Role of a Conserved Tyrosine Residue in the FMN-Heme Interdomain Electron Transfer in Inducible Nitric Oxide Synthase.
Role of a Conserved Tyrosine Residue in the FMN-Heme Interdomain Electron Transfer in Inducible Nitric Oxide Synthase.
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保守酪氨酸残基在诱导型一氧化氮合酶 FMN-血红素域间电子转移中的作用。
DOI:
10.1021/acs.jpca.6b08207
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发表时间:
2016
期刊:
影响因子:
--
通讯作者:
Feng,Changjian
中科院分区:
文献类型:
--
作者:
Chen,Li;Zheng,Huayu;Li,Wenbing;Li,Wei;Miao,Yubin;Feng,Changjian
The interdomain electron transfer (IET) between the flavin mononucleotide (FMN) and heme domains is essential in the biosynthesis of nitric oxide (NO) by the NO synthase (NOS) enzymes. A conserved tyrosine residue in the FMN domain (Y631 in human inducible NOS) was proposed to be a key part of the electron transfer pathway in the FMN/heme docked complex model. In the present study, the FMN–heme IET kinetics in the Y631F mutant and wild type of a bidomain oxygenase/FMN construct of human inducible NOS were determined by laser flash photolysis. The rate constant of the Y631F mutant is significantly decreased by ∼75% (compared to the wild type), showing that the tyrosine residue indeed facilitates the FMN–heme IET through the protein medium. The IET rate constant of the wild type protein decreases from 345 to 242 s–1on going from H2O to 95% D2O, giving a solvent kinetic isotope effect of 1.4. In contrast, no deuterium isotope effect was observed for the Tyr-to-Phe mutant. Moreover, an appreciable change in the wild type iNOS IET rate constant value was observed upon changing pH. These results indicate that the FMN–heme IET is proton coupled, in which the conserved tyrosine residue may play an important role.
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影响因子:
5.4
作者:
L. Stanberry;S. Kit;M. Myers
通讯作者:
M. Myers
DOI:
10.1093/infdis/143.2.281
发表时间:
1981
期刊:
The Journal of infectious diseases
影响因子:
--
作者:
Hugh J. Field;Andrew McMillan;Graham Darby
通讯作者:
Graham Darby
影响因子:
64.8
作者:
J. Smiley
通讯作者:
J. Smiley
影响因子:
3.7
作者:
R. Tenser;S. Ressel;M. E. Dunstan
通讯作者:
M. E. Dunstan
影响因子:
3.7
作者:
R. Tenser;M. E. Dunstan
通讯作者:
M. E. Dunstan