Reversibly acetylated lysine residues play important roles in the enzymatic activity of Escherichia coli N-hydroxyarylamine O-acetyltransferase

FEBS Journal

Volumn 280, Issue 9, 2013, Pages 1966-1979

  Zhang, Qunfang ^a,b   Gu, Jing ^a   Gong, Peng ^a   Wang, Xude ^a   Tu, Shun ^c,d   Bi, Lijun ^e   Yu, Ziniu ^b   Zhang, Zhiping ^a   Cui, Zongqiang ^a   Wei, Hongping ^a   Tao, Shengce ^c,d   Zhang, Xianen ^a  

^a WUHAN INSTITUTE OF VIROLOGY   (China)

^b HUAZHONG AGRICULTURAL UNIVERSITY   (China)

^c Shanghai Jiao Tong University   (China)

^d SHANGHAI JIAO TONG UNIVERSITY   (China)

^e INSTITUTE OF BIOPHYSICS   (China)

Author keywords

acetylation deacetylation; CobB; mutagenicity; NhoA; proteome microarray

Indexed keywords

ACYLTRANSFERASE; ESCHERICHIA COLI PROTEIN; LYSINE; N ACYLTRANSFERASE; N HYDROXYARYLAMINE O ACETYLTRANSFERASE; O ACYLTRANSFERASE; PROTEIN COBB; PROTEIN VARIANT; PROTEOME; UNCLASSIFIED DRUG;

ACETYLATION; AMINO ACID SUBSTITUTION; ARTICLE; CONTROLLED STUDY; DEACETYLATION; ENZYME ACTIVITY; ENZYME ANALYSIS; ENZYME STRUCTURE; ENZYME SUBSTRATE; ESCHERICHIA COLI; IN VITRO STUDY; MUTATION; NONHUMAN; PRIORITY JOURNAL; SITE DIRECTED MUTAGENESIS; STRUCTURE ANALYSIS;

ACETYLATION; ACETYLTRANSFERASES; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; KINETICS; LYSINE; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; PEPTIDE FRAGMENTS; PROTEIN ARRAY ANALYSIS; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEOME; SIRTUINS;

BACTERIA (MICROORGANISMS); ESCHERICHIA COLI;

EID: 84876921286     PISSN: 1742464X     EISSN: 17424658     Source Type: Journal    
DOI: 10.1111/febs.12216     Document Type: Article

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