KEGG   Homo sapiens (human): 9056
Entry
9056              CDS       T01001                                 
Symbol
SLC7A7, LAT3, LPI, MOP-2, Y+LAT1, y+LAT-1
Name
(RefSeq) Y+L amino acid transporter 1
  KO
K13867  solute carrier family 7 (L-type amino acid transporter), member 7
Organism
hsa  Homo sapiens (human)
Pathway
hsa04974  Protein digestion and absorption
Disease
H00899  Lysinuric protein intolerance
H01400  Secondary hyperammonemia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09154 Digestive system
   04974 Protein digestion and absorption
    9056 (SLC7A7)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    9056 (SLC7A7)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC7: Cationic amino acid transporter/glycoprotein-associated
   9056 (SLC7A7)
SSDB
Motif
Pfam: AA_permease_2 AA_permease SirB
Other DBs
NCBI-GeneID: 9056
NCBI-ProteinID: NP_001119577
OMIM: 603593
HGNC: 11065
UniProt: Q9UM01 A0A0S2Z502
Structure
Position
14:complement(22773222..22819791)
AA seq 511 aa
MVDSTEYEVASQPEVETSPLGDGASPGPEQVKLKKEISLLNGVCLIVGNMIGSGIFVSPK
GVLIYSASFGLSLVIWAVGGLFSVFGALCYAELGTTIKKSGASYAYILEAFGGFLAFIRL
WTSLLIIEPTSQAIIAITFANYMVQPLFPSCFAPYAASRLLAAACICLLTFINCAYVKWG
TLVQDIFTYAKVLALIAVIVAGIVRLGQGASTHFENSFEGSSFAVGDIALALYSALFSYS
GWDTLNYVTEEIKNPERNLPLSIGISMPIVTIIYILTNVAYYTVLDMRDILASDAVAVTF
ADQIFGIFNWIIPLSVALSCFGGLNASIVAASRLFFVGSREGHLPDAICMIHVERFTPVP
SLLFNGIMALIYLCVEDIFQLINYYSFSYWFFVGLSIVGQLYLRWKEPDRPRPLKLSVFF
PIVFCLCTIFLVAVPLYSDTINSLIGIAIALSGLPFYFLIIRVPEHKRPLYLRRIVGSAT
RYLQVLCMSVAAEMDLEDGGEMPKQRDPKSN
NT seq 1536 nt   +upstreamnt  +downstreamnt
atggttgacagcactgagtatgaagtggcctcccagcctgaggtggaaacctcccctttg
ggtgatggggccagcccagggccggagcaggtgaagctgaagaaggagatctcactgctt
aacggcgtgtgcctgattgtggggaacatgatcggctcgggcatctttgtttcccccaag
ggtgtgctcatatacagtgcctcctttggtctctctctggtcatctgggctgtcgggggc
ctcttctccgtctttggggccctttgttatgcggaactgggcaccaccattaagaaatct
ggggccagctatgcctatatcctggaggcctttggaggattccttgctttcatcagactc
tggacctccctgctcatcattgagcccaccagccaggccatcattgccatcacctttgcc
aactacatggtacagcctctcttcccgagctgcttcgccccttatgctgccagccgcctg
ctggctgctgcctgcatttgtctcttaaccttcattaactgtgcctatgtcaaatgggga
accctggtacaagatattttcacctatgctaaagtattggcactgatcgcggtcatcgtt
gcaggcattgttagacttggccagggagcctctactcattttgagaattcctttgagggt
tcatcatttgcagtgggtgacattgccctggcactgtactcagctctgttctcctactca
ggctgggacaccctcaactatgtcactgaagagatcaagaatcctgagaggaacctgccc
ctctccattggcatctccatgcccattgtcaccatcatctatatcttgaccaatgtggcc
tattatactgtgctagacatgagagacatcttggccagtgatgctgttgctgtgactttt
gcagatcagatatttggaatatttaactggataattccactgtcagttgcattatcctgt
tttggtggcctcaatgcctccattgtggctgcttctaggcttttctttgtgggctcaaga
gaaggccatctccctgatgccatctgcatgatccatgttgagcggttcacaccagtgcct
tctctgctcttcaatggtatcatggcattgatctacttgtgcgtggaagacatcttccag
ctcattaactactacagcttcagctactggttctttgtggggctttctattgtgggtcag
ctttatctgcgctggaaggagcctgatcgacctcgtcccctcaagctcagcgttttcttc
ccgattgtcttctgcctctgcaccatcttcctggtggctgttccactttacagtgatact
atcaactccctcatcggcattgccattgccctctcaggcctgcccttttacttcctcatc
atcagagtgccagaacataagcgaccgctttacctccgaaggatcgtggggtctgccaca
aggtacctccaggtcctgtgtatgtcagttgctgcagaaatggatttggaagatggagga
gagatgcccaagcaacgggatcccaaatctaactaa

  All links  
Disease (2)   
   OMIM (2)   
Gene (11)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (12)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (9)   
DNA sequence (61)   
   RefSeq(nuc) (9)   
   GenBank (26)   
   EMBL (26)   
3D Structure (5)   
   PDB (5)   
Protein domain (3)   
   Pfam (3)   
All databases (94)   

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