2GKD

Structural insight into self-sacrifice mechanism of enediyne resistance

2GKD の概要

• エントリーDOI: 10.2210/pdb2gkd/pdb
• 関連するPDBエントリー: 1ZXF 2GKC
• NMR情報: BMRB: 6726
• 分子名称: 5'-D(*GP*CP*AP*TP*AP*TP*GP*AP*TP*AP*G)-3', 5'-D(*CP*TP*AP*TP*CP*AP*TP*AP*TP*GP*C)-3', CalC (3 entities in total)
• 機能のキーワード: start domain protein, toxin-dna complex, toxin/dna
• 由来する生物種: Micromonospora echinospora
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 24620.50

構造登録者

Singh, S.,Thorson, J.S. (登録日: 2006-04-01, 公開日: 2006-08-22, 最終更新日: 2024-05-29)

主引用文献

Singh, S.,Hager, M.H.,Zhang, C.,Griffith, B.R.,Lee, M.S.,Hallenga, K.,Markley, J.L.,Thorson, J.S.
Structural insight into the self-sacrifice mechanism of enediyne resistance.
Acs Chem.Biol., 1:451-460, 2006

PubMed Abstract: The recent discovery of the first "self-sacrifice" mechanism for bacterial resistance to the enediyne antitumor antibiotics, where enediyne-induced proteolysis of the resistance protein CalC inactivates both the highly reactive metabolite and the resistance protein, revealed yet another ingenious bacterial mechanism for controlling reactive metabolites. As reported herein, the first 3D structures of CalC and CalC in complex with calicheamicin (CLM) divulge CalC to be a member of the steroidogenic acute regulatory protein (StAR)-related transfer (START) domain superfamily. In contrast to previous studies of proteins known to bind DNA-damaging natural products ( e.g ., bleomycins, mitomycins, and nine-membered chromoprotein enediynes), this is the first demonstrated involvement of a START domain fold. Consistent with the CalC self-sacrifice mechanism, CLM in complex with CalC is positioned for direct hydrogen abstraction from Gly113 to initiate the oxidative proteolysis-based resistance mechanism. These structural studies also illuminate, for the first time, a small DNA-binding region within CalC that may serve to localize CalC to the enediyne target (DNA). Given the role of START domains in nuclear/cytosolic transport and translocation, this structural study also may implicate START domains as post-endocytotic intracellular chaperones for enediyne-based therapeutics such as MyloTarg.

PubMed: 17168523
DOI: 10.1021/cb6002898

実験手法

SOLUTION NMR