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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5430
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pubmed:dateCreated |
1999-9-2
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pubmed:databankReference |
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pubmed:abstractText |
Isoleucyl-transfer RNA (tRNA) synthetase (IleRS) joins Ile to tRNA(Ile) at its synthetic active site and hydrolyzes incorrectly acylated amino acids at its editing active site. The 2.2 angstrom resolution crystal structure of Staphylococcus aureus IleRS complexed with tRNA(Ile) and Mupirocin shows the acceptor strand of the tRNA(Ile) in the continuously stacked, A-form conformation with the 3' terminal nucleotide in the editing active site. To position the 3' terminus in the synthetic active site, the acceptor strand must adopt the hairpinned conformation seen in tRNA(Gln) complexed with its synthetase. The amino acid editing activity of the IleRS may result from the incorrect products shuttling between the synthetic and editing active sites, which is reminiscent of the editing mechanism of DNA polymerases.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Monophosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Amino Acids,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Directed DNA Polymerase,
http://linkedlifedata.com/resource/pubmed/chemical/Glutamate-tRNA Ligase,
http://linkedlifedata.com/resource/pubmed/chemical/Isoleucine,
http://linkedlifedata.com/resource/pubmed/chemical/Isoleucine-tRNA Ligase,
http://linkedlifedata.com/resource/pubmed/chemical/Mupirocin,
http://linkedlifedata.com/resource/pubmed/chemical/Oligopeptides,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Transfer, Gln,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Transfer, Ile
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0036-8075
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
13
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pubmed:volume |
285
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1074-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:10446055-Acylation,
pubmed-meshheading:10446055-Adenosine Monophosphate,
pubmed-meshheading:10446055-Amino Acids,
pubmed-meshheading:10446055-Binding Sites,
pubmed-meshheading:10446055-Crystallography, X-Ray,
pubmed-meshheading:10446055-DNA-Directed DNA Polymerase,
pubmed-meshheading:10446055-Glutamate-tRNA Ligase,
pubmed-meshheading:10446055-Isoleucine,
pubmed-meshheading:10446055-Isoleucine-tRNA Ligase,
pubmed-meshheading:10446055-Models, Molecular,
pubmed-meshheading:10446055-Mupirocin,
pubmed-meshheading:10446055-Nucleic Acid Conformation,
pubmed-meshheading:10446055-Oligopeptides,
pubmed-meshheading:10446055-Protein Conformation,
pubmed-meshheading:10446055-Protein Structure, Secondary,
pubmed-meshheading:10446055-RNA, Transfer, Gln,
pubmed-meshheading:10446055-RNA, Transfer, Ile,
pubmed-meshheading:10446055-Staphylococcus aureus,
pubmed-meshheading:10446055-Substrate Specificity
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pubmed:year |
1999
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pubmed:articleTitle |
Insights into editing from an ile-tRNA synthetase structure with tRNAile and mupirocin.
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pubmed:affiliation |
Department of Molecular Biophysics, Yale University, and Howard Hughes Medical Institute, New Haven, CT 06520-8114, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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