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Details on Person Defective CP does not oxidise Fe2+ to Fe3+

Class:IdFailedReaction:5621402
_displayNameDefective CP does not oxidise Fe2+ to Fe3+
_doReleaseTRUE
_timestamp2016-09-23 20:29:49
authored[InstanceEdit:5621442] Jassal, Bijay, 2014-08-29
catalystActivity[CatalystActivity:9631863] ferroxidase activity of CP mutants:6xCu2+:SLC40A1 [plasma membrane]
compartment[Compartment:984] extracellular region
[Compartment:876] plasma membrane
created[InstanceEdit:5621442] Jassal, Bijay, 2014-08-29
disease[Disease:5623594] aceruloplasminemia
edited[InstanceEdit:5621442] Jassal, Bijay, 2014-08-29
entityFunctionalStatus[EntityFunctionalStatus:5621379] loss_of_function of CP mutants:6xCu2+:SLC40A1 [plasma membrane]
input[SimpleEntity:435347] Fe2+ [extracellular region]
[SimpleEntity:435347] Fe2+ [extracellular region]
[SimpleEntity:435347] Fe2+ [extracellular region]
[SimpleEntity:435347] Fe2+ [extracellular region]
[SimpleEntity:351626] H+ [extracellular region]
[SimpleEntity:351626] H+ [extracellular region]
[SimpleEntity:351626] H+ [extracellular region]
[SimpleEntity:351626] H+ [extracellular region]
[SimpleEntity:352327] O2 [extracellular region]
isChimericFALSE
literatureReference[LiteratureReference:5621420] Characterization of a nonsense mutation in the ceruloplasmin gene resulting in diabetes and neurodegenerative disease
[LiteratureReference:5621411] Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus
[LiteratureReference:5621433] Hereditary ceruloplasmin deficiency with hemosiderosis
[LiteratureReference:5621427] Aceruloplasminemia: molecular characterization of this disorder of iron metabolism
modified[InstanceEdit:5623578] Jassal, Bijay, 2014-09-17
[InstanceEdit:5623756] Jassal, Bijay, 2014-09-19
[InstanceEdit:6789777] Jassal, Bijay, 2015-08-04
[InstanceEdit:6789873] Jassal, Bijay, 2015-08-05
[InstanceEdit:8940224] D'Eustachio, Peter, 2016-09-23
[InstanceEdit:9631717] Wu, G, 2018-12-12
[InstanceEdit:9830342] Matthews, Lisa, 2023-03-08
nameDefective CP does not oxidise Fe2+ to Fe3+
normalReaction
releaseDate2015-09-22
releaseStatusNEW
reviewed[InstanceEdit:6789776] Broer, Stefan, 2015-08-04
reviewStatus[ReviewStatus:9821382] five stars
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:6797125] R-HSA-5621402.4
summation[Summation:5621421] Ceruloplasmin (CP), synthesised in the liver and secreted in...
(hasEvent)[Pathway:5619060] Defective CP causes aceruloplasminemia (ACERULOP) [Homo sapiens]
(updatedInstance)[_UpdateTracker:9778441] Update Tracker - [FailedReaction:5621402] Defective CP does not oxidise Fe2+ to Fe3+ - v68:[addCatalystActivity]
[_UpdateTracker:9782212] Update Tracker - [FailedReaction:5621402] Defective CP does not oxidise Fe2+ to Fe3+ - v59:[add_removeLiteratureReference]
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