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ADAM17 and MAD2L2
Data Source:
HPRD
(in vitro, in vivo)
ADAM17
MAD2L2
Description
ADAM metallopeptidase domain 17
mitotic arrest deficient 2 like 2
Image
GO Annotations
Cellular Component
Cytoplasm
Cytosol
Plasma Membrane
Integral Component Of Plasma Membrane
Cell-cell Junction
Focal Adhesion
Cell Surface
Actin Cytoskeleton
Membrane
Apical Plasma Membrane
Ruffle Membrane
Membrane Raft
Nucleus
Nucleoplasm
Anaphase-promoting Complex
Chromosome
Nucleolus
Spindle
Cytosol
Zeta DNA Polymerase Complex
Site Of Double-strand Break
Molecular Function
Endopeptidase Activity
Metalloendopeptidase Activity
Notch Binding
Interleukin-6 Receptor Binding
Integrin Binding
Protein Binding
Peptidase Activity
Metallopeptidase Activity
SH3 Domain Binding
PDZ Domain Binding
Metal Ion Binding
Metalloendopeptidase Activity Involved In Amyloid Precursor Protein Catabolic Process
RNA Polymerase II Activating Transcription Factor Binding
Protein Binding
JUN Kinase Binding
Biological Process
Response To Hypoxia
Positive Regulation Of Protein Phosphorylation
Neutrophil Mediated Immunity
Germinal Center Formation
Positive Regulation Of Leukocyte Chemotaxis
Proteolysis
Membrane Protein Ectodomain Proteolysis
Cell Adhesion
Epidermal Growth Factor Receptor Signaling Pathway
Notch Signaling Pathway
Notch Receptor Processing
Positive Regulation Of Cell Population Proliferation
Positive Regulation Of T Cell Chemotaxis
Protein Processing
B Cell Differentiation
Positive Regulation Of Cell Growth
Positive Regulation Of Cell Migration
Positive Regulation Of Transforming Growth Factor Beta Receptor Signaling Pathway
Negative Regulation Of Transforming Growth Factor Beta Receptor Signaling Pathway
Membrane Protein Intracellular Domain Proteolysis
Response To Lipopolysaccharide
Positive Regulation Of Chemokine Production
Regulation Of Mast Cell Apoptotic Process
T Cell Differentiation In Thymus
Tumor Necrosis Factor-mediated Signaling Pathway
Cell Adhesion Mediated By Integrin
Wound Healing, Spreading Of Epidermal Cells
Receptor Transactivation
Response To Drug
Amyloid Precursor Protein Catabolic Process
Positive Regulation Of Blood Vessel Endothelial Cell Migration
Positive Regulation Of Cyclin-dependent Protein Serine/threonine Kinase Activity
Positive Regulation Of Epidermal Growth Factor-activated Receptor Activity
Spleen Development
Cell Motility
Defense Response To Gram-positive Bacterium
Positive Regulation Of Cellular Component Movement
Cellular Response To High Density Lipoprotein Particle Stimulus
Negative Regulation Of Cold-induced Thermogenesis
Positive Regulation Of G1/S Transition Of Mitotic Cell Cycle
Positive Regulation Of Tumor Necrosis Factor-mediated Signaling Pathway
Positive Regulation Of Vascular Endothelial Cell Proliferation
Negative Regulation Of Transcription By RNA Polymerase II
Regulation Of Cell Growth
Double-strand Break Repair
Actin Filament Organization
Mitotic Spindle Assembly Checkpoint
Negative Regulation Of Epithelial To Mesenchymal Transition
Negative Regulation Of Transcription By Competitive Promoter Binding
Positive Regulation Of Peptidyl-serine Phosphorylation
Negative Regulation Of Protein Catabolic Process
Error-prone Translesion Synthesis
DNA Damage Response, Signal Transduction Resulting In Transcription
Negative Regulation Of DNA-binding Transcription Factor Activity
Positive Regulation Of Isotype Switching
Positive Regulation Of Transcription, DNA-templated
Cell Division
Negative Regulation Of Canonical Wnt Signaling Pathway
Negative Regulation Of Ubiquitin Protein Ligase Activity
Negative Regulation Of Double-strand Break Repair Via Homologous Recombination
Negative Regulation Of Cell-cell Adhesion Mediated By Cadherin
Negative Regulation Of Transcription Regulatory Region DNA Binding
Positive Regulation Of Double-strand Break Repair Via Nonhomologous End Joining
Pathways
Nuclear signaling by ERBB4
Collagen degradation
Signaling by EGFR
Regulated proteolysis of p75NTR
Activated NOTCH1 Transmits Signal to the Nucleus
Constitutive Signaling by NOTCH1 PEST Domain Mutants
Constitutive Signaling by NOTCH1 t(7;9)(NOTCH1:M1580_K2555) Translocation Mutant
Constitutive Signaling by NOTCH1 HD Domain Mutants
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants
Release of Hh-Np from the secreting cell
TNF signaling
CD163 mediating an anti-inflammatory response
Growth hormone receptor signaling
Translesion synthesis by REV1
Translesion synthesis by POLK
Translesion synthesis by POLI
Drugs
(3S)-1-{[4-(but-2-yn-1-yloxy)phenyl]sulfonyl}pyrrolidine-3-thiol
3-{[4-(but-2-yn-1-yloxy)phenyl]sulfonyl}propane-1-thiol
4-({4-[(4-AMINOBUT-2-YNYL)OXY]PHENYL}SULFONYL)-N-HYDROXY-2,2-DIMETHYLTHIOMORPHOLINE-3-CARBOXAMIDE
(2R)-N-HYDROXY-2-[(3S)-3-METHYL-3-{4-[(2-METHYLQUINOLIN-4-YL)METHOXY]PHENYL}-2-OXOPYRROLIDIN-1-YL]PROPANAMIDE
methyl (1R,2S)-2-(hydroxycarbamoyl)-1-{4-[(2-methylquinolin-4-yl)methoxy]benzyl}cyclopropanecarboxylate
(1S,3R,6S)-4-oxo-6-{4-[(2-phenylquinolin-4-yl)methoxy]phenyl}-5-azaspiro[2.4]heptane-1-carboxylic acid
N-{[4-(but-2-yn-1-yloxy)phenyl]sulfonyl}-5-methyl-D-tryptophan
(3S)-4-{[4-(BUT-2-YNYLOXY)PHENYL]SULFONYL}-N-HYDROXY-2,2-DIMETHYLTHIOMORPHOLINE-3-CARBOXAMIDE
Diseases
GWAS
Birth weight (
31043758
)
Offspring birth weight (
31043758
)
Arterial stiffness (brachial-femoral pulse wave velocity) (
32790701
)
Visceral adipose tissue adjusted for BMI (
22589738
)
Interacting Genes
14 interacting genes:
DLG1
ERBB4
FHL2
MAD2L1
MAD2L2
NOTCH1
PTPN3
SH3D19
TGFA
TIMP3
TNF
TNFRSF1A
TNFRSF1B
TNFSF11
47 interacting genes:
ADAM15
ADAM17
ADAM9
C20orf85
CAMK2B
CDC20
CDH1
DEPDC5
ELK1
FAM217B
FTO
FZR1
GSC2
IKZF1
IKZF3
INCA1
KCTD9
KRT34
MAD2L1
MAD2L1BP
MBD3L1
MYBPC2
PLAGL2
POLDIP2
PPM1B
PRCC
PRR5L
PRRC2A
RAB11FIP4
RBBP6
REL
REV1
REV3L
SFI1
SHLD1
TCF4
THAP6
TRIM27
TRIM54
TRIM7
YPEL3
YY1AP1
ZBED1
ZMYND12
ZNF511
ZNF558
ZNF655
Entrez ID
6868
10459
HPRD ID
04703
07246
Ensembl ID
ENSG00000151694
ENSG00000116670
Uniprot IDs
B2RNB2
P78536
A0A024R4I4
Q9UI95
PDB IDs
1BKC
1ZXC
2A8H
2DDF
2FV5
2FV9
2I47
2M2F
2OI0
3B92
3CKI
3E8R
3EDZ
3EWJ
3G42
3KMC
3KME
3L0T
3L0V
3LE9
3LEA
3LGP
3O64
3ABD
3ABE
3VU7
4EXT
4GK0
4GK5
5XPT
5XPU
6BC8
6BCD
6BI7
6K07
6K08
6KEA
6KTO
6NIF
Enriched GO Terms of Interacting Partners
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