作者
Chi Ho Chan, Sean A Newmister, Keenan Talyor, Kathy R Claas, Ivan Rayment, Jorge C Escalante-Semerena
发表日期
2014/1/1
期刊
Biochimica et Biophysica Acta (BBA)-General Subjects
卷号
1840
期号
1
页码范围
464-475
出版商
Elsevier
简介
Background
Cobamide diversity arises from the nature of the nucleotide base. Nicotinate mononucleotide (NaMN):base phosphoribosyltransferases (CobT) synthesize α-linked riboside monophosphates from diverse nucleotide base substrates (e.g., benzimidazoles, purines, phenolics) that are incorporated into cobamides.
Methods
Structural investigations of two members of the CobT family of enzymes in complex with various substrate bases as well as in vivo and vitro activity analyses of enzyme variants were performed to elucidate the roles of key amino acid residues important for substrate recognition.
Results
Results of in vitro and in vivo studies of active-site variants of the Salmonella enterica CobT (SeCobT) enzyme suggest that a catalytic base may not be required for catalysis. This idea is supported by the analyses of crystal structures that show that two glutamate residues function primarily to maintain an …
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