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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q9Y2W1 THRAP3 Thyroid hormone receptor-associated protein 3 … Homo sapiens (Human) 955 aa

Protein Details: Q9Y2W1 (THRAP3)

Protein Information
AccessionQ9Y2W1
Protein NamesThyroid hormone receptor-associated protein 3 (BCLAF1 and THRAP3 family member 2) (Thyroid hormone receptor-associated protein complex 150 kDa component) (Trap150)
Gene SymbolTHRAP3
OrganismHomo sapiens (Human)
Length955 aa
IsoformsNo isoforms
Related PMIDs 25914232 31251020 31382980
Database SourcesSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MSKTNKSKSG11SRSSRSRSAS21RSRSRSFSKS31RSRSRSLSRS41RKRRLSSRSR
51-10051SRSYSPAHNR61ERNHPRVYQN71RDFRGHNRGY81RRPYYFRGRN91RGFYPWGQYN
101-150101RGGYGNYRSN111WQNYRQAYSP121RRGRSRSRSP131KRRSPSPRSR141SHSRNSDKSS
151-200151SDRSRRSSSS161RSSSNHSRVE171SSKRKSAKEK181KSSSKDSRPS191QAAGDNQGDE
201-250201AKEQTFSGGT211SQDTKASESS221KPWPDATYGT231GSASRASAVS241ELSPRERSPA
251-300251LKSPLQSVVV261RRRSPRPSPV271PKPSPPLSST281SQMGSTLPSG291AGYQSGTHQG
301-350301QFDHGSGSLS311PSKKSPVGKS321PPSTGSTYGS331SQKEESAASG341GAAYTKRYLE
351-400351EQKTENGKDK361EQKQTNTDKE371KIKEKGSFSD381TGLGDGKMKS391DSFAPKTDSE
401-450401KPFRGSQSPK411RYKLRDDFEK421KMADFHKEEM431DDQDKDKAKG441RKESEFDDEP
451-500451KFMSKVIGAN461KNQEEEKSGK471WEGLVYAPPG481KEKQRKTEEL491EEESFPERSK
501-550501KEDRGKRSEG511GHRGFVPEKN521FRVTAYKAVQ531EKSSSPPPRK541TSESRDKLGA
551-600551KGDFPTGKSS561FSITREAQVN571VRMDSFDEDL581ARPSGLLAQE591RKLCRDLVHS
601-650601NKKEQEFRSI611FQHIQSAQSQ621RSPSELFAQH631IVTIVHHVKE641HHFGSSGMTL
651-700651HERFTKYLKR661GTEQEAAKNK671KSPEIHRRID681ISPSTFRKHG691LAHDEMKSPR
701-750701EPGYKAEGKY711KDDPVDLRLD721IERRKKHKER731DLKRGKSRES741VDSRDSSHSR
751-800751ERSAEKTEKT761HKGSKKQKKH771RRARDRSRSS781SSSSQSSHSY791KAEEYTEETE
801-850801EREESTTGFD811KSRLGTKDFV821GPSERGGGRA831RGTFQFRARG841RGWGRGNYSG
851-900851NNNNNSNNDF861QKRNREEEWD871PEYTPKSKKY881YLHDDREGEG891SDKWVSRGRG
901-950901RGAFPRGRGR911FMFRKSSTSP921KWAHDKFSGE931EGEIEDDESG941TENREEKDNI
951-955951QPTTE
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
594 - - -
GPS-Palm: 0.89
Deep-Palm: 0.96
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): 0.400
2
LNCaP
Specificity: 0.400
2/2 (100.0%)
2
CEM 174 cell
Specificity: 0.400
2/2 (100.0%)
1
U937 cell
Specificity: 0.200
1/1 (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
12 R → C 0.002141 SNP Missense Mutation SKCM
13 S → C 0.001764 SNP Missense Mutation LUAD
23 R → C 0.001887 SNP Missense Mutation UCEC
25 R → C 0.002141 SNP Missense Mutation SKCM
39 R → C 0.002427 SNP Missense Mutation BLCA
50 R → C 0.002141 SNP Missense Mutation SKCM
143 S → C 0.002506 SNP Missense Mutation COAD
266 R → C 0.001969 SNP Missense Mutation HNSC
270 V → Cfs*40 0.002288 DEL Frame Shift Del STAD
575 S → C 0.002427 SNP Missense Mutation BLCA
575 S → C 0.002033 SNP Missense Mutation LUSC
608 R → C 0.002288 SNP Missense Mutation STAD
608 R → C 0.002141 SNP Missense Mutation SKCM
819 F → Cfs*5 0.002294 DEL Frame Shift Del OV
873 Y → C 0.002288 SNP Missense Mutation STAD
886 R → C 0.002288 SNP Missense Mutation STAD