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Structural insights into a low-spin myoglobin variant with bis-histidine coordination from molecular modeling

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成果类型:
期刊论文
作者:
Lin, Ying-Wu*
通讯作者:
Lin, Ying-Wu
作者机构:
[Lin, Ying-Wu] Univ S China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China.
通讯机构:
[Lin, Ying-Wu] U
Univ S China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China.
语种:
英文
关键词:
six-coordinate;low-spin heme;hydrogen bond;protein design;MD simulation
期刊:
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS
ISSN:
0887-3585
年:
2011
卷:
79
期:
3
页码:
679-684
机构署名:
本校为第一且通讯机构
院系归属:
化学化工学院
摘要:
Rational design of functional enzymes is a powerful strategy to gain deep insights into more complex native enzymes, such as nitric oxide reductase (NOR). Recently, we engineered a functional model of NOR by creating a two His and one Glu (2-His-1-Glu) non-heme iron center in sperm whale myoglobin (swMb L29E, F43H, H64, called FeBMb(-His)). It was found that FeBMb(-His) adopts a low-spin state with bis-His coordination in the absence of metal ions binding to the designed metal center. However, no structural information was available for the var...

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