KEGG   Homo sapiens (human): 29928
Entry
29928             CDS       T01001                                 
Symbol
TIMM22, COXPD43, TEX4, TIM22
Name
(RefSeq) translocase of inner mitochondrial membrane 22
  KO
K17790  mitochondrial import inner membrane translocase subunit TIM22
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
   03029 Mitochondrial biogenesis [BR:hsa03029]
    29928 (TIMM22)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    29928 (TIMM22)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial protein import machinery
  Inner mambrane
   TIM22 complex
    29928 (TIMM22)
Transporters [BR:hsa02000]
 Other transporters
  Primary active transporters [TC:3]
   29928 (TIMM22)
SSDB
Motif
Pfam: Tim17
Other DBs
NCBI-GeneID: 29928
NCBI-ProteinID: NP_037469
OMIM: 607251
HGNC: 17317
Ensembl: ENSG00000177370
UniProt: Q9Y584
Structure
Position
17:997129..1003671
AA seq 194 aa
MAAAAPNAGGSAPETAGSAEAPLQYSLLLQYLVGDKRQPRLLEPGSLGGIPSPAKSEEQK
MIEKAMESCAFKAALACVGGFVLGGAFGVFTAGIDTNVGFDPKDPYRTPTAKEVLKDMGQ
RGMSYAKNFAIVGAMFSCTECLIESYRGTSDWKNSVISGCITGGAIGFRAGLKAGAIGCG
GFAAFSAAIDYYLR
NT seq 585 nt   +upstreamnt  +downstreamnt
atggcggcggccgcccccaatgccggaggctcggcccctgagacagcgggttccgccgaa
gctccgctgcagtacagcctgctcctgcagtacctggtgggtgacaagcgtcagccccgg
ctcctggagcctgggagcctgggcgggatcccaagtccagccaagagtgaggagcagaag
atgatcgagaaggcgatggaaagctgcgctttcaaggctgcgctggcctgcgtgggagga
tttgtcttaggaggtgcatttggggtgtttaccgctggcatcgataccaacgtgggcttt
gaccctaaggatccttaccgtacaccgactgcaaaagaagtgctgaaagacatggggcag
agaggaatgtcctatgccaaaaatttcgccattgtgggagccatgttttcttgtactgag
tgtttgatagaatcttaccggggaacatcagactggaagaacagtgtcatcagtggctgc
atcacgggaggagctattggtttcagagctggcttaaaggctggggccattggttgtgga
ggttttgctgctttctctgctgcgattgattattacctccggtga

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