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Structure prediction and analysis of MxaF from obligate facultative and restricted facultative methylobacterium

机译:专性兼性和限制性兼性甲基杆菌对MxaF的结构预测和分析

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摘要

Methylobacteria are ubiquitous in the biosphere which are capable of growing on C1 compounds such as formate, formaldehyde, methanol and methylamine as well as on a wide range of multi-carbon growth substrates such as C2, C3 and C4 compounds due to the methylotrophic enzymes methanol dehydrogenase (MDH). MDH is performing these functions with the help of a key protein mxaF. Unfortunately, detailed structural analysis and homology modeling of mxaF is remains undefined. Hence, the objective of this research is the characterization and three dimensional modeling of mxaF protein from three different methylotrophs by using I-TASSER server. The predicted model were further optimize and validate by Profile 3D, Errat, Verifiy3-D and PROCHECK server. Predicted and best evaluated models have been successfully deposited to PMDB database with PMDB ID PM0077505, PM0077506 and PM0077507. Active site identification revealed 11, 13 and 14 putative functional site residues in respected models. It may play a major role during protein-protein, and protein-cofactor interactions. This study can provide us an ab-initio and detail information to understand the structure, mechanism of action and regulation of mxaF protein.
机译:甲基细菌在生物圈中无处不在,由于甲基营养酶甲醇,能够在C1化合物(例如甲酸盐,甲醛,甲醇和甲胺)以及各种多碳生长底物(例如C2,C3和C4化合物)上生长脱氢酶(MDH)。 MDH在关键蛋白mxaF的帮助下执行这些功能。不幸的是,mxaF的详细结构分析和同源性建模仍然不确定。因此,本研究的目的是使用I-TASSER服务器对来自三种不同甲基营养菌的mxaF蛋白进行表征和三维建模。通过Profile 3D,Errat,Verifiy3-D和PROCHECK服务器进一步优化和验证了预测的模型。预测和最佳评估的模型已成功存储到PMDB数据库中,其中PMDB ID为PM0077505,PM0077506和PM0077507。活性部位鉴定揭示了在所关注模型中11、13和14个假定的功能部位残基。它可能在蛋白质-蛋白质和蛋白质-辅因子相互作用中起主要作用。这项研究可以为我们提供从头开始的详细信息,以了解mxaF蛋白的结构,作用机理和调控。

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