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Details on Person D'Eustachio, Peter, 2023-06-13
| Class:Id | InstanceEdit:9837348 |
| _displayName | D'Eustachio, Peter, 2023-06-13 |
| _timestamp | 2023-06-13 21:01:20 |
| author | [Person:140934] D'Eustachio, Peter |
| dateTime | 2023-06-13 21:01:08 |
| (created) | [Summation:9837327] Daugherty et al. (2002) identified a candidate monofunctiona... [CatalystActivityReference:9837328] acyl-coenzyme A diphosphatase activity of Nudt8 [mitochondrial matrix] Nudt8 is a novel CoA diphosphohydrolase that resides in the mitochondria [LiteratureReference:9837329] Regulation of coenzyme A levels by degradation: the 'Ins and Outs' [CatalystActivity:9837330] coenzyme A transmembrane transporter activity of SLC25A42 [mitochondrial inner membrane] [Summation:9837331] Nudt8 in the mitochondrial matrix catalyzes the hydrolysis o... [EntityWithAccessionedSequence:9837332] Nudt8 [mitochondrial matrix] [Mus musculus] [Reaction:9837333] SLC25A42 exchanges cytosolic CoA-SH for mitochondrial matrix ADP [Homo sapiens] [Person:9837334] Vickers, Schuyler D [LiteratureReference:9837335] Nudt8 is a novel CoA diphosphohydrolase that resides in the mitochondria [CatalystActivity:9837336] coenzyme A diphosphatase activity of Nudt8 [mitochondrial matrix] |
| (modified) | [Reaction:196754] COASY transfers an adenylyl group from ATP to PPANT [Homo sapiens] [Reaction:196773] COASY phosphorylates DP-CoA [Homo sapiens] [SimpleEntity:196778] DP-CoA [cytosol] [Pathway:196783] Coenzyme A biosynthesis [Homo sapiens] [Summation:199184] Graves disease carrier protein (SLC25A16), associated with t... [Reaction:199216] SLC25A16 transports cytosolic CoA-SH to mitochondrial matrix [Homo sapiens] [Pathway:199220] Vitamin B5 (pantothenate) metabolism [Homo sapiens] [CatalystActivity:199228] coenzyme A transmembrane transporter activity of SLC25A16 [mitochondrial inner 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 [EntityWithAccessionedSequence:5216033] SLC25A42 [mitochondrial inner membrane] [Homo sapiens] |
| (structureModified) | [Reaction:196754] COASY transfers an adenylyl group from ATP to PPANT [Homo sapiens] [Reaction:196773] COASY phosphorylates DP-CoA [Homo sapiens] [Pathway:196783] Coenzyme A biosynthesis [Homo sapiens] [Pathway:199220] Vitamin B5 (pantothenate) metabolism [Homo sapiens] |
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No pathways have been reviewed or authored by D'Eustachio, Peter, 2023-06-13 (9837348)