OPLAH S323R [cytosol]

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
26873
3158061
3158062
3158064
3158066
3158067
3158068
3158069
3158071
3158072
3158073
3158075
3158076
3158077
3158079
3158080
3158081
3158082
3158083
3158084
3158085
3158086
3158089
3158091
3158092
3158093
3158094
3158095
3158096
3158097
3158098
3158099
34969_s_at
34970_r_at
74666_s_at
74668_r_at
8153625
A_23_P170186
GE56385
GO:0000166
GO:0003674
GO:0003824
GO:0005515
GO:0005524
GO:0005575
GO:0005622
GO:0005737
GO:0005829
GO:0006749
GO:0006750
GO:0006790
GO:0008150
GO:0009058
GO:0016787
GO:0016810
GO:0017168
GO:0034641
GO:0042802
GO:0043167
GO:0051186
Hs.305882.0.S1_3p_s_at
ILMN_1711030
ILMN_1728366
ILMN_1738539
PH_hs_0032590
TC08001740.hg
Participant Of
Other forms of this molecule
Modified Residues
Name
L-serine 323 replaced with L-arginine
Coordinate
323
PsiMod
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
OpenTargets
IntEnz
GeneCards
PRO
Orphanet
HMDB Protein
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