KEGG   Ursus arctos (brown bear): 113245581
Entry
113245581         CDS       T05909                                 
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3
  KO
K15041  voltage-dependent anion channel protein 3
Organism
uah  Ursus arctos (brown bear)
Pathway
uah04020  Calcium signaling pathway
uah04022  cGMP-PKG signaling pathway
uah04216  Ferroptosis
uah04217  Necroptosis
uah04218  Cellular senescence
uah04613  Neutrophil extracellular trap formation
uah04621  NOD-like receptor signaling pathway
uah04979  Cholesterol metabolism
uah05010  Alzheimer disease
uah05012  Parkinson disease
uah05016  Huntington disease
uah05017  Spinocerebellar ataxia
uah05020  Prion disease
uah05022  Pathways of neurodegeneration - multiple diseases
uah05161  Hepatitis B
uah05166  Human T-cell leukemia virus 1 infection
uah05203  Viral carcinogenesis
uah05208  Chemical carcinogenesis - reactive oxygen species
uah05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:uah00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    113245581 (VDAC3)
   04022 cGMP-PKG signaling pathway
    113245581 (VDAC3)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    113245581 (VDAC3)
   04217 Necroptosis
    113245581 (VDAC3)
   04218 Cellular senescence
    113245581 (VDAC3)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    113245581 (VDAC3)
   04621 NOD-like receptor signaling pathway
    113245581 (VDAC3)
  09154 Digestive system
   04979 Cholesterol metabolism
    113245581 (VDAC3)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    113245581 (VDAC3)
   05203 Viral carcinogenesis
    113245581 (VDAC3)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    113245581 (VDAC3)
   05161 Hepatitis B
    113245581 (VDAC3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    113245581 (VDAC3)
   05012 Parkinson disease
    113245581 (VDAC3)
   05016 Huntington disease
    113245581 (VDAC3)
   05017 Spinocerebellar ataxia
    113245581 (VDAC3)
   05020 Prion disease
    113245581 (VDAC3)
   05022 Pathways of neurodegeneration - multiple diseases
    113245581 (VDAC3)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    113245581 (VDAC3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:uah03029]
    113245581 (VDAC3)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:uah04040]
    113245581 (VDAC3)
Mitochondrial biogenesis [BR:uah03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    113245581 (VDAC3)
Ion channels [BR:uah04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   113245581 (VDAC3)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 113245581
NCBI-ProteinID: XP_026341510
LinkDB
Position
Unknown
AA seq 283 aa
MCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLKTKSCSGVEFSTSGHAYTDTGKASGNLET
KYKVCNYGLTFTQKWNTDNTLGTEISLENKLAEGLKLTLDTIFVPNTGKKSGKLKASYKR
DCFSLGSNVDIDFSGPTIYGWAVLAFEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQL
HTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLSAKVNNA
SLIGLGYTQTLRPGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq 852 nt   +upstreamnt  +downstreamnt
atgtgtaacacaccgacttactgtgacctaggaaaggccgccaaggatgtcttcaataaa
ggatatggatttggcatggtcaagatagatctgaaaaccaagtcatgtagtggagtggaa
ttttctacttctggtcatgcttacactgatacagggaaagcgtcaggaaacctagagacc
aaatataaggtctgtaactatggacttaccttcacccagaagtggaacacagacaatact
cttggaacagaaatctctttggagaataagttggctgaaggattgaaactgactcttgat
accatatttgtaccgaacacaggaaagaagagtggaaaattgaaggcctcttacaaacgg
gattgtttcagtcttggcagtaatgttgatatagatttttctggaccaaccatctatggc
tgggctgtgttagcctttgaaggttggcttgctggctatcagatgagttttgacacagcc
aaatccaaactgtcacagaataatttcgccctgggttacaaggctgcagacttccagctg
cacactcacgtgaatgatggcactgaatttggcgggtctatctaccagaaggttaacgag
aagattgaaacgtcgataaaccttgcttggacggccggcagtaacaatacccgtttcggc
atcgctgctaagtacaagctggactgtaggacttctctgtctgctaaagtaaataatgcc
agcctgattggactgggttatactcagacccttcgaccaggtgtcaaactgaccctatca
gctttaattgacggaaagaacttcaatgcaggaggtcacaaggttggattgggatttgaa
ctagaagcttaa

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