KEGG   Mustela lutreola (European mink): 131836545
Entry
131836545         CDS       T09578                                 
Name
(RefSeq) voltage-dependent anion-selective channel protein 1-like
  KO
K05862  voltage-dependent anion channel protein 1
Organism
mlk  Mustela lutreola (European mink)
Pathway
mlk04020  Calcium signaling pathway
mlk04022  cGMP-PKG signaling pathway
mlk04217  Necroptosis
mlk04218  Cellular senescence
mlk04613  Neutrophil extracellular trap formation
mlk04621  NOD-like receptor signaling pathway
mlk04979  Cholesterol metabolism
mlk05010  Alzheimer disease
mlk05012  Parkinson disease
mlk05014  Amyotrophic lateral sclerosis
mlk05016  Huntington disease
mlk05017  Spinocerebellar ataxia
mlk05020  Prion disease
mlk05022  Pathways of neurodegeneration - multiple diseases
mlk05164  Influenza A
mlk05166  Human T-cell leukemia virus 1 infection
mlk05208  Chemical carcinogenesis - reactive oxygen species
mlk05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:mlk00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    131836545
   04022 cGMP-PKG signaling pathway
    131836545
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    131836545
   04218 Cellular senescence
    131836545
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    131836545
   04621 NOD-like receptor signaling pathway
    131836545
  09154 Digestive system
   04979 Cholesterol metabolism
    131836545
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    131836545
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    131836545
   05164 Influenza A
    131836545
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    131836545
   05012 Parkinson disease
    131836545
   05014 Amyotrophic lateral sclerosis
    131836545
   05016 Huntington disease
    131836545
   05017 Spinocerebellar ataxia
    131836545
   05020 Prion disease
    131836545
   05022 Pathways of neurodegeneration - multiple diseases
    131836545
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    131836545
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:mlk03029]
    131836545
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:mlk04040]
    131836545
Mitochondrial biogenesis [BR:mlk03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    131836545
Ion channels [BR:mlk04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   131836545
SSDB
Motif
Pfam: Porin_3 OMP_b-brl
Other DBs
NCBI-GeneID: 131836545
NCBI-ProteinID: XP_059038038
LinkDB
Position
7:105135506..105137015
AA seq 277 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTQTTKVTGSLET
KYRWTEYDLTFTEKWNTDNMLGTEITVEDQLARGLKLTFDSSFSPNTGEKNAKIKTGYKR
EHINLGCDVDFDIAGPSVRVAVVLGYEGCLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLTWTAGNSNTRFGIAAKYQINPDACFSSLIGLG
YTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 834 nt   +upstreamnt  +downstreamnt
atggctgtgcctcccacgtatgctgatcttggcaaatctgccagggatgtcttcaccaag
ggttatggatttggcttaataaaacttgacttgaaaacaaaatctgagaatggactggaa
tttacaagctcaggttcagccaacactcagaccaccaaagtgacgggcagtctggaaacc
aagtataggtggaccgaatatgatctgacgtttacagagaaatggaacactgacaacatg
ctaggcacagagatcactgtggaagatcagcttgcacgtggactgaagctgacctttgat
tcatccttctcaccaaacacaggggaaaaaaatgcaaaaatcaagacagggtataagcgg
gagcacatcaacttgggctgcgatgtggatttcgacattgccggtccttcagtccgggtt
gccgtggtgctgggctatgaaggctgcctggctggctaccagatgaattttgagactgcg
aagtctcgagtgacccagagcaacttcgcggttggctacaagactgacgagttccagctc
cacactaatgtaaatgatgggacagagtttggtggctccatttatcagaaggtgaacaag
aagttagagaccgctgtcaatctgacctggactgcaggaaatagtaacactcgctttgga
atagcagccaaatatcagatcaaccctgatgcctgcttctccagcctgataggtttagga
tacactcagaccctaaagccaggtatcaaactgacgctatcagctctgctggatggcaag
aatgtcaatgctggcggccacaagcttggtctaggactggaatttcaggcataa

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