Loxodonta africana (African savanna elephant): 100667571
Help
Entry
100667571 CDS
T04351
Symbol
IRF3
Name
(RefSeq) interferon regulatory factor 3
KO
K05411
interferon regulatory factor 3
Organism
lav
Loxodonta africana (African savanna elephant)
Pathway
lav04620
Toll-like receptor signaling pathway
lav04621
NOD-like receptor signaling pathway
lav04622
RIG-I-like receptor signaling pathway
lav04623
Cytosolic DNA-sensing pathway
lav04936
Alcoholic liver disease
lav05133
Pertussis
lav05135
Yersinia infection
lav05160
Hepatitis C
lav05161
Hepatitis B
lav05162
Measles
lav05163
Human cytomegalovirus infection
lav05164
Influenza A
lav05165
Human papillomavirus infection
lav05167
Kaposi sarcoma-associated herpesvirus infection
lav05168
Herpes simplex virus 1 infection
lav05169
Epstein-Barr virus infection
lav05170
Human immunodeficiency virus 1 infection
lav05171
Coronavirus disease - COVID-19
lav05203
Viral carcinogenesis
lav05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
lav00001
]
09150 Organismal Systems
09151 Immune system
04620 Toll-like receptor signaling pathway
100667571 (IRF3)
04621 NOD-like receptor signaling pathway
100667571 (IRF3)
04622 RIG-I-like receptor signaling pathway
100667571 (IRF3)
04623 Cytosolic DNA-sensing pathway
100667571 (IRF3)
09160 Human Diseases
09161 Cancer: overview
05203 Viral carcinogenesis
100667571 (IRF3)
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
100667571 (IRF3)
05161 Hepatitis B
100667571 (IRF3)
05160 Hepatitis C
100667571 (IRF3)
05171 Coronavirus disease - COVID-19
100667571 (IRF3)
05164 Influenza A
100667571 (IRF3)
05162 Measles
100667571 (IRF3)
05168 Herpes simplex virus 1 infection
100667571 (IRF3)
05163 Human cytomegalovirus infection
100667571 (IRF3)
05167 Kaposi sarcoma-associated herpesvirus infection
100667571 (IRF3)
05169 Epstein-Barr virus infection
100667571 (IRF3)
05165 Human papillomavirus infection
100667571 (IRF3)
09171 Infectious disease: bacterial
05135 Yersinia infection
100667571 (IRF3)
05133 Pertussis
100667571 (IRF3)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
100667571 (IRF3)
09167 Endocrine and metabolic disease
04936 Alcoholic liver disease
100667571 (IRF3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
lav03000
]
100667571 (IRF3)
04131 Membrane trafficking [BR:
lav04131
]
100667571 (IRF3)
Transcription factors [BR:
lav03000
]
Eukaryotic type
Helix-turn-helix
Tryptophan clusters interferon-regulating factors
100667571 (IRF3)
Membrane trafficking [BR:
lav04131
]
Autophagy
Other autophagy associated proteins
TRIM-directed selective autophagy
100667571 (IRF3)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
IRF-3
Motif
Other DBs
NCBI-GeneID:
100667571
NCBI-ProteinID:
XP_023398997
LinkDB
All DBs
Position
Unknown
AA seq
275 aa
AA seq
DB search
MVLASVPDGGPSGLAVASEQPPQLLLSPNIDVLPPCPNLASSENPLRQLLVPEEEWEFEV
TAFYRGRQVFQQAVFCPGGLRLVGSEAADNTLPGQLMMLPDPGVALTDKGATSFVRRVLS
SLGGGLALWRAGQQLWARRLGHCRTYWAAGEELLPDGTHGPDGEVPKDREGVVFNLGPFV
ADLIAFIEGSKRSPRYTLWFCIGELWPQDQPWTKKLVMVKVVPTCLRVLLDMARVEGASS
LETTMDLHISNSHPLSLTSDQYKAYLQDLAEDMDF
NT seq
828 nt
NT seq
+upstream
nt +downstream
nt
atggtcttggcctcagtcccagatggggggccctcaggactggctgtggcctctgagcag
ccccctcagctcttgctgagccccaacattgacgttcttcctccctgcccaaacctggca
tcctcggaaaacccactgaggcagctgctggtccccgaggaagagtgggagtttgaggtg
accgccttctaccggggccgccaagtcttccagcaggctgtcttctgcccaggtggcctg
cggctggtgggatcagaagcagcagacaatacactgcctgggcagctgatgatgctgcct
gaccctggggtggccctgacagacaagggggcgacaagcttcgtgaggcgtgtgctgagc
tccctaggcggggggcttgctctgtggagggcagggcaacagctctgggcccgaaggctg
gggcactgccgtacatactgggctgcgggtgaggagctgctccctgatggcactcacggg
ccagacggagaggtccccaaagacagagaaggagtcgtgttcaacctgggaccttttgtg
gcagatctgattgccttcatcgaaggaagcaaacgctcaccccgctacaccctctggttc
tgcattggggagttatggccccaggaccagccgtggaccaagaagctggtgatggtcaag
gtagttcccacatgcctccgggtcctgctagacatggcccgggtggagggtgcctcctca
ctggagactaccatggacctgcacatttctaacagccacccgctctccctcacctcagac
cagtacaaggcctatctgcaggacctggccgaggacatggatttctaa
DBGET
integrated database retrieval system