Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person Stephan, Ralf, 2024-04-06

Class:IdInstanceEdit:9907327
_displayNameStephan, Ralf, 2024-04-06
_timestamp2024-04-06 07:50:08
author[Person:804962] Stephan, Ralf
dateTime2024-04-06 07:50:03
(modified)[Reaction:70745] isovaleryl-CoA + FAD => beta-methylcrotonyl-CoA + FADH2 [Homo sapiens]
[Reaction:70773] beta-methylcrotonyl-CoA + ATP + HCO3- <=> beta-methylglutaconyl-CoA + ADP + orthophosphate + H2O (MCCA) [Homo sapiens]
[Reaction:70785] beta-methylglutaconyl-CoA + H2O <=> beta-hydroxy-beta-methylglutaryl-CoA [Homo sapiens]
[Reaction:70800] alpha-methylbutyryl-CoA + FAD => tiglyl-CoA + FADH2 [Homo sapiens]
[Reaction:70859] isobutyryl-CoA + FAD => methacrylyl-CoA + FADH2 [Homo sapiens]
[Pathway:70895] Branched-chain amino acid catabolism [Homo sapiens]
[PathwayDiagram:6788658] Diagram of Branched-chain amino acid catabolism, Loss-of-function mutations in BCKDHA or BCKDHB cause MSUD, Loss-of-function mutations in DBT cause MSUD2, Loss-of-function mutations in DLD cause MSUD3/DLDD, H139Hfs13* PPM1K causes a mild variant of MSUD, Branched-chain ketoacid dehydrogenase kinase deficiency, Isovaleric acidemia, 3-Methylcrotonyl-CoA carboxylase deficiency, 3-methylglutaconic aciduria, Beta-ketothiolase deficiency, Mitochondrial short-chain enoyl-CoA hydratase deficiency 1, and 3-hydroxyisobutyryl-CoA hydrolase deficiency
[FailedReaction:9865115] DBT loss-of-function mutants don't synthesize BCAA-CoA [Homo sapiens]
[FailedReaction:9865121] BCKDHA or BCKDHB loss-of-function mutants don't synthesize BCAA-CoA [Homo sapiens]
(structureModified)[Pathway:70895] Branched-chain amino acid catabolism [Homo sapiens]
[Change default viewing format]
No pathways have been reviewed or authored by Stephan, Ralf, 2024-04-06 (9907327)
Follow Reactome