KEGG   Trachypithecus francoisi (Francois's langur): 117098307
Entry
117098307         CDS       T07225                                 
Name
(RefSeq) voltage-dependent anion-selective channel protein 1-like
  KO
K05862  voltage-dependent anion channel protein 1
Organism
tfn  Trachypithecus francoisi (Francois's langur)
Pathway
tfn04020  Calcium signaling pathway
tfn04022  cGMP-PKG signaling pathway
tfn04217  Necroptosis
tfn04218  Cellular senescence
tfn04613  Neutrophil extracellular trap formation
tfn04621  NOD-like receptor signaling pathway
tfn04979  Cholesterol metabolism
tfn05010  Alzheimer disease
tfn05012  Parkinson disease
tfn05014  Amyotrophic lateral sclerosis
tfn05016  Huntington disease
tfn05017  Spinocerebellar ataxia
tfn05020  Prion disease
tfn05022  Pathways of neurodegeneration - multiple diseases
tfn05164  Influenza A
tfn05166  Human T-cell leukemia virus 1 infection
tfn05208  Chemical carcinogenesis - reactive oxygen species
tfn05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:tfn00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    117098307
   04022 cGMP-PKG signaling pathway
    117098307
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    117098307
   04218 Cellular senescence
    117098307
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    117098307
   04621 NOD-like receptor signaling pathway
    117098307
  09154 Digestive system
   04979 Cholesterol metabolism
    117098307
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    117098307
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    117098307
   05164 Influenza A
    117098307
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    117098307
   05012 Parkinson disease
    117098307
   05014 Amyotrophic lateral sclerosis
    117098307
   05016 Huntington disease
    117098307
   05017 Spinocerebellar ataxia
    117098307
   05020 Prion disease
    117098307
   05022 Pathways of neurodegeneration - multiple diseases
    117098307
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    117098307
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:tfn03029]
    117098307
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:tfn04040]
    117098307
Mitochondrial biogenesis [BR:tfn03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    117098307
Ion channels [BR:tfn04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   117098307
SSDB
Motif
Pfam: Porin_3 DUF3007
Other DBs
NCBI-GeneID: 117098307
NCBI-ProteinID: XP_033092589
LinkDB
Position
Unknown
AA seq 148 aa
MDFDIAGSSTQGALVLGYEGWLASYQMNVENAKSRVTQRNSAVGYKTDEFQLHTKVNDRT
EFGSSIYQKVNNKLETTINLAWTAGNSNTSFGIAAKYLIDPDACFSAKVNNSSLRGLRYT
QTLKPGIKLTLSALLDGKNVNAGGHKLG
NT seq 447 nt   +upstreamnt  +downstreamnt
atggattttgacattgctgggtcctcaacccagggtgctctggtgctgggttacgagggc
tggctggccagctaccagatgaatgttgagaatgcaaagtcccgagtgacccagaggaac
agtgcagttggctacaagactgatgaattccagcttcacactaaagtgaacgataggaca
gagtttggcagctccatttaccagaaggtgaacaacaagttggagactactatcaatctc
gcctggacagcaggaaacagcaacactagcttcggaatagcagccaagtatctgatcgac
cccgatgcctgcttctcagctaaagtgaacaactccagcctgagaggtttaagatacact
cagaccctaaagccaggtatcaaactgacactgtcagctctcctggatggcaagaatgtc
aatgctggtggtcacaagcttggttga

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