KEGG   Homo sapiens (human): 84706
Entry
84706             CDS       T01001                                 
Symbol
GPT2, ALT2, GPT_2, MRT49, NEDSPM
Name
(RefSeq) glutamic--pyruvic transaminase 2
  KO
K00814  alanine transaminase [EC:2.6.1.2]
Organism
hsa  Homo sapiens (human)
Pathway
hsa00220  Arginine biosynthesis
hsa00250  Alanine, aspartate and glutamate metabolism
hsa01100  Metabolic pathways
hsa01200  Carbon metabolism
hsa01210  2-Oxocarboxylic acid metabolism
hsa01230  Biosynthesis of amino acids
Disease
H00768  Autosomal recessive intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09105 Amino acid metabolism
   00250 Alanine, aspartate and glutamate metabolism
    84706 (GPT2)
   00220 Arginine biosynthesis
    84706 (GPT2)
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   01007 Amino acid related enzymes [BR:hsa01007]
    84706 (GPT2)
Enzymes [BR:hsa01000]
 2. Transferases
  2.6  Transferring nitrogenous groups
   2.6.1  Transaminases
    2.6.1.2  alanine transaminase
     84706 (GPT2)
Amino acid related enzymes [BR:hsa01007]
 Aminotransferase (transaminase)
  Class I
   84706 (GPT2)
SSDB
Motif
Pfam: Aminotran_1_2
Other DBs
NCBI-GeneID: 84706
NCBI-ProteinID: NP_597700
OMIM: 138210
HGNC: 18062
Ensembl: ENSG00000166123
UniProt: Q8TD30
Structure
Position
16:46884362..46931289
AA seq 523 aa
MQRAAALVRRGCGPRTPSSWGRSQSSAAAEASAVLKVRPERSRRERILTLESMNPQVKAV
EYAVRGPIVLKAGEIELELQRGIKKPFTEVIRANIGDAQAMGQQPITFLRQVMALCTYPN
LLDSPSFPEDAKKRARRILQACGGNSLGSYSASQGVNCIREDVAAYITRRDGGVPADPDN
IYLTTGASDGISTILKILVSGGGKSRTGVMIPIPQYPLYSAVISELDAIQVNYYLDEENC
WALNVNELRRAVQEAKDHCDPKVLCIINPGNPTGQVQSRKCIEDVIHFAWEEKLFLLADE
VYQDNVYSPDCRFHSFKKVLYEMGPEYSSNVELASFHSTSKGYMGECGYRGGYMEVINLH
PEIKGQLVKLLSVRLCPPVSGQAAMDIVVNPPVAGEESFEQFSREKESVLGNLAKKAKLT
EDLFNQVPGIHCNPLQGAMYAFPRIFIPAKAVEAAQAHQMAPDMFYCMKLLEETGICVVP
GSGFGQREGTYHFRMTILPPVEKLKTVLQKVKDFHINFLEKYA
NT seq 1572 nt   +upstreamnt  +downstreamnt
atgcagcgggcggcggcgctggtccggcggggctgtggtccccggacccccagctcctgg
ggccgcagccagagcagcgcggccgccgaggcctcggcggtgctcaaggtgcggcccgag
cgcagccggcgcgagcgcatcctcacgctggagtccatgaacccgcaggtgaaggcggtg
gagtacgccgtgcggggacccatcgtgctcaaggccggcgagatcgagctcgagctgcag
cggggtatcaaaaagccattcacagaggtcatccgagccaacatcggggacgcccaggct
atggggcagcagccaatcaccttcctccggcaggtgatggcactatgcacctacccaaac
ctgctggacagccccagcttcccagaagatgctaagaaacgtgcccggcggatcctgcag
gcttgtggcgggaacagcctggggtcctacagtgctagccagggtgtcaactgcatccgt
gaagatgtggctgcctacatcaccaggagggatggcggtgtgcctgcggaccccgacaac
atctacctgaccacgggagctagtgacggcatttctacgatcctgaagatcctcgtctcc
gggggcggcaagtcacggacaggtgtgatgatccccatcccacaatatcccctctattca
gctgtcatctctgagctcgacgccatccaggtgaattactacctggacgaggagaactgc
tgggcgctgaatgtgaatgagctccggcgggcggtgcaggaggccaaagaccactgtgat
cctaaggtgctctgcataatcaaccctgggaaccccacaggccaggtacaaagcagaaag
tgcatagaagatgtgatccactttgcctgggaagagaagctctttctcctggctgatgag
gtgtaccaggacaacgtgtactctccagattgcagattccactccttcaagaaggtgctg
tacgagatggggcccgagtactccagcaacgtggagctcgcctccttccactccacctcc
aagggctacatgggcgagtgtggttacagaggaggctacatggaggtgatcaacctgcac
cctgagatcaagggccagctggtgaagctgctgtcggtgcgcctgtgccccccagtgtct
gggcaggccgccatggacattgtcgtgaaccccccggtggcaggagaggagtcctttgag
caattcagccgagagaaggagtcggtcctgggtaatctggccaaaaaagcaaagctgacg
gaagacctgtttaaccaagtcccaggaattcactgcaaccccttgcagggggccatgtac
gccttccctcggatcttcattcctgccaaagctgtggaggctgctcaggcccatcaaatg
gctccagacatgttctactgcatgaagctcctggaggagactggcatctgtgtcgtgccc
ggcagtggctttgggcagagggaaggcacttaccacttcaggatgactatcctccctcca
gtggagaagctgaaaacggtgctgcagaaggtgaaagacttccacatcaacttcctggag
aagtacgcgtga

  All links  
Disease (2)   
   OMIM (2)   
Gene (22)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (11)   
   OC (1)   
Protein sequence (17)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (15)   
DNA sequence (35)   
   RefSeq(nuc) (15)   
   GenBank (10)   
   EMBL (10)   
3D Structure (1)   
   PDB (1)   
Protein domain (1)   
   Pfam (1)   
All databases (78)   

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