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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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| Vydáno v: | Appl Microbiol Biotechnol |
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| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer Berlin Heidelberg
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6208970/ https://ncbi.nlm.nih.gov/pubmed/30136203 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00253-018-9299-4 |
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