KEGG   Prionailurus bengalensis (leopard cat): 122490092
Entry
122490092         CDS       T07574                                 
Name
(RefSeq) LOW QUALITY PROTEIN: voltage-dependent anion-selective channel protein 3-like
  KO
K15041  voltage-dependent anion channel protein 3
Organism
pbg  Prionailurus bengalensis (leopard cat)
Pathway
pbg04020  Calcium signaling pathway
pbg04022  cGMP-PKG signaling pathway
pbg04216  Ferroptosis
pbg04217  Necroptosis
pbg04218  Cellular senescence
pbg04613  Neutrophil extracellular trap formation
pbg04621  NOD-like receptor signaling pathway
pbg04979  Cholesterol metabolism
pbg05010  Alzheimer disease
pbg05012  Parkinson disease
pbg05016  Huntington disease
pbg05017  Spinocerebellar ataxia
pbg05020  Prion disease
pbg05022  Pathways of neurodegeneration - multiple diseases
pbg05161  Hepatitis B
pbg05166  Human T-cell leukemia virus 1 infection
pbg05203  Viral carcinogenesis
pbg05208  Chemical carcinogenesis - reactive oxygen species
pbg05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:pbg00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    122490092
   04022 cGMP-PKG signaling pathway
    122490092
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    122490092
   04217 Necroptosis
    122490092
   04218 Cellular senescence
    122490092
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    122490092
   04621 NOD-like receptor signaling pathway
    122490092
  09154 Digestive system
   04979 Cholesterol metabolism
    122490092
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    122490092
   05203 Viral carcinogenesis
    122490092
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    122490092
   05161 Hepatitis B
    122490092
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122490092
   05012 Parkinson disease
    122490092
   05016 Huntington disease
    122490092
   05017 Spinocerebellar ataxia
    122490092
   05020 Prion disease
    122490092
   05022 Pathways of neurodegeneration - multiple diseases
    122490092
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    122490092
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:pbg03029]
    122490092
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:pbg04040]
    122490092
Mitochondrial biogenesis [BR:pbg03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    122490092
Ion channels [BR:pbg04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   122490092
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 122490092
NCBI-ProteinID: XP_043448539
LinkDB
Position
B2:complement(135377444..135378585)
AA seq 294 aa
MVECCLGGVETSPLVGGICNTLTYCDLGKAAKDDFNKGYGFGSVKVRLRTKSCRGVEFST
SGHAYTDTEQTSGNLETTYKVCSYGLAFTQKWNIDDTLGTEIASQNKLAEGSKRTLDTVF
APNPGKKSGKWKASYKWDCFSLGSNVDADFSGPTIFGFGGWLAGSQTSFDTARSKLPQNG
VALGYTAADFQLHMHVSDGPEFGGSVYQEVNGKIGTSINIAWMAGSNNTXDCRTFLSAIG
NKTSPTGLGYTQTLGPGVKLTLPAFTDRKNVNAGGHEVGLGFEREAYCGFEESI
NT seq 884 nt   +upstreamnt  +downstreamnt
atggtagagtgttgccttggcggagtggagaccagccctctggttggaggtatatgtaac
acactgacttactgtgacctagggaaggctgccaaagatgacttcaacaaaggctatgga
tttggctcggtcaaagtacgtctgagaactaagtcttgtaggggggtggaattttctact
tctggtcatgcttacactgacacagagcaaacgtcaggcaacctagagaccacgtataag
gtctgtagctacggacttgccttcacccagaaatggaacatagacgatactcttggaaca
gaaattgcttcacagaataagttggctgaagggtcgaaacgtactctcgataccgtattt
gcaccgaacccaggaaagaagagtgggaaatggaaggcctcctacaaatgggattgtttc
agtctcggcagtaatgttgatgcagatttttccggaccgaccatctttggctttggaggt
tggcttgctggctctcagacgagttttgacacagccagatccaaactgccacagaatggt
gtcgccctgggttacacagctgccgacttccagctgcacatgcatgtgagtgatggccct
gaatttggagggtctgtctaccaggaggttaatgggaagattggaacatcaatcaacatt
gcttggatggctggcagtaacaatacccggactgtagaacttttctatctgctataggaa
ataagacgagcccgaccggactgggttatactcagacccttggaccaggagtcaaactga
ccctaccagctttcacggacagaaagaacgtcaatgcaggaggccacgaggttgggctgg
gatttgaacgagaagcctattgtggttttgaggaaagcatctga

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