Disulfide isomerization within the C-terminus of cabrotoxin decelerates by thiol compounds and trinitrophenylation, but accelerates by modification of carboxyl groups

Archives of Biochemistry and Biophysics

Volumn 358, Issue 1, 1998, Pages 164-170

  Chang, Long Sen ^a   Lin, Shinne Ren ^a   Chang, Chun Chang ^a   Yang, Chen Chung ^b  

^a KAOHSIUNG MEDICAL UNIVERSITY   (Taiwan)

^b NATIONAL TSING HUA UNIVERSITY   (Taiwan)

Author keywords

Chemical modification of Lys residues and carboxyl groups; Cobrotoxin; Disulfide isomerization; Glutathione

Indexed keywords

COBROTOXIN; CYSTAMINE; GLUTATHIONE; GLUTATHIONE DISULFIDE; MERCAPTAMINE; THIOL DERIVATIVE; TRINITROPHENYL;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CHEMICAL MODIFICATION; ISOMERISM; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0032189441     PISSN: 00039861     EISSN: None     Source Type: Journal    
DOI: 10.1006/abbi.1998.0815     Document Type: Article

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