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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
O94832 MYO1D; KIAA0727 Unconventional myosin-Id Homo sapiens (Human) 1006 aa

Protein Details: O94832 (MYO1D)

Protein Information
Accession O94832
Protein Names Unconventional myosin-Id
Gene Symbol MYO1D; KIAA0727
Organism Homo sapiens (Human)
Length 1006 aa
Isoforms No isoforms
Related PMIDs 31251020 32944167 36430497
Database Sources CysModDB dbPTM SwissPalm
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.837
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
36
LNCaP cells
Specificity: 0.837
36/46 (78.3%)
4
PC3 cells
Specificity: 0.093
4/4 (100.0%)
3
Cerebral cortex
Specificity: 0.070
3/4 (75.0%)
0
Jurkat T cells
Specificity: 0.000
0/25 (0.0%)
0
U937 cells
Specificity: 0.000
0/1 (0.0%)
0
DU145 cells
Specificity: 0.000
0/2 (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
1-501MAEQESLEFG11KADFVLMDTV21SMPEFMANLR31LRFEKGRIYT41FIGEVVVSVN
51-10051PYKLLNIYGR61DTIEQYKGRE71LYERPPHLFA81IADAAYKAMK91RRSKDTCIVI
101-150101SGESGAGKTE111ASKYIMQYIA121AITNPSQRAE131VERVKNMLLK141SNCVLEAFGN
151-200151AKTNRNDNSS161RFGKYMDINF171DFKGDPIGGH181INNYLLEKSR191VIVQQPGERS
201-250201FHSFYQLLQG211GSEQMLRSLH221LQKSLSSYNY231IHVGAQLKSS241INDAAEFRVV
251-300251ADAMKVIGFK261PEEIQTVYKI271LAAILHLGNL281KFVVDGDTPL291IENGKVVSII
301-350301AELLSTKTDM311VEKALLYRTV321ATGRDIIDKQ331HTEQEASYGR341DAFAKAIYER
351-400351LFCWIVTRIN361DIIEVKNYDT371TIHGKNTVIG381VLDIYGFEIF391DNNSFEQFCI
401-450401NYCNEKLQQL411FIQLVLKQEQ421EEYQREGIPW431KHIDYFNNQI441IVDLVEQQHK
451-500451GIIAILDDAC461MNVGKVTDEM471FLEALNSKLG481KHAHFSSRKL491CASDKILEFD
501-550501RDFRIRHYAG511DVVYSVIGFI521DKNKDTLFQD531FKRLMYNSSN541PVLKNMWPEG
551-600551KLSITEVTKR561PLTAATLFKN571SMIALVDNLA581SKEPYYVRCI591KPNDKKSPQI
601-650601FDDERCRHQV611EYLGLLENVR621VRRAGFAFRQ631TYEKFLHRYK641MISEFTWPNH
651-700651DLPSDKEAVK661KLIERCGFQD671DVAYGKTKIF681IRTPRTLFTL691EELRAQMLIR
701-750701IVLFLQKVWR711GTLARMRYKR721TKAALTIIRY731YRRYKVKSYI741HEVARRFHGV
751-800751KTMRDYGKHV761KWPSPPKVLR771RFEEALQTIF781NRWRASQLIK791SIPASDLPQV
801-850801RAKVAAVEML811KGQRADLGLQ821RAWEGNYLAS831KPDTPQTSGT841FVPVANELKR
851-900851KDKYMNVLFS861CHVRKVNRFS871KVEDRAIFVT881DRHLYKMDPT891KQYKVMKTIP
901-950901LYNLTGLSVS911NGKDQLVVFH921TKDNKDLIVC931LFSKQPTHES941RIGELVGVLV
951-1000951NHFKSEKRHL961QVNVTNPVQC971SLHGKKCTVS981VETRLNQPQP991DFTKNRSGFI
1001-10061001LSVPGN
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
97 Prediction (Low) - -
143 Prediction (High) - -
353 Prediction (High) - -
460 Prediction (Low) - -
491 CYSMODDB SWISSPALM DBPTM Prediction (Low) Myosin head (motor domain) -
589 Prediction (Low) - -
861 Prediction (High) - -
930 Prediction (Low) - -
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
69 R → C 0.001887 SNP Missense Mutation UCEC
148 F → _G149insPKASNCVLEAF 0.002141 INS In Frame Ins SKCM
350 R → C 0.001887 SNP Missense Mutation UCEC
588 R → C 0.002545 SNP Missense Mutation GBM
588 R → C 0.003774 SNP Missense Mutation UCEC
605 R → C 0.002506 SNP Missense Mutation COAD
622 R → C 0.001014 SNP Missense Mutation BRCA
622 R → C 0.004577 SNP Missense Mutation STAD
622 R → C 0.002506 SNP Missense Mutation COAD
622 R → C 0.006993 SNP Missense Mutation LAML
622 R → C 0.003460 SNP Missense Mutation CESC
629 R → C 0.002747 SNP Missense Mutation LIHC
770 R → C 0.001887 SNP Missense Mutation UCEC
864 R → C 0.002141 SNP Missense Mutation SKCM
882 R → C 0.001887 SNP Missense Mutation UCEC