMODYNAMICS;

CATALYTIC DOMAIN; DEUTERIUM EXCHANGE MEASUREMENT; HUMANS; HYDROGEN BONDING; MASS SPECTROMETRY; MOLECULAR DYNAMICS SIMULATION; NEUROPEPTIDES; PRINCIPAL COMPONENT ANALYSIS; PROTEIN MULTIMERIZATION; PROTEIN STRUCTURE, QUATERNARY; PROTEIN STRUCTURE, SECONDARY; PROTEOLYSIS; SERPINS; THERMODYNAMICS;

EID: 80053356669     PISSN: 00063495     EISSN: 15420086     Source Type: Journal    
DOI: 10.1016/j.bpj.2011.08.037     Document Type: Article

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