KEGG   Homo sapiens (human): 84705
Entry
84705             CDS       T01001                                 
Symbol
GTPBP3, COXPD23, GTPBG3, MSS1, MTGP1, THDF1
Name
(RefSeq) 5-taurinomethyluridine-[tRNA] synthase subunit GTPB3, mitochondrial isoform V
  KO
K03650  tRNA modification GTPase [EC:3.6.-.-]
Organism
hsa  Homo sapiens (human)
Disease
H00891  Combined oxidative phosphorylation deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03016 Transfer RNA biogenesis [BR:hsa03016]
    84705 (GTPBP3)
Transfer RNA biogenesis [BR:hsa03016]
 Eukaryotic type
  tRNA modification factors
   Other tRNA modification factors
    84705 (GTPBP3)
 Prokaryotic type
   Methyltransferases
    84705 (GTPBP3)
SSDB
Motif
Pfam: MnmE_helical TrmE_N MMR_HSR1 Dynamin_N FeoB_N AAA_28 AAA_18 NTPase_P4 MCM RuvB_N SRPRB AAA_16
Other DBs
NCBI-GeneID: 84705
NCBI-ProteinID: NP_116009
OMIM: 608536
HGNC: 14880
Ensembl: ENSP00000313818.7
UniProt: Q969Y2
Position
19:17334982..17342731
AA seq 492 aa
MWRGLWTLAAQAARGPRRLCTRRSSGAPAPGSGATIFALSSGQGRCGIAVIRTSGPASGH
ALRILTAPRDLPLARHASLRLLSDPRSGEPLDRALVLWFPGPQSFTGEDCVEFHVHGGPA
VVSGVLQALGSVPGLRPAEAGEFTRRAFANGKLNLTEVEGLADLIHAETEAQRRQALRQL
DGELGHLCRGWAETLTKALAHVEAYIDFGEDDNLEEGVLEQADIEVRALQVALGAHLRDA
RRGQRLRSGVHVVVTGPPNAGKSSLVNLLSRKPVSIVSPEPGTTRDVLETPVDLAGFPVL
LSDTAGLREGVGPVEQEGVRRARERLEQADLILAMLDASDLASPSSCNFLATVVASVGAQ
SPSDSSQRLLLVLNKSDLLSPEGPGPGPDLPPHLLLSCLTGEGLDGLLEALRKELAAVCG
DPSTDPPLLTRARHQHHLQGCLDALGHYKQSKDLALAAEALRVARGHLTRLTGGGGTEEI
LDIIFQDFCVGK
NT seq 1479 nt   +upstreamnt  +downstreamnt
atgtggcgggggctttggaccctggcggcccaagcggcacgtgggcctcgcagattgtgc
acgcgccggagcagcggcgcaccagcccccggctccggcgccaccatcttcgcgctaagc
tctggccaaggccgctgcggcatcgcagtgatccggaccagcggccccgccagcggccac
gccctccgaattctcacagcaccccgagacctgccccttgctcgccacgccagcctgcgc
ctgctcagcgatccccgctccggggagcctctggaccgcgcactggtgctctggttccca
ggtccccagagtttcaccggtgaggactgcgtggagttccacgtgcatggaggcccggca
gtggtgagcggcgtcctgcaggccttgggcagcgtgccagggcttcgaccggcggaggca
ggcgagttcaccagacgggcgttcgccaatgggaagctgaacctgaccgaagtggagggg
ctggcggaccttatccacgcggaaacagaggcgcagcggcggcaggccctcaggcagctg
gacggagagctgggccacctctgccgtggctgggccgagaccctcaccaaagctctggcc
cacgtggaggcctatatcgatttcggcgaggatgacaacctggaggagggggtcctggag
caagccgacatcgaagtacgggcactgcaggtggccctgggtgcacatctacgagatgcc
aggcgcgggcagaggctccgctcaggggtgcacgtagtggtcactggaccccccaatgcg
ggcaagagcagcctagtgaacctgctcagtcggaagcctgtgtccatcgtgtccccggag
ccagggaccacccgtgacgtgctggagaccccagtcgacctggccggatttcctgtgctg
ctgagcgacacggctgggttgcgggagggcgtggggcccgtggagcaggagggcgtgcgg
cgcgcccgggagaggctagagcaggctgacctcattctggccatgctggatgcttctgac
ctggcctctccctccagttgcaacttcctggccaccgtcgtagcctctgtgggagcccag
agccccagtgacagcagccagcgcctcctcctggtgctgaacaagtcggacctgctgtcc
ccggagggcccaggtcccggtcctgacctgcccccgcacctgctgctgtcctgtctgacg
ggagaggggctggacggcctcctggaggcgctgaggaaggagctagctgcagtgtgtggg
gacccgtccacagatcccccgctgctgacccgagcaaggcaccagcaccacctccagggt
tgcctggatgccctcggccactacaagcagtcaaaagacctggccctggcggcagaggcg
ctgcgggtggcccggggtcacctgacccggctcacaggtggagggggtaccgaggagatc
ctggacatcatcttccaggacttctgtgtgggcaagtga

  All links  
Disease (2)   
   OMIM (2)   
Gene (12)   
   RefGene (5)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (6)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (4)   
DNA sequence (46)   
   RefSeq(nuc) (4)   
   GenBank (21)   
   EMBL (21)   
Protein domain (12)   
   Pfam (12)   
All databases (78)   

Download RDF
DBGET integrated database retrieval system