Search Database

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
AccessionP02786
Protein NamesTransferrin receptor protein 1 (TR) (TfR) (TfR1) (Trfr) (T9) (Transferrin receptor 1) (p90) (CD antigen CD71) [Cleaved into: Transferrin receptor protein 1, serum form (sTfR)]
Gene SymbolTFRC
OrganismHomo sapiens (Human)
Length760 aa
IsoformsNo isoforms
Related PMIDs 19137006 19801377 21076176 22496122 24357059 25914232 26111759 29575903 29733200 31251020 31382980 32651440 32944167 33636221 36430497 31251020 (mass) 32651440 (mass) 36430497 (mass)
Database SourcesCysModDBdbPTMSwissPalm
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
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 Database Domains Literature (PMID/Cell-Tissue) Mass(PMID/Cell-Tissue) Prediction Scores
62 SWISSPALM DBPTM CYSMODDB - - -
GPS-Palm: 0.83
Deep-Palm: 0.55
67 SWISSPALM DBPTM CYSMODDB -
HeLa (37611173)
-
GPS-Palm: 0.80
Deep-Palm: 0.62
89 - - -
GPS-Palm: 0.79
Deep-Palm: 0.86
98 - - -
Deep-Palm: 0.93
353 -
HeLa (29575903)
LNCaP (31251020)
Deep-Palm: 0.90
363 -
HeLa (29575903)
-
Deep-Palm: 0.59
556 - - -
Deep-Palm: 0.28
558 - - -
Deep-Palm: 0.18
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): 0.138
4
LNCaP
Specificity: 0.133
4/4 (100.0%)
4
Primary T cell
Specificity: 0.133
4/4 (100.0%)
4
PC3
Specificity: 0.133
4/4 (100.0%)
3
Jurkat T cell
Specificity: 0.100
3/3 (100.0%)
3
CEM 174 cell
Specificity: 0.100
3/3 (100.0%)
2
HAP1 cell
Specificity: 0.067
2/2 (100.0%)
2
HeLa cell
Specificity: 0.067
2/2 (100.0%)
1
U937 cell
Specificity: 0.033
1/1 (100.0%)
1
EC cell
Specificity: 0.033
1/1 (100.0%)
1
293T cell
Specificity: 0.033
1/1 (100.0%)
1
cerebral cortex
Specificity: 0.033
1/1 (100.0%)
1
heart
Specificity: 0.033
1/1 (100.0%)
1
HUVECs
Specificity: 0.033
1/1 (100.0%)
1
DU145 cell
Specificity: 0.033
1/1 (100.0%)
Mass Spectrometry Data - Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 1.000
1
LNCaP cells (Mass)
Specificity: 0.033
1/4 (25.0%)
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
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