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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
20
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pubmed:dateCreated |
2006-9-28
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pubmed:databankReference |
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pubmed:abstractText |
The 1.8 A resolution de novo structure of nucleoside 2-deoxyribosyltransferase (EC 2.4.2.6) from Trypanosoma brucei (TbNDRT) has been determined by SADa phasing in an unliganded state and several ligand-bound states. This enzyme is important in the salvage pathway of nucleoside recycling. To identify novel lead compounds, we exploited "fragment cocktail soaks". Out of 304 compounds tried in 31 cocktails, four compounds could be identified crystallographically in the active site. In addition, we demonstrated that very short soaks of approximately 10 s are sufficient even for rather hydrophobic ligands to bind in the active site groove, which is promising for the application of similar soaking experiments to less robust crystals of other proteins.
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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 |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0022-2623
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pubmed:author |
pubmed-author:AndersonLori ALA,
pubmed-author:BoniEricaE,
pubmed-author:BoschJürgenJ,
pubmed-author:BucknerFrederick SFS,
pubmed-author:DeTittaGeorgeG,
pubmed-author:EarnestThomas NTN,
pubmed-author:FanErkangE,
pubmed-author:GuldeStaceyS,
pubmed-author:HolWim G JWG,
pubmed-author:KalyuzhniyOleksandrO,
pubmed-author:LauricellaAngelaA,
pubmed-author:LuftJoseph RJR,
pubmed-author:MehlinChristopherC,
pubmed-author:MerrittEthan AEA,
pubmed-author:MylerPeter JPJ,
pubmed-author:NeelyHelen MHM,
pubmed-author:RiechersAaronA,
pubmed-author:RobienMark AMA,
pubmed-author:RossJenniJ,
pubmed-author:SchoenfeldLoriL,
pubmed-author:SoltisMichaelM,
pubmed-author:Van VoorhisWesley CWC,
pubmed-author:VerlindeChristophe L M JCL,
pubmed-author:WortheyElizabeth AEA,
pubmed-author:ZuckerFrankF
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pubmed:issnType |
Print
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pubmed:day |
5
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5939-46
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:17004709-Amino Acid Sequence,
pubmed-meshheading:17004709-Animals,
pubmed-meshheading:17004709-Benzyl Alcohols,
pubmed-meshheading:17004709-Binding Sites,
pubmed-meshheading:17004709-Crystallography, X-Ray,
pubmed-meshheading:17004709-Indoles,
pubmed-meshheading:17004709-Isoquinolines,
pubmed-meshheading:17004709-Ligands,
pubmed-meshheading:17004709-Models, Molecular,
pubmed-meshheading:17004709-Molecular Sequence Data,
pubmed-meshheading:17004709-Molecular Structure,
pubmed-meshheading:17004709-Pentosyltransferases,
pubmed-meshheading:17004709-Quinolines,
pubmed-meshheading:17004709-Structure-Activity Relationship,
pubmed-meshheading:17004709-Trypanocidal Agents,
pubmed-meshheading:17004709-Trypanosoma brucei brucei
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pubmed:year |
2006
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pubmed:articleTitle |
Using fragment cocktail crystallography to assist inhibitor design of Trypanosoma brucei nucleoside 2-deoxyribosyltransferase.
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pubmed:affiliation |
Department of Biochemistry, Division of Infectious Disease, and Howard Hughes Medical Institute, University of Washington, Seattle, Washington 98195, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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