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蛋白酶体抑制剂N-{N-[N-乙酰基-(S)-亮氨酰]-(S)-亮氨酰}正亮氨酸醛(ALLN)的晶体结构

Crystal structure of N-{N-[N-acetyl-(S)-leuc-yl]-(S)-leuc-yl}norleucinal (ALLN), an inhibitor of proteasome.

作者信息

Czerwinski Andrzej, Basava Channa, Dauter Miroslawa, Dauter Zbigniew

机构信息

Peptides International, Inc., 11621 Electron Drive, Louisville, KY 40299, USA.

Leidos Biomedical Research Inc., Basic Science Program, Argonne National Laboratory, Argonne, IL 60439, USA.

出版信息

Acta Crystallogr E Crystallogr Commun. 2015 Feb 7;71(Pt 3):254-7. doi: 10.1107/S2056989015002091. eCollection 2015 Mar 1.

DOI:10.1107/S2056989015002091
PMID:25844180
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4350719/
Abstract

The title compound, C20H37N3O4, also known by the acronym ALLN, is a tripeptidic inhibitor of the proteolytic activity of the proteasomes, enzyme complexes implicated in several neurodegenerative diseases and other disorders, including cancer. The crystal structure of ALLN, solved from synchrotron radiation diffraction data, revealed the mol-ecules in extended conformation of the backbone and engaging all peptide N and O atoms in inter-molecular hydrogen bonds forming an infinite anti-parallel β-sheet.

摘要

标题化合物C20H37N3O4,其简称为ALLN,是蛋白酶体蛋白水解活性的三肽抑制剂,蛋白酶体是一种与多种神经退行性疾病及其他病症(包括癌症)相关的酶复合物。通过同步辐射衍射数据解析得到的ALLN晶体结构表明,分子主链呈伸展构象,且所有肽的N原子和O原子参与分子间氢键形成无限的反平行β-折叠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf1/4350719/9336563312a7/e-71-00254-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf1/4350719/5dc03a16a573/e-71-00254-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf1/4350719/305661e6e4fb/e-71-00254-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf1/4350719/9336563312a7/e-71-00254-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf1/4350719/5dc03a16a573/e-71-00254-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf1/4350719/305661e6e4fb/e-71-00254-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf1/4350719/9336563312a7/e-71-00254-fig3.jpg

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本文引用的文献

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Development of proteasome inhibitors as research tools and cancer drugs.蛋白酶体抑制剂作为研究工具和癌症药物的开发。
J Cell Biol. 2012 Nov 12;199(4):583-8. doi: 10.1083/jcb.201210077.
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The proteasome in health and disease.蛋白酶体在健康和疾病中的作用。
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Covalent complexes of proteasome model with peptide aldehyde inhibitors MG132 and MG101: docking and molecular dynamics study.蛋白酶体模型与肽醛抑制剂 MG132 和 MG101 的共价复合物:对接和分子动力学研究。
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