1WW3

Crystallographic studies on two bioisosteric analogues, N-acetyl-beta-D-glucopyranosylamine and N-trifluoroacetyl-beta-D-glucopyranosylamine, potent inhibitors of muscle glycogen phosphorylase

1WW3 の概要

• エントリーDOI: 10.2210/pdb1ww3/pdb
• 関連するPDBエントリー: 1WW2 2PRJ
• 分子名称: Glycogen phosphorylase, muscle form, N-(trifluoroacetyl)-beta-D-glucopyranosylamine, PYRIDOXAL-5'-PHOSPHATE, ... (4 entities in total)
• 機能のキーワード: glycogenolysis, type 2 diabetes, transferase
• 由来する生物種: Oryctolagus cuniculus (rabbit)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 97813.52

構造登録者

Anagnostou, E.,Kosmopoulou, M.N.,Chrysina, E.D.,Leonidas, D.D.,Hadjiloi, T.,Tiraidis, C.,Zographos, S.E.,Gyorgydeak, Z.,Somsak, L.,Docsa, T.,Gergely, P.,Kolisis, F.N.,Oikonomakos, N.G. (登録日: 2004-12-31, 公開日: 2005-12-13, 最終更新日: 2023-10-25)

主引用文献

Anagnostou, E.,Kosmopoulou, M.N.,Chrysina, E.D.,Leonidas, D.D.,Hadjiloi, T.,Tiraidis, C.,Zographos, S.E.,Gyorgydeak, Z.,Somsak, L.,Docsa, T.,Gergely, P.,Kolisis, F.N.,Oikonomakos, N.G.
Crystallographic studies on two bioisosteric analogues, N-acetyl-beta-d-glucopyranosylamine and N-trifluoroacetyl-beta-d-glucopyranosylamine, potent inhibitors of muscle glycogen phosphorylase
Bioorg.Med.Chem., 14:181-189, 2006

PubMed Abstract: Structure-based inhibitor design has led to the discovery of a number of potent inhibitors of glycogen phosphorylase b (GPb), N-acyl derivatives of beta-D-glucopyranosylamine, that bind at the catalytic site of the enzyme. The first good inhibitor in this class of compounds, N-acetyl-beta-D-glucopyranosylamine (NAG) (K(i) = 32 microM), has been previously characterized by biochemical, biological and crystallographic experiments at 2.3 angstroms resolution. Bioisosteric replacement of the acetyl group by trifluoroacetyl group resulted in an inhibitor, N-trifluoroacetyl-beta-D-glucopyranosylamine (NFAG), with a K(i) = 75 microM. To elucidate the structural basis of its reduced potency, we determined the ligand structure in complex with GPb at 1.8 angstroms resolution. To compare the binding mode of N-trifluoroacetyl derivative with that of the lead molecule, we also determined the structure of GPb-NAG complex at a higher resolution (1.9 angstroms). NFAG can be accommodated in the catalytic site of T-state GPb at approximately the same position as that of NAG and stabilize the T-state conformation of the 280 s loop by making several favourable contacts to Asn284 of this loop. The difference observed in the K(i) values of the two analogues can be interpreted in terms of subtle conformational changes of protein residues and shifts of water molecules in the vicinity of the catalytic site, variations in van der Waals interaction, and desolvation effects.

PubMed: 16213146
DOI: 10.1016/j.bmc.2005.08.010

実験手法

X-RAY DIFFRACTION (1.8 Å)