Homo sapiens (human): 6490
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Entry
6490 CDS
T01001
Symbol
PMEL, D12S53E, HMB-45, HMB45, ME20, ME20-M, ME20M, P1, P100, PMEL17, SI, SIL, SILV, gp100
Name
(RefSeq) premelanosome protein
KO
K17304
melanocyte protein PMEL
Organism
hsa
Homo sapiens (human)
Drug target
Tebentafusp:
D12296
<US>
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04147 Exosome [BR:
hsa04147
]
6490 (PMEL)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of melanoma cells
6490 (PMEL)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PKAT_KLD
PKD
PKD_4
Motif
Other DBs
NCBI-GeneID:
6490
NCBI-ProteinID:
NP_008859
OMIM:
155550
HGNC:
10880
Ensembl:
ENSG00000185664
UniProt:
P40967
Structure
PDB
LinkDB
All DBs
Position
12:complement(55954105..55966709)
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AA seq
661 aa
AA seq
DB search
MDLVLKRCLLHLAVIGALLAVGATKVPRNQDWLGVSRQLRTKAWNRQLYPEWTEAQRLDC
WRGGQVSLKVSNDGPTLIGANASFSIALNFPGSQKVLPDGQVIWVNNTIINGSQVWGGQP
VYPQETDDACIFPDGGPCPSGSWSQKRSFVYVWKTWGQYWQVLGGPVSGLSIGTGRAMLG
THTMEVTVYHRRGSRSYVPLAHSSSAFTITDQVPFSVSVSQLRALDGGNKHFLRNQPLTF
ALQLHDPSGYLAEADLSYTWDFGDSSGTLISRALVVTHTYLEPGPVTAQVVLQAAIPLTS
CGSSPVPGTTDGHRPTAEAPNTTAGQVPTTEVVGTTPGQAPTAEPSGTTSVQVPTTEVIS
TAPVQMPTAESTGMTPEKVPVSEVMGTTLAEMSTPEATGMTPAEVSIVVLSGTTAAQVTT
TEWVETTARELPIPEPEGPDASSIMSTESITGSLGPLLDGTATLRLVKRQVPLDCVLYRY
GSFSVTLDIVQGIESAEILQAVPSGEGDAFELTVSCQGGLPKEACMEISSPGCQPPAQRL
CQPVLPSPACQLVLHQILKGGSGTYCLNVSLADTNSLAVVSTQLIMPGQEAGLGQVPLIV
GILLVLMAVVLASLIYRRRLMKQDFSVPQLPHSSSHWLRLPRIFCSCPIGENSPLLSGQQ
V
NT seq
1986 nt
NT seq
+upstream
nt +downstream
nt
atggatctggtgctaaaaagatgccttcttcatttggctgtgataggtgctttgctggct
gtgggggctacaaaagtacccagaaaccaggactggcttggtgtctcaaggcaactcaga
accaaagcctggaacaggcagctgtatccagagtggacagaagcccagagacttgactgc
tggagaggtggtcaagtgtccctcaaggtcagtaatgatgggcctacactgattggtgca
aatgcctccttctctattgccttgaacttccctggaagccaaaaggtattgccagatggg
caggttatctgggtcaacaataccatcatcaatgggagccaggtgtggggaggacagcca
gtgtatccccaggaaactgacgatgcctgcatcttccctgatggtggaccttgcccatct
ggctcttggtctcagaagagaagctttgtttatgtctggaagacctggggccaatactgg
caagttctagggggcccagtgtctgggctgagcattgggacaggcagggcaatgctgggc
acacacaccatggaagtgactgtctaccatcgccggggatcccggagctatgtgcctctt
gctcattccagctcagccttcaccattactgaccaggtgcctttctccgtgagcgtgtcc
cagttgcgggccttggatggagggaacaagcacttcctgagaaatcagcctctgaccttt
gccctccagctccatgaccccagtggctatctggctgaagctgacctctcctacacctgg
gactttggagacagtagtggaaccctgatctctcgggcacttgtggtcactcatacttac
ctggagcctggcccagtcactgcccaggtggtcctgcaggctgccattcctctcacctcc
tgtggctcctccccagttccaggcaccacagatgggcacaggccaactgcagaggcccct
aacaccacagctggccaagtgcctactacagaagttgtgggtactacacctggtcaggcg
ccaactgcagagccctctggaaccacatctgtgcaggtgccaaccactgaagtcataagc
actgcacctgtgcagatgccaactgcagagagcacaggtatgacacctgagaaggtgcca
gtttcagaggtcatgggtaccacactggcagagatgtcaactccagaggctacaggtatg
acacctgcagaggtatcaattgtggtgctttctggaaccacagctgcacaggtaacaact
acagagtgggtggagaccacagctagagagctacctatccctgagcctgaaggtccagat
gccagctcaatcatgtctacggaaagtattacaggttccctgggccccctgctggatggt
acagccaccttaaggctggtgaagagacaagtccccctggattgtgttctgtatcgatat
ggttccttttccgtcaccctggacattgtccagggtattgaaagtgccgagatcctgcag
gctgtgccgtccggtgagggggatgcatttgagctgactgtgtcctgccaaggcgggctg
cccaaggaagcctgcatggagatctcatcgccagggtgccagccccctgcccagcggctg
tgccagcctgtgctacccagcccagcctgccagctggttctgcaccagatactgaagggt
ggctcggggacatactgcctcaatgtgtctctggctgataccaacagcctggcagtggtc
agcacccagcttatcatgcctggtcaagaagcaggccttgggcaggttccgctgatcgtg
ggcatcttgctggtgttgatggctgtggtccttgcatctctgatatataggcgcagactt
atgaagcaagacttctccgtaccccagttgccacatagcagcagtcactggctgcgtcta
ccccgcatcttctgctcttgtcccattggtgagaacagccccctcctcagtgggcagcag
gtctga
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