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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 Jassal, B, 2013-05-09

Class:IdInstanceEdit:3323152
_displayNameJassal, B, 2013-05-09
_timestamp2013-05-09 10:19:56
author[Person:73447] Jassal, Bijay
dateTime2013-05-09 14:16:06
(authored)[BlackBoxEvent:3323111] Cytosolic carboxylases translocate to mitochondrial matrix [Homo sapiens]
[Pathway:3323169] Defects in biotin (Btn) metabolism [Homo sapiens]
[FailedReaction:3323184] Defective HLCS does not biotinylate ACACA:Mn2+ [Homo sapiens]
[FailedReaction:9035987] Defective HLCS does not biotinylate 6xMCCC1:6xMCCC2 [Homo sapiens]
[FailedReaction:9035988] Defective HLCS does not biotinylate PC:Mn2+ [Homo sapiens]
[FailedReaction:9035990] Defective HLCS does not biotinylate 6x(PCCA:PCCB) [Homo sapiens]
(created)[EntityWithAccessionedSequence:3323099] MUT G703R [mitochondrial matrix] [Homo sapiens]
[Person:3323100] Polyak, S W
[DefinedSet:3323101] hCBXs [cytosol] [Homo sapiens]
[Person:3323102] Crane, A M
[ReplacedResidue:3323103] L-tryptophan 105 replaced with L-arginine
[Person:3323104] Malvagia, S
[Person:3323105] Shaag, A
[EntityWithAccessionedSequence:3323106] MUT W105R [mitochondrial matrix] [Homo sapiens]
[Person:3323107] Wallace, J C
[LiteratureReference:3323108] Genetic characterization of a MUT locus mutation discriminating heterogeneity in mut0 and mut- methylmalonic aciduria by interallelic complementation
List all 91 refering instances
(edited)[BlackBoxEvent:3323111] Cytosolic carboxylases translocate to mitochondrial matrix [Homo sapiens]
[Pathway:3323169] Defects in biotin (Btn) metabolism [Homo sapiens]
[FailedReaction:3323184] Defective HLCS does not biotinylate ACACA:Mn2+ [Homo sapiens]
[FailedReaction:9035987] Defective HLCS does not biotinylate 6xMCCC1:6xMCCC2 [Homo sapiens]
[FailedReaction:9035988] Defective HLCS does not biotinylate PC:Mn2+ [Homo sapiens]
[FailedReaction:9035990] Defective HLCS does not biotinylate 6x(PCCA:PCCB) [Homo sapiens]
(modified)[EntityWithAccessionedSequence:70748] Btn-MCCC1 [mitochondrial matrix] [Homo sapiens]
[EntityWithAccessionedSequence:70769] MCCC2 [mitochondrial matrix] [Homo sapiens]
[Complex:70770] 6x(Btn-MCCC1:MCCC2) [mitochondrial matrix] [Homo sapiens]
[EntityWithAccessionedSequence:71021] PCCA [cytosol] [Homo sapiens]
[EntityWithAccessionedSequence:71024] PCCB [cytosol] [Homo sapiens]
[Complex:71025] Btn-PCCA:PCCB [mitochondrial matrix] [Homo sapiens]
[Pathway:196780] Biotin transport and metabolism [Homo sapiens]
[Reaction:2993447] HLCS biotinylates 6x(PCCA:PCCB) [Homo sapiens]
[Complex:2993798] 4x(PC:Mn2+) [cytosol] [Homo sapiens]
[Reaction:2993799] HLCS biotinylates 6xMCCC1:6xMCCC2 [Homo sapiens]
List all 23 refering instances
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No pathways have been reviewed or authored by Jassal, B, 2013-05-09 (3323152)