KEGG   Dipodomys spectabilis (banner-tailed kangaroo rat): 122101658
Entry
122101658         CDS       T07891                                 
Name
(RefSeq) voltage-dependent anion-selective channel protein 3-like
  KO
K15041  voltage-dependent anion channel protein 3
Organism
dsp  Dipodomys spectabilis (banner-tailed kangaroo rat)
Pathway
dsp04020  Calcium signaling pathway
dsp04022  cGMP-PKG signaling pathway
dsp04216  Ferroptosis
dsp04217  Necroptosis
dsp04218  Cellular senescence
dsp04613  Neutrophil extracellular trap formation
dsp04621  NOD-like receptor signaling pathway
dsp04979  Cholesterol metabolism
dsp05010  Alzheimer disease
dsp05012  Parkinson disease
dsp05016  Huntington disease
dsp05017  Spinocerebellar ataxia
dsp05020  Prion disease
dsp05022  Pathways of neurodegeneration - multiple diseases
dsp05161  Hepatitis B
dsp05166  Human T-cell leukemia virus 1 infection
dsp05203  Viral carcinogenesis
dsp05208  Chemical carcinogenesis - reactive oxygen species
dsp05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:dsp00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    122101658
   04022 cGMP-PKG signaling pathway
    122101658
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    122101658
   04217 Necroptosis
    122101658
   04218 Cellular senescence
    122101658
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    122101658
   04621 NOD-like receptor signaling pathway
    122101658
  09154 Digestive system
   04979 Cholesterol metabolism
    122101658
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    122101658
   05203 Viral carcinogenesis
    122101658
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    122101658
   05161 Hepatitis B
    122101658
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122101658
   05012 Parkinson disease
    122101658
   05016 Huntington disease
    122101658
   05017 Spinocerebellar ataxia
    122101658
   05020 Prion disease
    122101658
   05022 Pathways of neurodegeneration - multiple diseases
    122101658
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    122101658
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:dsp03029]
    122101658
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:dsp04040]
    122101658
Mitochondrial biogenesis [BR:dsp03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    122101658
Ion channels [BR:dsp04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   122101658
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 122101658
NCBI-ProteinID: XP_042528057
LinkDB
Position
Unknown
AA seq 283 aa
MCNTPTYCDLGKAAKDIFNKGYGFGMVKINLRTKSCSGVEFSTSGHAYTDTGKVSGNLET
KYKVCNYGLTFTQKWNTDNTLGTEISLENKLAEGLKLTLDTIFVPNTGKKSGKLKASYKW
DCYRLGSNVDIDFSGPTIYGWAVLGFEGWLAGYHMSFDTAKSKLSQNDFALGYKAADFQL
HTHVNDDPEFGGSIYQKVDEKIETSINLAWMAGSSNTHFGIAAKYKLDCRTSLFAKVNYA
SLIGLGYTQTLQPGVKLTLSALVDGKNFNAGGHKVGLGFELEA
NT seq 852 nt   +upstreamnt  +downstreamnt
atgtgtaacacaccaacttactgtgacctaggaaaggctgccaaagatatcttcaacaag
ggatatgggtttggcatggtcaaaataaatctgagaaccaagtcttgtagtggagtggaa
ttttctacttcgggtcatgcatatactgatacagggaaagtgtcaggcaatctagagacc
aagtataaggtctgtaactatggacttaccttcacccaaaaatggaacacagacaatact
cttgggacagagatctctttggagaataaattggctgaagggttgaaactgactcttgat
accatatttgtaccgaacacagggaagaagagtgggaaattgaaggcttcttataaatgg
gattgttaccgtcttggcagtaatgtggatatagatttttctggaccaaccatctatggc
tgggctgtgttgggttttgaaggttggcttgctggctatcatatgagttttgacacagcc
aaatccaaactgtctcagaatgattttgccctgggctacaaggctgcagacttccagctg
catactcatgtgaatgatgaccctgaatttggaggctccatctaccagaaagttgatgag
aagattgaaacatcaataaatcttgcatggatggctggtagcagcaatacccattttggc
attgctgctaaatacaagctggattgtagaacttctctatttgctaaagtaaattatgcc
agcctgattggactgggatatactcagactcttcagccaggagtcaaactgaccctatca
gcgttagttgatgggaagaatttcaacgcaggagggcacaaggttgggttgggatttgaa
ctggaagcttag

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