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Volumn 332, Issue 3, 2005, Pages 897-903

Affinity selection to papain yields potent peptide inhibitors of cathepsins L, B, H, and K

Author keywords

Affinity selection; Cathepsins; Inhibitor; Papain; Peptide; Phage display; Selective elution

Indexed keywords

CATHEPSIN B; CATHEPSIN H; CATHEPSIN K; CATHEPSIN L; CYSTEINE PROTEINASE INHIBITOR; CYSTEINYLASPARAGINYLALANYLALANYLGLYCYLTYROSYLASPARAGINYLCYSTEINYLGLYCYL GLYCYLGLYCYLSERINAMIDE; CYSTEINYLASPARAGINYLTRYPTOPHYLTHREONYLLEUCYLGLYCYLGLYCYLTYROSYLLYSYL CYSTEINYLGLYCYLGLYCYLGLYCYLSERINAMIDE; CYSTEINYLTRYPTOPHYLGLUTAMYLTRYPTOPHYLGLYCYLGLYCYLTRYPTOPHYLHISTIDYL CYSTEINYLGLYCYLGLYCYLSERYLSERINE; CYSTEINYLTRYPTOPHYLSERYLMETHIONYLMETHIONYLGLYCYLPHENYLALANYLGLUTAMINYL CYSTEINYLGLYCYLGLYCYLSERINAMIDE; GLYCYLASPARAGINYLTRYPTOPHYLTHREONYLLEUCYLGLYCYLGLYCYLTYROSYLLYSYLGLYCYL GLYCINE; PAPAIN; UNCLASSIFIED DRUG;

EID: 19744374543     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbrc.2005.05.028     Document Type: Article
Times cited : (31)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.