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TitleComplexes of HIV-1 reverse transcriptase with inhibitors of the HEPT series reveal conformational changes relevant to the design of potent non-nucleoside inhibitors.
Journal, issue, pagesJ. Med. Chem., Vol. 39, Page 1589-1600, Year 1996
Publish dateMar 16, 1996 (structure data deposition date)
AuthorsHopkins, A.L. / Ren, J. / Esnouf, R.M. / Willcox, B.E. / Jones, E.Y. / Ross, C. / Miyasaka, T. / Walker, R.T. / Tanaka, H. / Stammers, D.K. / Stuart, D.I.
External linksJ. Med. Chem. / PubMed:8648598
MethodsX-ray diffraction
Resolution2.55 Å
Structure data

PDB-1rt1:
CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE COMPLEXED WITH MKC-442
Method: X-RAY DIFFRACTION / Resolution: 2.55 Å

PDB-1rt2:
CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE COMPLEXED WITH TNK-651
Method: X-RAY DIFFRACTION / Resolution: 2.55 Å

Chemicals

ChemComp-MKC:
6-BENZYL-1-ETHOXYMETHYL-5-ISOPROPYL URACIL / inhibitor*YM

ChemComp-HOH:
WATER

ChemComp-TNK:
6-BENZYL-1-BENZYLOXYMETHYL-5-ISOPROPYL URACIL

Source
  • human immunodeficiency virus 1
KeywordsNUCLEOTIDYLTRANSFERASE / HIV-1 REVERSE TRANSCRIPTASE

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