Rousettus aegyptiacus (Egyptian rousette): 107506795
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Entry
107506795 CDS
T06036
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
KO
K05862
voltage-dependent anion channel protein 1
Organism
ray
Rousettus aegyptiacus (Egyptian rousette)
Pathway
ray04020
Calcium signaling pathway
ray04022
cGMP-PKG signaling pathway
ray04217
Necroptosis
ray04218
Cellular senescence
ray04613
Neutrophil extracellular trap formation
ray04621
NOD-like receptor signaling pathway
ray04979
Cholesterol metabolism
ray05010
Alzheimer disease
ray05012
Parkinson disease
ray05014
Amyotrophic lateral sclerosis
ray05016
Huntington disease
ray05017
Spinocerebellar ataxia
ray05020
Prion disease
ray05022
Pathways of neurodegeneration - multiple diseases
ray05164
Influenza A
ray05166
Human T-cell leukemia virus 1 infection
ray05208
Chemical carcinogenesis - reactive oxygen species
ray05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
ray00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
107506795 (VDAC1)
04022 cGMP-PKG signaling pathway
107506795 (VDAC1)
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
107506795 (VDAC1)
04218 Cellular senescence
107506795 (VDAC1)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
107506795 (VDAC1)
04621 NOD-like receptor signaling pathway
107506795 (VDAC1)
09154 Digestive system
04979 Cholesterol metabolism
107506795 (VDAC1)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
107506795 (VDAC1)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
107506795 (VDAC1)
05164 Influenza A
107506795 (VDAC1)
09164 Neurodegenerative disease
05010 Alzheimer disease
107506795 (VDAC1)
05012 Parkinson disease
107506795 (VDAC1)
05014 Amyotrophic lateral sclerosis
107506795 (VDAC1)
05016 Huntington disease
107506795 (VDAC1)
05017 Spinocerebellar ataxia
107506795 (VDAC1)
05020 Prion disease
107506795 (VDAC1)
05022 Pathways of neurodegeneration - multiple diseases
107506795 (VDAC1)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
107506795 (VDAC1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
ray03029
]
107506795 (VDAC1)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
ray04040
]
107506795 (VDAC1)
Mitochondrial biogenesis [BR:
ray03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
107506795 (VDAC1)
Ion channels [BR:
ray04040
]
Chloride channels
Maxi chloride channel (VDAC)
107506795 (VDAC1)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
107506795
NCBI-ProteinID:
XP_015993127
UniProt:
A0A7J8FNU7
LinkDB
All DBs
Position
Unknown
AA seq
283 aa
AA seq
DB search
MAVPPTYVDLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSVRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq
852 nt
NT seq
+upstream
nt +downstream
nt
atggctgtgcctcccacatatgttgatcttggcaaatctgccagggatgtcttcaccaag
ggctatggattcggcttaataaaacttgatttgaaaacaaaatctgagaatggactggaa
tttacaagctcaggttctgccaacactgagaccaccaaagtgacaggcagtttggaaacc
aagtacagatggactgaatatggtctgacgtttacggagaaatggaacactgacaacaca
ctcggcacggagattactgtggaagatcagcttgcccgtggactgaagctgaccttcgac
tcatccttctcaccaaacactgggaaaaaaaatgctaaaatcaagacagggtacaagcgg
gagcacatcaacctgggctgcgacgtggatttcgacatcgccgggccttcggtccggggc
gccctggtgctgggttatgagggttggctggccggctaccagatgaattttgagaccgcc
aagtctcgagtgacccagagcaactttgcggttggctacaagactgatgaattccagctt
cacactaatgtaaacgacgggacagagtttggtggctccatttatcagaaggtgaacaag
aagttggagactgctgttaatctcgcctggacagcagggaatagcaacactcgctttggg
atagcagccaagtatcagatcgaccctgacgcctgcttctcggctaaagtgaacaactcc
agccttataggcttaggatacactcagaccctaaagccaggtatcaaactgacgctgtca
gctctgctggatggcaagaatgtcaacgctggtggccacaagcttggtctaggactggaa
tttcaagcataa
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