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 Defective MAT1A does not transfer Ado from ATP to L-Met

Class:IdFailedReaction:5603087
_displayNameDefective MAT1A does not transfer Ado from ATP to L-Met
_doReleaseTRUE
_timestamp2019-02-25 17:10:57
authored[InstanceEdit:5603083] Jassal, Bijay, 2014-06-27
catalystActivity[CatalystActivity:9638105] methionine adenosyltransferase activity of MAT1A mutant multimers [cytosol]
compartment[Compartment:70101] cytosol
created[InstanceEdit:5603083] Jassal, Bijay, 2014-06-27
disease[Disease:5579115] hypermethioninemia
edited[InstanceEdit:5603083] Jassal, Bijay, 2014-06-27
entityFunctionalStatus[EntityFunctionalStatus:5603113] loss_of_function of MAT1A mutant multimers [cytosol]
input[SimpleEntity:113592] ATP [cytosol]
[SimpleEntity:29356] H2O [cytosol]
[SimpleEntity:174390] L-Met [cytosol]
isChimericFALSE
literatureReference[LiteratureReference:5603116] Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency
[LiteratureReference:5603110] Normal brain myelination in a patient homozygous for a mutation that encodes a severely truncated methionine adenosyltransferase I/III
modified[InstanceEdit:5603368] Jassal, Bijay, 2014-07-01
[InstanceEdit:5623544] Jassal, Bijay, 2014-09-15
[InstanceEdit:5627273] Jassal, Bijay, 2014-10-17
[InstanceEdit:5633253] Matthews, Lisa, 2014-10-31
[InstanceEdit:5634120] Jassal, Bijay, 2014-11-03
[InstanceEdit:5635755] Matthews, Lisa, 2014-11-07
[InstanceEdit:9638107] Jassal, Bijay, 2019-02-25
[InstanceEdit:9830342] Matthews, Lisa, 2023-03-08
nameDefective MAT1A does not transfer Ado from ATP to L-Met
normalReaction
releaseDate2014-12-11
reviewed[InstanceEdit:5634119] Nakaki, Toshio, 2014-11-03
reviewStatus[ReviewStatus:9821382] five stars
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:5622286] R-HSA-5603087.3
summation[Summation:5603075] S-adenosylmethionine (AdoMet, SAM) is an important methyl do...
systematicNameMAT1A mutants do not transfer Ado from ATP to L-Met
(hasEvent)[Pathway:5579024] Defective MAT1A causes MATD [Homo sapiens]
(updatedInstance)[_UpdateTracker:9778623] Update Tracker - [FailedReaction:5603087] Defective MAT1A does not transfer Ado from ATP to L-Met - v68:[addCatalystActivity]
[Change default viewing format]
No pathways have been reviewed or authored by Defective MAT1A does not transfer Ado from ATP to L-Met (5603087)