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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
A2VCT2 OGDH 2-oxoglutarate dehydrogenase complex component E1 … Homo sapiens (Human) 636 aa

Protein Details: A2VCT2 (OGDH)

Protein Information
AccessionA2VCT2
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)
Length636 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
1-501CIQPGEAQPN11VDKLVEDHLA21VQSLIRAYQV31RGHHIAKLDP41LGISCVNFDD
51-10051APVTVSSNVD61LAVFKERLRM71LTVGGFYGLD81ESDLDKVFHL91PTTTFIGGQE
101-150101SALPLREIIR111RLEMAYCQHI121GVEFMFINDL131EQCQWIRQKF141ETPGIMQFTN
151-200151EEKRTLLARL161VRSTRFEEFL171QRKWSSEKRF181GLEGCEVLIP191ALKTIIDKSS
201-250201ENGVDYVIMG211MPHRGRLNVL221ANVIRKELEQ231IFCQFDSKLE241AADEGSGDVK
251-300251YHLGMYHRRI261NRVTDRNITL271SLVANPSHLE281AADPVVMGKT291KAEQFYCGDT
301-350301EGKKVMSILL311HGDAAFAGQG321IVYETFHLSD331LPSYTTHGTV341HVVVNNQIGF
351-400351TTDPRMARSS361PYPTDVARVV371NAPIFHVNSD381DPEAVMYVCK391VAAEWRSTFH
401-450401KDVVVDLVCY411RRNGHNEMDE421PMFTQPLMYK431QIRKQKPVLQ441KYAELLVSQG
451-500451VVNQPEYEEE461ISKYDKICEE471AFARSKDEKI481LHIKHWLDSP491WPGFFTLDGQ
501-550501PRSMSCPSTG511LTEDILTHIG521NVASSVPVEN531FTIHGGLSRI541LKTRGEMVKN
551-600551RTVDWALAEY561MAFGSLLKEG571IHIRLSGQDV581ERGTFSHRHH591VLHDQNVDKR
601-636601TCIPMNHLWP611NQAPYTVCNS621SLSEYGVLGF631ELCFTR
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
1 - - -
GPS-Palm: 0.94
Deep-Palm: 0.03
45 TPP helical domain - -
Deep-Palm: 0.78
117 - - -
GPS-Palm: 0.73
Deep-Palm: 0.70
133 - - -
GPS-Palm: 0.82
Deep-Palm: 0.05
185 - -
cerebral cortex (36430497)
LNCaP (31251020)
GPS-Palm: 0.91
Deep-Palm: 0.97
233 - -
LNCaP (31251020)
GPS-Palm: 0.81
Deep-Palm: 0.94
297 - -
cerebral cortex (36430497)
GPS-Palm: 0.69
Deep-Palm: 0.91
389 - -
cerebral cortex (36430497)
LNCaP (31251020)
Unknown (32651440)
Deep-Palm: 0.11
409 - -
cerebral cortex (36430497)
LNCaP (31251020)
GPS-Palm: 0.87
Deep-Palm: 0.38
468 - -
cerebral cortex (36430497)
GPS-Palm: 0.84
Deep-Palm: 0.61
506 - -
cerebral cortex (36430497)
GPS-Palm: 0.78
Deep-Palm: 0.77
602 - - -
Deep-Palm: 0.04
618 - - -
Deep-Palm: 0.27
633 - - -
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