2RF7

Crystal structure of the escherichia coli nrfa mutant Q263E

2RF7 の概要

• エントリーDOI: 10.2210/pdb2rf7/pdb
• 関連するPDBエントリー: 2RDZ
• 分子名称: Cytochrome c-552, CALCIUM ION, HEME C, ... (5 entities in total)
• 機能のキーワード: oxidoreductase, calcium ligand, electron transport, heme, iron, metal-binding, periplasm, transport
• 由来する生物種: Escherichia coli K12
• 細胞内の位置: Periplasm: P0ABK9
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 211809.16

構造登録者

Clarke, T.A.,Richardson, D.J.,Hemmings, A.M. (登録日: 2007-09-28, 公開日: 2008-03-25, 最終更新日: 2023-08-30)

主引用文献

Clarke, T.A.,Kemp, G.L.,Wonderen, J.H.,Doyle, R.M.,Cole, J.A.,Tovell, N.,Cheesman, M.R.,Butt, J.N.,Richardson, D.J.,Hemmings, A.M.
Role of a Conserved Glutamine Residue in Tuning the Catalytic Activity of Escherichia coli Cytochrome c Nitrite Reductase.
Biochemistry, 47:3789-3799, 2008

PubMed Abstract: The pentaheme cytochrome c nitrite reductase (NrfA) of Escherichia coli is responsible for nitrite reduction during anaerobic respiration when nitrate is scarce. The NrfA active site consists of a hexacoordinate high-spin heme with a lysine ligand on the proximal side and water/hydroxide or substrate on the distal side. There are four further highly conserved active site residues including a glutamine (Q263) positioned 8 A from the heme iron for which the side chain, unusually, coordinates a conserved, essential calcium ion. Mutation of this glutamine to the more usual calcium ligand, glutamate, results in an increase in the K m for nitrite by around 10-fold, while V max is unaltered. Protein film voltammetry showed that lower potentials were required to detect activity from NrfA Q263E when compared with native enzyme, consistent with the introduction of a negative charge into the vicinity of the active site heme. EPR and MCD spectroscopic studies revealed the high spin state of the active site to be preserved, indicating that a water/hydroxide molecule is still coordinated to the heme in the resting state of the enzyme. Comparison of the X-ray crystal structures of the as-prepared, oxidized native and mutant enzymes showed an increased bond distance between the active site heme Fe(III) iron and the distal ligand in the latter as well as changes to the structure and mobility of the active site water molecule network. These results suggest that an important function of the unusual Q263-calcium ion pair is to increase substrate affinity through its role in supporting a network of hydrogen bonded water molecules stabilizing the active site heme distal ligand.

PubMed: 18311941
DOI: 10.1021/bi702175w

実験手法

X-RAY DIFFRACTION (2.04 Å)