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Volumn 73, Issue 7, 2009, Pages 1683-1684
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The hydrophobicity in a chemically modified side-chain of cysteine residues of thanatin is related to antimicrobial activity against Micrococcus luteus
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Author keywords
Antimicrobial peptide; Chemical modification; Thanatin
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Indexed keywords
ANTI-MICROBIAL ACTIVITY;
ANTIMICROBIAL PEPTIDE;
CHEMICALLY MODIFIED;
CYSTEINE RESIDUES;
ETHYL GROUPS;
METHYL GROUP;
MICROCOCCUS LUTEUS;
OCTYL GROUPS;
SIDE-CHAIN;
THANATIN;
WILD TYPES;
AMINES;
HYDROCARBONS;
HYDROPHOBICITY;
PEPTIDES;
CHEMICAL MODIFICATION;
ANTIINFECTIVE AGENT;
ANTIMICROBIAL CATIONIC PEPTIDE;
CYCLOPEPTIDE;
CYSTEINE;
THANATIN;
AMINO ACID SEQUENCE;
ARTICLE;
CHEMICAL PHENOMENA;
CHEMISTRY;
DRUG EFFECT;
MICROBIOLOGICAL EXAMINATION;
MICROCOCCUS LUTEUS;
MOLECULAR GENETICS;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
AMINO ACID SEQUENCE;
ANTI-INFECTIVE AGENTS;
ANTIMICROBIAL CATIONIC PEPTIDES;
CYSTEINE;
HYDROPHOBIC AND HYDROPHILIC INTERACTIONS;
MICROBIAL SENSITIVITY TESTS;
MICROCOCCUS LUTEUS;
MOLECULAR SEQUENCE DATA;
PEPTIDES, CYCLIC;
STRUCTURE-ACTIVITY RELATIONSHIP;
MICROCOCCUS LUTEUS;
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EID: 68649115070
PISSN: 09168451
EISSN: 13476947
Source Type: Journal
DOI: 10.1271/bbb.90183 Document Type: Article |
Times cited : (5)
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References (9)
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