1MU2

CRYSTAL STRUCTURE OF HIV-2 REVERSE TRANSCRIPTASE

1MU2 の概要

• エントリーDOI: 10.2210/pdb1mu2/pdb
• 分子名称: HIV-2 RT, SULFATE ION, GLYCEROL, ... (5 entities in total)
• 機能のキーワード: hiv-2 reverse transcriptase, aids, polymerase, drug design, transferase
• 由来する生物種: Human immunodeficiency virus 2; 詳細
• 細胞内の位置: Matrix protein p17: Virion (Potential). Capsid protein p24: Virion (Potential). Nucleocapsid protein p7: Virion (Potential). Reverse transcriptase/ribonuclease H: Virion (Potential). Integrase: Virion (Potential): P04584 P04584
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 116925.14

構造登録者

Ren, J.,Bird, L.E.,Chamberlain, P.P.,Stewart-Jones, G.B.,Stuart, D.I.,Stammers, D.K. (登録日: 2002-09-23, 公開日: 2002-10-30, 最終更新日: 2023-10-25)

主引用文献

Ren, J.,Bird, L.E.,Chamberlain, P.P.,Stewart-Jones, G.B.,Stuart, D.I.,Stammers, D.K.
Structure of HIV-2 reverse transcriptase at 2.35-A resolution and the mechanism of resistance to non-nucleoside inhibitors
Proc.Natl.Acad.Sci.USA, 99:14410-14415, 2002

PubMed Abstract: The HIV-2 serotype of HIV is a cause of disease in parts of the West African population, and there is evidence for its spread to Europe and Asia. HIV-2 reverse transcriptase (RT) demonstrates an intrinsic resistance to non-nucleoside RT inhibitors (NNRTIs), one of two classes of anti-AIDS drugs that target the viral RT. We report the crystal structure of HIV-2 RT to 2.35 A resolution, which reveals molecular details of the resistance to NNRTIs. HIV-2 RT has a similar overall fold to HIV-1 RT but has structural differences within the "NNRTI pocket" at both conserved and nonconserved residues. The structure points to the role of sequence differences that can give rise to unfavorable inhibitor contacts or destabilization of part of the binding pocket at positions 101, 106, 138, 181, 188, and 190. We also present evidence that the conformation of Ile-181 compared with the HIV-1 Tyr-181 could be a significant contributory factor to this inherent drug resistance of HIV-2 to NNRTIs. The availability of a refined structure of HIV-2 RT will provide a stimulus for the structure-based design of novel non-nucleoside inhibitors that could be used against HIV-2 infection.

PubMed: 12386343
DOI: 10.1073/pnas.222366699

実験手法

X-RAY DIFFRACTION (2.35 Å)