Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q15029-3 EFTUD2 116 kDa U5 small nuclear … Homo sapiens (Human) 962 aa

Protein Details: Q15029-3 (EFTUD2)

Protein Information
AccessionQ15029-3
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)
Length962 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
1-501MDTDLYDEFG11NYIGPELDSD21EDDDELGRET31KDLDEMDDDD41DDDDVGDHDD
51-10051DHPGMEVVLH61EDKKYYPTAE71EVYGPEVETI81VQEEDTQPLT91EPIIKPVKTK
101-150101KFTLMEQTLP111VTVYEMDFLA121DLMDNSELIR131NVTLCGHLHH141GKTHPEIRKR
151-200151YDQDLCYTDI161LFTEQERGVG171IKSTPVTVVL181PDTKGKSYLF191NIMDTPGHVN
201-250201FSDEVTAGLR211ISDGVVLFID221AAEGVMLNTE231RLIKHAVQER241LAVTVCINKI
251-300251DRLILELKLP261PTDAYYKLRH271IVDEVNGLIS281MYSTDENLIL291SPLLGNVCFS
301-350301SSQYSICFTL311GSFAKIYADT321FGDINYQEFA331KRLWGDIYFN341PKTRKFTKKA
351-400351PTSSSQRSFV361EFILEPLYKI371LAQVVGDVDT381SLPRTLDELG391IHLTKEELKL
401-450401NIRPLLRLVC411KKFFGEFTGF421VDMCVQHIPS431PKVGAKPKIE441HTYTGGVDSD
451-500451LGEAMSDCDP461DGPLMCHTTK471MYSTDDGVQF481HAFGRVLSGT491IHAGQPVKVL
501-550501GENYTLEDEE511DSQICTVGRL521WISVARYHIE531VNRVPAGNWV541LIEGVDQPIV
551-600551KTATITEPRG561NEEAQIFRPL571KFNTTSVIKI581AVEPVNPSEL591PKMLDGLRKV
601-650601NKSYPSLTTK611VEESGEHVIL621GTGELYLDCV631MHDLRKMYSE641IDIKVADPVV
651-700651TFCETVVETS661SLKCFAETPN671KKNKITMIAE681PLEKGLAEDI691ENEVVQITWN
701-750701RKKLGEFFQT711KYDWDLLAAR721SIWAFGPDAT731GPNILVDDTL741PSEVDKALLG
751-800751SVKDSIVQGF761QWGTREGPLC771DELIRNVKFK781ILDAVVAQEP791LHRGGGQIIP
801-850801TARRVVYSAF811LMATPRLMEP821YYFVEVQAPA831DCVSAVYTVL841ARRRGHVTQD
851-900851APIPGSPLYT861IKAFIPAIDS871FGFETDLRTH881TQGQAFSLSV891FHHWQIVPGD
901-950901PLDKSIVIRP911LEPQPAPHLA921REFMIKTRRR931KGLSEDVSIS941KFFDDPMLLE
951-962951LAKQDVVLNY961PM
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
246 - - -
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
770 - - -
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