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5THO

Crystal Structure of Mycobacterium Tuberculosis Proteasome in complex with N,C-capped Dipeptide Inhibitor PKS2205

5THO の概要
エントリーDOI10.2210/pdb5tho/pdb
関連するBIRD辞書のPRD_IDPRD_002250
分子名称Proteasome subunit alpha, Proteasome subunit beta, N,N-diethyl-N~2~-(3-phenylpropanoyl)-L-asparaginyl-O-methyl-N-[(naphthalen-1-yl)methyl]-L-serinamide, ... (4 entities in total)
機能のキーワードdipeptide inhibitor, proteasome, mycobacterium tuberculosis, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
由来する生物種Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra)
詳細
タンパク質・核酸の鎖数28
化学式量合計725296.92
構造登録者
Hsu, H.C.,Li, H. (登録日: 2016-09-30, 公開日: 2017-01-11, 最終更新日: 2023-10-04)
主引用文献Hsu, H.C.,Singh, P.K.,Fan, H.,Wang, R.,Sukenick, G.,Nathan, C.,Lin, G.,Li, H.
Structural Basis for the Species-Selective Binding of N,C-Capped Dipeptides to the Mycobacterium tuberculosis Proteasome.
Biochemistry, 56:324-333, 2017
Cited by
PubMed Abstract: The Mycobacterium tuberculosis (Mtb) 20S proteasome is vital for the pathogen to survive under nitrosative stress in vitro and to persist in mice. To qualify for drug development, inhibitors targeting Mtb 20S must spare both the human constitutive proteasome (c-20S) and immunoproteasome (i-20S). We recently reported members of a family of noncovalently binding dipeptide proteasome inhibitors that are highly potent and selective for Mtb 20S over human c-20S and i-20S. To understand the structural basis of their potency and selectivity, we have studied the structure-activity relationship of six derivatives and solved their cocrystal structures with Mtb 20S. The dipeptide inhibitors form an antiparallel β-strand with the active site β-strands. Selectivity is conferred by several features of Mtb 20S relative to its mouse counterparts, including a larger S1 pocket, additional hydrogen bonds in the S3 pocket, and hydrophobic interactions in the S4 pocket. Serine-20 and glutamine-22 of Mtb 20S interact with the dipeptides and confer Mtb-specific inhibition over c-20S and i-20S. The Mtb 20S and mammalian i-20S have a serine-27 that interacts strongly with the dipeptides, potentially explaining the higher inhibitory activity of the dipeptides toward i-20S over c-20S. This detailed structural knowledge will aid in optimizing the dipeptides as anti-tuberculosis drugs.
PubMed: 27976853
DOI: 10.1021/acs.biochem.6b01107
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3.002 Å)
構造検証レポート
Validation report summary of 5tho
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-04-09に公開中

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