KEGG   Mustela nigripes (black-footed ferret): 132028515
Entry
132028515         CDS       T09425                                 
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1 isoform X1
  KO
K05862  voltage-dependent anion channel protein 1
Organism
mnp  Mustela nigripes (black-footed ferret)
Pathway
mnp04020  Calcium signaling pathway
mnp04022  cGMP-PKG signaling pathway
mnp04217  Necroptosis
mnp04218  Cellular senescence
mnp04613  Neutrophil extracellular trap formation
mnp04621  NOD-like receptor signaling pathway
mnp04979  Cholesterol metabolism
mnp05010  Alzheimer disease
mnp05012  Parkinson disease
mnp05014  Amyotrophic lateral sclerosis
mnp05016  Huntington disease
mnp05017  Spinocerebellar ataxia
mnp05020  Prion disease
mnp05022  Pathways of neurodegeneration - multiple diseases
mnp05164  Influenza A
mnp05166  Human T-cell leukemia virus 1 infection
mnp05208  Chemical carcinogenesis - reactive oxygen species
mnp05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:mnp00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    132028515 (VDAC1)
   04022 cGMP-PKG signaling pathway
    132028515 (VDAC1)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    132028515 (VDAC1)
   04218 Cellular senescence
    132028515 (VDAC1)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    132028515 (VDAC1)
   04621 NOD-like receptor signaling pathway
    132028515 (VDAC1)
  09154 Digestive system
   04979 Cholesterol metabolism
    132028515 (VDAC1)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    132028515 (VDAC1)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    132028515 (VDAC1)
   05164 Influenza A
    132028515 (VDAC1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    132028515 (VDAC1)
   05012 Parkinson disease
    132028515 (VDAC1)
   05014 Amyotrophic lateral sclerosis
    132028515 (VDAC1)
   05016 Huntington disease
    132028515 (VDAC1)
   05017 Spinocerebellar ataxia
    132028515 (VDAC1)
   05020 Prion disease
    132028515 (VDAC1)
   05022 Pathways of neurodegeneration - multiple diseases
    132028515 (VDAC1)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    132028515 (VDAC1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:mnp03029]
    132028515 (VDAC1)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:mnp04040]
    132028515 (VDAC1)
Mitochondrial biogenesis [BR:mnp03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    132028515 (VDAC1)
Ion channels [BR:mnp04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   132028515 (VDAC1)
SSDB
Motif
Pfam: Porin_3 Nsp2_AV
Other DBs
NCBI-GeneID: 132028515
NCBI-ProteinID: XP_059273551
LinkDB
Position
12:complement(71684869..71713818)
AA seq 321 aa
MGGRHACPRARTHLAHVSPHAASFPCPGTRSSHACPHTQCAHAPVAGTESAGSRRWPCLP
RMLILANLPGMSSPRVMEFTSSGSANTETTKVTGSLETKYRWTEYGLTFTEKWNTDNTLG
TEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKREHINLGCDVDFDIAGPSVRGAV
VLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQLHTNVNDGTEFGGSIYQKVNKKL
ETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNSSLIGLGYTQTLKPGIKLTLSAL
LDGKNVNAGGHKLGLGLEFQA
NT seq 966 nt   +upstreamnt  +downstreamnt
atgggcggccggcacgcgtgtccccgcgcacgcacacatcttgcgcacgtcagtcctcac
gccgcctcgttcccgtgcccgggcacacgcagctctcacgcgtgcccgcatacccaatgc
gcacacgcaccggtggcgggcactgagagcgcaggaagcagaagatggccgtgcctccca
cgtatgctgatcttggcaaatctgccagggatgtcttcaccaagggttatggaatttaca
agctcaggttcagccaacactgagaccaccaaagtgacgggcagtctggaaaccaagtac
aggtggaccgaatatggtctgacgtttacagagaaatggaacactgacaacacgctaggc
acagagatcactgtggaagatcagcttgcacgtggactgaagctgacctttgattcatcc
ttctcaccaaacacagggaaaaaaaatgcaaaaatcaagacagggtataagcgggagcac
atcaacctaggctgcgatgtggatttcgacattgccggtccttcagtccggggtgccgtg
gtgctgggctatgaaggctggctggctggctaccagatgaattttgagactgcgaagtct
cgagtgacccagagcaacttcgcggttggctacaagactgacgagttccagctccacact
aatgtaaatgatgggacagagtttggtggctccatttatcagaaggtgaacaagaagtta
gagactgctgtcaatctggcctggactgcaggaaatagtaacactcgctttggaatagca
gccaaatatcagatcgaccctgacgcctgcttctcggctaaagtgaacaactccagcctg
ataggtttaggatacactcagaccctaaagccaggtatcaaactgacgctatcagctctg
ctggatggcaagaatgtcaatgctggcggccacaagcttggtctaggactggaatttcag
gcataa

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