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Structure paper

TitleStructural insights into mechanisms of non-nucleoside drug resistance for HIV-1 reverse transcriptases mutated at codons 101 or 138.
Journal, issue, pagesFebs J., Vol. 273, Page 3850-3860, Year 2006
Publish dateJul 12, 2006 (structure data deposition date)
AuthorsRen, J. / Nichols, C.E. / Stamp, A. / Chamberlain, P.P. / Ferris, R. / Weaver, K.L. / Short, S.A. / Stammers, D.K.
External linksFebs J. / PubMed:16911530
MethodsX-ray diffraction
Resolution2.5 - 3 Å
Structure data

PDB-2hnd:
Crystal Structure of K101E Mutant HIV-1 Reverse Transcriptase in Complex with Nevirapine
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

PDB-2hny:
Crystal Structure of E138K Mutant HIV-1 Reverse Transcriptase in Complex with Nevirapine
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

PDB-2hnz:
Crystal Structure of E138K Mutant HIV-1 Reverse Transcriptase in Complex with PETT-2
Method: X-RAY DIFFRACTION / Resolution: 3 Å

Chemicals

ChemComp-PO4:
PHOSPHATE ION

ChemComp-MG:
Unknown entry

ChemComp-NVP:
11-CYCLOPROPYL-5,11-DIHYDRO-4-METHYL-6H-DIPYRIDO[3,2-B:2',3'-E][1,4]DIAZEPIN-6-ONE / medication, antiretroviral*YM

ChemComp-HOH:
WATER

ChemComp-PC0:
1-[2-(4-ETHOXY-3-FLUOROPYRIDIN-2-YL)ETHYL]-3-(5-METHYLPYRIDIN-2-YL)THIOUREA

Source
  • human immunodeficiency virus 1
KeywordsTRANSFERASE / HIV-1 REVERSE TRANSCRIPTASE / AIDS / NON-NUCLEOSIDE INHIBITOR / NEVIRAPINE / DRUG RESISTANCE MUTATIONS / DRUG DESIGN / PETT-2

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