Search Database
Select Protein (1 found)
| UniProt ID | Gene Symbol | Protein Name | Organism | Length | Action |
|---|---|---|---|---|---|
| Q96BY7 | ATG2B; C14orf103 | Autophagy-related protein 2 homolog B | Homo sapiens (Human) | 2078 aa |
Protein Details: Q96BY7 (ATG2B)
Protein Information
| Accession | Q96BY7 |
|---|---|
| Protein Names | Autophagy-related protein 2 homolog B |
| Gene Symbol | ATG2B; C14orf103 |
| Organism | Homo sapiens (Human) |
| Length | 2078 aa |
| Isoforms | No isoforms |
| Related PMIDs | 37611173 |
| Database Sources | No database sources |
These studies detected palmitoylation of this protein in the samples.
Protein Sequence
Single Types:
Experimental Database High Prediction Medium Prediction Low Prediction
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
All Three Exp + DB Exp + High Pred Exp + Med Pred Exp + Low Pred DB + High Pred DB + Med Pred DB + Low Pred Cysteine
1-501MPWPFSESIK11KRACRYLLQR21YLGHFLQEKL31SLEQLSLDLY41QGTGSLAQVP
51-10051LDKWCLNEIL61ESADAPLEVT71EGFIQSISLS81VPWGSLLQDN91CALEVRGLEM
101-150101VFRPRPRPAT111GSEPMYWSSF121MTSSMQLAKE131CLSQKLTDEQ141GEGSQPFEGL
151-200151EKFAETIETV161LRRVKVTFID171TVLRIEHVPE181NSKTGTALEI191RIERTVYCDE
201-250201TADESSGINV211HQPTAFAHKL221LQLSGVSLFW231DEFSASAKSS241PVCSTAPVET
251-300251EPKLSPSWNP261KIIYEPHPQL271TRNLPEIAPS281DPVQIGRLIG291RLELSLTLKQ
301-350301NEVLPGAKLD311VDGQIDSIHL321LLSPRQVHLL331LDMLAAIAGP341ENSSKIGLAN
351-400351KDRKNRPMQQ361EDEYRIQMEL371NRYYLRKDSL381SVGVSSEQSF391YETETARTPS
401-450401SREEEVFFSM411ADMDMSHSLS421SLPPLGDPPN431MDLELSLTST441YTNTPAGSPL
451-500451SATVLQPTWG461EFLDHHKEQP471VRGSTFPSNL481VHPTPLQKTS491LPSRSVSVDE
501-550501SRPELIFRLA511VGTFSISVLH521IDPLSPPETS531QNLNPLTPMA541VAFFTCIEKI
551-600551DPARFSTEDF561KSFRAVFAEA571CSHDHLRFIG581TGIKVSYEQR591QRSASRYFST
601-650601DMSIGQMEFL611ECLFPTDFHS621VPPHYTELLT631FHSKEETGSH641SPVCLQLHYK
651-700651HSENRGPQGN661QARLSSVPHK671AELQIKLNPV681CCELDISIVD691RLNSLLQPQK
701-750701LATVEMMASH711MYTSYNKHIS721LHKAFTEVFL731DDSHSPANCR741ISVQVATPAL
751-800751NLSVRFPIPD761LRSDQERGPW771FKKSLQKEIL781YLAFTDLEFK791TEFIGGSTPE
801-850801QIKLELTFRE811LIGSFQEEKG821DPSIKFFHVS831SGVDGDTTSS841DDFDWPRIVL
851-900851KINPPAMHSI861LERIAAEEEE871ENDGHYQEEE881EGGAHSLKDV891CDLRRPAPSP
901-950901FSSRRVMFEN911EQMVMPGDPV921EMTEFQDKAI931SNSHYVLELT941LPNIYVTLPN
951-1000951KSFYEKLYNR961IFNDLLLWEP971TAPSPVETFE981NISYGIGLSV991ASQLINTFNK
1001-10501001DSFSAFKSAV1011HYDEESGSEE1021ETLQYFSTVD1031PNYRSRRKKK1041LDSQNKNSQS
1051-11001051FLSVLLNINH1061GLIAVFTDVK1071QDNGDLLENK1081HGEFWLEFNS1091GSLFCVTKYE
1101-11501101GFDDKHYICL1111HSSSFSLYHK1121GIVNGVILPT1131ETRLPSSTRP1141HWLEPTIYSS
1151-12001151EEDGLSKTSS1161DGVGGDSLNM1171LSVAVKILSD1181KSESNTKEFL1191IAVGLKGATL
1201-12501201QHRMLPSGLS1211WHEQILYFLN1221IADEPVLGYN1231PPTSFTTFHV1241HLWSCALDYR
1251-13001251PLYLPIRSLL1261TVETFSVSSS1271VALDKSSSTL1281RIILDEAALH1291LSDKCNTVTI
1301-13501301NLSRDYVRVM1311DMGLLELTIT1321AVKSDSDGEQ1331TEPRFELHCS1341SDVVHIRTCS
1351-14001351DSCAALMNLI1361QYIASYGDLQ1371TPNKADMKPG1381AFQRRSKVDS1391SGRSSSRGPV
1401-14501401LPEADQQMLR1411DLMSDAMEEI1421DMQQGTSSVK1431PQANGVLDEK1441SQIQEPCCSD
1451-15001451LFLFPDESGN1461VSQESGPTYA1471SFSHHFISDA1481MTGVPTENDD1491FCILFAPKAA
1501-15501501MQEKEEEPVI1511KIMVDDAIVI1521RDNYFSLPVN1531KTDTSKAPLH1541FPIPVIRYVV
1551-16001551KEVSLVWHLY1561GGKDFGIVPP1571TSPAKSYISP1581HSSPSHTPTR1591HGRNTVCGGK
1601-16501601GRNHDFLMEI1611QLSKVKFQHE1621VYPPCKPDCD1631SSLSEHPVSR1641QVFIVQDLEI
1651-17001651RDRLATSQMN1661KFLYLYCSKE1671MPRKAHSNML1681TVKALHVCPE1691SGRSPQECCL
1701-17501701RVSLMPLRLN1711IDQDALFFLK1721DFFTSLSAEV1731ELQMTPDPEV1741KKSPGADVTC
1751-18001751SLPRHLSTSK1761EPNLVISFSG1771PKQPSQNDSA1781NSVEVVNGME1791EKNFSAEEAS
1801-18501801FRDQPVFFRE1811FRFTSEVPIR1821LDYHGKHVSM1831DQGTLAGILI1841GLAQLNCSEL
1851-19001851KLKRLSYRHG1861LLGVDKLFSY1871AITEWLNDIK1881KNQLPGILGG1891VGPMHSLVQL
1901-19501901VQGLKDLVWL1911PIEQYRKDGR1921IVRGFQRGAA1931SFGTSTAMAA1941LELTNRMVQT
1951-20001951IQAAAETAYD1961MVSPGTLSIE1971PKKTKRFPHH1981RLAHQPVDLR1991EGVAKAYSVV
2001-20502001KEGITDTAQT2011IYETAAREHE2021SRGVTGAVGE2031VLRQIPPAVV2041KPLIVATEAT
2051-20782051SNVLGGMRNQ2061IRPDVRQDES2071QKWRHGDD
Palmitoylation Sites Details
| Position | Sources | Domains | Experimental PMIDs |
|---|---|---|---|
| 14 | Prediction (Medium) | - | - |
| 55 | Prediction (Low) | - | - |
| 91 | Prediction (Medium) | - | - |
| 131 | Prediction (Medium) | - | - |
| 243 | Prediction (Low) | - | - |
| 546 | Experimental Prediction (Medium) | - | 37611173 |
| 571 | Prediction (Low) | - | - |
| 682 | Prediction (Medium) | - | - |
| 891 | Prediction (Low) | - | - |
| 1597 | Prediction (Medium) | - | - |
| 1625 | Experimental | Autophagy-related protein 2 | 37611173 |
| 1629 | Experimental | Autophagy-related protein 2 | 37611173 |
| 1667 | Prediction (High) | - | - |
| 1688 | Prediction (Low) | - | - |
| 1698 | Prediction (Low) | - | - |
| 1699 | Prediction (Medium) | - | - |
| 1750 | Prediction (Medium) | - | - |
| 1847 | Prediction (High) | - | - |
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 |
|---|---|---|---|---|---|
| 14 | C → Afs*17 | 0.002427 | DEL | Frame Shift Del | BLCA |
| 107 | R → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 131 | C → C | 0.002288 | SNP | Silent | STAD |
| 343 | S → C | 0.010870 | SNP | Missense Mutation | ACC |
| 753 | S → C | 0.002427 | SNP | Missense Mutation | BLCA |
| 755 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 770 | W → C | 0.001014 | SNP | Missense Mutation | BRCA |
| 826 | F → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1043 | S → C | 0.003460 | SNP | Missense Mutation | CESC |
| 1094 | F → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1238 | F → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1308 | R → C | 0.002141 | SNP | Missense Mutation | SKCM |
| 1340 | S → C | 0.002294 | SNP | Missense Mutation | OV |
| 1362 | Y → C | 0.002033 | SNP | Missense Mutation | LUSC |
| 1547 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1622 | Y → C | 0.005618 | SNP | Missense Mutation | PAAD |
| 1625 | C → Y | 0.001887 | SNP | Missense Mutation | UCEC |
| 1653 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1662 | F → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 1688 | C → Y | 0.001887 | SNP | Missense Mutation | UCEC |
| 2074 | R → C | 0.001887 | SNP | Missense Mutation | UCEC |
| 2074 | R → C | 0.005435 | SNP | Missense Mutation | ESCA |