KEGG   Cervus canadensis (wapiti): 122439923
Entry
122439923         CDS       T07554                                 
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
  KO
K05862  voltage-dependent anion channel protein 1
Organism
ccad  Cervus canadensis (wapiti)
Pathway
ccad04020  Calcium signaling pathway
ccad04022  cGMP-PKG signaling pathway
ccad04217  Necroptosis
ccad04218  Cellular senescence
ccad04613  Neutrophil extracellular trap formation
ccad04621  NOD-like receptor signaling pathway
ccad04979  Cholesterol metabolism
ccad05010  Alzheimer disease
ccad05012  Parkinson disease
ccad05014  Amyotrophic lateral sclerosis
ccad05016  Huntington disease
ccad05017  Spinocerebellar ataxia
ccad05020  Prion disease
ccad05022  Pathways of neurodegeneration - multiple diseases
ccad05164  Influenza A
ccad05166  Human T-cell leukemia virus 1 infection
ccad05208  Chemical carcinogenesis - reactive oxygen species
ccad05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ccad00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    122439923 (VDAC1)
   04022 cGMP-PKG signaling pathway
    122439923 (VDAC1)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    122439923 (VDAC1)
   04218 Cellular senescence
    122439923 (VDAC1)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    122439923 (VDAC1)
   04621 NOD-like receptor signaling pathway
    122439923 (VDAC1)
  09154 Digestive system
   04979 Cholesterol metabolism
    122439923 (VDAC1)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    122439923 (VDAC1)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    122439923 (VDAC1)
   05164 Influenza A
    122439923 (VDAC1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122439923 (VDAC1)
   05012 Parkinson disease
    122439923 (VDAC1)
   05014 Amyotrophic lateral sclerosis
    122439923 (VDAC1)
   05016 Huntington disease
    122439923 (VDAC1)
   05017 Spinocerebellar ataxia
    122439923 (VDAC1)
   05020 Prion disease
    122439923 (VDAC1)
   05022 Pathways of neurodegeneration - multiple diseases
    122439923 (VDAC1)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    122439923 (VDAC1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ccad03029]
    122439923 (VDAC1)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:ccad04040]
    122439923 (VDAC1)
Mitochondrial biogenesis [BR:ccad03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    122439923 (VDAC1)
Ion channels [BR:ccad04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   122439923 (VDAC1)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 122439923
NCBI-ProteinID: XP_043321444
LinkDB
Position
4:62948418..62978847
AA seq 283 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggctgtgcctcccacgtatgctgatcttggcaaatctgccagggatgtcttcacaaag
ggctatggatttggcttaataaaacttgatctgaaaacaaaatccgagaatggattggaa
tttacgagctcaggttcagccaacactgagaccaccaaagtgacgggcagcctggaaacc
aagtacagatggactgaatatggcctgacgtttacagagaaatggaacacggacaacacg
ctgggcacggagatcactgtggaggaccagcttgcgcgtggcctgaagctgaccttcgat
tcatccttctcaccaaacactgggaaaaaaaacgctaaaattaagacagggtacaagcgg
gaacatatcaacctgggctgtgacgtggattttgatatagccggtccttccatccggggc
gctctggtgctgggttatgaaggctggctggctggctaccagatgaattttgagaccgca
aagtctcgagtgactcagagcaactttgcggttggctacaagaccgatgagttccagctt
cacactaatgtaaatgatggaacagagtttggtggctccatttatcagaaggtgaacaag
aagctggagactgctgttaatctggcctggacagcaggaaacagtaacactcgcttcgga
atagcagccaagtaccagattgacccagacgcctgcttctcggctaaagtgaacaactcc
agcctgataggattaggatatactcagaccctaaagccaggtatcaaactgacactgtcg
gctctgctggatggcaagaatgtcaatgctggtggccacaagcttggtctaggactggag
tttcaagcataa

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