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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q13308-2 PTK7 Isoform 2 of Inactive tyrosine-protein … Homo sapiens (Human) 1030 aa

Protein Details: Q13308-2 (PTK7)

Protein Information
Accession Q13308-2
Protein Names Isoform 2 of Inactive tyrosine-protein kinase 7
Gene Symbol PTK7
Organism Homo sapiens (Human)
Length 1030 aa
Isoforms
Related PMIDs 19801377 31251020 32651440 32944167
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.870
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
40
LNCaP cells
Specificity: 0.870
40/46 (87.0%)
3
PC3 cells
Specificity: 0.065
3/4 (75.0%)
2
DU145 cells
Specificity: 0.043
2/2 (100.0%)
1
Jurkat T cells
Specificity: 0.022
1/25 (4.0%)
0
U937 cells
Specificity: 0.000
0/1 (0.0%)
0
HeLa cells
Specificity: 0.000
0/1 (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
1-501MGAARGSPAR11PRRLPLLSVL21LLPLLGGTQT31AIVFIKQPSS41QDALQGRRAL
51-10051LRCEVEAPGP61VHVYWLLDGA71PVQDTERRFA81QGSSLSFAAV91DRLQDSGTFQ
101-150101CVARDDVTGE111EARSANASFN121IKWIEAGPVV131LKHPASEAEI141QPQTQVTLRC
151-200151HIDGHPRPTY161QWFRDGTPLS171DGQSNHTVSS181KERNLTLRPA191GPEHSGLYSC
201-250201CAHSAFGQAC211SSQNFTLSIA221DESFARVVLA231PQDVVVARYE241EAMFHCQFSA
251-300251QPPPSLQWLF261EDETPITNRS271RPPHLRRATV281FANGSLLLTQ291VRPRNAGIYR
301-350301CIGQGQRGPP311IILEATLHLA321EIEDMPLFEP331RVFTAGSEER341VTCLPPKGLP
351-400351EPSVWWEHAG361VRLPTHGRVY371QKGHELVLAN381IAESDAGVYT391CHAANLAGQR
401-450401RQDVNITVAT411VPSWLKKPQD421SQLEEGKPGY431LDCLTQATPK441PTVVWYRNQM
451-500451LISEDSRFEV461FKNGTLRINS471VEVYDGTWYR481CMSSTPAGSI491EAQARVQVLD
501-550501GSSLPEWVTD511NAGTLHFARV521TRDDAGNYTC531IASNGPQGQI541RAHVQLTVAV
551-600551FITFKVEPER561TTVYQGHTAL571LQCEAQGDPK581PLIQWKGKDR591ILDPTKLGPR
601-650601MHIFQNGSLV611IHDVAPEDSG621RYTCIAGNSC631NIKHTEAPLY641VVDKPVPEES
651-700651EGPGSPPPYK661MIQTIGLSVG671AAVAYIIAVL681GLMFYCKKRC691KAKRLQKQPE
701-750701GEEPEMECLN711GGPLQNGQPS721AEIQEEVALT731SLGSGPAATN741KRHSTSDKMH
751-800751FPRSSLQPIT761TLGKSEFGEV771FLAKAQGLEE781GVAETLVLVK791SLQSKDEQQQ
801-850801LDFRRELEMF811GKLNHANVVR821LLGLCREAEP831HYMVLEYVDL841GDLKQFLRIS
851-900851KSKDEKLKSQ861PLSTKQKVAL871CTQVALGMEH881LSNNRFVHKD891LAARNCLVSA
901-950901QRQVKVSALG911LSKDVYNSEY921YHFRQAWVPL931RWMSPEAILE941GDFSTKSDVW
951-1000951AFGVLMWEVF961THGEMPHGGQ971ADDEVLADLQ981AGKARLPQPE991GCPSKLYRLM
1001-10301001QRCWALSPKD1011RPSFSEIASA1021LGDSTVDSKP
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
686 Prediction (High) - -
690 Prediction (High) - -
896 Prediction (High) - -
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
149 R → C 0.002506 SNP Missense Mutation COAD
162 W → C 0.001764 SNP Missense Mutation LUAD
201 C → C 0.001887 SNP Silent UCEC
340 R → C 0.001887 SNP Missense Mutation UCEC
391 C → S 0.002294 SNP Missense Mutation OV
429 G → C 0.001764 SNP Missense Mutation LUAD
581 R → C 0.004283 SNP Missense Mutation SKCM
581 R → C 0.003460 SNP Missense Mutation CESC
613 C → C 0.002020 SNP Silent PRAD
925 R → C 0.002506 SNP Missense Mutation COAD
964 R → C 0.002141 SNP Missense Mutation SKCM
964 R → C 0.001887 SNP Missense Mutation UCEC
990 W → C 0.001764 SNP Missense Mutation LUAD