2R8N
Structural Analysis of the Unbound Form of HIV-1 Subtype C Protease
2R8N の概要
| エントリーDOI | 10.2210/pdb2r8n/pdb |
| 分子名称 | Pol protein, GLYCEROL (3 entities in total) |
| 機能のキーワード | hiv-1 subtype c, aspartyl protease, hydrolase, multifunctional enzyme, nucleotidyltransferase, protease, rna-directed dna polymerase, transferase |
| 由来する生物種 | Human immunodeficiency virus 1 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 10935.98 |
| 構造登録者 | Coman, R.M.,Robbins, A.H.,McKenna, R.,Dunn, B.M. (登録日: 2007-09-11, 公開日: 2008-07-29, 最終更新日: 2024-02-21) |
| 主引用文献 | Coman, R.M.,Robbins, A.H.,Goodenow, M.M.,Dunn, B.M.,McKenna, R. High-resolution structure of unbound human immunodeficiency virus 1 subtype C protease: implications of flap dynamics and drug resistance. Acta Crystallogr.,Sect.D, 64:754-763, 2008 Cited by PubMed Abstract: The X-ray crystal structure of the unbound state of human immunodeficiency virus 1 (HIV-1) subtype C protease (C PR) has been determined to 1.20 angstroms resolution in the tetragonal space group P4(1)2(1)2, with one monomer per asymmetric unit and unit-cell parameters a = 46.7, c = 100.8 angstroms, allowing full anisotropic least-squares refinement. The refined model has a conventional R factor of 14.1% for all reflections and estimated standard deviations in bond lengths and angles for all main-chain non-H atoms of 0.014 angstroms and 0.030 degrees , respectively. The structure is compared with three unbound subtype B proteases (B PRs) to identify structural changes arising from the naturally occurring polymorphisms and delineate their implications in antiretroviral drug resistance/susceptibility. The unbound C PR exhibits a larger distance between the tips of the flaps, a downward displacement of the 36-41 loop and an increased thermal stability of the 10s loop when compared with the B PR structures. The C PR structure presents the highest resolution of the unbound state of a non-subtype-B PR and adds to the understanding of flap dynamics and drug resistance. PubMed: 18566511DOI: 10.1107/S090744490801278X 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.2 Å) |
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