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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q02218-2 OGDH 2-oxoglutarate dehydrogenase complex component E1 … Homo sapiens (Human) 1019 aa

Protein Details: Q02218-2 (OGDH)

Protein Information
AccessionQ02218-2
Protein Names2-oxoglutarate dehydrogenase complex component E1 (E1o) (HsOGDH) (OGDC-E1) (OGDH-E1) (EC 1.2.4.2) (2-oxoglutarate dehydrogenase, mitochondrial) (Alpha-ketoglutarate dehydrogenase) (Alpha-KGDH-E1) (Thiamine diphosphate (ThDP)-dependent 2-oxoglutarate dehydrogenase)
Gene SymbolOGDH
OrganismHomo sapiens (Human)
Length1019 aa
Isoforms
Related PMIDs 36430497
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MFHLRTCAAK11LRPLTASQTV21KTFSQNRPAA31ARTFQQIRCY41SAPVAAEPFL
51-10051SGTSSNYVEE61MYCAWLENPK71SVHKSWDIFF81RNTNAGAPPG91TAYQSPLPLS
101-150101RGSLAAVAHA111QSLVEAQPNV121DKLVEDHLAV131QSLIRAYQVR141GHHIAKLDPL
151-200151GISCVNFDDA161PVTVSSNVGF171YGLDESDLDK181VFHLPTTTFI191GGQESALPLR
201-250201EIIRRLEMAY211CQHIGVEFMF221INDLEQCQWI231RQKFETPGIM241QFTNEEKRTL
251-300251LARLVRSTRF261EEFLQRKWSS271EKRFGLEGCE281VLIPALKTII291DKSSENGVDY
301-350301VIMGMPHRGR311LNVLANVIRK321ELEQIFCQFD331SKLEAADEGS341GDVKYHLGMY
351-400351HRRINRVTDR361NITLSLVANP371SHLEAADPVV381MGKTKAEQFY391CGDTEGKKVM
401-450401SILLHGDAAF411AGQGIVYETF421HLSDLPSYTT431HGTVHVVVNN441QIGFTTDPRM
451-500451ARSSPYPTDV461ARVVNAPIFH471VNSDDPEAVM481YVCKVAAEWR491STFHKDVVVD
501-550501LVCYRRNGHN511EMDEPMFTQP521LMYKQIRKQK531PVLQKYAELL541VSQGVVNQPE
551-600551YEEEISKYDK561ICEEAFARSK571DEKILHIKHW581LDSPWPGFFT591LDGQPRSMSC
601-650601PSTGLTEDIL611THIGNVASSV621PVENFTIHGG631LSRILKTRGE641MVKNRTVDWA
651-700651LAEYMAFGSL661LKEGIHIRLS671GQDVERGTFS681HRHHVLHDQN691VDKRTCIPMN
701-750701HLWPNQAPYT711VCNSSLSEYG721VLGFELGFAM731ASPNALVLWE741AQFGDFHNTA
751-800751QCIIDQFICP761GQAKWVRQNG771IVLLLPHGME781GMGPEHSSAR791PERFLQMCND
801-850801DPDVLPDLKE811ANFDINQLYD821CNWVVVNCST831PGNFFHVLRR841QILLPFRKPL
851-900851IIFTPKSLLR861HPEARSSFDE871MLPGTHFQRV881IPEDGPAAQN891PENVKRLLFC
901-950901TGKVYYDLTR911ERKARDMVGQ921VAITRIEQLS931PFPFDLLLKE941VQKYPNAELA
951-1000951WCQEEHKNQG961YYDYVKPRLR971TTISRAKPVW981YAGRDPAAAP991ATGNKKTHLT
1001-10191001ELQRLLDTAF1011DLDVFKNFS
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
7 - - -
GPS-Palm: 0.91
Deep-Palm: 0.06
39 - - -
Deep-Palm: 0.81
63 - - -
Deep-Palm: 0.08
215 - - -
Deep-Palm: 0.70
231 - - -
Deep-Palm: 0.05
279 - - -
GPS-Palm: 0.91
283 - - -
Deep-Palm: 0.97
331 - - -
Deep-Palm: 0.94
395 - - -
Deep-Palm: 0.91
487 - - -
Deep-Palm: 0.11
507 - - -
Deep-Palm: 0.38
566 - - -
Deep-Palm: 0.61
604 - - -
Deep-Palm: 0.77
700 - - -
Deep-Palm: 0.04
716 - - -
Deep-Palm: 0.58
756 - - -
Deep-Palm: 0.11
763 - - -
Deep-Palm: 0.11
802 - - -
Deep-Palm: 0.85
825 - - -
Deep-Palm: 0.06
832 - - -
Deep-Palm: 0.09
904 - - -
Deep-Palm: 0.96
956 - - -
Deep-Palm: 0.79
Score Interpretation:
GPS-Palm: Thresholds - High (≥0.8920), Medium (≥0.7766), Low (≥0.6484), Very Low (<0.6484)
Deep-Palm: Higher score indicates higher probability of palmitoylation (High ≥0.9)
Tissue/Cell Line Expression
Literature Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
4
cerebral cortex
Specificity: 1.000
4/4 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.000
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID). Blue bars: Literature data, Orange bars: Mass Spectrometry data. The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples.
Conservation score for cysteine
PhyloP for Cysteine
PhastCons Conservation Scores for Cysteine
TCGA Cysteine Mutation Information

Note: Mutations indicate amino acid changes that may create potential palmitoylation sites.

Position Amino Acid Change Frequency Type Function Cancer Type
41 S → C 0.001014 SNP Missense Mutation BRCA
81 R → C 0.002141 SNP Missense Mutation SKCM
81 R → C 0.001887 SNP Missense Mutation UCEC
277 R → C 0.001887 SNP Missense Mutation UCEC
283 C → C 0.001887 SNP Silent UCEC
604 C → C 0.001764 SNP Silent LUAD
653 W → C 0.001014 SNP Missense Mutation BRCA
686 R → C 0.001887 SNP Missense Mutation UCEC
700 C → S 0.001764 SNP Missense Mutation LUAD
713 Y → C 0.002976 SNP Missense Mutation KIRC
769 W → C 0.001014 SNP Missense Mutation BRCA
794 R → C 0.001887 SNP Missense Mutation UCEC
864 R → C 0.002506 SNP Missense Mutation COAD
904 C → C 0.001969 SNP Silent LGG
909 Y → C 0.001887 SNP Missense Mutation UCEC