Ursus americanus (American black bear): 123790351
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Entry
123790351 CDS
T07931
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
KO
K05862
voltage-dependent anion channel protein 1
Organism
uar
Ursus americanus (American black bear)
Pathway
uar04020
Calcium signaling pathway
uar04022
cGMP-PKG signaling pathway
uar04217
Necroptosis
uar04218
Cellular senescence
uar04613
Neutrophil extracellular trap formation
uar04621
NOD-like receptor signaling pathway
uar04979
Cholesterol metabolism
uar05010
Alzheimer disease
uar05012
Parkinson disease
uar05014
Amyotrophic lateral sclerosis
uar05016
Huntington disease
uar05017
Spinocerebellar ataxia
uar05020
Prion disease
uar05022
Pathways of neurodegeneration - multiple diseases
uar05164
Influenza A
uar05166
Human T-cell leukemia virus 1 infection
uar05208
Chemical carcinogenesis - reactive oxygen species
uar05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
uar00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
123790351 (VDAC1)
04022 cGMP-PKG signaling pathway
123790351 (VDAC1)
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
123790351 (VDAC1)
04218 Cellular senescence
123790351 (VDAC1)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
123790351 (VDAC1)
04621 NOD-like receptor signaling pathway
123790351 (VDAC1)
09154 Digestive system
04979 Cholesterol metabolism
123790351 (VDAC1)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
123790351 (VDAC1)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
123790351 (VDAC1)
05164 Influenza A
123790351 (VDAC1)
09164 Neurodegenerative disease
05010 Alzheimer disease
123790351 (VDAC1)
05012 Parkinson disease
123790351 (VDAC1)
05014 Amyotrophic lateral sclerosis
123790351 (VDAC1)
05016 Huntington disease
123790351 (VDAC1)
05017 Spinocerebellar ataxia
123790351 (VDAC1)
05020 Prion disease
123790351 (VDAC1)
05022 Pathways of neurodegeneration - multiple diseases
123790351 (VDAC1)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
123790351 (VDAC1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
uar03029
]
123790351 (VDAC1)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
uar04040
]
123790351 (VDAC1)
Mitochondrial biogenesis [BR:
uar03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
123790351 (VDAC1)
Ion channels [BR:
uar04040
]
Chloride channels
Maxi chloride channel (VDAC)
123790351 (VDAC1)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
123790351
NCBI-ProteinID:
XP_045650660
LinkDB
All DBs
Position
Unknown
AA seq
283 aa
AA seq
DB search
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSVRGALVLGYEGWLAGYQMNFETSKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq
852 nt
NT seq
+upstream
nt +downstream
nt
atggctgtgcctcccacgtatgctgatcttggcaaatctgccagggatgtcttcaccaag
ggttacggatttggcttaataaaacttgacttgaaaacaaaatctgagaatggactggaa
tttacaagctcaggttcagccaacactgagaccaccaaagtgacgggcagtctagaaacc
aagtacagatggaccgaatatggtttgacgtttacagaaaaatggaacactgacaacaca
ctaggcacagagatcactgtggaagatcagcttgcacgtggactgaagctgacctttgat
tcatccttctcaccaaacacagggaaaaaaaatgctaaaatcaagacagggtataagcgg
gagcacatcaacctgggctgcgacgtggatttcgacattgccggtccttcggtccggggc
gctttggtgctgggctatgaaggctggctggccggctaccagatgaattttgagacttcg
aagtctcgagtgacccagagcaactttgcggttggctacaagactgacgagttccagctc
cacactaacgtaaacgatgggacagagttcggtggctccatttatcagaaggtgaacaag
aagttagagactgctgtcaatctggcctggacagcaggaaatagtaacactcgctttgga
atagcggccaagtatcagatcgaccctgacgcctgcttctcggctaaagtgaacaactcc
agcctgataggtttaggatacactcagaccctaaagccaggtatcaaactgacgctatcg
gctcttctggatggcaagaatgtcaatgctggcggccacaagcttggtctaggactggaa
tttcaggcataa
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