KEGG   Homo sapiens (human): 3916
Entry
3916              CDS       T01001                                 
Symbol
LAMP1, CD107a, LAMPA, LGP120
Name
(RefSeq) lysosomal associated membrane protein 1
  KO
K06528  lysosomal-associated membrane protein 1/2
Organism
hsa  Homo sapiens (human)
Pathway
hsa03272  Virion - Hepatitis viruses
hsa03273  Virion - Lassa virus and SFTS virus
hsa04140  Autophagy - animal
hsa04142  Lysosome
hsa04145  Phagosome
hsa05152  Tuberculosis
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09125 Information processing in viruses
   03273 Virion - Lassa virus and SFTS virus
    3916 (LAMP1)
   03272 Virion - Hepatitis viruses
    3916 (LAMP1)
 09140 Cellular Processes
  09141 Transport and catabolism
   04145 Phagosome
    3916 (LAMP1)
   04142 Lysosome
    3916 (LAMP1)
   04140 Autophagy - animal
    3916 (LAMP1)
 09160 Human Diseases
  09171 Infectious disease: bacterial
   05152 Tuberculosis
    3916 (LAMP1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    3916 (LAMP1)
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:hsa04147]
    3916 (LAMP1)
   04090 CD molecules [BR:hsa04090]
    3916 (LAMP1)
Membrane trafficking [BR:hsa04131]
 Endosome - Lysosome transport
  Others
   Lysosomal membrane proteins
    3916 (LAMP1)
 Autophagy
  Chaperone mediated autophagy (CMA)
   Cargo receptors
    3916 (LAMP1)
  Other autophagy associated proteins
   RNautophagy/DNautophagy
    3916 (LAMP1)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of hepatic cells
   3916 (LAMP1)
CD molecules [BR:hsa04090]
 Proteins
  3916 (LAMP1)
SSDB
Motif
Pfam: Lamp2-like_luminal Lamp2_2nd
Other DBs
NCBI-GeneID: 3916
NCBI-ProteinID: NP_005552
OMIM: 153330
HGNC: 6499
Ensembl: ENSG00000185896
UniProt: P11279
Structure
LinkDB
Position
13:113297239..113323672
AA seq 417 aa
MAAPGSARRPLLLLLLLLLLGLMHCASAAMFMVKNGNGTACIMANFSAAFSVNYDTKSGP
KNMTFDLPSDATVVLNRSSCGKENTSDPSLVIAFGRGHTLTLNFTRNATRYSVQLMSFVY
NLSDTHLFPNASSKEIKTVESITDIRADIDKKYRCVSGTQVHMNNVTVTLHDATIQAYLS
NSSFSRGETRCEQDRPSPTTAPPAPPSPSPSPVPKSPSVDKYNVSGTNGTCLLASMGLQL
NLTYERKDNTTVTRLLNINPNKTSASGSCGAHLVTLELHSEGTTVLLFQFGMNASSSRFF
LQGIQLNTILPDARDPAFKAANGSLRALQATVGNSYKCNAEEHVRVTKAFSVNIFKVWVQ
AFKVEGGQFGSVEECLLDENSMLIPIAVGGALAGLVLIVLIAYLVGRKRSHAGYQTI
NT seq 1254 nt   +upstreamnt  +downstreamnt
atggcggcccccggcagcgcccggcgacccctgctgctgctactgctgttgctgctgctc
ggcctcatgcattgtgcgtcagcagcaatgtttatggtgaaaaatggcaacgggaccgcg
tgcataatggccaacttctctgctgccttctcagtgaactacgacaccaagagtggccct
aagaacatgacctttgacctgccatcagatgccacagtggtgctcaaccgcagctcctgt
ggaaaagagaacacttctgaccccagtctcgtgattgcttttggaagaggacatacactc
actctcaatttcacgagaaatgcaacacgttacagcgtccagctcatgagttttgtttat
aacttgtcagacacacaccttttccccaatgcgagctccaaagaaatcaagactgtggaa
tctataactgacatcagggcagatatagataaaaaatacagatgtgttagtggcacccag
gtccacatgaacaacgtgaccgtaacgctccatgatgccaccatccaggcgtacctttcc
aacagcagcttcagccggggagagacacgctgtgaacaagacaggccttccccaaccaca
gcgccccctgcgccacccagcccctcgccctcacccgtgcccaagagcccctctgtggac
aagtacaacgtgagcggcaccaacgggacctgcctgctggccagcatggggctgcagctg
aacctcacctatgagaggaaggacaacacgacggtgacaaggcttctcaacatcaacccc
aacaagacctcggccagcgggagctgcggcgcccacctggtgactctggagctgcacagc
gagggcaccaccgtcctgctcttccagttcgggatgaatgcaagttctagccggtttttc
ctacaaggaatccagttgaatacaattcttcctgacgccagagaccctgcctttaaagct
gccaacggctccctgcgagcgctgcaggccacagtcggcaattcctacaagtgcaacgcg
gaggagcacgtccgtgtcacgaaggcgttttcagtcaatatattcaaagtgtgggtccag
gctttcaaggtggaaggtggccagtttggctctgtggaggagtgtctgctggacgagaac
agcatgctgatccccatcgctgtgggtggtgccctggcggggctggtcctcatcgtcctc
atcgcctacctcgtcggcaggaagaggagtcacgcaggctaccagactatctag

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