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OPLAH S323R

Stable Identifier
R-HSA-5603264
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
5-oxoprolinase, OPLA_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
OPLAH
Chain
chain:1-1288
Reference Transcript
Other Identifiers
0005390239
11755485_a_at
17082453
222025_s_at
26562
26873
28260
34969_s_at
34970_r_at
52429
74666_s_at
74668_r_at
8153625
A_23_P170186
AAB81519
AAI42673
AB122018
AH005594
AL096750
BAD13434
BC142672
CAB46426
CCDS75802
ENSG00000178814
ENSP00000480476
ENST00000618853
EntrezGene:26873
GE56385
GO:0000166
GO:0003824
GO:0005524
GO:0005829
GO:0006749
GO:0006750
GO:0016787
GO:0017168
HGNC:8149
HPA026562
HPA028260
HPA052429
Hs.305882
Hs.305882.0.S1_3p_s_at
ILMN_1711030
ILMN_1728366
ILMN_1738539
IPR002821
IPR003692
IPR008040
MIM:260005
MIM:614243
NM_017570
NP_060040
OPLAH
OPLAH-204
PF01968
PF02538
PF05378
PH_hs_0032590
TC08001740.hg
uc033cce.2
UPI000035154E
XM_011516960
XP_011515262
XR_001745509
Participant Of
Other forms of this molecule
Modified Residues
Name
L-serine 323 replaced with L-arginine
Coordinate
323
PsiMod HEY
A protein modification that effectively converts a source amino acid residue to an L-arginine.
A protein modification that effectively removes or replaces an L-serine.
Disease
Name Identifier Synonyms
inherited metabolic disorder 655 Metabolic hereditary disorder, Inborn Errors of Metabolism, inborn metabolism disorder
Cross References
RefSeq
Brenda
GeneCards
PRO
Orphanet
HMDB Protein