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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
H0Y7C1 ATP1A2 Sodium/potassium-transporting ATPase subunit alpha Homo sapiens (Human) 714 aa

Protein Details: H0Y7C1 (ATP1A2)

Protein Information
Accession H0Y7C1
Protein Names Sodium/potassium-transporting ATPase subunit alpha
Gene Symbol ATP1A2
Organism Homo sapiens (Human)
Length 714 aa
Isoforms No isoforms
Related PMIDs 21076176 29575903 31251020
Database Sources CysModDB dbPTM SwissPalm
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.923
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
36
LNCaP cells
Specificity: 0.923
36/46 (78.3%)
2
Jurkat T cells
Specificity: 0.051
2/25 (8.0%)
1
HeLa cells
Specificity: 0.026
1/1 (100.0%)
0
U937 cells
Specificity: 0.000
0/1 (0.0%)
0
DU145 cells
Specificity: 0.000
0/2 (0.0%)
0
PC3 cells
Specificity: 0.000
0/4 (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
1-501XQLITGVAVF11LGVSFFVLSL21ILGYSWLEAV31IFLIGIIVAN41VPEGLLATVT
51-10051VCLTLTAKRM61ARKNCLVKNL71EAVETLGSTS81TICSDKTGTL91TQNRMTVAHM
101-150101WFDNQIHEAD111TTEDQSGATF121DKRSPTWTAL131SRIAGLCNRA141VFKAGQENIS
151-200151VSKRDTAGDA161SESALLKCIE171LSCGSVRKMR181DRNPKVAEIP191FNSTNKYQLS
201-250201IHEREDSPQS211HVLVMKGAPE221RILDRCSTIL231VQGKEIPLDK241EMQDAFQNAY
251-300251MELGGLGERV261LGFCQLNLPS271GKFPRGFKFD281TDELNFPTEK291LCFVGLMSMI
301-350301DPPRAAVPDA311VGKCRSAGIK321VIMVTGDHPI331TAKAIAKGVG341IISEGNETVE
351-400351DIAARLNIPM361SQVNPREAKA371CVVHGSDLKD381MTSEQLDEIL391KNHTEIVFAR
401-450401TSPQQKLIIV411EGCQRQGAIV421AVTGDGVNDS431PALKKADIGI441AMGISGSDVS
451-500451KQAADMILLD461DNFASIVTGV471EEGRLIFDNL481KKSIAYTLTS491NIPEITPFLL
501-550501FIIANIPLPL511GTVTILCIDL521GTDMVPAISL531AYEAAESDIM541KRQPRNSQTD
551-600551KLVNERLISM561AYGQIENGFL571PSRLLGIRLD581WDDRTMNDLE591DSYGQEWTYE
601-650601QRKVVEFTCH611TAFFASIVVV621QWADLIICKT631RRNSVFQQGM641KNKILIFGLL
651-700651EETALAAFLS661YCPGMGVALR671MYPLKVTWWF681CAFPYSLLIF691IYDEVRKLIL
701-714701RRYPGGWVEK711ETYY
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
52 Prediction (Medium) - -
65 Prediction (High) - -
83 Prediction (Low) - -
137 Prediction (Medium) - -
168 Prediction (Low) - -
173 Prediction (High) - -
226 Prediction (Medium) - -
264 Prediction (Medium) - -
314 Prediction (Medium) - -
371 Prediction (Medium) - -
413 CYSMODDB SWISSPALM DBPTM Prediction (High) - -
628 Prediction (High) - -
662 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
51 R → C 0.002288 SNP Missense Mutation STAD
143 C → G 0.002506 SNP Missense Mutation COAD
247 C → C 0.002033 SNP Silent LUSC
267 R → C 0.002288 SNP Missense Mutation STAD
267 R → C 0.001969 SNP Missense Mutation HNSC
428 R → C 0.002506 SNP Missense Mutation COAD
486 Y → C 0.001887 SNP Missense Mutation UCEC
510 R → C 0.001969 SNP Missense Mutation HNSC
548 R → C 0.002976 SNP Missense Mutation KIRC
664 G → C 0.001764 SNP Missense Mutation LUAD
861 G → C 0.001764 SNP Missense Mutation LUAD
861 G → C 0.001887 SNP Missense Mutation UCEC
976 R → C 0.001969 SNP Missense Mutation HNSC