Macaca mulatta (rhesus monkey): 707169
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Entry
707169 CDS
T01028
Symbol
ARAF
Name
(RefSeq) serine/threonine-protein kinase A-Raf
KO
K08845
A-Raf proto-oncogene serine/threonine-protein kinase [EC:
2.7.11.1
]
Organism
mcc
Macaca mulatta (rhesus monkey)
Pathway
mcc01521
EGFR tyrosine kinase inhibitor resistance
mcc01522
Endocrine resistance
mcc04010
MAPK signaling pathway
mcc04012
ErbB signaling pathway
mcc04068
FoxO signaling pathway
mcc04270
Vascular smooth muscle contraction
mcc04650
Natural killer cell mediated cytotoxicity
mcc04720
Long-term potentiation
mcc04726
Serotonergic synapse
mcc04730
Long-term depression
mcc04810
Regulation of actin cytoskeleton
mcc04910
Insulin signaling pathway
mcc04914
Progesterone-mediated oocyte maturation
mcc04928
Parathyroid hormone synthesis, secretion and action
mcc05010
Alzheimer disease
mcc05022
Pathways of neurodegeneration - multiple diseases
mcc05034
Alcoholism
mcc05160
Hepatitis C
mcc05161
Hepatitis B
mcc05200
Pathways in cancer
mcc05205
Proteoglycans in cancer
mcc05208
Chemical carcinogenesis - reactive oxygen species
mcc05210
Colorectal cancer
mcc05211
Renal cell carcinoma
mcc05212
Pancreatic cancer
mcc05213
Endometrial cancer
mcc05214
Glioma
mcc05215
Prostate cancer
mcc05218
Melanoma
mcc05219
Bladder cancer
mcc05220
Chronic myeloid leukemia
mcc05221
Acute myeloid leukemia
mcc05223
Non-small cell lung cancer
mcc05224
Breast cancer
mcc05225
Hepatocellular carcinoma
mcc05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
mcc00001
]
09130 Environmental Information Processing
09132 Signal transduction
04010 MAPK signaling pathway
707169 (ARAF)
04012 ErbB signaling pathway
707169 (ARAF)
04068 FoxO signaling pathway
707169 (ARAF)
09140 Cellular Processes
09142 Cell motility
04810 Regulation of actin cytoskeleton
707169 (ARAF)
09150 Organismal Systems
09151 Immune system
04650 Natural killer cell mediated cytotoxicity
707169 (ARAF)
09152 Endocrine system
04910 Insulin signaling pathway
707169 (ARAF)
04914 Progesterone-mediated oocyte maturation
707169 (ARAF)
04928 Parathyroid hormone synthesis, secretion and action
707169 (ARAF)
09153 Circulatory system
04270 Vascular smooth muscle contraction
707169 (ARAF)
09156 Nervous system
04726 Serotonergic synapse
707169 (ARAF)
04720 Long-term potentiation
707169 (ARAF)
04730 Long-term depression
707169 (ARAF)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
707169 (ARAF)
05205 Proteoglycans in cancer
707169 (ARAF)
05208 Chemical carcinogenesis - reactive oxygen species
707169 (ARAF)
09162 Cancer: specific types
05210 Colorectal cancer
707169 (ARAF)
05212 Pancreatic cancer
707169 (ARAF)
05225 Hepatocellular carcinoma
707169 (ARAF)
05226 Gastric cancer
707169 (ARAF)
05214 Glioma
707169 (ARAF)
05221 Acute myeloid leukemia
707169 (ARAF)
05220 Chronic myeloid leukemia
707169 (ARAF)
05218 Melanoma
707169 (ARAF)
05211 Renal cell carcinoma
707169 (ARAF)
05219 Bladder cancer
707169 (ARAF)
05215 Prostate cancer
707169 (ARAF)
05213 Endometrial cancer
707169 (ARAF)
05224 Breast cancer
707169 (ARAF)
05223 Non-small cell lung cancer
707169 (ARAF)
09172 Infectious disease: viral
05161 Hepatitis B
707169 (ARAF)
05160 Hepatitis C
707169 (ARAF)
09164 Neurodegenerative disease
05010 Alzheimer disease
707169 (ARAF)
05022 Pathways of neurodegeneration - multiple diseases
707169 (ARAF)
09165 Substance dependence
05034 Alcoholism
707169 (ARAF)
09176 Drug resistance: antineoplastic
01521 EGFR tyrosine kinase inhibitor resistance
707169 (ARAF)
01522 Endocrine resistance
707169 (ARAF)
09180 Brite Hierarchies
09181 Protein families: metabolism
01001 Protein kinases [BR:
mcc01001
]
707169 (ARAF)
Enzymes [BR:
mcc01000
]
2. Transferases
2.7 Transferring phosphorus-containing groups
2.7.11 Protein-serine/threonine kinases
2.7.11.1 non-specific serine/threonine protein kinase
707169 (ARAF)
Protein kinases [BR:
mcc01001
]
Serine/threonine kinases: TKL group
RAF family [OT]
707169 (ARAF)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PK_Tyr_Ser-Thr
Pkinase
RBD
C1_1
Kinase-like
zf-RING-like
ABC1
Pkinase_fungal
TUG-UBL1
Kdo
Motif
Other DBs
NCBI-GeneID:
707169
NCBI-ProteinID:
XP_014982783
Ensembl:
ENSMMUG00000011418
UniProt:
H9FU32
LinkDB
All DBs
Position
X:47507237..47518253
Genome browser
AA seq
606 aa
AA seq
DB search
MEPPRGPPANGAEPSRAVGTVKVYLPNKQRTVVTVRDGMSVYDSLDKALKVRGLNQDCCV
VYRLIKGRKTVTAWDTAIAPLDGEELIVEVLEDVPLTMHNFVRKTFFSLAFCDFCLKFLF
HGFRCQTCGYKFHQHCSSKVPTVCVDMSTNRQQFYHSVQDLSGGSRQHEAPSNRPLNELL
TPQGPRPHTQHCDPEHFPFPAPANAPLQRIRSTSTPNVHMVSTTAPMDSNLIQLTGQSFS
TDAASSRGGGDGTPRGSPSPASVSSGRKSPHSKSPAEQRERKSLADDKKKVKNLGYRDSG
YYWEVPPSEVQLLKRIGTGSFGTVFRGRWHGDVAVKVLKVSQPTAEQAQAFKNEMQVLRK
TRHVNILLFMGFMTRPGFAIITQWCEGSSLYHHLHVADTRFDMVQLIDVARQTAQGMDYL
HAKNIIHRDLKSNNIFLHEGLTVKIGDFGLATVKTRWSGAQPLEQPSGSVLWMAAEVIRM
QDPNPYSFQSDVYAYGVVLYELMTGSLPYSHIGCRDQIIFMVGRGYLSPDLSKISSNCPK
AMRRLLSDCLKFQREERPLFPQILATIELLQRSLPKIERSASEPSLHRTQADELPACLLS
AARLVP
NT seq
1821 nt
NT seq
+upstream
nt +downstream
nt
atggagccaccacggggcccccctgccaatggggccgagccgtcccgggcagtgggcacc
gtcaaagtgtacctgcccaacaagcaacgcacggtggtgactgtccgggatggcatgagt
gtctacgactctctagacaaggccctgaaggtgcggggtctaaatcaggactgctgtgtg
gtctaccgactcatcaagggacgaaagacagtcactgcctgggacacagccattgctccc
ctggatggcgaggagctcattgtcgaggtccttgaagatgtcccgctgaccatgcacaat
tttgtacggaagaccttcttcagcctggcattctgtgacttctgccttaagtttctgttc
catggcttccgttgccaaacctgtggctacaagttccaccagcattgttcctccaaggtc
cccacagtctgtgttgacatgagtaccaaccgccaacagttctaccacagtgtccaggat
ttgtccggaggctccagacaacatgaggctccctcgaaccgccccctgaatgagttgcta
accccccagggtcccaggcctcacactcagcactgtgacccggagcacttccccttccct
gccccggccaacgcccccctgcagcgcatccgctccacatccactcccaacgtccatatg
gtcagcaccacggcccccatggactccaacctcatccagctcactggccagagtttcagc
actgatgctgccagtagtagaggaggtggtgatggaaccccccgggggagccccagccca
gccagcgtgtcctcggggaggaagtccccacattccaagtcaccagcagagcagcgtgag
cggaagtctttggccgatgacaagaagaaagtgaagaacctggggtaccgggactcaggc
tattactgggaagtaccacccagtgaggtgcagctgctgaagaggatcgggacgggctcg
tttggcaccgtgtttcgagggcggtggcatggcgatgtggctgtgaaggtgctcaaggtg
tcccagcccacagctgagcaggcccaagctttcaagaatgagatgcaggtgctcaggaag
acgcgacatgtcaacatcttgctgtttatgggcttcatgacccggccgggattcgccatc
atcacacagtggtgtgaaggctccagcctctaccatcacctgcatgtggccgacacgcgc
ttcgacatggtccagctcatcgacgtggcccggcagactgcccagggcatggactacctc
catgccaagaacatcatccaccgagatctcaagtctaacaacatcttcctacatgagggg
ctcacggtgaagatcggtgactttggcttggccacagtgaagactcgatggagcggggcc
cagcccttggagcagccctcaggctctgtgctgtggatggcagctgaggtgatccgtatg
caggacccgaacccctacagcttccagtcagatgtctatgcctacggggttgtgctctac
gagctcatgactggctcactgccttacagccacattggctgccgtgaccagattatcttt
atggtgggccgtggctatctgtccccggacctcagcaaaatctctagcaactgccccaag
gccatgcggcgcctgctgtctgactgcctcaagttccagcgggaggaacggcccctcttc
ccccagatcctggccacaattgagctgctgcaacggtcactccccaagattgagcggagt
gcctcggaaccctccttgcaccgcacccaggctgatgagttgcctgcctgcctactcagc
gcagcccgccttgtgccttag
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