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Details on Person Jassal, Bijay, 2019-04-04
| Class:Id | InstanceEdit:9641161 |
| _displayName | Jassal, Bijay, 2019-04-04 |
| _timestamp | 2019-04-04 14:51:49 |
| author | [Person:73447] Jassal, Bijay |
| dateTime | 2019-04-04 18:49:02 |
| (created) | [ReferenceMolecule:9641153] riboflavin cyclic 4',5'-phosphate(2-) [ChEBI:76202] [SimpleEntity:9641154] PAP [peroxisomal matrix] [DefinedSet:9641155] CoA-SH,FAD,NAD+ [cytosol] [Summation:9641156] Mitochondrial folate transporter/carrier (encoded by SLC25A3... [LiteratureReference:9641157] The human gene SLC25A17 encodes a peroxisomal transporter of coenzyme A, FAD and NAD+ [DefinedSet:9641158] PAP,FMN,AMP [cytosol] [Reaction:9641159] TKFC:2Mg2+ dimer cleaves FAD to AMP and cFMN [Homo sapiens] [CatalystActivity:9641160] FAD-AMP lyase (cyclizing) activity of TKFC:2Mg2+ dimer [cytosol] [Person:9641162] Spaan, András N [CatalystActivity:9641163] FAD transmembrane transporter activity of SLC25A32 [mitochondrial inner membrane] |
| (edited) | [Reaction:9641159] TKFC:2Mg2+ dimer cleaves FAD to AMP and cFMN [Homo sapiens] [Reaction:9641164] SLC25A17 exchanges FAD, CoA-SH, NAD+ for PAP, FMN, AMP [Homo sapiens] [Reaction:9641169] SLC25A17 exchanges PAP, FMN, AMP for FAD, CoA-SH, NAD+ [Homo sapiens] [BlackBoxEvent:9641175] SLC25A32 transports FAD from cytosol to mitochondrial matrix [Homo sapiens] |
| (modified) | [CatalystActivity:70346] triokinase activity of TKFC:2Mg2+ dimer [cytosol] [Pathway:196843] Vitamin B2 (riboflavin) metabolism [Homo sapiens] [PathwayDiagram:532187] Diagram of Metabolism of water-soluble vitamins and cofactors, Defective AMN causes MGA1, Defective CD320 causes MMATC, Defective CUBN causes MGA1, Defective CBLIF causes IFD, Defective MMAA causes MMA, cblA type, Defective MMAB causes MMA, cblB type, Defective MMACHC causes MAHCC, Defective MMADHC causes MMAHCD, Defective MTR causes HMAG, Defective MTRR causes HMAE, Defective TCN2 causes TCN2 deficiency, Defective HLCS causes multiple carboxylase deficiency, Defective BTD causes biotidinase deficiency, and Defective ABCD4 causes MAHCJ [EntityWithAccessionedSequence:918185] TKFC [cytosol] [Homo sapiens] [Complex:5652070] TKFC:2Mg2+ dimer [cytosol] [Homo sapiens] |
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No pathways have been reviewed or authored by Jassal, Bijay, 2019-04-04 (9641161)