4YUW

Crystal structure of Trypanosoma cruzi spermidine synthase in complex with trans-4-methylcyclohexylamine

4YUW の概要

• エントリーDOI: 10.2210/pdb4yuw/pdb
• 関連するPDBエントリー: 4YUV 4YUX 4YUY 4YUZ 4YV0 4YV1 4YV2
• 分子名称: Spermidine synthase, putative, 5'-[(S)-(3-AMINOPROPYL)(METHYL)-LAMBDA~4~-SULFANYL]-5'-DEOXYADENOSINE, trans-4-methylcyclohexanamine, ... (4 entities in total)
• 機能のキーワード: methyltransferase, polyamine synthesis, transferase
• 由来する生物種: Trypanosoma cruzi (strain CL Brener)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 69146.74

構造登録者

Amano, Y.,Tateishi, Y. (登録日: 2015-03-19, 公開日: 2015-09-09, 最終更新日: 2023-11-08)

主引用文献

Amano, Y.,Namatame, I.,Tateishi, Y.,Honboh, K.,Tanabe, E.,Niimi, T.,Sakashita, H.
Structural insights into the novel inhibition mechanism of Trypanosoma cruzi spermidine synthase.
Acta Crystallogr.,Sect.D, 71:1879-1889, 2015

PubMed Abstract: Trypanosoma cruzi causes Chagas disease, a severe disease affecting 8-10 million people in Latin America. While nifurtimox and benznidazole are used to treat this disease, their efficacy is limited and adverse effects are observed. New therapeutic targets and novel drugs are therefore urgently required. Enzymes in the polyamine-trypanothione pathway are promising targets for the treatment of Chagas disease. Spermidine synthase is a key enzyme in this pathway that catalyzes the transfer of an aminopropyl group from decarboxylated S-adenosylmethionine (dcSAM) to putrescine. Fragment-based drug discovery was therefore conducted to identify novel, potent inhibitors of spermidine synthase from T. cruzi (TcSpdSyn). Here, crystal structures of TcSpdSyn in complex with dcSAM, trans-4-methylcyclohexylamine and hit compounds from fragment screening are reported. The structure of dcSAM complexed with TcSpdSyn indicates that dcSAM stabilizes the conformation of the `gatekeeping' loop to form the putrescine-binding pocket. The structures of fragments bound to TcSpdSyn revealed two fragment-binding sites: the putrescine-binding pocket and the dimer interface. The putrescine-binding pocket was extended by an induced-fit mechanism. The crystal structures indicate that the conformation of the dimer interface is required to stabilize the gatekeeping loop and that fragments binding to this interface inhibit TcSpdSyn by disrupting its conformation. These results suggest that utilizing the dynamic structural changes in TcSpdSyn that occur upon inhibitor binding will facilitate the development of more selective and potent inhibitors.

PubMed: 26327378
DOI: 10.1107/S1399004715013048

実験手法

X-RAY DIFFRACTION (1.97 Å)