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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
E9PFG7 OGDH 2-oxoglutarate dehydrogenase complex component E1 … Homo sapiens (Human) 873 aa

Protein Details: E9PFG7 (OGDH)

Protein Information
Accession E9PFG7
Protein Names 2-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 Symbol OGDH
Organism Homo sapiens (Human)
Length 873 aa
Isoforms No isoforms
Related PMIDs 19801377 32944167
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.750
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
3
PC3 cells
Specificity: 0.750
3/4 (75.0%)
1
DU145 cells
Specificity: 0.250
1/2 (50.0%)
0
Jurkat T cells
Specificity: 0.000
0/25 (0.0%)
0
U937 cells
Specificity: 0.000
0/1 (0.0%)
0
HeLa cells
Specificity: 0.000
0/1 (0.0%)
0
LNCaP cells
Specificity: 0.000
0/46 (0.0%)
0
T cells
Specificity: 0.000
0/4 (0.0%)
0
HAP1 cells
Specificity: 0.000
0/10 (0.0%)
0
293T cells
Specificity: 0.000
0/10 (0.0%)
0
CEMx174 cells
Specificity: 0.000
0/3 (0.0%)
0
Endothelial cells
Specificity: 0.000
0/2 (0.0%)
0
Prefrontal cortex
Specificity: 0.000
0/1 (0.0%)
0
Cerebral cortex
Specificity: 0.000
0/4 (0.0%)
0
Liver membrane
Specificity: 0.000
0/1 (0.0%)
Palmitoylation Distribution by Study and Tissue/Cell Line
Chart Explanation: Each bar represents a study (PMID). The colored bottom segment shows palmitoylated samples, while the gray top segment shows non-palmitoylated samples. Bars are grouped by tissue/cell line for easy comparison.
Protein Sequence
Single Types:
Experimental Database High Prediction Medium Prediction Low Prediction
Combined Types:
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
1-501MFHLRTCAAK11LRPLTASQTV21KTFSQNRPAA31ARTFQQIRCY41SAPVAAEPFL
51-10051SGTSSNYVEE61MYCAWLENPK71SVHKGSMAWM81SLTSTRSSTC91PPPLSSGDRN
101-150101QHFLCGRSSV111GWRFEEFLQR121KWSSEKRFGL131EGCEVLIPAL141KTIIDKSSEN
151-200151GVDYVIMGMP161HRGRLNVLAN171VIRKELEQIF181CQFDSKLEAA191DEGSGDVKYH
201-250201LGMYHRRINR211VTDRNITLSL221VANPSHLEAA231DPVVMGKTKA241EQFYCGDTEG
251-300251KKVMSILLHG261DAAFAGQGIV271YETFHLSDLP281SYTTHGTVHV291VVNNQIGFTT
301-350301DPRMARSSPY311PTDVARVVNA321PIFHVNSDDP331EAVMYVCKVA341AEWRSTFHKD
351-400351VVVDLVCYRR361NGHNEMDEPM371FTQPLMYKQI381RKQKPVLQKY391AELLVSQGVV
401-450401NQPEYEEEIS411KYDKICEEAF421ARSKDEKILH431IKHWLDSPWP441GFFTLDGQPR
451-500451SMSCPSTGLT461EDILTHIGNV471ASSVPVENFT481IHGGLSRILK491TRGEMVKNRT
501-550501VDWALAEYMA511FGSLLKEGIH521IRLSGQDVER531GTFSHRHHVL541HDQNVDKRTC
551-600551IPMNHLWPNQ561APYTVCNSSL571SEYGVLGFEL581GFAMASPNAL591VLWEAQFGDF
601-650601HNTAQCIIDQ611FICPGQAKWV621RQNGIVLLLP631HGMEGMGPEH641SSARPERFLQ
651-700651MCNDDPDVLP661DLKEANFDIN671QLYDCNWVVV681NCSTPGNFFH691VLRRQILLPF
701-750701RKPLIIFTPK711SLLRHPEARS721SFDEMLPGTH731FQRVIPEDGP741AAQNPENVKR
751-800751LLFCTGKVYY761DLTRERKARD771MVGQVAITRI781EQLSPFPFDL791LLKEVQKYPN
801-850801AELAWCQEEH811KNQGYYDYVK821PRLRTTISRA831KPVWYAGRDP841AAAPATGNKK
851-873851THLTELQRLL861DTAFDLDVFK871NFS
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
7 Prediction (High) - -
39 Prediction (Low) - -
105 Prediction (Low) - -
133 Prediction (High) - -
181 Prediction (Medium) - -
245 Prediction (Low) - -
357 Prediction (Medium) - -
416 Prediction (Medium) - -
454 Prediction (Medium) - -
613 Prediction (Low) - -
754 Prediction (Medium) - -
Conservation Scores
PhyloP
PhastCons
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