X-ray structure of simian immunodeficiency virus integrase containing the core and C-terminal domain (residues 50-293) - An initial glance of the viral DNA binding platform

被引:90
作者
Chen, ZG [1 ]
Yan, YW [1 ]
Munshi, S [1 ]
Li, Y [1 ]
Zugay-Murphy, J [1 ]
Xu, B [1 ]
Witmer, M [1 ]
Felock, P [1 ]
Wolfe, A [1 ]
Sardana, V [1 ]
Emini, EA [1 ]
Hazuda, D [1 ]
Kuo, LC [1 ]
机构
[1] Merck Res Labs, Dept Antiviral Res, West Point, PA 19486 USA
关键词
SIV; integrase; X-ray crystal structure;
D O I
10.1006/jmbi.1999.3451
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The crystal structure of simian immunodeficiency virus (SIV) integrase that contains in a single polypeptide the core and the C-terminal deoxyoligonucleotide binding domain has been determined at 3 Angstrom resolution with an X-value of 0.203 in the space group P2(1)2(1)2(1). Four integrase core domains and one C-terminal domain are found to be well defined in the asymmetric unit. The segment extending from residues 114 to 121 assumes the same position as seen in the integrase core domain of avian sarcoma virus as well as human immunodeficiency virus type-1 (HIV-1) crystallized in the absence of sodium cacodylate. The flexible loop in the active site, composed of residues 141-151, remains incompletely defined, but the location of the essential Glu152 residue is unambiguous. The residues from 210-218 that Link the core and C-terminal domains can be traced as an extension from the core with a short gap at residues 214-215. The C-alpha folding of the C-terminal domain is similar to the solution structure of this domain from HIV-1 integrase. However, the dimeric form seen in the NMR structure cannot exist as related by the non-crystallographic symmetry in the SIV integrase crystal. The two flexible loops of the C-terminal domain, residues 228-236 and residues 244-249, are much better fixed in the crystal structure than in the NMR structure with the former in the immediate vicinity of the flexible loop of the core domain. The interface between the two domains encompasses a solvent-exclusion area of 1500 Angstrom(2). Residues from both domains purportedly involved in DNA binding are narrowly distributed on the same face of the molecule. They include Asp64, Asp116, Glu152 and Lys159 from the core and Arg231, Leu234, Arg262, Arg263 and Lys264 from the C-terminal domain. A model for DNA binding is proposed to bridge the two domains by tethering the 228-236 loop of the C-terminal domain and the flexible loop of the core. (C) 2000 Academic Press.
引用
收藏
页码:521 / 533
页数:13
相关论文
共 42 条
[1]   THE CCP4 SUITE - PROGRAMS FOR PROTEIN CRYSTALLOGRAPHY [J].
BAILEY, S .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1994, 50 :760-763
[2]  
Brunger A. T., 1992, X PLOR VERSION 3 1 S
[3]   The catalytic domain of human immunodeficiency virus integrase: Ordered active site in the F185H mutant [J].
Bujacz, G ;
Alexandratos, J ;
ZhouLiu, Q ;
ClementMella, C ;
Wlodawer, A .
FEBS LETTERS, 1996, 398 (2-3) :175-178
[4]   The catalytic domain of avian sarcoma virus integrase: Conformation of the active-site residues in the presence of divalent cations [J].
Bujacz, G ;
Jaskolski, M ;
Alexandratos, J ;
Wlodawer, A ;
Merkel, G ;
Katz, RA ;
Skalka, AM .
STRUCTURE, 1996, 4 (01) :89-96
[5]  
BURKE CJ, 1992, J BIOL CHEM, V267, P9639
[6]   DOMAINS OF THE INTEGRASE PROTEIN OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 RESPONSIBLE FOR POLYNUCLEOTIDYL TRANSFER AND ZINC-BINDING [J].
BUSHMAN, FD ;
ENGELMAN, A ;
PALMER, I ;
WINGFIELD, P ;
CRAIGIE, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3428-3432
[7]   Solution structure of the N-terminal zinc binding domain of HIV-1 integrase [J].
Cai, ML ;
Zheng, RL ;
Caffrey, M ;
Craigie, R ;
Clore, GM ;
Gronenborn, AM .
NATURE STRUCTURAL BIOLOGY, 1997, 4 (07) :567-577
[8]   RIBBONS 2 0 [J].
CARSON, M .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1991, 24 :958-&
[9]   IDENTIFICATION OF AMINO-ACID-RESIDUES CRITICAL FOR ENDONUCLEASE AND INTEGRATION ACTIVITIES OF HIV-1 IN PROTEIN INVITRO [J].
DRELICH, M ;
WILHELM, R ;
MOUS, J .
VIROLOGY, 1992, 188 (02) :459-468
[10]   A mutation in integrase can compensate for mutations in the simian immunodeficiency virus att site [J].
Du, ZJ ;
Ilyinskii, PO ;
Lally, K ;
Desrosiers, RC ;
Engelman, A .
JOURNAL OF VIROLOGY, 1997, 71 (11) :8124-8132