Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| P48634 | PRRC2A | Protein PRRC2A (HLA-B-associated transcript 2) … | Homo sapiens (Human) | 2157 aa |
Protein Details: P48634 (PRRC2A)
Protein Information
| Accession | P48634 |
|---|---|
| Protein Names | Protein PRRC2A (HLA-B-associated transcript 2) (Large proline-rich protein BAT2) (Proline-rich and coiled-coil-containing protein 2A) (Protein G2) |
| Gene Symbol | PRRC2A |
| Organism | Homo sapiens (Human) |
| Length | 2157 aa |
| Isoforms | No isoforms |
| Related PMIDs | No related PMIDs |
| Database Sources | CysModDBdbPTMSwissPalm |
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Types:
Experimental Database High Prediction Non-palmitylated Cys
Experimental Database High Prediction Non-palmitylated Cys
1-501MSDRSGPTAK11GKDGKKYSSL21NLFDTYKGKS31LEIQKPAVAP41RHGLQSLGKV
51-10051AIARRMPPPA61NLPSLKAENK71GNDPNVSLVP81KDGTGWASKQ91EQSDPKSSDA
101-150101STAQPPESQP111LPASQTPASN121QPKRPPAAPE131NTPLVPSGVK141SWAQASVTHG
151-200151AHGDGGRASS161LLSRFSREEF171PTLQAAGDQD181KAAKERESAE191QSSGPGPSLR
201-250201PQNSTTWRDG211GGRGPDELEG221PDSKLHHGHD231PRGGLQPSGP241PQFPPYRGMM
251-300251PPFMYPPYLP261FPPPYGPQGP271YRYPTPDGPS281RFPRVAGPRG291SGPPMRLVEP
301-350301VGRPSILKED311NLKEFDQLDQ321ENDDGWAGAH331EEVDYTEKLK341FSDEEDGRDS
351-400351DEEGAEGHRD361SQSASGEERP371PEADGKKGNS381PNSEPPTPKT391AWAETSRPPE
401-450401TEPGPPAPKP411PLPPPHRGPA421GNWGPPGDYP431DRGGPPCKPP441APEDEDEAWR
451-500451QRRKQSSSEI461SLAVERARRR471REEEERRMQE481ERRAACAEKL491KRLDEKFGAP
501-550501DKRLKAEPAA511PPAAPSTPAP521PPAVPKELPA531PPAPPPASAP541TPETEPEEPA
551-600551QAPPAQSTPT561PGVAAAPTLV571SGGGSTSSTS581SGSFEASPVE591PQLPSKEGPE
601-650601PPEEVPPPTT611PPVPKVEPKG621DGIGPTRQPP631SQGLGYPKYQ641KSLPPRFQRQ
651-700651QQEQLLKQQQ661QHQWQQHQQG671SAPPTPVPPS681PPQPVTLGAV691PAPQAPPPPP
701-750701KALYPGALGR711PPPMPPMNFD721PRWMMIPPYV731DPRLLQGRPP741LDFYPPGVHP
751-800751SGLVPRERSD761SGGSSSEPFD771RHAPAMLRER781GTPPVDPKLA791WVGDVFTATP
801-850801AEPRPLTSPL811RQAADEDDKG821MRSETPPVPP831PPPYLASYPG841FPENGAPGPP
851-900851ISRFPLEEPG861PRPLPWPPGS871DEVAKIQTPP881PKKEPPKEET891AQLTGPEAGR
901-950901KPARGVGSGG911QGPPPPRRES921RTETRWGPRP931GSSRRGIPPE941EPGAPPRRAG
951-1000951PIKKPPPPTK961VEELPPKPLE971QGDETPKPPK981PDPLKITKGK991LGGPKETPPN
1001-10501001GNLSPAPRLR1011RDYSYERVGP1021TSCRGRGRGE1031YFARGRGFRG1041TYGGRGRGAR
1051-11001051SREFRSYREF1061RGDDGRGGGT1071GGPNHPPAPR1081GRTASETRSE1091GSEYEEIPKR
1101-11501101RRQRGSETGS1111ETHESDLAPS1121DKEAPTPKEG1131TLTQVPLAPP1141PPGAPPSPAP
1151-12001151ARFTARGGRV1161FTPRGVPSRR1171GRGGGRPPPQ1181VCPGWSPPAK1191SLAPKKPPTG
1201-12501201PLPPSKEPLK1211EKLIPGPLSP1221VARGGSNGGS1231NVGMEDGERP1241RRRRHGRAQQ
1251-13001251QDKPPRFRRL1261KQERENAARG1271SEGKPSLTLP1281ASAPGPEEAL1291TTVTVAPAPR
1301-13501301RAAAKSPDLS1311NQNSDQANEE1321WETASESSDF1331TSERRGDKEA1341PPPVLLTPKA
1351-14001351VGTPGGGGGG1361AVPGISAMSR1371GDLSQRAKDL1381SKRSFSSQRP1391GMERQNRRPG
1401-14501401PGGKAGSSGS1411SSGGGGGGPG1421GRTGPGRGDK1431RSWPSPKNRS1441RPPEERPPGL
1451-15001451PLPPPPPSSS1461AVFRLDQVIH1471SNPAGIQQAL1481AQLSSRQGSV1491TAPGGHPRHK
1501-15501501PGLPQAPQGP1511SPRPPTRYEP1521QRVNSGLSSD1531PHFEEPGPMV1541RGVGGTPRDS
1551-16001551AGVSPFPPKR1561RERPPRKPEL1571LQEESLPPPH1581SSGFLGSKPE1591GPGPQAESRD
1601-16501601TGTEALTPHI1611WNRLHTATSR1621KSYRPSSMEP1631WMEPLSPFED1641VAGTEMSQSD
1651-17001651SGVDLSGDSQ1661VSSGPCSQRS1671SPDGGLKGAA1681EGPPKRPGGS1691SPLNAVPCEG
1701-17501701PPGSEPPRRP1711PPAPHDGDRK1721ELPREQPLPP1731GPIGTERSQR1741TDRGTEPGPI
1751-18001751RPSHRPGPPV1761QFGTSDKDSD1771LRLVVGDSLK1781AEKELTASVT1791EAIPVSRDWE
1801-18501801LLPSAAASAE1811PQSKNLDSGH1821CVPEPSSSGQ1831RLYPEVFYGS1841AGPSSSQISG
1851-19001851GAMDSQLHPN1861SGGFRPGTPS1871LHPYRSQPLY1881LPPGPAPPSA1891LLSGLALKGQ
1901-19501901FLDFSTMQAT1911ELGKLPAGGV1921LYPPPSFLYS1931PAFCPSPLPD1941TSLLQVRQDL
1951-20001951PSPSDFYSTP1961LQPGGQSGFL1971PSGAPAQQML1981LPMVDSQLPV1991VNFGSLPPAP
2001-20502001PPAPPPLSLL2011PVGPALQPPS2021LAVRPPPAPA2031TRVLPSPARP2041FPASLGRAEL
2051-21002051HPVELKPFQD2061YQKLSSNLGG2071PGSSRTPPTG2081RSFSGLNSRL2091KATPSTYSGV
2101-21502101FRTQRVDLYQ2111QASPPDALRW2121IPKPWERTGP2131PPREGPSRRA2141EEPGSRGDKE
2151-21572151PGLPPPR
Palmitoylation Sites Details
| Position | Database | Domains | Literature (PMID/Cell-Tissue) | Mass(PMID/Cell-Tissue) | Prediction Scores |
|---|---|---|---|---|---|
| 437 | - | - | - |
Deep-Palm: 0.39
|
|
| 486 | SWISSPALM DBPTM CYSMODDB | - | - | - |
GPS-Palm: 0.89
Deep-Palm: 0.98
|
| 1023 | - | - | - |
GPS-Palm: 0.83
Deep-Palm: 0.81
|
|
| 1182 | - | - | - |
GPS-Palm: 0.76
Deep-Palm: 0.95
|
|
| 1666 | - | - | - |
Deep-Palm: 0.96
|
|
| 1698 | - | - | - |
Deep-Palm: 0.92
|
|
| 1821 | - | - | - |
Deep-Palm: 0.79
|
|
| 1934 | - | - | - |
Deep-Palm: 0.94
|
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)
• 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)
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 |
|---|---|---|---|---|---|
| 482 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 482 | R → C | 0.005618 | SNP | Missense Mutation | PAAD |
| 486 | C → W | 0.002033 | SNP | Missense Mutation | THCA |
| 486 | C → C | 0.001887 | SNP | Silent | UCEC |
| 516 | S → C | 0.002033 | SNP | Missense Mutation | THCA |
| 627 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 737 | G → C | 0.001764 | SNP | Missense Mutation | LUAD |
| 758 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 904 | R → C | 0.002294 | SNP | Missense Mutation | OV |
| 934 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 934 | R → C | 0.003774 | SNP | Missense Mutation | UCEC |
| 1152 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 1464 | R → C | 0.002506 | SNP | Missense Mutation | COAD |
| 1475 | G → C | 0.002294 | SNP | Missense Mutation | OV |
| 1560 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1602 | G → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1666 | C → C | 0.001887 | SNP | Silent | UCEC |
| 1926 | S → C | 0.002427 | SNP | Missense Mutation | BLCA |
| 1947 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 2089 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 2119 | R → C | 0.002288 | SNP | Missense Mutation | STAD |
| 2157 | R → C | 0.002288 | SNP | Missense Mutation | STAD |