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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A2VCT3 OGDH 2-oxoglutarate dehydrogenase complex component E1 … Homo sapiens (Human) 640 aa

Protein Details: A2VCT3 (OGDH)

Protein Information
AccessionA2VCT3
Protein Names2-oxoglutarate dehydrogenase complex component E1 (EC 1.2.4.2) (2-oxoglutarate dehydrogenase, mitochondrial) (Alpha-ketoglutarate dehydrogenase) (Thiamine diphosphate (ThDP)-dependent 2-oxoglutarate dehydrogenase)
Gene SymbolOGDH
OrganismHomo sapiens (Human)
Length640 aa
IsoformsNo isoforms
Related PMIDs 36430497 31251020 (mass) 32651440 (mass) 36430497 (mass)
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501CSTPGEAQPN11VDKLVEDHLA21VQSLIRAYQI31RGHHVAQLDP41LGILDADLDS
51-10051SVPADIISST61DKLDLAVFKE71RLRMLTVGGF81YGLDESDLDK91VFHLPTTTFI
101-150101GGQESALPLR111EIIRRLEMAY121CQHIGVEFMF131INDLEQCQWI141RQKFETPGIM
151-200151QFTNEEKRTL161LARLVRSTRF171EEFLQRKWSS181EKRFGLEGCE191VLIPALKTII
201-250201DKSSENGVDY211VIMGMPHRGR221LNVLANVIRK231ELEQIFCQFD241SKLEAADEGS
251-300251GDVKYHLGMY261HRRINRVTDR271NITLSLVANP281SHLEAADPVV291MGKTKAEQFY
301-350301CGDTEGKKVM311SILLHGDAAF321AGQGIVYETF331HLSDLPSYTT341HGTVHVVVNN
351-400351QIGFTTDPRM361ARSSPYPTDV371ARVVNAPIFH381VNSDDPEAVM391YVCKVAAEWR
401-450401STFHKDVVVD411LVCYRRNGHN421EMDEPMFTQP431LMYKQIRKQK441PVLQKYAELL
451-500451VSQGVVNQPE461YEEEISKYDK471ICEEAFARSK481DEKILHIKHW491LDSPWPGFFT
501-550501LDGQPRSMSC511PSTGLTEDIL521THIGNVASSV531PVENFTIHGG541LSRILKTRGE
551-600551MVKNRTVDWA561LAEYMAFGSL571LKEGIHIRLS581GQDVERGTFS591HRHHVLHDQN
601-640601VDKRTCIPMN611HLWPNQAPYT621VCNSSLSEYG631VLGFELCFTR
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
1 - - -
GPS-Palm: 0.94
Deep-Palm: 0.02
121 - - -
GPS-Palm: 0.73
Deep-Palm: 0.70
137 - - -
GPS-Palm: 0.82
Deep-Palm: 0.05
189 - -
cerebral cortex (36430497)
LNCaP (31251020)
GPS-Palm: 0.91
Deep-Palm: 0.97
237 - -
LNCaP (31251020)
GPS-Palm: 0.81
Deep-Palm: 0.94
301 - -
cerebral cortex (36430497)
GPS-Palm: 0.69
Deep-Palm: 0.91
393 - -
cerebral cortex (36430497)
LNCaP (31251020)
Unknown (32651440)
Deep-Palm: 0.11
413 - -
cerebral cortex (36430497)
LNCaP (31251020)
GPS-Palm: 0.87
Deep-Palm: 0.38
472 - -
cerebral cortex (36430497)
GPS-Palm: 0.84
Deep-Palm: 0.61
510 - -
cerebral cortex (36430497)
GPS-Palm: 0.78
Deep-Palm: 0.77
606 - - -
Deep-Palm: 0.04
622 - - -
Deep-Palm: 0.27
637 - - -
GPS-Palm: 0.97
Deep-Palm: 0.03
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: 0.500
4/4 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
4
Cerebral Cortex (Mass)
Specificity: 0.500
4/4 (100.0%)
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.
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