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.
Details on Person alpha-methylbutyryl-CoA + FAD => tiglyl-CoA + FADH2
Class:Id Reaction:70800
_displayName alpha-methylbutyryl-CoA + FAD => tiglyl-CoA + FADH2
_doRelease TRUE
_timestamp 2024-08-02 17:57:01
catalystActivity [CatalystActivity:70798] acyl-CoA dehydrogenase activity of ACADSB tetramer [mitochondrial matrix]
catalystActivityReference [CatalystActivityReference:9643583] acyl-CoA dehydrogenase activity of ACADSB tetramer [mitochondrial matrix] Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism
compartment [Compartment:5460] mitochondrial matrix
crossReference [DatabaseIdentifier:9917126] RHEA:43781
input [SimpleEntity:70718] 2MBUT-CoA [mitochondrial matrix] [SimpleEntity:113596] FAD [mitochondrial matrix] [SimpleEntity:113529] H+ [mitochondrial matrix]
internalReviewed [InstanceEdit:9917225] D'Eustachio, Peter, 2024-08-01
literatureReference [LiteratureReference:70801] Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism [LiteratureReference:70813] 2-Methylbutyryl-coenzyme A dehydrogenase deficiency: a new inborn error of L-isoleucine metabolism
modified [InstanceEdit:113517] Schmidt, EE, 2004-06-09 05:19:12 [InstanceEdit:163376] Vastrik, I, 2005-04-29 06:26:51 [InstanceEdit:508267] D'Eustachio, P, 2010-02-11 [InstanceEdit:508376] D'Eustachio, P, 2010-02-11 [InstanceEdit:517476] D'Eustachio, P, 2010-02-18 [InstanceEdit:8946993] Shorser, Solomon, 2016-11-07 [InstanceEdit:9643047] Wu, G, 2019-04-04 [InstanceEdit:9830342] Matthews, Lisa, 2023-03-08 [InstanceEdit:9907327] Stephan, Ralf, 2024-04-06 [InstanceEdit:9908873] Stephan, Ralf, 2024-04-23 [InstanceEdit:9917131] Stephan, Ralf, 2024-07-30 [InstanceEdit:9917363] D'Eustachio, Peter, 2024-08-02
name alpha-methylbutyryl-CoA + FAD => tiglyl-CoA + FADH2
output [SimpleEntity:70799] tiglyl-CoA [mitochondrial matrix] [SimpleEntity:31649] FADH2 [mitochondrial matrix]
precedingEvent
previousReviewStatus [ReviewStatus:9821385] four stars
releaseDate 2004-07-06
reviewed [InstanceEdit:9917333] Hill, David P, 2024-08-02
reviewStatus [ReviewStatus:9821382] five stars
species [Species:48887] Homo sapiens
stableIdentifier [StableIdentifier:359751] R-HSA-70800.6
structureModified [InstanceEdit:9917131] Stephan, Ralf, 2024-07-30
summation [Summation:178469] Mitochondrial 2-methyl branched-chain acyl-CoA dehydrogenase...
(hasEvent) [Pathway:70895] Branched-chain amino acid catabolism [Homo sapiens]
(precedingEvent) [Reaction:70830] tiglyl-CoA + H2O <=> alpha-methyl-beta-hydroxybutyryl-CoA [Homo sapiens]
(updatedInstance) [_UpdateTracker:9790952] Update Tracker - [Reaction:70800] alpha-methylbutyryl-CoA + FAD => tiglyl-CoA + FADH2 - v32:[modifyText] [_UpdateTracker:9919411] Update Tracker - [Reaction:70800] alpha-methylbutyryl-CoA + FAD => tiglyl-CoA + FADH2 - v90:[modifyText, removeInput]
[Change default viewing format]
List...
Protein identifiers
ChEBI identifiers
KEGG COMPOUND identifiers
No pathways have been reviewed or authored by alpha-methylbutyryl-CoA + FAD => tiglyl-CoA + FADH2 (70800)