KEGG   Rhinopithecus roxellana (golden snub-nosed monkey): 104659812
Entry
104659812         CDS       T03989                                 
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
  KO
K05862  voltage-dependent anion channel protein 1
Organism
rro  Rhinopithecus roxellana (golden snub-nosed monkey)
Pathway
rro04020  Calcium signaling pathway
rro04022  cGMP-PKG signaling pathway
rro04217  Necroptosis
rro04218  Cellular senescence
rro04613  Neutrophil extracellular trap formation
rro04621  NOD-like receptor signaling pathway
rro04979  Cholesterol metabolism
rro05010  Alzheimer disease
rro05012  Parkinson disease
rro05014  Amyotrophic lateral sclerosis
rro05016  Huntington disease
rro05017  Spinocerebellar ataxia
rro05020  Prion disease
rro05022  Pathways of neurodegeneration - multiple diseases
rro05164  Influenza A
rro05166  Human T-cell leukemia virus 1 infection
rro05208  Chemical carcinogenesis - reactive oxygen species
rro05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:rro00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    104659812 (VDAC1)
   04022 cGMP-PKG signaling pathway
    104659812 (VDAC1)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    104659812 (VDAC1)
   04218 Cellular senescence
    104659812 (VDAC1)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    104659812 (VDAC1)
   04621 NOD-like receptor signaling pathway
    104659812 (VDAC1)
  09154 Digestive system
   04979 Cholesterol metabolism
    104659812 (VDAC1)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    104659812 (VDAC1)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    104659812 (VDAC1)
   05164 Influenza A
    104659812 (VDAC1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    104659812 (VDAC1)
   05012 Parkinson disease
    104659812 (VDAC1)
   05014 Amyotrophic lateral sclerosis
    104659812 (VDAC1)
   05016 Huntington disease
    104659812 (VDAC1)
   05017 Spinocerebellar ataxia
    104659812 (VDAC1)
   05020 Prion disease
    104659812 (VDAC1)
   05022 Pathways of neurodegeneration - multiple diseases
    104659812 (VDAC1)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    104659812 (VDAC1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:rro03029]
    104659812 (VDAC1)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:rro04040]
    104659812 (VDAC1)
Mitochondrial biogenesis [BR:rro03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    104659812 (VDAC1)
Ion channels [BR:rro04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   104659812 (VDAC1)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 104659812
NCBI-ProteinID: XP_010358255
UniProt: A0A2K6NQM2
LinkDB
Position
3:complement(150546157..150581088)
AA seq 283 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDMDFDIAGPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggctgtgccacccacgtatgccgatcttggcaaatctgccagggatgtcttcaccaag
ggctatggatttggcttaataaagcttgatttgaaaacaaaatctgagaatggattggaa
tttacaagctcaggctcagccaacactgagaccaccaaagtaacaggcagtctggaaacc
aagtacagatggactgagtacggcctgacgtttacagagaaatggaacaccgacaataca
ctaggcaccgagattactgtggaagatcagcttgcacgtggactgaagctgaccttcgat
tcatccttctcacctaacactgggaaaaaaaatgctaaaatcaagacagggtacaagcgg
gagcacattaacctgggctgtgacatggatttcgacattgctggaccttccatccggggt
gctctagtgctgggttacgagggctggctggcgggttaccagatgaattttgagactgca
aaatcccgagtgacccagagcaactttgcagttggctacaagactgatgaattccagctt
cacactaatgtgaatgacgggacagagtttggtggctccatttaccagaaagtgaacaag
aagttggagaccgctgtcaatctcgcctggacagcaggaaacagtaacacgcgcttcgga
atagcagccaagtatcagattgaccctgacgcctgcttctcggctaaagtgaacaactcc
agcctgataggtttaggatacactcagactctaaagccaggtatcaaactgacactgtca
gctcttctggatggcaagaacgtcaatgctggtggccacaagcttggtctaggactggaa
tttcaagcataa

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