KEGG   Ursus americanus (American black bear): 123790351
Entry
123790351         CDS       T07931                                 
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
  KO
K05862  voltage-dependent anion channel protein 1
Organism
uar  Ursus americanus (American black bear)
Pathway
uar04020  Calcium signaling pathway
uar04022  cGMP-PKG signaling pathway
uar04217  Necroptosis
uar04218  Cellular senescence
uar04613  Neutrophil extracellular trap formation
uar04621  NOD-like receptor signaling pathway
uar04979  Cholesterol metabolism
uar05010  Alzheimer disease
uar05012  Parkinson disease
uar05014  Amyotrophic lateral sclerosis
uar05016  Huntington disease
uar05017  Spinocerebellar ataxia
uar05020  Prion disease
uar05022  Pathways of neurodegeneration - multiple diseases
uar05164  Influenza A
uar05166  Human T-cell leukemia virus 1 infection
uar05208  Chemical carcinogenesis - reactive oxygen species
uar05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:uar00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    123790351 (VDAC1)
   04022 cGMP-PKG signaling pathway
    123790351 (VDAC1)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    123790351 (VDAC1)
   04218 Cellular senescence
    123790351 (VDAC1)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    123790351 (VDAC1)
   04621 NOD-like receptor signaling pathway
    123790351 (VDAC1)
  09154 Digestive system
   04979 Cholesterol metabolism
    123790351 (VDAC1)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    123790351 (VDAC1)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    123790351 (VDAC1)
   05164 Influenza A
    123790351 (VDAC1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    123790351 (VDAC1)
   05012 Parkinson disease
    123790351 (VDAC1)
   05014 Amyotrophic lateral sclerosis
    123790351 (VDAC1)
   05016 Huntington disease
    123790351 (VDAC1)
   05017 Spinocerebellar ataxia
    123790351 (VDAC1)
   05020 Prion disease
    123790351 (VDAC1)
   05022 Pathways of neurodegeneration - multiple diseases
    123790351 (VDAC1)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    123790351 (VDAC1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:uar03029]
    123790351 (VDAC1)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:uar04040]
    123790351 (VDAC1)
Mitochondrial biogenesis [BR:uar03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    123790351 (VDAC1)
Ion channels [BR:uar04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   123790351 (VDAC1)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 123790351
NCBI-ProteinID: XP_045650660
UniProt: A0A452QQM5
LinkDB
Position
Unknown
AA seq 283 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSVRGALVLGYEGWLAGYQMNFETSKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggctgtgcctcccacgtatgctgatcttggcaaatctgccagggatgtcttcaccaag
ggttacggatttggcttaataaaacttgacttgaaaacaaaatctgagaatggactggaa
tttacaagctcaggttcagccaacactgagaccaccaaagtgacgggcagtctagaaacc
aagtacagatggaccgaatatggtttgacgtttacagaaaaatggaacactgacaacaca
ctaggcacagagatcactgtggaagatcagcttgcacgtggactgaagctgacctttgat
tcatccttctcaccaaacacagggaaaaaaaatgctaaaatcaagacagggtataagcgg
gagcacatcaacctgggctgcgacgtggatttcgacattgccggtccttcggtccggggc
gctttggtgctgggctatgaaggctggctggccggctaccagatgaattttgagacttcg
aagtctcgagtgacccagagcaactttgcggttggctacaagactgacgagttccagctc
cacactaacgtaaacgatgggacagagttcggtggctccatttatcagaaggtgaacaag
aagttagagactgctgtcaatctggcctggacagcaggaaatagtaacactcgctttgga
atagcggccaagtatcagatcgaccctgacgcctgcttctcggctaaagtgaacaactcc
agcctgataggtttaggatacactcagaccctaaagccaggtatcaaactgacgctatcg
gctcttctggatggcaagaatgtcaatgctggcggccacaagcttggtctaggactggaa
tttcaggcataa

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