Inscribing the perimeter of the PagP hydrocarbon ruler by site-specific chemical alkylation

Biochemistry

Volumn 49, Issue 42, 2010, Pages 9046-9057

  Khan, M Adil ^a   Moktar, Joel ^a   Mott, Patrick J ^a   Vu, Mary ^a   McKie, Aaron H ^b   Pinter, Thomas ^b   Hof, Fraser ^b   Bishop, Russell E ^a  

^a MCMASTER UNIVERSITY   (Canada)

^b UNIVERSITY OF VICTORIA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLATION; ESCHERICHIA COLI; FUNCTIONAL GROUPS; PHOSPHOLIPIDS; SELENIUM COMPOUNDS; VAN DER WAALS FORCES;

ACYL CHAIN; ANTIMICROBIAL PEPTIDE; BI-LAYER; CHEMICAL ALKYLATION; GAUCHE CONFORMER; LIPID A; METHYL GROUP; MICELLAR PROPERTIES; N-PROPYL; NORLEUCINE; OUTER MEMBRANE; PALMITOYLATION; PALMITOYLTRANSFERASE; PHOSPHATIDYLCHOLINE; SELENOMETHIONINE; SIDE CHAINS; SITE-SPECIFIC; SULFHYDRYL GROUPS; THIOETHERS; VAN DER WAALS;

AROMATIC HYDROCARBONS;

GLYCINE; HYDROCARBON; METHIONINE; NORLEUCINE; PAGP ENZYME; PHOSPHATIDYLCHOLINE; SELENOMETHIONINE; UNCLASSIFIED DRUG; ACYLTRANSFERASE; ESCHERICHIA COLI PROTEIN; LIPID A; MUTANT PROTEIN; OUTER MEMBRANE PROTEIN; PAGP PROTEIN, E COLI; PRIMER DNA; RECOMBINANT PROTEIN;

ALKYLATION; ARTICLE; ELECTROSPRAY MASS SPECTROMETRY; PRIORITY JOURNAL; PROTEIN STRUCTURE; AMINO ACID SUBSTITUTION; BINDING SITE; CHEMICAL STRUCTURE; CHEMISTRY; CIRCULAR DICHROISM; ESCHERICHIA COLI; GENETICS; METABOLISM; NUCLEAR MAGNETIC RESONANCE; NUCLEOTIDE SEQUENCE; PROTEIN CONFORMATION; PROTEIN STABILITY; SITE DIRECTED MUTAGENESIS;

ESCHERICHIA COLI;

ACYLTRANSFERASES; ALKYLATION; AMINO ACID SUBSTITUTION; BACTERIAL OUTER MEMBRANE PROTEINS; BASE SEQUENCE; BINDING SITES; CIRCULAR DICHROISM; DNA PRIMERS; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; LIPID A; MODELS, MOLECULAR; MUTAGENESIS, SITE-DIRECTED; MUTANT PROTEINS; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PROTEIN CONFORMATION; PROTEIN STABILITY; RECOMBINANT PROTEINS; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION;

EID: 77958111818     PISSN: 00062960     EISSN: 15204995     Source Type: Journal    
DOI: 10.1021/bi1011496     Document Type: Article

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