Abstract

AbstractCitrus canker, caused by the bacterium Xanthomonas citri subsp. citri (XAC) is one of the most important diseases in citrus, presenting a significant impact on the Brazilian economy. A promising target enzyme for such disease control is phosphomannose isomerase (PMI). Phosphomannose isomerase is an enzyme that catalyses the interconversion of fructose-6-phosphate (F6P) and mannose-6-phosphate (M6P) and allows the synthesis of GDP-mannose in eukaryotic organisms. In Xanthomonas sp., phosphomannose isomerase is related to the production of xanthan gum, which is a defense mechanism of bacteria to prevent dehydration in harmful environments. Due to the lack of a resolved protein structure, a PMI model was created using the protein homology modeling method and, after protein selection by a BLASTp algorithm and subsequent alignment using ClustalOmega, the model was built using the MODELLER Software. The model was analysed and validated using the WhatIf, ProCheck, Errat, Prove and Verify-3D softwares. The Xanthomonas PMI model proved reliable through the validation and evaluation tests.KeywordsCitrus cankerPhosphomannose isomerase (PMI)Homology modeling

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