Xh. Ji et al., LOCATION OF A POTENTIAL TRANSPORT BINDING-SITE IN A SIGMA-CLASS GLUTATHIONE TRANSFERASE BY X-RAY CRYSTALLOGRAPHY, Proceedings of the National Academy of Sciences of the United Statesof America, 93(16), 1996, pp. 8208-8213
The crystal structure of the sigma class glutathione transferase from
squid digestive gland ire complex with S-(3-iodobenzyl)glutathione rev
eals a third binding site for the glutathione conjugate besides the tw
o in the active sites of the dimer, The additional binding site is nea
r the crystallographic two-fold axis between the two alpha 4-turn-alph
a 5 motifs. The principal binding interactions with the conjugate incl
ude specific electrostatic interactions between the peptide and tile t
wo subunits and a hydrophobic cavity found across the two-fold axis th
at accommodates the 3-iodobenzyl group. Thus, two identical, symmetry-
related but mutually exclusive binding modes for the third conjugate a
re observed, The hydrophobic pocket is about 14 Angstrom from the hydr
oxyl group of Tyr-7 in the active site. This site is a potential trans
port binding site for hydrophobic molecules or their glutathione conju
gates.