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Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
P02786 TFRC Transferrin receptor protein 1 (TR) … Homo sapiens (Human) 760 aa

Protein Details: P02786 (TFRC)

Protein Information
Accession P02786
Protein Names Transferrin receptor protein 1 (TR) (TfR) (TfR1) (Trfr) (T9) (p90) (CD antigen CD71) [Cleaved into: Transferrin receptor protein 1, serum form (sTfR)]
Gene Symbol TFRC
Organism Homo sapiens (Human)
Length 760 aa
Isoforms No isoforms
Related PMIDs 19801377 21076176 22496122 24357059 25914232 26111759 29575903 29733200 31251020 31382980 32651440 32944167 33636221 36430497 37611173
Database Sources CysModDB dbPTM SwissPalm
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.523
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
46
LNCaP cells
Specificity: 0.523
46/46 (100.0%)
10
HAP1 cells
Specificity: 0.114
10/10 (100.0%)
7
Jurkat T cells
Specificity: 0.080
7/25 (28.0%)
6
293T cells
Specificity: 0.068
6/10 (60.0%)
4
PC3 cells
Specificity: 0.045
4/4 (100.0%)
4
T cells
Specificity: 0.045
4/4 (100.0%)
3
CEMx174 cells
Specificity: 0.034
3/3 (100.0%)
2
DU145 cells
Specificity: 0.023
2/2 (100.0%)
2
Endothelial cells
Specificity: 0.023
2/2 (100.0%)
1
U937 cells
Specificity: 0.011
1/1 (100.0%)
1
HeLa cells
Specificity: 0.011
1/1 (100.0%)
1
Cerebral cortex
Specificity: 0.011
1/4 (25.0%)
1
Liver membrane
Specificity: 0.011
1/1 (100.0%)
0
Prefrontal cortex
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
1-501MMDQARSAFS11NLFGGEPLSY21TRFSLARQVD31GDNSHVEMKL41AVDEEENADN
51-10051NTKANVTKPK61RCSGSICYGT71IAVIVFFLIG81FMIGYLGYCK91GVEPKTECER
101-150101LAGTESPVRE111EPGEDFPAAR121RLYWDDLKRK131LSEKLDSTDF141TGTIKLLNEN
151-200151SYVPREAGSQ161KDENLALYVE171NQFREFKLSK181VWRDQHFVKI191QVKDSAQNSV
201-250201IIVDKNGRLV211YLVENPGGYV221AYSKAATVTG231KLVHANFGTK241KDFEDLYTPV
251-300251NGSIVIVRAG261KITFAEKVAN271AESLNAIGVL281IYMDQTKFPI291VNAELSFFGH
301-350301AHLGTGDPYT311PGFPSFNHTQ321FPPSRSSGLP331NIPVQTISRA341AAEKLFGNME
351-400351GDCPSDWKTD361STCRMVTSES371KNVKLTVSNV381LKEIKILNIF391GVIKGFVEPD
401-450401HYVVVGAQRD411AWGPGAAKSG421VGTALLLKLA431QMFSDMVLKD441GFQPSRSIIF
451-500451ASWSAGDFGS461VGATEWLEGY471LSSLHLKAFT481YINLDKAVLG491TSNFKVSASP
501-550501LLYTLIEKTM511QNVKHPVTGQ521FLYQDSNWAS531KVEKLTLDNA541AFPFLAYSGI
551-600551PAVSFCFCED561TDYPYLGTTM571DTYKELIERI581PELNKVARAA591AEVAGQFVIK
601-650601LTHDVELNLD611YERYNSQLLS621FVRDLNQYRA631DIKEMGLSLQ641WLYSARGDFF
651-700651RATSRLTTDF661GNAEKTDRFV671MKKLNDRVMR681VEYHFLSPYV691SPKESPFRHV
701-750701FWGSGSHTLP711ALLENLKLRK721QNNGAFNETL731FRNQLALATW741TIQGAANALS
751-760751GDVWDIDNEF
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
62 CYSMODDB SWISSPALM DBPTM Prediction (Medium) - -
67 Experimental CYSMODDB SWISSPALM DBPTM Prediction (Medium) - 37611173
89 Prediction (Medium) - -
353 Experimental - 29575903
363 Experimental - 29575903
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
152 Y → C 0.001969 SNP Missense Mutation HNSC
174 R → C 0.007299 SNP Missense Mutation READ
174 R → C 0.002141 SNP Missense Mutation SKCM
174 R → C 0.003774 SNP Missense Mutation UCEC
321 F → delinsLEYVALILIC 0.002294 INS In Frame Ins OV
338 S → C 0.001764 SNP Missense Mutation LUAD
646 R → C 0.002427 SNP Missense Mutation BLCA
719 R → C 0.001887 SNP Missense Mutation UCEC
719 R → C 0.005435 SNP Missense Mutation ESCA
719 R → C 0.003460 SNP Missense Mutation CESC