SOH-C326-OGG1 S326C [nucleoplasm]

Stable Identifier
R-HSA-9658815
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
nucleoplasm
Icon
SOH-C326-OGG1 S326C [nucleoplasm] icon
SOH-C326-OGG1 S326C [nucleoplasm] icon
Locations in the PathwayBrowser
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Literature References
PubMed ID Title Journal Year
24632493 hOGG1-Cys326 variant cells are hypersensitive to DNA repair inhibition by nitric oxide

Radicella, JP, Hall, J, Pauly, K, Epe, B, Bravard, A, Moritz, E

Carcinogenesis 2014
External Reference Information
External Reference
UniProt:O15527 OGG1
Gene Names
OGG1, MMH, MUTM, OGH1
Chain
chain:1-345
Reference Genes
BioGPS Gene:4968 OGG1
COSMIC (genes):OGG1 OGG1
CTD Gene:4968 OGG1
dbSNP Gene:4968 OGG1
ENSEMBL:ENSG00000114026 OGG1
HGNC:8125 OGG1
KEGG Gene (Homo sapiens):4968 OGG1
Monarch:4968 OGG1
NCBI Gene:4968 OGG1
OMIM:601982 OGG1
UCSC:O15527 OGG1
Reference Transcript
Other Identifiers
0002060524
0004810403
11727607_a_at
11727608_x_at
11727696_x_at
11740749_a_at
16937329
205301_s_at
205760_s_at
2609907
2609908
2609909
2609910
2609913
2609914
2609916
2609917
2609918
2609920
2609921
2609922
2609923
2609924
2609925
2609926
2609927
2609929
2609930
2609931
34146_at
34147_g_at
38333_at
38334_g_at
38335_at
4968
8077635
AB000410_s_at
A_14_P200082
A_23_P212196
A_23_P344392
A_24_P414183
GE58739
GO:0002526
GO:0003674
GO:0003677
GO:0003684
GO:0003824
GO:0004518
GO:0004519
GO:0005515
GO:0005575
GO:0005622
GO:0005634
GO:0005654
GO:0005737
GO:0005739
GO:0005759
GO:0005829
GO:0006259
GO:0006281
GO:0006284
GO:0006285
GO:0006287
GO:0006289
GO:0006355
GO:0006950
GO:0006974
GO:0006979
GO:0007568
GO:0008017
GO:0008092
GO:0008150
GO:0008152
GO:0008219
GO:0008534
GO:0009056
GO:0009058
GO:0009314
GO:0009416
GO:0016363
GO:0016607
GO:0016787
GO:0016798
GO:0016829
GO:0019104
GO:0032355
GO:0032357
GO:0032991
GO:0033683
GO:0034039
GO:0034641
GO:0034655
GO:0042493
GO:0043066
GO:0043226
GO:0044281
GO:0045007
GO:0045008
GO:0045471
GO:0051593
GO:0071276
GO:0140078
GO:1901291
HMNXSV003027366
HMNXSV003040435
HMNXSV003055999
ILMN_1706652
ILMN_1808340
ILMN_2352609
PH_hs_0024314
TC03000042.hg
TC03002210.hg
g8670531_3p_a_at
g8670533_3p_a_at
Participates
as a member of
as an output of
Other forms of this molecule
OGG1 A53T [nucleoplasm]
OGG1 A288V [nucleoplasm]
OGG1 S326C [nucleoplasm]
OGG1 K249Q [nucleoplasm]
OGG1 D268A [nucleoplasm]
OGG1 D268N [nucleoplasm]
OGG1 R154H [nucleoplasm]
OGG1 R46Q [nucleoplasm]
OGG1 R229Q [nucleoplasm]
OGG1 R131Q [nucleoplasm]
OGG1 P266fs139* [nucleoplasm]
OGG1 R46L [nucleoplasm]
OGG1 R131G [nucleoplasm]
OGG1 [nucleoplasm]
Modified Residues
Name
L-serine 326 replaced with L-cysteine
Coordinate
326
PsiMod
L-serine removal [MOD:01646]
A protein modification that effectively removes or replaces an L-serine.
L-cysteine residue [MOD:00014]
A protein modification that effectively converts a source amino acid residue to an L-cysteine.
Name
L-cysteine sulfenic acid at 326
Coordinate
326
PsiMod Name
L-cysteine sulfenic acid
PsiMod Definition
A protein modification that effectively monooxygenates an L-cysteine residue to L-cysteine sulfenic acid.
Disease
Name Identifier Synonyms
cancer DOID:162 malignant tumor, malignant neoplasm, primary cancer
Cross References
RefSeq
Guide to Pharmacology - Targets
OpenTargets
IntEnz
HPA
GeneCards
Ensembl
PRO
Pharos - Targets
PDB
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