7JUJ

Cruzain bound to Gallinamide inhibitor

7JUJ の概要

• エントリーDOI: 10.2210/pdb7juj/pdb
• 分子名称: Cruzipain, gallinamide A, bound form, POTASSIUM ION, ... (4 entities in total)
• 機能のキーワード: cysteine protease, cruzain, gallinamide, hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
• 由来する生物種: Trypanosoma cruzi
• タンパク質・核酸の鎖数: 6
• 化学式量合計: 140406.87

構造登録者

Silva, E.B.,Sharma, V.,Alvarez, L.H.,Gerwick, W.H.,McKerrow, J.H.,Podust, L.M. (登録日: 2020-08-19, 公開日: 2021-08-25, 最終更新日: 2024-10-23)

主引用文献

Barbosa Da Silva, E.,Sharma, V.,Hernandez-Alvarez, L.,Tang, A.H.,Stoye, A.,O'Donoghue, A.J.,Gerwick, W.H.,Payne, R.J.,McKerrow, J.H.,Podust, L.M.
Intramolecular Interactions Enhance the Potency of Gallinamide A Analogues against Trypanosoma cruzi .
J.Med.Chem., 65:4255-4269, 2022

PubMed Abstract: Gallinamide A, a metabolite of the marine cyanobacterium sp., selectively inhibits cathepsin L-like cysteine proteases. We evaluated the potency of gallinamide A and 23 synthetic analogues against intracellular amastigotes and the cysteine protease, cruzain. We determined the co-crystal structures of cruzain with gallinamide A and two synthetic analogues at ∼2 Å. SAR data revealed that the N-terminal end of gallinamide A is loosely bound and weakly contributes in drug-target interactions. At the C-terminus, the intramolecular π-π stacking interactions between the aromatic substituents at P1' and P1 restrict the bioactive conformation of the inhibitors, thus minimizing the entropic loss associated with target binding. Molecular dynamics simulations showed that in the absence of an aromatic group at P1, the substituent at P1' interacts with tryptophan-184. The P1-P1' interactions had no effect on anti-cruzain activity, whereas anti- potency increased by ∼fivefold, likely due to an increase in solubility/permeability of the analogues.

PubMed: 35188371
DOI: 10.1021/acs.jmedchem.1c02063

実験手法

X-RAY DIFFRACTION (2.2 Å)