KEGG   Rousettus aegyptiacus (Egyptian rousette): 107501347
Entry
107501347         CDS       T06036                                 
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3 isoform X1
  KO
K15041  voltage-dependent anion channel protein 3
Organism
ray  Rousettus aegyptiacus (Egyptian rousette)
Pathway
ray04020  Calcium signaling pathway
ray04022  cGMP-PKG signaling pathway
ray04216  Ferroptosis
ray04217  Necroptosis
ray04218  Cellular senescence
ray04613  Neutrophil extracellular trap formation
ray04621  NOD-like receptor signaling pathway
ray04979  Cholesterol metabolism
ray05010  Alzheimer disease
ray05012  Parkinson disease
ray05016  Huntington disease
ray05017  Spinocerebellar ataxia
ray05020  Prion disease
ray05022  Pathways of neurodegeneration - multiple diseases
ray05161  Hepatitis B
ray05166  Human T-cell leukemia virus 1 infection
ray05203  Viral carcinogenesis
ray05208  Chemical carcinogenesis - reactive oxygen species
ray05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ray00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    107501347 (VDAC3)
   04022 cGMP-PKG signaling pathway
    107501347 (VDAC3)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    107501347 (VDAC3)
   04217 Necroptosis
    107501347 (VDAC3)
   04218 Cellular senescence
    107501347 (VDAC3)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    107501347 (VDAC3)
   04621 NOD-like receptor signaling pathway
    107501347 (VDAC3)
  09154 Digestive system
   04979 Cholesterol metabolism
    107501347 (VDAC3)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    107501347 (VDAC3)
   05203 Viral carcinogenesis
    107501347 (VDAC3)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    107501347 (VDAC3)
   05161 Hepatitis B
    107501347 (VDAC3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    107501347 (VDAC3)
   05012 Parkinson disease
    107501347 (VDAC3)
   05016 Huntington disease
    107501347 (VDAC3)
   05017 Spinocerebellar ataxia
    107501347 (VDAC3)
   05020 Prion disease
    107501347 (VDAC3)
   05022 Pathways of neurodegeneration - multiple diseases
    107501347 (VDAC3)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    107501347 (VDAC3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ray03029]
    107501347 (VDAC3)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:ray04040]
    107501347 (VDAC3)
Mitochondrial biogenesis [BR:ray03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    107501347 (VDAC3)
Ion channels [BR:ray04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   107501347 (VDAC3)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 107501347
NCBI-ProteinID: XP_015982898
LinkDB
Position
Unknown
AA seq 284 aa
MCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLRTKSCSGVMEFSTSGHAYTDTGKASGNLE
TKYKVCNYGLTFTQKWNTDNTLGTEISWENKLAEGLKLTLDTIFVPNTGKKSGKLKASYK
RDCFSLGSNVDIDFSGPTIYGWAVLALEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQ
LHTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLSAKVNN
ASLIGLGYTQTLRPGVKLTLSALVDGKNFNAGGHKVGLGFELEA
NT seq 855 nt   +upstreamnt  +downstreamnt
atgtgtaacacaccgacttactgtgacctaggaaaggctgccaaggatgtcttcaacaaa
ggatatgggtttggcatggtcaaaatagatctgagaaccaagtcatgtagtggagtgatg
gaattttctacttctggtcatgcttacactgatacagggaaagcgtcaggcaacctagag
accaaatataaggtctgtaactatggacttaccttcacccaaaaatggaacacagacaat
actcttggaacagaaatctcttgggagaataagttggccgaagggttgaaactgactctt
gataccatctttgtaccaaacacagggaagaagagtgggaaattgaaggcttcctataaa
cgggattgtttcagtcttggcagcaatgttgatatagatttttctggaccaaccatctat
ggctgggctgtgttagcccttgaaggttggcttgctggctatcagatgagttttgacaca
gccaaatctaaactgtcacagaataatttcgccctgggttataaggctgcagatttccag
ctgcacactcatgtgaatgatggcactgaatttggagggtctatctaccagaaggttaat
gaaaagattgaaacatcaataaacctcgcttggacagctggcagtaacaacacccgtttc
ggcatcgctgctaaatacaagctggattgtagaacttctttatctgctaaagtaaataat
gcaagcctgattggacttggttatactcagacccttcgaccaggagtcaaactgaccctg
tcagctttagtcgatggaaagaacttcaatgcaggcggtcacaaggttgggttgggattc
gaactagaagcttaa

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