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Dataset Title Dataset ID Primary Publications Keywords
Potent and Selective Phosphodiesterase 10A Inhibitors PDB:4FCB Novel triazines as potent and selective phosphodiesterase 10A inhibitors.
Hydrolase/Hydrolase inhibitor
Binding Sites
Cyclic AMP
Cyclic GMP
Ligands
Phosphodiesterase Inhibitors
Hydrolase-Hydrolase inhibitor complex
Crystal structure of the major cat allergen Fel d 1 (1+2) PDB:1ZKR Crystal structure of the major cat allergen Fel d 1 (1+2)
ALLERGEN
CAT ALLERGEN
UTEROGLOBIN
SECRETOGLOBIN
ALLERGEN
Highly Potent, Selective, and Orally Active Phosphodiestarase 10A Inhibitors PDB:3SNI Highly Potent, Selective, and Orally Active Phosphodiesterase 10A Inhibitors.
HYDROLASE/HYDROLASE INHIBITOR
Hydrolase
Hydrolase inhibitor
Zn Binding
HYDROLASE-HYDROLASE INHIBITOR complex
The crystal structure of the P132R, Y133G mutant of Pyrococcus furiosus phosphoglucose isomerase in complex with manganese and 5-phospho-D-arabinonate. PDB:4LTA Correlated mutation analysis as a tool for smart library design to improve protein performance.
ISOMERASE
Cupin Fold
Isomerase
Glucose 6-phosphate and Fructose 6-phosphate binding
INTERLEUKIN-4 / RECEPTOR ALPHA CHAIN COMPLEX PDB:1IAR Crystal structure of the interleukin-4/receptor alpha chain complex reveals a mosaic binding interface.
CYTOKINE/RECEPTOR
CYTOKINE RECEPTOR
INTERLEUKIN-4
CYTOKINE-RECEPTOR COMPLEX
Crystal Structure of an iodinated insulin analog PDB:5EMS Extending Halogen-based Medicinal Chemistry to Proteins: IODO-INSULIN AS A CASE STUDY.
HORMONE
insulin
hormone
non-standard modification
protein design
protein engineering
Crystal structure of rat phosphodiesterase 10A in complex with ligand WEB-3 PDB:3LXG Discovery of imidazo[1,5-a]pyrido[3,2-e]pyrazines as a new class of phosphodiesterase 10A inhibitiors.
HYDROLASE
PHOSPHODIESTERASE 10A; CATALYTIC DOMAIN
Allosteric enzyme
cAMP
cAMP-binding
cGMP
cGMP-binding
Hydrolase
Metal-binding
Nucleotide-binding
Structure of Helicobacter pylori adhesin BabA determined by SeMet SAD PDB:4ZH0 Structural basis of Lewis(b) antigen binding by the Helicobacter pylori adhesin BabA.
S
blood group antigen binding
Structural characterization of the tetrameric form of the major cat allergen fel D 1 PDB:2EJN Structural characterization of the tetrameric form of the major cat allergen Fel d 1
ALLERGEN
ALLERGEN
CAT ALLERGEN
UTEROGLOBIN
SECRETOGLOBIN
The crystal structure of the P132A, Y133D mutant of Pyrococcus furiosus phosphoglucose isomerase in complex with manganese. PDB:4LUL Correlated mutation analysis as a tool for smart library design to improve protein performance.
ISOMERASE
Cupin Fold
Isomerase
Glucose 6-phsphate and Fructose 6-phosphate binding protein
The crystal structure of the P132V mutant of Pyrococcus furiosus phosphoglucose isomerase in complex with manganese and fructose-6- phosphate. PDB:4LUM Correlated mutation analysis as a tool for smart library design to improve protein performance.
ISOMERASE
Cupin Fold
Isomerase
Glucose 6-phosphate and Fructose 6-phosphate binding protein
Highly Potent, Selective, and Orally Active Phosphodiestarase 10A Inhibitors PDB:3SN7 Highly Potent, Selective, and Orally Active Phosphodiesterase 10A Inhibitors.
HYDROLASE/HYDROLASE INHIBITOR
Hydrolase
Hydrolase inhibitor
Zn Binding
HYDROLASE-HYDROLASE INHIBITOR complex
Structural basis of Lewisb antigen binding by the Helicobacter pylori adhesin BabA PDB:4ZH7 Structural basis of Lewis(b) antigen binding by the Helicobacter pylori adhesin BabA.
S
blood group antigen binding
Potent and Selective Phosphodiesterase 10A Inhibitors PDB:4FCD Novel triazines as potent and selective phosphodiesterase 10A inhibitors.
Hydrolase/Hydrolase inhibitor
Binding Sites
Cyclic AMP
Cyclic GMP
Humans
Hydrolysis
Ligands
Phosphodiesterase Inhibitors
Phosphoric Diester Hydrolases
Recombinant Proteins
Structure-Activity Relationship
Hydrolase-Hydrolase inhibitor complex
Highly Potent, Selective, and Orally Active Phosphodiestarase 10A Inhibitors PDB:3SNL Highly Potent, Selective, and Orally Active Phosphodiesterase 10A Inhibitors.
HYDROLASE/HYDROLASE INHIBITOR
Hydrolase
Hydrolase inhibitor
Zn Binding
HYDROLASE-HYDROLASE INHIBITOR complex
Crystal structure of Fel d 1- the major cat allergen PDB:1PUO The crystal structure of the major cat allergen Fel d 1, a member of the secretoglobin family.
ALLERGEN
cat allergen
uteroglobin
secretoglobin
ALLERGEN
The crystal structure of the P132A, Y133G mutant of Pyrococcus furiosus phosphoglucose isomerase in complex with manganese and 5-phospho-D-arabinonate. PDB:4LUK Correlated mutation analysis as a tool for smart library design to improve protein performance.
ISOMERASE
Cupin Fold
Isomerase
Glucose 6-phsphate and Fructose 6-phosphate binding protein