Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q08043 ACTN3 Alpha-actinin-3 (Alpha-actinin skeletal muscle isoform … Homo sapiens (Human) 901 aa

Protein Details: Q08043 (ACTN3)

Protein Information
AccessionQ08043
Protein NamesAlpha-actinin-3 (Alpha-actinin skeletal muscle isoform 3) (F-actin cross-linking protein)
Gene SymbolACTN3
OrganismHomo sapiens (Human)
Length901 aa
IsoformsNo isoforms
Related PMIDs 31251020
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
1-501MMMVMQPEGL11GAGEGRFAGG21GGGGEYMEQE31EDWDRDLLLD41PAWEKQQRKT
51-10051FTAWCNSHLR61KAGTQIENIE71EDFRNGLKLM81LLLEVISGER91LPRPDKGKMR
101-150101FHKIANVNKA111LDFIASKGVK121LVSIGAEEIV131DGNLKMTLGM141IWTIILRFAI
151-200151QDISVEETSA161KEGLLLWCQR171KTAPYRNVNV181QNFHTSWKDG191LALCALIHRH
201-250201RPDLIDYAKL211RKDDPIGNLN221TAFEVAEKYL231DIPKMLDAED241IVNTPKPDEK
251-300251AIMTYVSCFY261HAFAGAEQAE271TAANRICKVL281AVNQENEKLM291EEYEKLASEL
301-350301LEWIRRTVPW311LENRVGEPSM321SAMQRKLEDF331RDYRRLHKPP341RIQEKCQLEI
351-400351NFNTLQTKLR361LSHRPAFMPS371EGKLVSDIAN381AWRGLEQVEK391GYEDWLLSEI
401-450401RRLQRLQHLA411EKFRQKASLH421EAWTRGKEEM431LSQRDYDSAL441LQEVRALLRR
451-500451HEAFESDLAA461HQDRVEHIAA471LAQELNELDY481HEAASVNSRC491QAICDQWDNL
501-550501GTLTQKRRDA511LERMEKLLET521IDRLQLEFAR531RAAPFNNWLD541GAVEDLQDVW
551-600551LVHSVEETQS561LLTAHDQFKA571TLPEADRERG581AIMGIQGEIQ591KICQTYGLRP
601-650601CSTNPYITLS611PQDINTKWDM621VRKLVPSCDQ631TLQEELARQQ641VNERLRRQFA
651-700651AQANAIGPWI661QAKVEEVGRL671AAGLAGSLEE681QMAGLRQQEQ691NIINYKTNID
701-750701RLEGDHQLLQ711ESLVFDNKHT721VYSMEHIRVG731WEQLLTSIAR741TINEVENQVL
751-800751TRDAKGLSQE761QLNEFRASFN771HFDRKQNGMM781EPDDFRACLI791SMGYDLGEVE
801-850801FARIMTMVDP811NAAGVVTFQA821FIDFMTRETA831ETDTTEQVVA841SFKILAGDKN
851-900851YITPEELRRE861LPAKQAEYCI871RRMVPYKGSG881APAGALDYVA891FSSALYGESD
901-901901L
Palmitoylation Sites Details
Position Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
55 - - -
GPS-Palm: 0.87
Deep-Palm: 0.72
168 SWISSPALM DBPTM CYSMODDB Calponin homology (CH) domain
HeLa (29575903)
-
GPS-Palm: 0.96
Deep-Palm: 0.96
194 - - -
GPS-Palm: 0.88
Deep-Palm: 0.92
258 - - -
Deep-Palm: 0.73
277 - - -
GPS-Palm: 0.73
Deep-Palm: 0.96
346 SWISSPALM DBPTM CYSMODDB - -
Unknown (32651440)
Deep-Palm: 0.87
490 - - -
Deep-Palm: 0.23
494 - - -
Deep-Palm: 0.36
593 - - -
GPS-Palm: 0.86
Deep-Palm: 0.49
601 - - -
GPS-Palm: 0.75
Deep-Palm: 0.36
628 - - -
GPS-Palm: 0.85
Deep-Palm: 0.87
788 - - -
GPS-Palm: 0.78
Deep-Palm: 0.34
869 - - -
GPS-Palm: 0.84
Deep-Palm: 0.98
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): 1.000
3
LNCaP
Specificity: 1.000
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
74 R → C 0.001887 SNP Missense Mutation UCEC
100 R → C 0.002747 SNP Missense Mutation LIHC
100 R → C 0.002427 SNP Missense Mutation BLCA
176 R → C 0.002506 SNP Missense Mutation COAD
325 R → C 0.001887 SNP Missense Mutation UCEC
372 G → C 0.002294 SNP Missense Mutation OV
402 R → C 0.001887 SNP Missense Mutation UCEC
436 Y → C 0.002033 SNP Missense Mutation LUSC
494 C → C 0.008130 SNP Silent THYM
628 C → Y 0.001887 SNP Missense Mutation UCEC
803 R → C 0.002545 SNP Missense Mutation GBM