8B9Y

Cysteine Synthase from Trypanosoma cruzi with PLP and OAS

8B9Y の概要

• エントリーDOI: 10.2210/pdb8b9y/pdb
• 分子名称: Cysteine synthase, putative, O-ACETYLSERINE, alpha-D-ribofuranose, ... (6 entities in total)
• 機能のキーワード: chagas disease, amino acid synthesis, o-acetyl l-serine, pyridoxal 5-phosphate, transferase
• 由来する生物種: Trypanosoma cruzi
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 148069.92

構造登録者

Sowerby, K.V.,Pohl, E. (登録日: 2022-10-10, 公開日: 2023-05-31, 最終更新日: 2024-02-07)

主引用文献

Sowerby, K.,Freitag-Pohl, S.,Murillo, A.M.,Silber, A.M.,Pohl, E.
Cysteine synthase: multiple structures of a key enzyme in cysteine synthesis and a potential drug target for Chagas disease and leishmaniasis.
Acta Crystallogr D Struct Biol, 79:518-530, 2023

PubMed Abstract: Chagas disease is a neglected tropical disease (NTD) caused by Trypanosoma cruzi, whilst leishmaniasis, which is caused by over 20 species of Leishmania, represents a group of NTDs endemic to most countries in the tropical and subtropical belt of the planet. These diseases remain a significant health problem both in endemic countries and globally. These parasites and other trypanosomatids, including T. theileri, a bovine pathogen, rely on cysteine biosynthesis for the production of trypanothione, which is essential for parasite survival in hosts. The de novo pathway of cysteine biosynthesis requires the conversion of O-acetyl-L-serine into L-cysteine, which is catalysed by cysteine synthase (CS). These enzymes present potential for drug development against T. cruzi, Leishmania spp. and T. theileri. To enable these possibilities, biochemical and crystallographic studies of CS from T. cruzi (TcCS), L. infantum (LiCS) and T. theileri (TthCS) were conducted. Crystal structures of the three enzymes were determined at resolutions of 1.80 Å for TcCS, 1.75 Å for LiCS and 2.75 Å for TthCS. These three homodimeric structures show the same overall fold and demonstrate that the active-site geometry is conserved, supporting a common reaction mechanism. Detailed structural analysis revealed reaction intermediates of the de novo pathway ranging from an apo structure of LiCS and holo structures of both TcCS and TthCS to the substrate-bound structure of TcCS. These structures will allow exploration of the active site for the design of novel inhibitors. Additionally, unexpected binding sites discovered at the dimer interface represent new potential for the development of protein-protein inhibitors.

PubMed: 37204818
DOI: 10.1107/S2059798323003613

実験手法

X-RAY DIFFRACTION (1.8 Å)