KEGG   Homo sapiens (human): 206358
Entry
206358            CDS       T01001                                 
Symbol
SLC36A1, Dct1, LYAAT1, PAT1, TRAMD3
Name
(RefSeq) proton-coupled amino acid transporter 1 isoform a
  KO
K14209  solute carrier family 36 (proton-coupled amino acid transporter)
Organism
hsa  Homo sapiens (human)
Pathway
hsa04142  Lysosome
hsa04974  Protein digestion and absorption
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09141 Transport and catabolism
   04142 Lysosome
    206358 (SLC36A1)
 09150 Organismal Systems
  09154 Digestive system
   04974 Protein digestion and absorption
    206358 (SLC36A1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    206358 (SLC36A1)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    206358 (SLC36A1)
Membrane trafficking [BR:hsa04131]
 Autophagy
  Other autophagy associated proteins
   Others
    206358 (SLC36A1)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC36: Proton-coupled amino acid transporter
   206358 (SLC36A1)
SSDB
Motif
Pfam: Aa_trans Sld3_STD
Other DBs
NCBI-GeneID: 206358
NCBI-ProteinID: NP_510968
OMIM: 606561
HGNC: 18761
Ensembl: ENSP00000243389.3
UniProt: Q7Z2H8
Position
5:151344596..151556085
AA seq 476 aa
MSTQRLRNEDYHDYSSTDVSPEESPSEGLNNLSSPGSYQRFGQSNSTTWFQTLIHLLKGN
IGTGLLGLPLAVKNAGIVMGPISLLIIGIVAVHCMGILVKCAHHFCRRLNKSFVDYGDTV
MYGLESSPCSWLRNHAHWGRRVVDFFLIVTQLGFCCVYFVFLADNFKQVIEAANGTTNNC
HNNETVILTPTMDSRLYMLSFLPFLVLLVFIRNLRALSIFSLLANITMLVSLVMIYQFIV
QRIPDPSHLPLVAPWKTYPLFFGTAIFSFEGIGMVLPLENKMKDPRKFPLILYLGMVIVT
ILYISLGCLGYLQFGANIQGSITLNLPNCWLYQSVKLLYSIGIFFTYALQFYVPAEIIIP
FFVSRAPEHCELVVDLFVRTVLVCLTCILAILIPRLDLVISLVGSVSSSALALIIPPLLE
VTTFYSEGMSPLTIFKDALISILGFVGFVVGTYEALYELIQPSNAPIFINSTCAFI
NT seq 1431 nt   +upstreamnt  +downstreamnt
atgtccacgcagagacttcggaatgaagactaccacgactacagctccacggacgtgagc
cctgaggagagcccgtcggaaggcctcaacaacctctcctccccgggctcctaccagcgc
tttggtcaaagcaatagcacaacatggttccagaccttgatccacctgttaaaaggcaac
attggcacaggactcctgggactccctctggcggtgaaaaatgcaggcatcgtgatgggt
cccatcagcctgctgatcataggcatcgtggccgtgcactgcatgggtatcctggtgaaa
tgtgctcaccacttctgccgcaggctgaataaatcctttgtggattatggtgatactgtg
atgtatggactagaatccagcccctgctcctggctccggaaccacgcacactggggaaga
cgtgttgtggacttcttcctgattgtcacccagctgggattctgctgtgtctattttgtg
tttctggctgacaactttaaacaggtgatagaagcggccaatgggaccaccaataactgc
cacaacaatgagacggtgattctgacgcctaccatggactcgcgactctacatgctctcc
ttcctgcccttcctggtgctgctggttttcatcaggaacctccgagccctgtccatcttc
tccctgttggccaacatcaccatgctggtcagcttggtcatgatctaccagttcattgtt
cagaggatcccagaccccagccacctccccttggtggccccttggaagacctaccctctc
ttctttggcacagcgattttttcatttgaaggcattggaatggttctgcccctggaaaac
aaaatgaaggatcctcggaagttcccactcatcctgtacctgggcatggtcatcgtcacc
atcctctacatcagcctggggtgtctggggtacctgcaatttggagctaatatccaaggc
agcataaccctcaacctgcccaactgctggttgtaccagtcagttaagctgctgtactcc
atcgggatctttttcacctacgcactccagttctacgtcccggctgagatcatcatcccc
ttctttgtgtcccgagcgcccgagcactgtgagttagtggtggacctgtttgtgcgcaca
gtgctggtctgcctgacatgcatcttggccatcctcatcccccgcctggacctggtcatc
tccctggtgggctccgtgagcagcagcgccctggccctcatcatcccaccgctcctggag
gtcaccaccttctactcagagggcatgagccccctcaccatctttaaggacgccctgatc
agcatcctgggcttcgtgggctttgtggtggggacctatgaggctctctatgagctgatc
cagccaagcaatgctcccatcttcatcaattccacctgtgccttcatatag

  All links  
Disease (1)   
   OMIM (1)   
Gene (16)   
   RefGene (11)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (52)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (50)   
DNA sequence (84)   
   RefSeq(nuc) (50)   
   GenBank (17)   
   EMBL (17)   
Protein domain (2)   
   Pfam (2)   
All databases (155)   

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