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MAST1 and CYP2C8
Number of citations of the paper that reports this interaction (PMID
21163940
)
13
Data Source:
BioGRID
(two hybrid)
MAST1
CYP2C8
Gene Name
microtubule associated serine/threonine kinase 1
cytochrome P450, family 2, subfamily C, polypeptide 8
Image
Gene Ontology Annotations
Cellular Component
Cytoplasm
Cytoskeleton
Plasma Membrane
Cytoplasm
Endoplasmic Reticulum Membrane
Intracellular Membrane-bounded Organelle
Molecular Function
Magnesium Ion Binding
Protein Serine/threonine Kinase Activity
Protein Binding
ATP Binding
Monooxygenase Activity
Iron Ion Binding
Arachidonic Acid Epoxygenase Activity
Steroid Hydroxylase Activity
Oxidoreductase Activity, Acting On Paired Donors, With Incorporation Or Reduction Of Molecular Oxygen, Reduced Flavin Or Flavoprotein As One Donor, And Incorporation Of One Atom Of Oxygen
Oxygen Binding
Heme Binding
Caffeine Oxidase Activity
Aromatase Activity
Biological Process
Protein Phosphorylation
Cytoskeleton Organization
Intracellular Signal Transduction
Organic Acid Metabolic Process
Xenobiotic Metabolic Process
Drug Metabolic Process
Arachidonic Acid Metabolic Process
Epoxygenase P450 Pathway
Exogenous Drug Catabolic Process
Small Molecule Metabolic Process
Oxidation-reduction Process
Oxidative Demethylation
Omega-hydroxylase P450 Pathway
Pathways
Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B)
Metabolism of lipids and lipoproteins
Metabolic disorders of biological oxidation enzymes
Phase 1 - Functionalization of compounds
Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A)
Arachidonic acid metabolism
Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4)
Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56)
Cytochrome P450 - arranged by substrate type
CYP2E1 reactions
Biological oxidations
Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD)
Defective FMO3 causes Trimethylaminuria (TMAU)
Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR)
Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET)
Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX)
Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4)
Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA)
Defective CYP1B1 causes Glaucoma
Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5)
Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3)
Defective CYP19A1 causes Aromatase excess syndrome (AEXS)
Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5)
Defective CYP24A1 causes Hypercalcemia, infantile (HCAI)
Xenobiotics
Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE)
Defective MAOA causes Brunner syndrome (BRUNS)
Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency)
Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3)
Drugs
Diseases
GWAS
Immune response to smallpox vaccine (IL-6) (
22542470
)
Osteonecrosis of the jaw (
18594024
)
Response to clopidogrel therapy (
19706858
)
Warfarin maintenance dose (
23755828
)
Protein-Protein Interactions
37 interactors:
A2M
AP1M2
APOE
APP
BLMH
CDK5
CYP2C8
CYP2C9
DNAJB1
ECSIT
EGFR
ELAVL3
EXOC6
EXOSC1
FBXL12
FBXW4
GCDH
IFIT3
IFIT5
LONP1
LOXL4
MGEA5
NOS3
PAXIP1
PRAM1
PRDX2
PSEN2
PTEN
RAB3A
RAB3D
RAD23A
RNF32
RNLS
RPP30
SNTA1
SNTB2
STAMBPL1
11 interactors:
A2M
APOE
BLMH
DNAJB1
ECSIT
EXOC6
IFIT3
LONP1
MAST1
PSEN1
RNF32
Entrez ID
22983
1558
HPRD ID
17469
03083
Ensembl ID
ENSG00000105613
ENSG00000138115
Uniprot IDs
Q9Y2H9
B7Z1F5
P10632
PDB IDs
2M9X
3PS4
1PQ2
2NNH
2NNI
2NNJ
2VN0
Enriched GO Terms of Interacting Partners
?
Catabolic Process
Synapse Organization
Negative Regulation Of Protein Metabolic Process
Response To Stress
Negative Regulation Of Cellular Protein Metabolic Process
Response To Abiotic Stimulus
Negative Regulation Of Presynaptic Membrane Organization
Regulation Of Synaptic Plasticity
Regulation Of Synaptic Transmission
Regulation Of Oxidoreductase Activity
Synapse Assembly
Exocytosis
Regulation Of Cellular Protein Metabolic Process
Axon Development
Response To Stimulus
Regulation Of Presynaptic Membrane Organization
Regulation Of Nitric-oxide Synthase Activity
Regulation Of Protein Metabolic Process
Negative Regulation Of Dendritic Spine Development
Learning Or Memory
Regulation Of Proteolysis
Regulation Of Dendritic Spine Development
Negative Regulation Of Cell Death
Cognition
Omega-hydroxylase P450 Pathway
Synaptic Vesicle Exocytosis
Anatomical Structure Morphogenesis
Secretion By Cell
Vesicle Docking Involved In Exocytosis
Axonogenesis
Positive Regulation Of Exocytosis
Neuron Projection Development
Vesicle-mediated Transport
Glial Cell Differentiation
Protein Metabolic Process
Establishment Of Protein Localization
Regulation Of Epidermal Growth Factor Receptor Signaling Pathway
Cell Morphogenesis Involved In Neuron Differentiation
Negative Regulation Of Neuron Differentiation
Membrane Organization
Oxidative Demethylation
Protein Catabolic Process
Establishment Of Vesicle Localization
Oligodendrocyte Differentiation
Positive Regulation Of Catalytic Activity
Regulation Of ERBB Signaling Pathway
Vesicle Docking
Regulation Of Cellular Amino Acid Metabolic Process
Endothelial Cell Migration
Vesicle Localization
Regulation Of Inclusion Body Assembly
Response To Stress
Protein Metabolic Process
Exocytosis
Oxidation-dependent Protein Catabolic Process
Cajal-Retzius Cell Differentiation
Positive Regulation Of Low-density Lipoprotein Particle Receptor Catabolic Process
Positive Regulation Of Dendritic Spine Maintenance
Negative Regulation Of Dendritic Spine Maintenance
Negative Regulation Of Phospholipid Efflux
Negative Regulation Of Lipid Transport Across Blood Brain Barrier
Positive Regulation Of Lipid Transport Across Blood Brain Barrier
Beta-amyloid Formation
Positive Regulation Of Postsynaptic Membrane Organization
Negative Regulation Of Postsynaptic Membrane Organization
Regulation Of Oxidoreductase Activity
Response To Stimulus
Response To Oxidative Stress
Regulation Of Cellular Component Organization
Extracellular Matrix Disassembly
Establishment Of Localization In Cell
Positive Regulation Of Neurofibrillary Tangle Assembly
Smooth Endoplasmic Reticulum Calcium Ion Homeostasis
Negative Regulation Of Complement Activation, Lectin Pathway
Negative Regulation Of Presynaptic Membrane Organization
Positive Regulation Of Presynaptic Membrane Organization
Cellular Response To Stimulus
Secretion By Cell
Immune System Process
Negative Regulation Of Neuron Projection Development
Positive Regulation Of Phospholipid Efflux
Negative Regulation Of Cholesterol Biosynthetic Process
Regulation Of Mitochondrial DNA Replication
Regulation Of Postsynaptic Membrane Organization
Very-low-density Lipoprotein Particle Clearance
Negative Regulation Of Cell Projection Organization
Regulation Of Catalytic Activity
Synaptic Vesicle Targeting
Regulation Of Resting Membrane Potential
Cellular Localization
Positive Regulation Of Cellular Protein Catabolic Process
Maintenance Of Location In Cell
Regulation Of Axonogenesis
Secretion
Regulation Of Low-density Lipoprotein Particle Receptor Catabolic Process
Regulation Of Tau-protein Kinase Activity
Response To Aluminum Ion
Negative Regulation Of Cholesterol Efflux
N-methyl-D-aspartate Receptor Clustering
Regulation Of Presynaptic Membrane Organization
Tagcloud
?
allele
apolipoprotein
associations
cardiotoxicity
commonly
comt
conform
epsilon4
failed
fatigue
genetic
genotype
guidelines
il6
impairment
listed
lle655val
met
neuropathy
polymorphisms
reporting
strega
systematic
toxicities
transparent
underlying
val
variant
variants
Tagcloud (Difference)
?
allele
apolipoprotein
associations
cardiotoxicity
commonly
comt
conform
epsilon4
failed
fatigue
genetic
genotype
guidelines
il6
impairment
listed
lle655val
met
neuropathy
polymorphisms
reporting
strega
systematic
toxicities
transparent
underlying
val
variant
variants
Tagcloud (Intersection)
?