Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q9UIQ6-2 LNPEP Isoform 2 of Leucyl-cystinyl aminopeptidase Homo sapiens (Human) 1011 aa

Protein Details: Q9UIQ6-2 (LNPEP)

Protein Information
Accession Q9UIQ6-2
Protein Names Isoform 2 of Leucyl-cystinyl aminopeptidase
Gene Symbol LNPEP
Organism Homo sapiens (Human)
Length 1011 aa
Isoforms
Related PMIDs 19801377 21076176 31251020 32651440 32944167 36430497
Database Sources No database sources
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.294
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
5
Jurkat T cells
Specificity: 0.294
5/25 (20.0%)
4
LNCaP cells
Specificity: 0.235
4/46 (8.7%)
4
PC3 cells
Specificity: 0.235
4/4 (100.0%)
2
DU145 cells
Specificity: 0.118
2/2 (100.0%)
2
Cerebral cortex
Specificity: 0.118
2/4 (50.0%)
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
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
1-501MIENSMFEEE11PDVVDLAKEP21CLHPLEPDEV31EYEPRGSRLL41VRGLGEHEME
51-10051EDEEDYESSA61KLLGMSFMNR71SSGLRNSATG81YRQSPDGACS91VPSARTMVVC
101-150101AFVIVVAVSV111IMVIYLLPRC121TFTKEGCHKK131NQSIGLIQPF141ATNGKLFPWA
151-200151QIRLPTAVVP161LRYELSLHPN171LTSMTFRGSV181TISVQALQVT191WNIILHSTGH
201-250201NISRVTFMSA211VSSQEKQAEI221LEYAYHGQIA231IVAPEALLAG241HNYTLKIEYS
251-300251ANISSSYYGF261YGFSYTDESN271EKKYFAATQF281EPLAARSAFP291CFDEPAFKAT
301-350301FIIKIIRDEQ311YTALSNMPKK321SSVVLDDGLV331QDEFSESVKM341STYLVAFIVG
351-400351EMKNLSQDVN361GTLVSIYAVP371EKIGQVHYAL381ETTVKLLEFF391QNYFEIQYPL
401-450401KKLDLVAIPD411FEAGAMENWG421LLTFREETLL431YDSNTSSMAD441RKLVTKIIAH
451-500451ELAHQWFGNL461VTMKWWNDLW471LNEGFATFME481YFSLEKIFKE491LSSYEDFLDA
501-550501RFKTMKKDSL511NSSHPISSSV521QSSEQIEEMF531DSLSYFKGSS541LLLMLKTYLS
551-600551EDVFQHAVVL561YLHNHSYASI571QSDDLWDSFN581EVTNQTLDVK591RMMKTWTLQK
601-650601GFPLVTVQKK611GKELFIQQER621FFLNMKPEIQ631PSDTSYLWHI641PLSYVTEGRN
651-700651YSKYQSVSLL661DKKSGVINLT671EEVLWVKVNI681NMNGYYIVHY691ADDDWEALIH
701-750701QLKINPYVLS711DKDRANLINN721IFELAGLGKV731PLKRAFDLIN741YLGNENHTAP
751-800751ITEALFQTDL761IYNLLEKLGY771MDLASRLVTR781VFKLLQNQIQ791QQTWTDEGTP
801-850801SMRELRSALL811EFACTHNLGN821CSTTAMKLFD831DWMASNGTQS841LPTDVMTTVF
851-900851KVGAKTDKGW861SFLLGKYISI871GSEAEKNKIL881EALASSEDVR891KLYWLMKSSL
901-950901NGDNFRTQKL911SFIIRTVGRH921FPGHLLAWDF931VKENWNKLVQ941KFPLGSYTIQ
951-1000951NIVAGSTYLF961STKTHLSEVQ971AFFENQSEAT981FRLRCVQEAL991EVIQLNIQWM
1001-10111001EKNLKSLTWW1011L
Palmitoylation Sites Details

No known palmitoylation sites

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
134 C → S 0.002545 SNP Missense Mutation GBM
213 G → C 0.001887 SNP Missense Mutation UCEC
301 S → C 0.001969 SNP Missense Mutation HNSC
315 F → C 0.001887 SNP Missense Mutation UCEC
470 W → C 0.002747 SNP Missense Mutation LIHC
497 S → C 0.002288 SNP Missense Mutation STAD
506 S → C 0.002427 SNP Missense Mutation BLCA
581 Y → C 0.002427 SNP Missense Mutation BLCA
961 Y → C 0.001887 SNP Missense Mutation UCEC
998 R → C 0.001014 SNP Missense Mutation BRCA
998 R → C 0.002141 SNP Missense Mutation SKCM
998 R → C 0.001887 SNP Missense Mutation UCEC