2Y6P

Evidence for a Two-Metal-Ion-Mechanism in the Kdo- Cytidylyltransferase KdsB

2Y6P の概要

• エントリーDOI: 10.2210/pdb2y6p/pdb
• 分子名称: 3-DEOXY-MANNO-OCTULOSONATE CYTIDYLYLTRANSFERASE, CYTIDINE-5'-TRIPHOSPHATE, MAGNESIUM ION, ... (6 entities in total)
• 機能のキーワード: transferase, lipid a
• 由来する生物種: AQUIFEX AEOLICUS
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 83434.09

構造登録者

Schmidt, H.,Mesters, J.R.,Mamat, U.,Hilgenfeld, R. (登録日: 2011-01-25, 公開日: 2011-08-24, 最終更新日: 2024-05-08)

主引用文献

Schmidt, H.,Mesters, J.R.,Wu, J.,Woodard, R.W.,Hilgenfeld, R.,Mamat, U.
Evidence for a Two-Metal-Ion Mechanism in the Cytidyltransferase Kdsb, an Enzyme Involved in Lipopolysaccharide Biosynthesis.
Plos One, 6:23231-, 2011

PubMed Abstract: Lipopolysaccharide (LPS) is located on the surface of Gram-negative bacteria and is responsible for maintaining outer membrane stability, which is a prerequisite for cell survival. Furthermore, it represents an important barrier against hostile environmental factors such as antimicrobial peptides and the complement cascade during Gram-negative infections. The sugar 3-deoxy-D-manno-oct-2-ulosonic acid (Kdo) is an integral part of LPS and plays a key role in LPS functionality. Prior to its incorporation into the LPS molecule, Kdo has to be activated by the CMP-Kdo synthetase (CKS). Based on the presence of a single Mg²⁺ ion in the active site, detailed models of the reaction mechanism of CKS have been developed previously. Recently, a two-metal-ion hypothesis suggested the involvement of two Mg²⁺ ions in Kdo activation. To further investigate the mechanistic aspects of Kdo activation, we kinetically characterized the CKS from the hyperthermophilic organism Aquifex aeolicus. In addition, we determined the crystal structure of this enzyme at a resolution of 2.10 Å and provide evidence that two Mg²⁺ ions are part of the active site of the enzyme.

PubMed: 21826242
DOI: 10.1371/JOURNAL.PONE.0023231

実験手法

X-RAY DIFFRACTION (2.1 Å)