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Details on Person D'Eustachio, Peter, 2024-04-17
| Class:Id | InstanceEdit:9907889 |
| _displayName | D'Eustachio, Peter, 2024-04-17 |
| _timestamp | 2024-04-17 17:51:43 |
| author | [Person:140934] D'Eustachio, Peter |
| dateTime | 2024-04-17 17:51:40 |
| (created) | [DatabaseIdentifier:9907886] RHEA:22717 [ReferenceMolecule:9907887] (4Z,7Z,10Z,13Z,16Z,19Z)-22-hydroxydocosahexaenoate [ChEBI:77015] [DatabaseIdentifier:9907888] RHEA:25287 |
| (modified) | [Reaction:192061] CYP46A1 24-hydroxylates CHOL [Homo sapiens] [Reaction:194678] CYP51A1 demethylates LAN [Homo sapiens] [CatalystActivity:194693] oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen of CYP51A1 [endoplasmic reticulum membrane] [PathwayDiagram:500339] Diagram of Phase I - Functionalization of compounds, Defective CYP11A1 causes AICSR, Defective CYP11B1 causes AH4, Defective CYP11B2 causes CMO-1 deficiency, Defective CYP19A1 causes AEXS, Defective CYP1B1 causes Glaucoma, Defective CYP21A2 causes AH3, Defective CYP24A1 causes HCAI, Defective CYP26B1 causes RHFCA, Defective CYP26C1 causes FFDD4, Defective CYP2U1 causes SPG56, Defective CYP4F22 causes ARCI5, Defective CYP7B1 causes SPG5A and CBAS3, Defective FMO3 causes TMAU, Defective MAOA causes BRUNS, and Defective TBXAS1 causes GHDD [SimpleEntity:6786220] DHA [endoplasmic reticulum membrane] [SimpleEntity:6786225] HDoHE [endoplasmic reticulum membrane] [CatalystActivity:6786235] oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen of CYP4V2 [endoplasmic reticulum membrane] [Reaction:6786239] CYP4V2 omega-hydroxylates DHA to HDoHE [Homo sapiens] [SimpleEntity:9860950] DHA [nucleoplasm] |
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No pathways have been reviewed or authored by D'Eustachio, Peter, 2024-04-17 (9907889)