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EEF2K and PRKAA2
Number of citations of the paper that reports this interaction (PubMedID
11500364
)
231
Data Source:
HPRD
(in vivo, in vitro)
EEF2K
PRKAA2
Description
eukaryotic elongation factor 2 kinase
protein kinase AMP-activated catalytic subunit alpha 2
Image
GO Annotations
Cellular Component
Cytoplasm
Cytosol
Postsynaptic Density
Dendritic Spine
Cell
Nucleus
Nucleoplasm
Cytoplasm
Golgi Apparatus
Cytosol
Cytoplasmic Stress Granule
Nuclear Speck
Axon
Dendrite
Neuronal Cell Body
Molecular Function
Protein Kinase Activity
Elongation Factor-2 Kinase Activity
Calcium Ion Binding
Calmodulin Binding
ATP Binding
Translation Factor Activity, RNA Binding
Chromatin Binding
Protein Kinase Activity
Protein Serine/threonine Kinase Activity
AMP-activated Protein Kinase Activity
Protein Serine/threonine/tyrosine Kinase Activity
Protein Binding
ATP Binding
Histone Serine Kinase Activity
Metal Ion Binding
[hydroxymethylglutaryl-CoA Reductase (NADPH)] Kinase Activity
[acetyl-CoA Carboxylase] Kinase Activity
Biological Process
Response To Ischemia
Translational Elongation
Regulation Of Protein Autophosphorylation
Cellular Response To Insulin Stimulus
Negative Regulation Of Apoptotic Process
Positive Regulation Of Endocytosis
Protein Autophosphorylation
Positive Regulation Of Synapse Assembly
Positive Regulation Of Dendritic Spine Morphogenesis
Cellular Response To Calcium Ion
Cellular Response To CAMP
Cellular Response To Anoxia
Cellular Response To Brain-derived Neurotrophic Factor Stimulus
Response To Prolactin
Protein Phosphorylation
Fatty Acid Biosynthetic Process
Cholesterol Biosynthetic Process
Carnitine Shuttle
Cell Cycle Arrest
Signal Transduction
Lipid Biosynthetic Process
Positive Regulation Of Autophagy
Negative Regulation Of Gene Expression
Response To Muscle Activity
Wnt Signaling Pathway
Macroautophagy
Positive Regulation Of Macroautophagy
Regulation Of Macroautophagy
Cellular Response To Nutrient Levels
Negative Regulation Of TOR Signaling
Cellular Response To Oxidative Stress
Histone-serine Phosphorylation
Intracellular Signal Transduction
Cellular Response To Drug
Cellular Response To Glucose Starvation
Regulation Of Fatty Acid Biosynthetic Process
Glucose Homeostasis
Regulation Of Circadian Rhythm
Negative Regulation Of Apoptotic Process
Positive Regulation Of Glycolytic Process
Rhythmic Process
Fatty Acid Homeostasis
Regulation Of Stress Granule Assembly
Regulation Of Microtubule Cytoskeleton Organization
Cellular Response To Calcium Ion
Cellular Response To Glucose Stimulus
Cellular Response To Prostaglandin E Stimulus
Energy Homeostasis
Regulation Of Signal Transduction By P53 Class Mediator
Positive Regulation Of Cellular Protein Localization
Negative Regulation Of Tubulin Deacetylation
Positive Regulation Of Peptidyl-lysine Acetylation
Pathways
mTORC1-mediated signalling
Translocation of SLC2A4 (GLUT4) to the plasma membrane
Macroautophagy
AMPK inhibits chREBP transcriptional activation activity
AMPK inhibits chREBP transcriptional activation activity
Carnitine metabolism
Activation of PPARGC1A (PGC-1alpha) by phosphorylation
Energy dependent regulation of mTOR by LKB1-AMPK
TP53 Regulates Metabolic Genes
Regulation of TP53 Activity through Phosphorylation
Lipophagy
Activation of AMPK downstream of NMDARs
Drugs
Acetylsalicylic acid
Diseases
GWAS
Heel bone mineral density (
30598549
)
Lymphocyte counts (
22286170
)
Interacting Genes
17 interacting genes:
CDK1
EEF2
MAPK11
MAPK12
MAPK13
MAPK14
MAPK8
MAPK9
MAPKAPK2
MAPKAPK3
MAPKAPK5
PRKAA1
PRKAA2
PRKACA
RPS6KA1
RPS6KB1
RPS6KB2
52 interacting genes:
ABI2
ACACA
ACACB
AIMP2
APPBP2
C19orf47
CCNB1IP1
DNMT1
EEF2K
EPM2A
FOS
GLI1
HAT1
HMBOX1
HNF4A
HOMEZ
KCTD1
KIF24
KIFC3
KRT31
KRTAP10-3
L3MBTL3
LEP
MYOZ1
NECAB2
NONO
NOTCH2NLA
NRAP
NUTM1
PBXIP1
PFKFB2
PRKAB1
PRKAG1
RBBP7
RBPMS
RFX6
RPTOR
SNW1
STK11
TCF4
TFAP2A
TLE5
TMOD1
TRIP6
TSC22D4
UBE2I
USHBP1
USP10
VPS52
WWP1
ZBTB8A
ZNF397
Entrez ID
29904
5563
HPRD ID
07369
02735
Ensembl ID
ENSG00000103319
ENSG00000162409
Uniprot IDs
O00418
P54646
PDB IDs
5J8H
5KS5
6NX4
2H6D
2LTU
2YZA
3AQV
4CFE
4CFF
4ZHX
5EZV
5ISO
6B1U
6B2E
6BX6
Enriched GO Terms of Interacting Partners
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