KEGG   Puma concolor (puma): 112858617
Entry
112858617         CDS       T08890                                 
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3 isoform X1
  KO
K15041  voltage-dependent anion channel protein 3
Organism
pcoo  Puma concolor (puma)
Pathway
pcoo04020  Calcium signaling pathway
pcoo04022  cGMP-PKG signaling pathway
pcoo04216  Ferroptosis
pcoo04217  Necroptosis
pcoo04218  Cellular senescence
pcoo04613  Neutrophil extracellular trap formation
pcoo04621  NOD-like receptor signaling pathway
pcoo04979  Cholesterol metabolism
pcoo05010  Alzheimer disease
pcoo05012  Parkinson disease
pcoo05016  Huntington disease
pcoo05017  Spinocerebellar ataxia
pcoo05020  Prion disease
pcoo05022  Pathways of neurodegeneration - multiple diseases
pcoo05161  Hepatitis B
pcoo05166  Human T-cell leukemia virus 1 infection
pcoo05203  Viral carcinogenesis
pcoo05208  Chemical carcinogenesis - reactive oxygen species
pcoo05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:pcoo00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    112858617 (VDAC3)
   04022 cGMP-PKG signaling pathway
    112858617 (VDAC3)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    112858617 (VDAC3)
   04217 Necroptosis
    112858617 (VDAC3)
   04218 Cellular senescence
    112858617 (VDAC3)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    112858617 (VDAC3)
   04621 NOD-like receptor signaling pathway
    112858617 (VDAC3)
  09154 Digestive system
   04979 Cholesterol metabolism
    112858617 (VDAC3)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    112858617 (VDAC3)
   05203 Viral carcinogenesis
    112858617 (VDAC3)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    112858617 (VDAC3)
   05161 Hepatitis B
    112858617 (VDAC3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    112858617 (VDAC3)
   05012 Parkinson disease
    112858617 (VDAC3)
   05016 Huntington disease
    112858617 (VDAC3)
   05017 Spinocerebellar ataxia
    112858617 (VDAC3)
   05020 Prion disease
    112858617 (VDAC3)
   05022 Pathways of neurodegeneration - multiple diseases
    112858617 (VDAC3)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    112858617 (VDAC3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:pcoo03029]
    112858617 (VDAC3)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:pcoo04040]
    112858617 (VDAC3)
Mitochondrial biogenesis [BR:pcoo03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    112858617 (VDAC3)
Ion channels [BR:pcoo04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   112858617 (VDAC3)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 112858617
NCBI-ProteinID: XP_025777837
UniProt: A0A6P6HPZ8
LinkDB
Position
Unknown
AA seq 284 aa
MCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLRTKSCSGVMEFSTSGHAYTDTGKASGNLE
TKYKICNYGLTFTQKWNTDNTLGTEISLENKLAEGLKLTLDTIFVPNTGKKSGKLKASYK
RECFSLGSNVDIDFSGPTIYGWAVLAFEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQ
LHTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLSAKVNN
ASLIGLGYTQTLRPGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq 855 nt   +upstreamnt  +downstreamnt
atgtgtaacacaccaacttactgtgacctaggaaaggccgccaaggatgtcttcaacaaa
ggatatggatttggcatggtcaaaatagacctgagaaccaagtcttgtagtggagtgatg
gaattttctacttctggtcatgcttacactgatacaggaaaagcgtcaggcaacctagag
accaaatataagatctgtaactatggacttaccttcactcagaaatggaacacagataac
actcttggaacagaaatctctttggagaataagttggctgaagggttgaaactgactctt
gataccatatttgtaccgaacacaggaaagaagagtggaaaattaaaggcctcctataag
cgggaatgtttcagtctcggcagcaatgttgatatagatttttctggaccaaccatctat
ggctgggctgtgttagcctttgaaggttggcttgctggctatcagatgagtttcgacaca
gccaaatccaaactgtcacagaataatttcgctctgggttacaaggccgcagacttccag
ctgcacactcatgtgaatgacggcactgaatttggagggtctatctaccagaaggttaat
gagaagattgaaacatcaataaaccttgcttggacggctggcagtaacaatacccgtttt
ggcatcgctgctaaatacaagctggactgtagaacttctctatctgctaaagtaaataat
gccagcctgattggactgggttatactcagactcttcgaccaggagtcaaactgacccta
tcagctttaatcgacggaaagaacttcaatgcaggaggtcacaaggttgggttgggattt
gagctagaagcttaa

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