Linking cytochrome P450 enzymes from Mycobacterium tuberculosis to their cognate ferredoxin partners

Mycobacterium tuberculosis (Mtb) codes for 20 cytochrome P450 enzymes (CYPs), considered potential drug-targets due to their essential roles in bacterial viability and host infection. Catalytic activity of mycobacterial CYPs is dependent on electron transfer from a NAD (P)H-ferredoxin-reductase (FNR...

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Detalles Bibliográficos
Autores principales: Ortega Ugalde, Sandra, de Koning, Coen P., Wallraven, Kerstin, Bruyneel, Ben, Vermeulen, Nico P. E., Grossmann, Tom N., Bitter, Wilbert, Commandeur, Jan N. M., Vos, J. Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Biotechnologically Relevant Enzymes and Proteins
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208970/
https://www.ncbi.nlm.nih.gov/pubmed/30136203
http://dx.doi.org/10.1007/s00253-018-9299-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208970/
https://www.ncbi.nlm.nih.gov/pubmed/30136203
http://dx.doi.org/10.1007/s00253-018-9299-4

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