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1KEE

Inactivation of the Amidotransferase Activity of Carbamoyl Phosphate Synthetase by the Antibiotic Acivicin

1KEE の概要
エントリーDOI10.2210/pdb1kee/pdb
分子名称Carbamoyl-phosphate synthetase large chain, Carbamoyl-phosphate synthetase small chain, MANGANESE (II) ION, ... (10 entities in total)
機能のキーワードatp grasp, channeling, antibiotic, ligase
由来する生物種Escherichia coli
詳細
タンパク質・核酸の鎖数8
化学式量合計645960.47
構造登録者
Miles, B.W.,Thoden, J.B.,Holden, H.M.,Raushel, F.M. (登録日: 2001-11-15, 公開日: 2001-12-21, 最終更新日: 2023-08-16)
主引用文献Miles, B.W.,Thoden, J.B.,Holden, H.M.,Raushel, F.M.
Inactivation of the amidotransferase activity of carbamoyl phosphate synthetase by the antibiotic acivicin.
J.Biol.Chem., 277:4368-4373, 2002
Cited by
PubMed Abstract: Carbamoyl phosphate synthetase (CPS) from Escherichia coli catalyzes the formation of carbamoyl phosphate from 2 mol of ATP, bicarbonate, and glutamine. CPS was inactivated by the glutamine analog, acivicin. In the presence of ATP and bicarbonate the second-order rate constant for the inactivation of the glutamine-dependent activities was 4.0 x 10(4) m(-1) s(-1). In the absence of ATP and bicarbonate the second-order rate constant for inactivation of CPS was reduced by a factor of 200. The enzyme was protected against inactivation by the inclusion of glutamine in the reaction mixture. The ammonia-dependent activities were unaffected by the incubation of CPS with acivicin. These results are consistent with the covalent labeling of the glutamine-binding site located within the small amidotransferase subunit. The binding of ATP and bicarbonate to the large subunit of CPS must also induce a conformational change within the amidotransferase domain of the small subunit that enhances the nucleophilic character of the thiol group required for glutamine hydrolysis. The acivicin-inhibited enzyme was crystallized, and the three-dimensional structure was determined by x-ray diffraction techniques. The thiol group of Cys-269 was covalently attached to the dihydroisoxazole ring of acivicin with the displacement of a chloride ion.
PubMed: 11729189
DOI: 10.1074/jbc.M108582200
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.1 Å)
構造検証レポート
Validation report summary of 1kee
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2025-12-31に公開中

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