KEGG   Acinonyx jubatus (cheetah): 106984918
Entry
106984918         CDS       T04657                                 
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
  KO
K05862  voltage-dependent anion channel protein 1
Organism
aju  Acinonyx jubatus (cheetah)
Pathway
aju04020  Calcium signaling pathway
aju04022  cGMP-PKG signaling pathway
aju04217  Necroptosis
aju04218  Cellular senescence
aju04613  Neutrophil extracellular trap formation
aju04621  NOD-like receptor signaling pathway
aju04979  Cholesterol metabolism
aju05010  Alzheimer disease
aju05012  Parkinson disease
aju05014  Amyotrophic lateral sclerosis
aju05016  Huntington disease
aju05017  Spinocerebellar ataxia
aju05020  Prion disease
aju05022  Pathways of neurodegeneration - multiple diseases
aju05164  Influenza A
aju05166  Human T-cell leukemia virus 1 infection
aju05208  Chemical carcinogenesis - reactive oxygen species
aju05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:aju00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    106984918
   04022 cGMP-PKG signaling pathway
    106984918
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    106984918
   04218 Cellular senescence
    106984918
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    106984918
   04621 NOD-like receptor signaling pathway
    106984918
  09154 Digestive system
   04979 Cholesterol metabolism
    106984918
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    106984918
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    106984918
   05164 Influenza A
    106984918
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    106984918
   05012 Parkinson disease
    106984918
   05014 Amyotrophic lateral sclerosis
    106984918
   05016 Huntington disease
    106984918
   05017 Spinocerebellar ataxia
    106984918
   05020 Prion disease
    106984918
   05022 Pathways of neurodegeneration - multiple diseases
    106984918
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    106984918
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:aju03029]
    106984918
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:aju04040]
    106984918
Mitochondrial biogenesis [BR:aju03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    106984918
Ion channels [BR:aju04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   106984918
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 106984918
NCBI-ProteinID: XP_026932497
UniProt: A0A6J2AT46
LinkDB
Position
A1:complement(109510643..109537977)
AA seq 283 aa
MAVPPTYADLGKCARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggctgtgcctcccacgtatgctgatcttggcaaatgtgccagggatgtcttcaccaag
ggttatggatttggcttaatcaaacttgatttgaagacaaaatctgagaatggactggaa
tttacgagctcaggttctgccaacactgagaccaccaaagtgacgggcagtctggaaacc
aagtacagatggactgaatacggtctgacgtttacggagaaatggaacactgacaacaca
ttaggcacagagattactgtggaggatcagcttgcacgtggactgaagctgacctttgat
tcatccttctcaccaaacacagggaaaaaaaatgctaaaatcaagacagggtataagcgg
gagcacatcaacctgggctgtgacgtggatttcgacatcgccggcccttcgatccggggc
gctctggtactgggctatgagggctggctggctggctaccagatgaattttgagactgca
aagtctcgagtgacccagagcaactttgcagttggctacaagactgacgaattccagctc
cacactaacgtaaacgatgggacagagtttggtggctccatttatcagaaggtgaacaag
aagttagagaccgctgttaatctggcctggacagcaggaaatagtaacactcgctttgga
atagcggccaagtatcagatcgatcctgacgcctgcttctcggctaaagtgaacaactcc
agcctgataggtttaggatacactcagaccctaaagccaggtatcaaactgacgctctca
gctttgctggatggcaagaatgtcaatgctggtggccacaagcttggtctaggactggaa
tttcaggcataa

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