amide binding oor Frans

amide binding

Vertalings in die woordeboek Engels - Frans

liaison d'amine

en
Interacting selectively and non-covalently with an amide, any derivative of an oxoacid in which an acidic hydroxy group has been replaced by an amino or substituted amino group.
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PDZ2 from hPTP1E, amide exchange, ligand binding, NMR.
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One such agonist, gambogic amide, selectively binds to TrkA but not TrkB or C, robustly induces its tyrosine phosphorylation and downstream signaling activation including Akt and MAP kinases.
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The invention also relates to modulation of levels of fatty acid amides for treatment or amelioration of diseases or disorders by modulating binding of the fatty acid amides to fatty acid binding proteins.
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The present 1,2- or 1,3-diamine and amide compounds have high binding affinity to the sigma receptor.
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He died, the last prince, amid poems, phylacteries, and foot bindings.
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Glycylglycyl-L-histidine-N-methyl amide is a copper-binding tripeptide designed and synthesized to mimic the copper-transport site of human albumin.
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Antibodies that specifically bind to fatty acid amide hydrolases and methods of using the antibodies are provided herein.
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The main anion complexing agents are anion binding agents having amidic hydrogen bond donor(s) such as found in bis(amide)s.
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The amide/imide composition is preferably a non-halogenated, single-ring hydantoin that binds methyl amines to the amide or imide functional group of the hydantoin.
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Conformationally restrained oligomers containing amide or carbamate linkages for sequence-specific binding
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The peptides of the invention are characterized by a C-terminal, non-enzymatic originated amide or by a nitric oxide binding site.
La liste des tâches déléguées par l'autorité responsable est communiquée à l'autorité déléguée, qui en prend actepatents-wipo patents-wipo
At higher amounts of adsorbed amide, hydrogen bonding arises either from the self-association of amide molecules or from the binding of these to the surface phosphate anions.
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The binding sites were formed by an amide and a strongly complexing ligand such as an amine.
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A method of treating gastrointestinal cancers dependent on the prohormones amidated gastrin-17 and glycine extended G-17, comprising the administration to the patient of an anti-gastrin-17 immunogen which induces antibodies which bind and neutralize amidated and glycine-extended gastrin-17.
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Amide compounds, amide polymers, compositions including amide compounds and amide polymers may be used to bind target ions, such as phosphorous-containing compounds in the gastrointestinal tract of animals.
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The methods utilize water-soluble polymers having pendant derivatized amide, ester or ether functionalites for dispersing and binding various classes of ceramic materials.
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Short analogs of SRIF which are selective for SSTR1 in contrast to the other four SRIF receptors comprise a 6-member ring wherein D-Agl(NMe,2Np) and IAmp are flanked by residues having an aromatic side chain end wherein its C-terminus is amidated, inhibit the binding of a universal SRIF radioligand to the cloned human receptor SSTR1, but not to the other receptors.
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A ligand to GPR8, its DNA, etc. More particularly speaking, a polypeptide capable of binding to GPR8 or its amide or ester or salts thereof, DNA thereof, etc. are provided.
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Binding of nucleotide (e.g., ATP) to the donor site decreases the β-content and shifts the amide I band to higher wavenumbers, whereas binding of nucleotide (e.g., AMP) to the acceptor site does not produce any change in conformation of the protein.
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An aromatic ring in the structure is substituted with a radiohalogen atom and the substitution on the amide nitrogen atom is such that the compound binds to melanin.
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Novel 1,2,3,4-tetrahydroquinoxaline derivative which has, as substituent, phenyl group having sulfonic acid ester structure or sulfonic acid amide structure introduced therein and has glucocorticoid receptor-binding activity
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We have used two-dimensional 1H-15N heteronuclear single quantum correlation spectroscopy to measure the pH dependence of backbone amide group chemical shifts in the actin binding protein hisactophilin over the pH range 5.7-11.1.
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Certain YceI members could bind amphiphilic molecules and sequester toxic fatty acids or amides, while others interacted with isoprenoid lipids and chlorophenoxy herbicides.
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Linker sites, which can be represented by a chemical bond or by hydrophobic moieties like alkyl(ene) chains or hydrophilic moieties like amide structures connect the support to the binding domains and the binding domains to each other.
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Amid high expectations – and subsequent recriminations – that meeting failed to achieve a comprehensive, legally-binding agreement to reduce greenhouse-gas emissions.
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71 sinne gevind in 12 ms. Hulle kom uit baie bronne en word nie nagegaan nie.