KEGG   Myotis brandtii (Brandt's bat): 102263138
Entry
102263138         CDS       T02920                                 
Symbol
VDAC3
Name
(RefSeq) voltage dependent anion channel 3
  KO
K15041  voltage-dependent anion channel protein 3
Organism
myb  Myotis brandtii (Brandt's bat)
Pathway
myb04020  Calcium signaling pathway
myb04022  cGMP-PKG signaling pathway
myb04216  Ferroptosis
myb04217  Necroptosis
myb04218  Cellular senescence
myb04613  Neutrophil extracellular trap formation
myb04621  NOD-like receptor signaling pathway
myb04979  Cholesterol metabolism
myb05010  Alzheimer disease
myb05012  Parkinson disease
myb05016  Huntington disease
myb05017  Spinocerebellar ataxia
myb05020  Prion disease
myb05022  Pathways of neurodegeneration - multiple diseases
myb05161  Hepatitis B
myb05166  Human T-cell leukemia virus 1 infection
myb05203  Viral carcinogenesis
myb05208  Chemical carcinogenesis - reactive oxygen species
myb05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:myb00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    102263138 (VDAC3)
   04022 cGMP-PKG signaling pathway
    102263138 (VDAC3)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    102263138 (VDAC3)
   04217 Necroptosis
    102263138 (VDAC3)
   04218 Cellular senescence
    102263138 (VDAC3)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    102263138 (VDAC3)
   04621 NOD-like receptor signaling pathway
    102263138 (VDAC3)
  09154 Digestive system
   04979 Cholesterol metabolism
    102263138 (VDAC3)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    102263138 (VDAC3)
   05203 Viral carcinogenesis
    102263138 (VDAC3)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    102263138 (VDAC3)
   05161 Hepatitis B
    102263138 (VDAC3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102263138 (VDAC3)
   05012 Parkinson disease
    102263138 (VDAC3)
   05016 Huntington disease
    102263138 (VDAC3)
   05017 Spinocerebellar ataxia
    102263138 (VDAC3)
   05020 Prion disease
    102263138 (VDAC3)
   05022 Pathways of neurodegeneration - multiple diseases
    102263138 (VDAC3)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    102263138 (VDAC3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:myb03029]
    102263138 (VDAC3)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:myb04040]
    102263138 (VDAC3)
Mitochondrial biogenesis [BR:myb03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    102263138 (VDAC3)
Ion channels [BR:myb04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   102263138 (VDAC3)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 102263138
NCBI-ProteinID: XP_005856531
LinkDB
Position
Un
AA seq 289 aa
MQPRHQMCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLRTKSCSGVEFSTSGHAYTDTGKA
SGNLETKYKICNYGLTFTQKWNTDNTLGTEISWENKLAEGLKLTLDTTFVPNTGKKSGKL
KASYKRDCFSLGSNVDIDFSGPTIYGWAVLGFEGWLAGYQMSFDTAKSKLSQNNFALGYK
AADFQLHTHVNDGTEFGGSIYQKVNEKTETSINLAWTAGSNNTRFGIAAKYKLDCRTSLA
AKVNNASLIGLGYTQTLRPGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq 870 nt   +upstreamnt  +downstreamnt
atgcaacctcggcaccagatgtgtaacacaccaacttactgtgacctaggaaaggctgcc
aaggatgtcttcaacaaaggatatgggtttggcatggtcaaaatagatctgagaaccaag
tcatgtagtggagtggaattttctacttctggtcatgcttatactgacacagggaaagca
tcaggcaacctagagacaaaatataagatctgtaactatggacttacattcacccaaaaa
tggaacacagacaatactcttggaacagaaatctcttgggagaataagttggctgaaggg
ttgaaactgactcttgataccacatttgtaccgaacacaggaaagaagagtgggaagttg
aaggcctcctacaaacgggattgtttcagtcttggcagtaatgtggatatagatttttct
ggcccaaccatctatggctgggctgtactaggctttgaaggttggcttgctggctatcag
atgagttttgacacagccaaatccaaactgtcacagaataattttgccctgggttacaag
gctgcagacttccagctgcacactcatgtgaatgatggcactgaatttggagggtctatc
taccagaaggttaatgagaagactgaaacgtcaataaaccttgcttggacagctggcagt
aacaacacccgttttggcatcgctgctaaatacaagttggattgtagaacttctctagct
gctaaagtaaataacgccagcctgattggactgggttatactcagactcttcgaccagga
gtcaaactgaccctatcagctttaatcgacggaaagaacttcaatgcaggaggtcacaag
gttgggttgggttttgaactagaagcttaa

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