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-methyl-beta-hydroxybutyryl-CoA + NAD+ <=> alpha-methylacetoacetyl-CoA + NADH + H+
Class:Id Reaction:70837
_displayName alpha-methyl-beta-hydroxybutyryl-CoA + NAD+ <=> alpha-methylacetoacetyl-CoA + NADH + H+
_doRelease TRUE
_timestamp 2024-10-28 22:29:20
catalystActivity [CatalystActivity:70835] (3S)-3-hydroxyacyl-CoA dehydrogenase (NAD+) activity of HSD17B10 tetramer [mitochondrial matrix]
catalystActivityReference [CatalystActivityReference:9643191] 3-hydroxyacyl-CoA dehydrogenase activity of HSD17B10 tetramer [mitochondrial matrix] 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency Is caused by mutations in the HADH2 gene
compartment [Compartment:5460] mitochondrial matrix
crossReference [DatabaseIdentifier:9917124] RHEA:13282
input [SimpleEntity:70829] aMbHBUT-CoA [mitochondrial matrix] [SimpleEntity:113526] NAD+ [mitochondrial matrix]
literatureReference [LiteratureReference:508368] Crystal structure of human ABAD/HSD10 with a bound inhibitor: implications for design of Alzheimer's disease therapeutics [LiteratureReference:70832] 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency Is caused by mutations in the HADH2 gene
modified [InstanceEdit:113517] Schmidt, EE, 2004-06-09 05:19:12 [InstanceEdit:163376] Vastrik, I, 2005-04-29 06:26:51 [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:9908873] Stephan, Ralf, 2024-04-23 [InstanceEdit:9917131] Stephan, Ralf, 2024-07-30 [InstanceEdit:9925948] D'Eustachio, Peter, 2024-10-28
name alpha-methyl-beta-hydroxybutyryl-CoA + NAD+ <=> alpha-methylacetoacetyl-CoA + NADH + H+ (2S,3S)-3-hydroxy-2-methylbutanoyl-CoA + NAD(+) => 2-methyl-3-oxobutanoyl-CoA + H(+) + NADH
negativePrecedingEvent [NegativePrecedingEvent:9908868] Futile Cycle: alpha-methylacetoacetyl-CoA + NADH + H+ <=> alpha-methyl-beta-hydroxybutyryl-CoA + NAD+
output [SimpleEntity:70836] 2MACA-CoA [mitochondrial matrix] [SimpleEntity:29362] NADH [mitochondrial matrix] [SimpleEntity:113529] H+ [mitochondrial matrix]
precedingEvent
releaseDate 2004-07-06
reverseReaction
reviewStatus [ReviewStatus:9821382] five stars
species [Species:48887] Homo sapiens
stableIdentifier [StableIdentifier:361984] R-HSA-70837.7
summation [Summation:178468] Mitochondrial 3-hydroxyacyl-CoA dehydrogenase type-2 (HSD17B...
(hasEvent) [Pathway:70895] Branched-chain amino acid catabolism [Homo sapiens]
(precedingEvent) [Reaction:70844] alpha-methylacetoacetyl-CoA + CoA => propionyl-CoA + acetyl-CoA [Homo sapiens] [NegativePrecedingEvent:9908875] Futile Cycle: alpha-methyl-beta-hydroxybutyryl-CoA + NAD+ <=> alpha-methylacetoacetyl-CoA + NADH + H+
(reverseReaction) [Reaction:508369] alpha-methylacetoacetyl-CoA + NADH + H+ <=> alpha-methyl-beta-hydroxybutyryl-CoA + NAD+ [Homo sapiens]
(updatedInstance) [_UpdateTracker:9790859] Update Tracker - [Reaction:70837] alpha-methyl-beta-hydroxybutyryl-CoA + NAD+ <=> alpha-methylacetoacetyl-CoA + NADH + H+ - v32:[add_removeLiteratureReference, modifyText]
[Change default viewing format]
List...
Protein identifiers
ChEBI identifiers
KEGG COMPOUND identifiers
No pathways have been reviewed or authored by alpha-methyl-beta-hydroxybutyryl-CoA + NAD+ <=> alpha-methylacetoacetyl-CoA + NADH + H+ (70837)