Search Database

Select Protein (1 found)

UniProt ID Gene Symbol Protein Name Organism Length Action
Q9UBG0 MRC2; CLEC13E; ENDO180; KIAA0709; UPARAP C-type mannose receptor 2 (C-type … Homo sapiens (Human) 1479 aa

Protein Details: Q9UBG0 (MRC2)

Protein Information
Accession Q9UBG0
Protein Names C-type mannose receptor 2 (C-type lectin domain family 13 member E) (Endocytic receptor 180) (Macrophage mannose receptor 2) (Urokinase-type plasminogen activator receptor-associated protein) (UPAR-associated protein) (Urokinase receptor-associated protein) (CD antigen CD280)
Gene Symbol MRC2; CLEC13E; ENDO180; KIAA0709; UPARAP
Organism Homo sapiens (Human)
Length 1479 aa
Isoforms No isoforms
Related PMIDs 31382980 33636221
Database Sources CysModDB dbPTM SwissPalm
These studies detected palmitoylation of this protein in the samples.
Tissue/Cell Line Expression
Tissue Specificity Index (TSI): 0.500
Bubble Size: Positive Samples Count Color Intensity: Positive Ratio
1
U937 cells
Specificity: 0.500
1/1 (100.0%)
1
Liver membrane
Specificity: 0.500
1/1 (100.0%)
0
Jurkat T cells
Specificity: 0.000
0/25 (0.0%)
0
DU145 cells
Specificity: 0.000
0/2 (0.0%)
0
HeLa cells
Specificity: 0.000
0/1 (0.0%)
0
LNCaP cells
Specificity: 0.000
0/46 (0.0%)
0
PC3 cells
Specificity: 0.000
0/4 (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
Cerebral cortex
Specificity: 0.000
0/4 (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
1-501MGPGRPAPAP11WPRHLLRCVL21LLGCLHLGRP31GAPGDAALPE41PNVFLIFSHG
51-10051LQGCLEAQGG61QVRVTPACNT71SLPAQRWKWV81SRNRLFNLGT91MQCLGTGWPG
101-150101TNTTASLGMY111ECDREALNLR121WHCRTLGDQL131SLLLGARTSN141ISKPGTLERG
151-200151DQTRSGQWRI161YGSEEDLCAL171PYHEVYTIQG181NSHGKPCTIP191FKYDNQWFHG
201-250201CTSTGREDGH211LWCATTQDYG221KDERWGFCPI231KSNDCETFWD241KDQLTDSCYQ
251-300251FNFQSTLSWR261EAWASCEQQG271ADLLSITEIH281EQTYINGLLT291GYSSTLWIGL
301-350301NDLDTSGGWQ311WSDNSPLKYL321NWESDQPDNP331SEENCGVIRT341ESSGGWQNRD
351-400351CSIALPYVCK361KKPNATAEPT371PPDRWANVKV381ECEPSWQPFQ391GHCYRLQAEK
401-450401RSWQESKKAC411LRGGGDLVSI421HSMAELEFIT431KQIKQEVEEL441WIGLNDLKLQ
451-500451MNFEWSDGSL461VSFTHWHPFE471PNNFRDSLED481CVTIWGPEGR491WNDSPCNQSL
501-550501PSICKKAGQL511SQGAAEEDHG521CRKGWTWHSP531SCYWLGEDQV541TYSEARRLCT
551-600551DHGSQLVTIT561NRFEQAFVSS571LIYNWEGEYF581WTALQDLNST591GSFFWLSGDE
601-650601VMYTHWNRDQ611PGYSRGGCVA621LATGSAMGLW631EVKNCTSFRA641RYICRQSLGT
651-700651PVTPELPGPD661PTPSLTGSCP671QGWASDTKLR681YCYKVFSSER691LQDKKSWVQA
701-750701QGACQELGAQ711LLSLASYEEE721HFVANMLNKI731FGESEPEIHE741QHWFWIGLNR
751-800751RDPRGGQSWR761WSDGVGFSYH771NFDRSRHDDD781DIRGCAVLDL791ASLQWVAMQC
801-850801DTQLDWICKI811PRGTDVREPD821DSPQGRREWL831RFQEAEYKFF841EHHSTWAQAQ
851-900851RICTWFQAEL861TSVHSQAELD871FLSHNLQKFS881RAQEQHWWIG891LHTSESDGRF
901-950901RWTDGSIINF911ISWAPGKPRP921VGKDKKCVYM931TASREDWGDQ941RCLTALPYIC
951-1000951KRSNVTKETQ961PPDLPTTALG971GCPSDWIQFL981NKCFQVQGQE991PQSRVKWSEA
1001-10501001QFSCEQQEAQ1011LVTITNPLEQ1021AFITASLPNV1031TFDLWIGLHA1041SQRDFQWVEQ
1051-11001051EPLMYANWAP1061GEPSGPSPAP1071SGNKPTSCAV1081VLHSPSAHFT1091GRWDDRSCTE
1101-11501101ETHGFICQKG1111TDPSLSPSPA1121ALPPAPGTEL1131SYLNGTFRLL1141QKPLRWHDAL
1151-12001151LLCESRNASL1161AYVPDPYTQA1171FLTQAARGLR1181TPLWIGLAGE1191EGSRRYSWVS
1201-12501201EEPLNYVGWQ1211DGEPQQPGGC1221TYVDVDGAWR1231TTSCDTKLQG1241AVCGVSSGPP
1251-13001251PPRRISYHGS1261CPQGLADSAW1271IPFREHCYSF1281HMELLLGHKE1291ARQRCQRAGG
1301-13501301AVLSILDEME1311NVFVWEHLQS1321YEGQSRGAWL1331GMNFNPKGGT1341LVWQDNTAVN
1351-14001351YSNWGPPGLG1361PSMLSHNSCY1371WIQSNSGLWR1381PGACTNITMG1391VVCKLPRAEQ
1401-14501401SSFSPSALPE1411NPAALVVVLM1421AVLLLLALLT1431AALILYRRRQ1441SIERGAFEGA
1451-14791451RYSRSSSSPT1461EATEKNILVS1471DMEMNEQQE
Palmitoylation Sites Details
Position Sources Domains Experimental PMIDs
24 Prediction (High) - -
54 Prediction (Low) - -
68 Prediction (Medium) - -
93 Prediction (Medium) - -
112 Prediction (Low) - -
123 Prediction (Low) - -
228 Prediction (Medium) - -
359 Prediction (Low) - -
410 Prediction (Medium) - -
481 Prediction (Low) - -
496 CYSMODDB SWISSPALM DBPTM - -
504 CYSMODDB SWISSPALM DBPTM - -
549 Prediction (Medium) - -
635 Prediction (Low) - -
644 Prediction (Low) - -
682 Prediction (Medium) - -
704 Prediction (Low) - -
785 Prediction (Low) - -
927 Prediction (Low) - -
942 Prediction (Low) - -
950 Prediction (High) - -
972 Prediction (Low) - -
1153 Prediction (Medium) - -
1295 Prediction (Medium) - -
1393 Prediction (Medium) - -
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
24 C → C 0.001014 SNP Silent BRCA
68 C → S 0.002288 SNP Missense Mutation STAD
93 C → Y 0.002747 SNP Missense Mutation LIHC
137 R → C 0.001887 SNP Missense Mutation UCEC
224 R → C 0.006944 SNP Missense Mutation TGCT
270 G → C 0.001764 SNP Missense Mutation LUAD
618 C → C 0.001887 SNP Silent UCEC
760 R → C 0.002288 SNP Missense Mutation STAD
760 R → C 0.001887 SNP Missense Mutation UCEC
769 Y → C 0.001887 SNP Missense Mutation UCEC
779 D → Cfs*68 0.002288 DEL Frame Shift Del STAD
800 C → Y 0.002976 SNP Missense Mutation KIRC
800 C → C 0.001887 SNP Silent UCEC
831 R → C 0.017544 SNP Missense Mutation UCS
927 C → Y 0.002033 SNP Missense Mutation LUSC
942 C → S 0.002294 SNP Missense Mutation OV
952 R → C 0.002506 SNP Missense Mutation COAD
1092 R → C 0.002288 SNP Missense Mutation STAD
1295 C → C 0.002020 SNP Silent PRAD
1369 C → F 0.006993 SNP Missense Mutation LAML