Examples of 'peptidyl' in a sentence
Meaning of "peptidyl"
peptidyl (noun) - relating to or characteristic of peptides, which are short chains of amino acids. This term is often used in biochemistry and molecular biology
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- Of or pertaining to peptides
How to use "peptidyl" in a sentence
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peptidyl
Additional examples include peptidyl derivatives of a compound.
Such peptidyl linkers may be any length.
The linker may be a peptidyl linker.
Peptidyl transferase activity is carried out by the ribosome.
Zestril is a peptidyl dipeptidase inhibitor.
As defined hereinabove or peptidyl residues.
Other peptidyl compounds have been described as renin inhibitors.
Endothelial cell peptidyl dipeptidase.
Additional peptidyl nitriles have been reported as protease inhibitors.
The large subunit contains the active site of peptidyl transferase.
Additional examples include peptidyl derivatives of a compound of the invention.
The peptidyl linkers can be altered to form derivatives as described herein.
Inhibitors that directly target peptidyl arginine deminiases and the like.
Various peptidyl aldehydes as the inhibitors are synthesized in the light of them.
The clear solution was added to the peptidyl resin and flushed with argon.
See also
A peptidyl chemotherapeutic agent.
Methods for the synthesis of such peptidyl derivatives are well established in the art.
The peptidyl amide bond surrogate is often referred to by the zwitterionic name.
Convertase inhibitors used according to the invention may be proteins or have peptidyl components.
VÃa a peptidyl bond or linker.
The coupling conditions may be any known to skilled practitioners for forming peptidyl bonds.
Fructosyl peptidyl oxidase and sensor for assaying a glycated protein.
These efforts have produced a number of small peptidyl compounds which directly inhibit thrombin.
The fructosyl peptidyl oxidase PnFPOX was capable of oxidizing fructosyl hexapeptide.
It prevents protein chain elongation by inhibiting the peptidyl transferase activity of the bacterial ribosome.
Peptidyl hormones may be naturally occurring or may be pharmacologically active derivatives of known hormones.
Another advantageous feature of the fructosyl peptidyl oxidase of the present invention is its thermostability.
Such a small peptidyl portion being capable of providing highly specific recognition of thrombin is unexpected.
The present invention provides previously unknown peptidyl boronic acid ester and acid compounds.
The fructosyl peptidyl oxidase of the invention is useful in assaying a glycated protein in a sample.
Compounds with lower clearance rates have improved pharmacokinetic properties relative to peptidyl ICE inhibitors.
The amino acids of the peptidyl residue are preferably selected from natural amino acids.
Figure 2 shows a purification procedure of the fructosyl peptidyl oxidase.
The data indicated that peptidyl proline biosynthesis was similar in nonelongating and elongating segments.
The compound may be either peptidyl or non-peptidyl.
The hydrophobic peptidyl segment or hydrophilic peptidyl segment of the amphiphilic peptide can be modified.
Figure 4 shows the thermostability of the fructosyl peptidyl oxidase.
Peptide and peptidyl inhibitors of ICE have been described.
In some embodiments, the proteasome inhibitor is a peptidyl boronic acid.
Certain peptidyl epoxy ketones such as EST are irreversible inhibitors of the proteasomes.
The Fmoc group was removed and the peptidyl resin washed several times with DCM.
ACE is a peptidyl dipeptidase which catalyzes the conversion of angiotensin I to angiotensin II.
As cysteine protease inhibitors, peptidyl aldehyde derivatives are well known.
In some embodiments, the linker is an amino acid or a peptidyl linker.
Mercaptoamide peptidyl derivatives have shown ACE inhibition in vitro and in vivo.
Figure 6 shows measurement of fructosyl hexapeptide using the fructosyl peptidyl oxidase.
In addition, the peptidyl drug may be a kinin.
In this case, an amino acid chain is the functional group transferred by a peptidyl transferase.
Pleuromutilins bind to the peptidyl transferase centre, as well as phenicols.
In some embodiments, the amide replacement linkage is present in the hydrophilic peptidyl segment.
