KEGG   Hylobates moloch (silvery gibbon): 116811837
Entry
116811837         CDS       T08803                                 
Name
(RefSeq) voltage-dependent anion-selective channel protein 1-like
  KO
K05862  voltage-dependent anion channel protein 1
Organism
hmh  Hylobates moloch (silvery gibbon)
Pathway
hmh04020  Calcium signaling pathway
hmh04022  cGMP-PKG signaling pathway
hmh04217  Necroptosis
hmh04218  Cellular senescence
hmh04613  Neutrophil extracellular trap formation
hmh04621  NOD-like receptor signaling pathway
hmh04979  Cholesterol metabolism
hmh05010  Alzheimer disease
hmh05012  Parkinson disease
hmh05014  Amyotrophic lateral sclerosis
hmh05016  Huntington disease
hmh05017  Spinocerebellar ataxia
hmh05020  Prion disease
hmh05022  Pathways of neurodegeneration - multiple diseases
hmh05164  Influenza A
hmh05166  Human T-cell leukemia virus 1 infection
hmh05208  Chemical carcinogenesis - reactive oxygen species
hmh05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:hmh00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    116811837
   04022 cGMP-PKG signaling pathway
    116811837
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    116811837
   04218 Cellular senescence
    116811837
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    116811837
   04621 NOD-like receptor signaling pathway
    116811837
  09154 Digestive system
   04979 Cholesterol metabolism
    116811837
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    116811837
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    116811837
   05164 Influenza A
    116811837
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    116811837
   05012 Parkinson disease
    116811837
   05014 Amyotrophic lateral sclerosis
    116811837
   05016 Huntington disease
    116811837
   05017 Spinocerebellar ataxia
    116811837
   05020 Prion disease
    116811837
   05022 Pathways of neurodegeneration - multiple diseases
    116811837
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    116811837
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hmh03029]
    116811837
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hmh04040]
    116811837
Mitochondrial biogenesis [BR:hmh03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    116811837
Ion channels [BR:hmh04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   116811837
SSDB
Motif
Pfam: Porin_3 Gp44_C
Other DBs
NCBI-GeneID: 116811837
NCBI-ProteinID: XP_032613123
LinkDB
Position
Unknown
AA seq 283 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKCENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGEKNAKIKTGYKR
EHINLGCYMDFDIAGPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETTVNLARTAGNSNRCFGIAAKYQIDPDACFSANVNNS
SLIGLGYTQTLKPGIKLTLSAILDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggctgtgccacctacgtatgccgatcttggcaaatctgccagggatgtcttcaccaag
ggctatggatttggcttaataaagcttgatttgaaaacaaaatgtgagaatggattggaa
tttacaagctcaggctcagccaacactgagaccaccaaagtgacgggcagtctggaaacc
aagtacagatggactgagtacggcctcacgtttacagagaaatggaacaccgacaataca
ctaggcactgagattactgtggaagatcagcttgcacgtggactgaagctgaccttcgat
tcatccttctcacctaacactggggaaaaaaatgctaaaatcaagacagggtacaagcgg
gagcacattaacctgggctgctacatggatttcgacattgctgggccttccatccggggt
gctctggtgctgggttacgagggctggctggccggctaccagatgaattttgagactgca
aaatcccgagtgacccagagcaactttgcagttggctacaagactgatgaattccagctt
cacactaatgtgaatgacgggacagagtttggcggctccatttaccagaaagtgaacaag
aagttggagaccactgtcaatcttgcccggacagcaggaaacagtaacaggtgcttcgga
atagcagccaagtatcagattgaccctgacgcctgcttctccgctaacgtgaacaactcc
agcctgataggtttaggatacactcagactctaaagccaggtatcaaactgacactgtca
gcaattctggatggcaagaacgtcaatgctggtggccacaagcttggtctaggactggaa
tttcaagcataa

DBGET integrated database retrieval system