KEGG   Mustela putorius furo (domestic ferret): 101679422
Entry
101679422         CDS       T07239                                 
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
  KO
K05862  voltage-dependent anion channel protein 1
Organism
mpuf  Mustela putorius furo (domestic ferret)
Pathway
mpuf04020  Calcium signaling pathway
mpuf04022  cGMP-PKG signaling pathway
mpuf04217  Necroptosis
mpuf04218  Cellular senescence
mpuf04613  Neutrophil extracellular trap formation
mpuf04621  NOD-like receptor signaling pathway
mpuf04979  Cholesterol metabolism
mpuf05010  Alzheimer disease
mpuf05012  Parkinson disease
mpuf05014  Amyotrophic lateral sclerosis
mpuf05016  Huntington disease
mpuf05017  Spinocerebellar ataxia
mpuf05020  Prion disease
mpuf05022  Pathways of neurodegeneration - multiple diseases
mpuf05164  Influenza A
mpuf05166  Human T-cell leukemia virus 1 infection
mpuf05208  Chemical carcinogenesis - reactive oxygen species
mpuf05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:mpuf00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    101679422 (VDAC1)
   04022 cGMP-PKG signaling pathway
    101679422 (VDAC1)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    101679422 (VDAC1)
   04218 Cellular senescence
    101679422 (VDAC1)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    101679422 (VDAC1)
   04621 NOD-like receptor signaling pathway
    101679422 (VDAC1)
  09154 Digestive system
   04979 Cholesterol metabolism
    101679422 (VDAC1)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101679422 (VDAC1)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    101679422 (VDAC1)
   05164 Influenza A
    101679422 (VDAC1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101679422 (VDAC1)
   05012 Parkinson disease
    101679422 (VDAC1)
   05014 Amyotrophic lateral sclerosis
    101679422 (VDAC1)
   05016 Huntington disease
    101679422 (VDAC1)
   05017 Spinocerebellar ataxia
    101679422 (VDAC1)
   05020 Prion disease
    101679422 (VDAC1)
   05022 Pathways of neurodegeneration - multiple diseases
    101679422 (VDAC1)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101679422 (VDAC1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:mpuf03029]
    101679422 (VDAC1)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:mpuf04040]
    101679422 (VDAC1)
Mitochondrial biogenesis [BR:mpuf03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    101679422 (VDAC1)
Ion channels [BR:mpuf04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   101679422 (VDAC1)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 101679422
NCBI-ProteinID: XP_004745034
Ensembl: ENSMPUG00000010220
UniProt: M3YFN8
LinkDB
Position
Unknown
AA seq 283 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSVRGAVVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggccgtgcctcccacgtacgctgatcttggcaaatctgccagggatgtcttcaccaag
ggttatggatttggcttaataaaacttgacttgaaaacaaaatctgagaatggactggaa
tttacaagctcaggttcagccaacactgagaccaccaaagtgacgggcagtctggaaacc
aagtacaggtggaccgaatatggtctgacgtttacagagaaatggaacactgacaacacg
ctaggcacagagatcactgtggaagatcagcttgcacgtggactgaagctgacctttgat
tcatccttctcaccaaacacagggaaaaaaaatgcaaaaatcaagacagggtataagcgg
gagcacatcaacctgggctgcgatgtggatttcgacattgccggtccttcagtccggggt
gccgtggtgctgggctatgaaggctggctggctggctaccagatgaattttgagactgcg
aagtctcgagtgacccagagcaacttcgcggttggctacaagactgacgagttccagctc
cacactaatgtaaatgatgggacagagtttggtggctccatttatcagaaggtgaacaag
aagttagagaccgctgtcaatctggcctggactgcaggaaatagtaacactcgctttgga
atagcagccaaatatcagatcgaccctgacgcctgcttctcggctaaagtgaacaactcc
agcctgataggtttaggatacactcagaccctaaagccaggtatcaaactgacgctatca
gctctgctggatggcaagaatgtcaatgctggcggccacaagcttggtctaggactggaa
tttcaggcataa

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