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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.

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Details on Person K273E ECHS1 [mitochondrial matrix]

Class:IdEntityWithAccessionedSequence:9916680
_displayNameK273E ECHS1 [mitochondrial matrix]
_timestamp2024-07-25 19:37:50
compartment[Compartment:5460] mitochondrial matrix
created[InstanceEdit:9916660] Rothfels, Karen, 2024-07-25
crossReference[DatabaseIdentifier:9916657] ClinGen:CA5765624
disease[Disease:9916658] mitochondrial short-chain enoyl-CoA hydratase 1 deficiency
endCoordinate290
hasModifiedResidue[ReplacedResidue:9916651] L-lysine 273 replaced with L-glutamic acid
literatureReference[LiteratureReference:9916618] Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement
nameK273E ECHS1
Enoyl-CoA hydratase, mitochondrial precursor
Short chain enoyl-CoA hydratase
Enoyl-CoA hydratase 1
referenceEntity[ReferenceGeneProduct:54126] UniProt:P30084 ECHS1 [Homo sapiens]
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:9916701] R-HSA-9916680.1
startCoordinate28
(hasCandidate)[CandidateSet:9916709] ECHS1 mutants [mitochondrial matrix] [Homo sapiens]
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No pathways have been reviewed or authored by K273E ECHS1 [mitochondrial matrix] (9916680)