Lepluart Jesse, Kirk Martin L
Department of Chemistry and Chemical Biology, The University of New Mexico, MSC03 2060, 1 University of New Mexico, Albuquerque, NM 87131, USA.
The Center for High Technology Materials, The University of New Mexico, Albuquerque, NM 87106, USA.
Molecules. 2025 Feb 14;30(4):871. doi: 10.3390/molecules30040871.
The determination of tungsten oxidation states and W-ligand bond lengths for pyranopterin tungsten enzymes can be negatively impacted by Fourier series termination effects and photodamage/photoreduction in the X-ray beam. As a result, a new set of bond valence sum (BVS) parameters have been derived from bond length data on W(+4) and W(+6) model compounds that were obtained from X-ray crystallography. These new W enzyme-specific BVS parameters have been used in the analysis of pyranopterin tungsten enzyme structural data. The results of this analysis indicate that there are potential issues with the enzyme crystal structures, including the number of ligating atoms to the tungsten atom, the W-ligand bond lengths, and the W oxidation state. We conclude that a BVS analysis of crystallographic and EXAFS structural data will help address these issues, and EXAFS should be more routinely employed in the determination of pyranopterin tungsten enzyme active site structures due to the increased accuracy of this technique for the determination of W-ligand bond distances.
对于吡喃蝶呤钨酶,钨氧化态和W-配体键长的测定可能会受到傅里叶级数终止效应以及X射线束中的光损伤/光还原的负面影响。因此,基于通过X射线晶体学获得的W(+4)和W(+6)模型化合物的键长数据,推导出了一组新的键价和(BVS)参数。这些新的针对钨酶的BVS参数已用于分析吡喃蝶呤钨酶的结构数据。该分析结果表明,酶晶体结构存在潜在问题,包括与钨原子配位的原子数量、W-配体键长以及W氧化态。我们得出结论,对晶体学和EXAFS结构数据进行BVS分析将有助于解决这些问题,并且由于EXAFS技术在测定W-配体键距方面的准确性提高,在测定吡喃蝶呤钨酶活性位点结构时应更常规地采用EXAFS。