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 SRD5A3 reduces polyprenal to dolichal
Class:Id Reaction:9937295
_displayName SRD5A3 reduces polyprenal to dolichal
_doRelease TRUE
_timestamp 2025-02-26 19:05:09
authored [InstanceEdit:9937271] D'Eustachio, Peter, 2025-01-29
catalystActivity [CatalystActivity:9937303] polyprenal reductase activity of SRD5A3 [endoplasmic reticulum membrane]
catalystActivityReference [CatalystActivityReference:9937313] polyprenal reductase activity of SRD5A3 [endoplasmic reticulum membrane] A pseudoautosomal glycosylation disorder prompts the revision of dolichol biosynthesis
compartment [Compartment:5263266] cytoplasmic side of endoplasmic reticulum membrane [Compartment:70101] cytosol [Compartment:12045] endoplasmic reticulum membrane
created [InstanceEdit:9937296] D'Eustachio, Peter, 2025-01-30
crossReference [DatabaseIdentifier:9937285] RHEA:80729
edited [InstanceEdit:9938253] D'Eustachio, Peter, 2025-02-11
input [SimpleEntity:9937308] pNAL [cytoplasmic side of endoplasmic reticulum membrane] [SimpleEntity:70106] H+ [cytosol] [SimpleEntity:29364] NADPH [cytosol]
isChimeric FALSE
literatureReference [LiteratureReference:4420007] SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder [LiteratureReference:4420042] Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3 [LiteratureReference:4420017] SRD5A3-CDG: a patient with a novel mutation [LiteratureReference:9937278] A pseudoautosomal glycosylation disorder prompts the revision of dolichol biosynthesis
modified [InstanceEdit:9937320] D'Eustachio, Peter, 2025-01-30 [InstanceEdit:9937325] D'Eustachio, Peter, 2025-01-30 [InstanceEdit:9939398] D'Eustachio, Peter, 2025-02-26 [InstanceEdit:9939400] D'Eustachio, Peter, 2025-02-26
name SRD5A3 reduces polyprenal to dolichal a di-trans,poly-cis-polyprenal + NADPH + H(+) => a di-trans,poly-cis-dolichal + NADP(+)
output [SimpleEntity:29366] NADP+ [cytosol] [SimpleEntity:9937289] DCHAL [cytoplasmic side of endoplasmic reticulum membrane]
precedingEvent
releaseDate 2025-03-26
reviewed [InstanceEdit:9939401] Hill, David P, 2025-02-26
reviewStatus [ReviewStatus:9821382] five stars
species [Species:48887] Homo sapiens
stableIdentifier [StableIdentifier:9937316] R-HSA-9937295.1
summation [Summation:9937290] SRD5A3 (Polyprenal reductase) associated with the cytoplasmi...
(hasEvent) [Pathway:446199] Synthesis of dolichyl-phosphate [Homo sapiens]
(normalReaction) [FailedReaction:4755572] Defective SRD5A3 does not reduce pPNOL to DCHOL [Homo sapiens]
(precedingEvent) [Reaction:9937340] DHRSX reduces dolichal to dolichol [Homo sapiens]
(replacementInstances) [_Deleted:9937351] Deletion of instance: 4419979
[Change default viewing format]
List...
Protein identifiers
ChEBI identifiers
KEGG COMPOUND identifiers
No pathways have been reviewed or authored by SRD5A3 reduces polyprenal to dolichal (9937295)