Human Orphan Cytochrome P450 2U1 Catalyzes the ω-Hydroxylation of Leukotriene B(4)

Cytochrome P450 2U1 (CYP2U1) identified from the human genome remains poorly known since few data are presently available on its physiological function(s) and substrate(s) specificity. CYP2U1 mutations are associated with complicated forms of hereditary spastic paraplegia, alterations of mitochondri...

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Detalles Bibliográficos
Autores principales: Nouri, Khawla, Pietrancosta, Nicolas, Le Corre, Laurent, Dansette, Patrick M., Mansuy, Daniel, Boucher, Jean-Luc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9739833/
https://www.ncbi.nlm.nih.gov/pubmed/36498943
http://dx.doi.org/10.3390/ijms232314615

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9739833/
https://www.ncbi.nlm.nih.gov/pubmed/36498943
http://dx.doi.org/10.3390/ijms232314615

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