KEGG   Macaca thibetana thibetana (Pere David's macaque): 126960768
Entry
126960768         CDS       T08579                                 
Name
(RefSeq) voltage-dependent anion-selective channel protein 3
  KO
K15041  voltage-dependent anion channel protein 3
Organism
mthb  Macaca thibetana thibetana (Pere David's macaque)
Pathway
mthb04020  Calcium signaling pathway
mthb04022  cGMP-PKG signaling pathway
mthb04216  Ferroptosis
mthb04217  Necroptosis
mthb04218  Cellular senescence
mthb04613  Neutrophil extracellular trap formation
mthb04621  NOD-like receptor signaling pathway
mthb04979  Cholesterol metabolism
mthb05010  Alzheimer disease
mthb05012  Parkinson disease
mthb05016  Huntington disease
mthb05017  Spinocerebellar ataxia
mthb05020  Prion disease
mthb05022  Pathways of neurodegeneration - multiple diseases
mthb05161  Hepatitis B
mthb05166  Human T-cell leukemia virus 1 infection
mthb05203  Viral carcinogenesis
mthb05208  Chemical carcinogenesis - reactive oxygen species
mthb05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:mthb00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    126960768
   04022 cGMP-PKG signaling pathway
    126960768
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    126960768
   04217 Necroptosis
    126960768
   04218 Cellular senescence
    126960768
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    126960768
   04621 NOD-like receptor signaling pathway
    126960768
  09154 Digestive system
   04979 Cholesterol metabolism
    126960768
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    126960768
   05203 Viral carcinogenesis
    126960768
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    126960768
   05161 Hepatitis B
    126960768
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    126960768
   05012 Parkinson disease
    126960768
   05016 Huntington disease
    126960768
   05017 Spinocerebellar ataxia
    126960768
   05020 Prion disease
    126960768
   05022 Pathways of neurodegeneration - multiple diseases
    126960768
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    126960768
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:mthb03029]
    126960768
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:mthb04040]
    126960768
Mitochondrial biogenesis [BR:mthb03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    126960768
Ion channels [BR:mthb04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   126960768
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 126960768
NCBI-ProteinID: XP_050656386
LinkDB
Position
8:complement(100856812..100871101)
AA seq 283 aa
MCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLKTKSCSGVEFSTSGHAYTDTGKASGNLET
KYKVCNYGLTFTQKWNTDNTLGTEISWENKLAEGLKLTLDTIFVPNTGKKSGKLKASYKR
DCFSVGSNVDIDFSGPTIYGWAVLAFEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQL
HTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLSAKVNNA
SLIGLGYTQTLRPGVKLTLSALIDGKNFSAGGHKVGLGFELEA
NT seq 852 nt   +upstreamnt  +downstreamnt
atgtgtaacacaccaacttactgtgacctaggaaaggctgctaaggatgtcttcaacaaa
ggatatggctttggcatggtcaagatagacctgaaaaccaagtcttgtagtggagtggaa
ttttctacttctggtcatgcttacactgatacagggaaagcatcaggcaacctagaaacc
aaatataaggtctgtaactatggacttaccttcacccaaaaatggaacacggacaatact
ctagggacagaaatctcttgggagaataagttggctgaagggttgaaactgactcttgat
accatatttgtaccgaacacaggaaagaagagtgggaaattgaaggcttcctataaacgg
gattgttttagtgttggcagtaatgttgatatagatttttctggaccaaccatctatggc
tgggctgtgttggccttcgaagggtggcttgctggctatcagatgagttttgacacagcc
aaatccaaactgtcacagaataatttcgccctgggttacaaggctgcggacttccagctg
cacacacatgtgaacgacggcactgagtttggaggttctatctaccagaaggttaatgag
aagattgaaacatccataaaccttgcttggacggctgggagtaacaacacccgttttggc
attgctgctaagtacaagctggattgtagaacttctctctctgctaaagtaaataatgcc
agcctgattggactgggttatactcagacccttcgaccaggagtcaaattgactttatca
gctttaatcgatgggaagaacttcagtgcaggaggtcacaaggttggcttgggatttgaa
ctggaagcttaa

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