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Details on Person Jassal, Bijay, 2013-03-01
| Class:Id | InstanceEdit:3204328 |
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| _displayName | Jassal, Bijay, 2013-03-01 |
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| _timestamp | 2014-07-19 00:43:37 |
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| author | [Person:73447] Jassal, Bijay |
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| dateTime | 2013-03-01 14:47:13 |
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| modified |
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| (authored) | [Reaction:3204311] AOX1 oxidises PXL to PDXate [Homo sapiens] |
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| (created) | [Reaction:3204311] AOX1 oxidises PXL to PDXate [Homo sapiens]
[Person:3204312] Alfaro, Joshua F
[Summation:3204313] Aldehyde oxidase (AOX1) is a complex molybdo-flavoprotein th...
[Person:3204314] Jones, Jeffrey P
[Complex:3204315] AOX1:cofactors [cytosol] [Homo sapiens]
[Complex:3204316] 2xAOX1:cofactors [cytosol] [Homo sapiens]
[LiteratureReference:3204317] The impact of single nucleotide polymorphisms on human aldehyde oxidase
[BlackBoxEvent:3204318] cob(II)alamin is transferred from MMACHC:MMADHC:cob(II)alamin to MTRR:MTR [Homo sapiens]
[Person:3204319] Leimkühler, Silke
[Person:3204320] Teutloff, Christian |
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| (edited) | [Reaction:3204311] AOX1 oxidises PXL to PDXate [Homo sapiens]
[BlackBoxEvent:3204318] cob(II)alamin is transferred from MMACHC:MMADHC:cob(II)alamin to MTRR:MTR [Homo sapiens] |
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| (modified) | [Complex:70770] 6x(Btn-MCCC1:MCCC2) [mitochondrial matrix] [Homo sapiens]
[CatalystActivity:70771] methylcrotonoyl-CoA carboxylase activity of 6x(Btn-MCCC1:MCCC2) [mitochondrial matrix]
[Complex:71026] 6x(Btn-PCCA:PCCB) [mitochondrial matrix] [Homo sapiens]
[CatalystActivity:71030] propionyl-CoA carboxylase activity of 6x(Btn-PCCA:PCCB) [mitochondrial matrix]
[Pathway:196741] Cobalamin (Cbl, vitamin B12) transport and metabolism [Homo sapiens]
[SimpleEntity:198803] MDASC [cytosol]
[DefinedSet:198841] SLC2A1,3 [plasma membrane] [Homo sapiens]
[CatalystActivity:198847] dehydroascorbic acid transmembrane transporter activity of SLC2A1,3 [plasma membrane]
[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
[Pathway:964975] Vitamin B6 activation to pyridoxal phosphate [Homo sapiens] |
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No pathways have been reviewed or authored by Jassal, Bijay, 2013-03-01 (3204328)
