KEGG   Myotis yumanensis (Yuma myotis): 139010489
Entry
139010489         CDS       T10762                                 
Symbol
VDAC1
Name
(RefSeq) non-selective voltage-gated ion channel VDAC1
  KO
K05862  voltage-dependent anion channel protein 1
Organism
myum  Myotis yumanensis (Yuma myotis)
Pathway
myum04020  Calcium signaling pathway
myum04022  cGMP-PKG signaling pathway
myum04217  Necroptosis
myum04218  Cellular senescence
myum04613  Neutrophil extracellular trap formation
myum04621  NOD-like receptor signaling pathway
myum04979  Cholesterol metabolism
myum05010  Alzheimer disease
myum05012  Parkinson disease
myum05014  Amyotrophic lateral sclerosis
myum05016  Huntington disease
myum05017  Spinocerebellar ataxia
myum05020  Prion disease
myum05022  Pathways of neurodegeneration - multiple diseases
myum05164  Influenza A
myum05166  Human T-cell leukemia virus 1 infection
myum05208  Chemical carcinogenesis - reactive oxygen species
myum05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:myum00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    139010489 (VDAC1)
   04022 cGMP-PKG signaling pathway
    139010489 (VDAC1)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    139010489 (VDAC1)
   04218 Cellular senescence
    139010489 (VDAC1)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    139010489 (VDAC1)
   04621 NOD-like receptor signaling pathway
    139010489 (VDAC1)
  09154 Digestive system
   04979 Cholesterol metabolism
    139010489 (VDAC1)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    139010489 (VDAC1)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    139010489 (VDAC1)
   05164 Influenza A
    139010489 (VDAC1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    139010489 (VDAC1)
   05012 Parkinson disease
    139010489 (VDAC1)
   05014 Amyotrophic lateral sclerosis
    139010489 (VDAC1)
   05016 Huntington disease
    139010489 (VDAC1)
   05017 Spinocerebellar ataxia
    139010489 (VDAC1)
   05020 Prion disease
    139010489 (VDAC1)
   05022 Pathways of neurodegeneration - multiple diseases
    139010489 (VDAC1)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    139010489 (VDAC1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:myum03029]
    139010489 (VDAC1)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:myum04040]
    139010489 (VDAC1)
Mitochondrial biogenesis [BR:myum03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    139010489 (VDAC1)
Ion channels [BR:myum04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   139010489 (VDAC1)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 139010489
NCBI-ProteinID: XP_070271103
LinkDB
Position
Unknown
AA seq 283 aa
MAVPPTYIDLGKSARDVFTKGYGFGLIKLELKTKSESGLEFTSSGSANTETTKVAGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDMAGPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPEACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggctgtgcctcccacgtatattgatcttggcaagtccgccagggacgtcttcaccaag
ggctatggatttggcttaataaagcttgagttgaaaacaaaatctgagagtggactggaa
tttacaagctcaggttcagccaacaccgagaccaccaaagtggcaggcagtctggaaacc
aagtacaggtggactgagtatggtctgacatttacggagaagtggaacacggacaacaca
ctaggcacggagattactgtggaagaccagcttgcacgtggactgaagctgacctttgat
tcatccttctccccaaacactgggaaaaaaaatgctaaaatcaagacagggtacaagcgg
gagcacatcaacctgggctgcgacgtggacttcgacatggccgggccttcgatccggggt
gccctggtgctgggctatgagggctggctggctggctaccagatgaattttgagacggcg
aagtctcgagtgacccagagcaactttgcggttggctacaagaccgatgaattccagctt
cacactaatgtgaacgacgggacggagtttggtggctccatttatcagaaggtgaataag
aagttggagaccgccgttaacctcgcctggacagcaggaaacagtaacactcgctttgga
atagcagccaagtatcagatcgaccccgaagcctgcttctcggctaaagtgaacaactcc
agcctgatagggttaggatacacccagacactaaagccaggtatcaaactgacgctgtca
gctctgctggatggcaagaatgtcaatgctggtggccacaagcttggtctaggactggaa
tttcaagcataa

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