KEGG   Bison bison bison (American bison): 104991863
Entry
104991863         CDS       T08726                                 
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
  KO
K05862  voltage-dependent anion channel protein 1
Organism
bbis  Bison bison bison (American bison)
Pathway
bbis04020  Calcium signaling pathway
bbis04022  cGMP-PKG signaling pathway
bbis04217  Necroptosis
bbis04218  Cellular senescence
bbis04613  Neutrophil extracellular trap formation
bbis04621  NOD-like receptor signaling pathway
bbis04979  Cholesterol metabolism
bbis05010  Alzheimer disease
bbis05012  Parkinson disease
bbis05014  Amyotrophic lateral sclerosis
bbis05016  Huntington disease
bbis05017  Spinocerebellar ataxia
bbis05020  Prion disease
bbis05022  Pathways of neurodegeneration - multiple diseases
bbis05164  Influenza A
bbis05166  Human T-cell leukemia virus 1 infection
bbis05208  Chemical carcinogenesis - reactive oxygen species
bbis05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:bbis00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    104991863 (VDAC1)
   04022 cGMP-PKG signaling pathway
    104991863 (VDAC1)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    104991863 (VDAC1)
   04218 Cellular senescence
    104991863 (VDAC1)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    104991863 (VDAC1)
   04621 NOD-like receptor signaling pathway
    104991863 (VDAC1)
  09154 Digestive system
   04979 Cholesterol metabolism
    104991863 (VDAC1)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    104991863 (VDAC1)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    104991863 (VDAC1)
   05164 Influenza A
    104991863 (VDAC1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    104991863 (VDAC1)
   05012 Parkinson disease
    104991863 (VDAC1)
   05014 Amyotrophic lateral sclerosis
    104991863 (VDAC1)
   05016 Huntington disease
    104991863 (VDAC1)
   05017 Spinocerebellar ataxia
    104991863 (VDAC1)
   05020 Prion disease
    104991863 (VDAC1)
   05022 Pathways of neurodegeneration - multiple diseases
    104991863 (VDAC1)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    104991863 (VDAC1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:bbis03029]
    104991863 (VDAC1)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:bbis04040]
    104991863 (VDAC1)
Mitochondrial biogenesis [BR:bbis03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    104991863 (VDAC1)
Ion channels [BR:bbis04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   104991863 (VDAC1)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 104991863
NCBI-ProteinID: XP_010842822
Ensembl: ENSBBBG00000004884
UniProt: A0A6P3HJ22
LinkDB
Position
Unknown
AA seq 283 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggctgtgcctcccacgtatgctgatcttggcaaatctgccagggatgtcttcaccaag
ggctatggatttggcttaataaaacttgatctgaaaacaaaatctgagaatggactggaa
tttacgagctcaggttcagccaacaccgagaccaccaaagtgacgggcagcctggaaacc
aagtacagatggactgaatatggtctgacgtttacagagaaatggaatactgacaacacg
ctgggcacggagattactgtggaagatcagcttgcacgtgggctgaagctgaccttcgat
tcatccttctcaccaaacactgggaaaaaaaatgctaaaatcaagacagggtacaagcgg
gaacatatcaacctgggctgcgatgtggattttgacatagctggtccttccatccggggc
gctctggtgctgggttatgaaggttggctggctggctaccagatgaattttgagactgca
aagtctcgagtgactcagagcaactttgcagttggctacaagaccgatgagttccagctt
cacactaatgtaaatgatggaacagagtttggtggctccatttatcagaaggtgaacaag
aagttggagaccgctgttaatctggcctggaccgcaggaaacagcaacactcgctttgga
atagcagccaagtaccagattgaccctgatgcctgcttctcggctaaagtgaacaactcc
agcctgataggattaggatatactcagaccctaaagccaggtatcaaactgacactctcg
gctctgctggatggcaagaacgtcaatgctggtggccacaagcttggtctaggactggag
tttcaagcataa

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