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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q15029-2 EFTUD2 116 kDa U5 small nuclear … Homo sapiens (Human) 937 aa

Protein Details: Q15029-2 (EFTUD2)

Protein Information
AccessionQ15029-2
Protein Names116 kDa U5 small nuclear ribonucleoprotein component (Elongation factor Tu GTP-binding domain-containing protein 2) (SNU114 homolog) (hSNU114) (U5 snRNP-specific protein, 116 kDa) (U5-116 kDa)
Gene SymbolEFTUD2
OrganismHomo sapiens (Human)
Length937 aa
Isoforms
Related PMIDs 31251020 36430497
Database SourcesNo database sources
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MDDDDDDDDV11GDHDDDHPGM21EVVLHEDKKY31YPTAEEVYGP41EVETIVQEED
51-10051TQPLTEPIIK61PVKTKKFTLM71EQTLPVTVYE81MDFLADLMDN91SELIRNVTLC
101-150101GHLHHGKTCF111VDCLIEQTHP121EIRKRYDQDL131CYTDILFTEQ141ERGVGIKSTP
151-200151VTVVLPDTKG161KSYLFNIMDT171PGHVNFSDEV181TAGLRISDGV191VLFIDAAEGV
201-250201MLNTERLIKH211AVQERLAVTV221CINKIDRLIL231ELKLPPTDAY241YKLRHIVDEV
251-300251NGLISMYSTD261ENLILSPLLG271NVCFSSSQYS281ICFTLGSFAK291IYADTFGDIN
301-350301YQEFAKRLWG311DIYFNPKTRK321FTKKAPTSSS331QRSFVEFILE341PLYKILAQVV
351-400351GDVDTSLPRT361LDELGIHLTK371EELKLNIRPL381LRLVCKKFFG391EFTGFVDMCV
401-450401QHIPSPKVGA411KPKIEHTYTG421GVDSDLGEAM431SDCDPDGPLM441CHTTKMYSTD
451-500451DGVQFHAFGR461VLSGTIHAGQ471PVKVLGENYT481LEDEEDSQIC491TVGRLWISVA
501-550501RYHIEVNRVP511AGNWVLIEGV521DQPIVKTATI531TEPRGNEEAQ541IFRPLKFNTT
551-600551SVIKIAVEPV561NPSELPKMLD571GLRKVNKSYP581SLTTKVEESG591EHVILGTGEL
601-650601YLDCVMHDLR611KMYSEIDIKV621ADPVVTFCET631VVETSSLKCF641AETPNKKNKI
651-700651TMIAEPLEKG661LAEDIENEVV671QITWNRKKLG681EFFQTKYDWD691LLAARSIWAF
701-750701GPDATGPNIL711VDDTLPSEVD721KALLGSVKDS731IVQGFQWGTR741EGPLCDELIR
751-800751NVKFKILDAV761VAQEPLHRGG771GQIIPTARRV781VYSAFLMATP791RLMEPYYFVE
801-850801VQAPADCVSA811VYTVLARRRG821HVTQDAPIPG831SPLYTIKAFI841PAIDSFGFET
851-900851DLRTHTQGQA861FSLSVFHHWQ871IVPGDPLDKS881IVIRPLEPQP891APHLAREFMI
901-937901KTRRRKGLSE911DVSISKFFDD921PMLLELAKQD931VVLNYPM
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
135 - - -
Deep-Palm: 0.62
144 - - -
Deep-Palm: 0.47
148 - - -
Deep-Palm: 0.35
166 - - -
Deep-Palm: 0.53
221 - - -
GPS-Palm: 0.92
256 - - -
Deep-Palm: 0.97
308 - - -
Deep-Palm: 0.92
317 - - -
Deep-Palm: 0.55
420 - - -
Deep-Palm: 0.97
434 - - -
Deep-Palm: 0.56
468 - - -
Deep-Palm: 0.12
476 - - -
Deep-Palm: 0.03
525 - - -
Deep-Palm: 0.89
639 - - -
Deep-Palm: 0.93
663 - - -
Deep-Palm: 0.76
674 - - -
Deep-Palm: 0.71
745 - - -
GPS-Palm: 0.90
780 - - -
Deep-Palm: 0.91
842 - - -
Deep-Palm: 0.84
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): 0.571
4
cerebral cortex
Specificity: 0.571
4/4 (100.0%)
3
LNCaP
Specificity: 0.429
3/3 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.000
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.
Conservation score for cysteine
PhyloP for Cysteine
PhastCons Conservation Scores for Cysteine
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
65 Y → C 0.001014 SNP Missense Mutation BRCA
220 R → C 0.002294 SNP Missense Mutation OV
279 R → C 0.001764 SNP Missense Mutation LUAD
413 R → C 0.002506 SNP Missense Mutation COAD
413 R → C 0.001887 SNP Missense Mutation UCEC
529 R → C 0.001969 SNP Missense Mutation HNSC
531 W → C 0.001887 SNP Missense Mutation UCEC
537 Y → C 0.002288 SNP Missense Mutation STAD
730 R → C 0.001014 SNP Missense Mutation BRCA
730 R → C 0.002141 SNP Missense Mutation SKCM
730 R → C 0.003774 SNP Missense Mutation UCEC
919 R → C 0.001014 SNP Missense Mutation BRCA
919 R → C 0.003460 SNP Missense Mutation CESC
939 R → C 0.002288 SNP Missense Mutation STAD
? ? → ? 0.001764 SNP Missense Mutation LUAD