Location of a potential transport binding site in a sigma class glutathione transferase by x-ray crystallography

被引:48
作者
Ji, XH
vonRosenvinge, EC
Johnson, WW
Armstrong, RN
Gilliland, GL
机构
[1] UNIV MARYLAND, MARYLAND BIOTECHNOL INST, CTR ADV RES BIOTECHNOL, ROCKVILLE, MD 20850 USA
[2] NIST, ROCKVILLE, MD 20850 USA
关键词
D O I
10.1073/pnas.93.16.8208
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The crystal structure of the sigma class glutathione transferase from squid digestive gland ire complex with S-(3-iodobenzyl)glutathione reveals a third binding site for the glutathione conjugate besides the two in the active sites of the dimer, The additional binding site is near the crystallographic two-fold axis between the two alpha 4-turn-alpha 5 motifs. The principal binding interactions with the conjugate include specific electrostatic interactions between the peptide and the two subunits and a hydrophobic cavity found across the two-fold axis that accommodates the 3-iodobenzyl group. Thus, two identical, symmetry-related but mutually exclusive binding modes for the third conjugate are observed, The hydrophobic pocket is about 14 Angstrom from the hydroxyl group of Tyr-7 in the active site. This site is a potential transport binding site for hydrophobic molecules or their glutathione conjugates.
引用
收藏
页码:8208 / 8213
页数:6
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