about
Thermodynamics and structural analysis of positive allosteric modulation of the ionotropic glutamate receptor GluA2Intersubunit Bridge Formation Governs Agonist Efficacy at Nicotinic Acetylcholine 4 2 Receptors: UNIQUE ROLE OF HALOGEN BONDING REVEALEDStructural analysis of the positive AMPA receptor modulators CX516 and Me-CX516 in complex with the GluA2 ligand-binding domainSynthesis, pharmacological and structural characterization, and thermodynamic aspects of GluA2-positive allosteric modulators with a 3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide scaffoldL-Asp is a useful tool in the purification of the ionotropic glutamate receptor A2 ligand-binding domainAcetylcholine-Binding Protein Engineered to Mimic the α4-α4 Binding Pocket in α4β2 Nicotinic Acetylcholine Receptors Reveals Interface Specific Interactions Important for Binding and ActivityStudies on Aryl-Substituted Phenylalanines: Synthesis, Activity, and Different Binding Modes at AMPA ReceptorsSer649 and Ser650 are the major determinants of protein kinase A-mediated activation of human hormone-sensitive lipase against lipid substrates.Quarternary structure and enzymological properties of the different hormone-sensitive lipase (HSL) isoforms.Perilipin 1 binds to aquaporin 7 in human adipocytes and controls its mobility via protein kinase A mediated phosphorylation.Enthalpy-Entropy Compensation in the Binding of Modulators at Ionotropic Glutamate Receptor GluA2.Phosphorylation of hormone-sensitive lipase by protein kinase A in vitro promotes an increase in its hydrophobic surface area.Invisible detergents for structure determination of membrane proteins by small-angle neutron scattering.
P50
Q27673244-9539F591-795E-435E-BEAB-9E9F463F3120Q27676179-E349B27F-256C-4504-8C18-C32027B877BBQ27685440-6E09C714-5E04-4D49-A233-55B26A35AC5EQ27687224-30100A8E-CD00-48CD-85DA-CB8BFC0AA349Q27689654-09F20BFE-8030-47FF-8294-C8F24DD41599Q27701563-3336CD69-96FD-49FA-8F5C-6BC4D43FB37EQ27703123-96E3A427-0805-490B-B2D8-1CB727121852Q33385449-D7C2E99F-CFA4-4095-9E16-BD7182074104Q33612270-D0509166-7DA5-4BB9-9803-5089A45FEBADQ36189281-27CC1EF5-7F9C-421C-AD26-B70F22DCDA3BQ41980060-E5609987-4657-41DE-A72D-C7D046356920Q43296305-0610C7B4-FCA5-41D0-8B86-56DB5CDF17D6Q47311421-887DB065-F20E-4338-A18D-870C680A287F
P50
description
researcher, ORCID id # 0000-0001-5925-5639
@en
wetenschapper
@nl
name
Christian Krintel
@ast
Christian Krintel
@en
Christian Krintel
@es
Christian Krintel
@nl
type
label
Christian Krintel
@ast
Christian Krintel
@en
Christian Krintel
@es
Christian Krintel
@nl
prefLabel
Christian Krintel
@ast
Christian Krintel
@en
Christian Krintel
@es
Christian Krintel
@nl
P106
P21
P31
P496
0000-0001-5925-5639