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GSS R267W [cytosol]
Stable Identifier
R-HSA-5602830
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
cytosol
Synonyms
Glutathione synthase
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Metabolic disorders of biological oxidation enzymes (Homo sapiens)
Defective GSS causes GSS deficiency (Homo sapiens)
Defective GSS does not synthesize GSH (Homo sapiens)
GSS mutants:GSS mutants:Mg2+:Mg2+ [cytosol] (Homo sapiens)
GSS mutants [cytosol] (Homo sapiens)
GSS R267W [cytosol] (Homo sapiens)
External Reference Information
External Reference
UniProt:P48637 GSS
Gene Names
GSS
Chain
initiator methionine:, chain:2-474
Reference Genes
BioGPS Gene:2937 GSS
COSMIC (genes):GSS GSS
CTD Gene:2937 GSS
dbSNP Gene:2937 GSS
ENSEMBL:ENSG00000100983 GSS
HGNC:4624 GSS
KEGG:hsa:2937 GSS
Monarch:2937 GSS
NCBI Gene:2937 GSS
OMIM:601002 GSS
UCSC:P48637 GSS
Reference Transcript
RefSeq:NM_001322494.1 GSS
RefSeq:NM_001322495.1 GSS
RefSeq:NM_000178.3 GSS
Other Identifiers
11715923_a_at
11746330_a_at
16918589
201415_PM_at
201415_at
211630_PM_s_at
211630_s_at
2937
38386_r_at
3903669
3903671
3903672
3903673
3903674
3903675
3903678
3903679
3903680
3903681
3903682
3903683
3903685
3903686
3903687
3903688
3903689
3903690
3903691
3903692
3903693
3903694
3903695
3903696
3903697
74726_at
8065817
A_23_P210920
GE59100
GE63329
GE84610
GO:0000287
GO:0003824
GO:0004363
GO:0005515
GO:0005524
GO:0005829
GO:0006520
GO:0006575
GO:0006750
GO:0006790
GO:0006979
GO:0007399
GO:0016874
GO:0042802
GO:0042803
GO:0043226
GO:0043295
GO:0046686
GO:0046872
GO:0048856
GO:0070062
HMNXSV003047596
ILMN_1683462
PH_hs_0004715
TC20000789.hg
U34683_at
g4504168_3p_at
g886283_3p_s_at
Participates
as a member of
GSS mutants [cytosol] (Homo sapiens)
Other forms of this molecule
GSS R125C [cytosol]
GSS R164Q [cytosol]
GSS R283C [cytosol]
GSS P314L [cytosol]
GSS [cytosol]
Modified Residues
Name
L-arginine 267 replaced with L-tryptophan
Coordinate
267
PsiMod
L-tryptophan residue [MOD:00027]
A protein modification that effectively converts a source amino acid residue to L-tryptophan.
L-arginine removal [MOD:01632]
A protein modification that effectively removes or replaces an L-arginine.
Disease
Name
Identifier
Synonyms
inherited metabolic disorder
DOID:655
Metabolic hereditary disorder, Inborn Errors of Metabolism, inborn metabolism disorder
Cross References
ENSEMBL
ENSP00000407517
,
ENSP00000495750
,
ENST00000451957
,
ENSP00000493903
,
ENST00000646735
,
ENST00000651619
,
ENST00000643188
,
ENST00000644793
,
ENSP00000493763
,
ENSP00000498303
OpenTargets
ENSG00000100983
IntEnz
6.3.2.3
HPA
ENSG00000100983-GSS
PRO
P48637
Pharos - Targets
P48637
Orphanet
GSS
HMDB Protein
HMDBP00791
PDB
8FBZ
,
2HGS
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