Examples of 'd-amino' in a sentence
Meaning of "d-amino"
D-amino refers to the structural configuration of amino acids where the amino group is on the right side of the carbon atom. This configuration is commonly found in certain peptides and proteins
How to use "d-amino" in a sentence
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d-amino
D-amino acids are normally used as a ingredients for synthetize.
Polypeptides comprising one or more d-amino acids are contemplated within the disclosure.
D-amino acid oxidases are ubiquitous flavoenzymes.
Pharmaceutical compositions and methods utilizing a d-amino acid and an antioxidant for treating neuropsychiatric disorders.
D-amino acids are not capable of proteolytic cleavage by proteolytic enzymes.
The library consisted of heptamers of D-amino acids.
D-amino acids may also be used in the transport polymers.
Examples of amino acid mimetics include D-amino acids.
D-amino acids may be substituted for some or all of the amino acid residues.
Pharmaceutical compositions and methods utilizing a D-amino acid.
D-amino acids are highly resistant to protease mediated degradation and have a low immunogenic response.
Peptides may also be prepared with D-amino acids.
The D-amino acid peptides can be chemically synthesized.
A selective herbicide composition comprising a D-amino acid is described.
Represents a D-amino acid residue or a group of the formula.
See also
In some cases the amino acid is a D-amino acid.
Many D-amino acid dehydrogenase gene sequences are known.
The polypeptides may also be produced using D-amino acids.
The D-amino acid oxidase activity usually exists in transformed cells.
A peptidic component of the compound is comprised entirely of D-amino acids.
Plants can not therefore use D-amino acids as a source of nitrogen.
In these compositions the peptide may comprise a D-amino acid.
Alternatively D-amino acid oxidase encoding sequences obtained are the same as in example 2.
Figure 2 shows examples of potential metabolic conversions of D-amino acids in organisms.
The D-amino acid oxidase may be used in either free or immobilized form.
Little or no growth was observed for plants grown on D-amino acid media.
As described above, no endogenous D-amino acid metabolising activity has been reported in plants.
Lower case letters are used to designate the corresponding D-amino acids.
D-amino acids may be used in MTS molecules having features of the invention.
In another embodiment, said metabolic enzyme is a D-amino acid transferase enzyme.
Many D-amino acid oxidase genes are available in databases for molecular cloning.
Fmoc derivatives of many non-trivial as well as D-amino acids are commercially available.
These sequences are preferably inverted sequences ; more preferably comprising D-amino acids.
This model polypeptide drug is composed of D-amino acids and is excreted unchanged in urine.
The polypeptides of the invention may also be produced using D-amino acids.
Further mutant variants of D-amino acid oxidase are created using various methods of mutagenesis.
In another embodiment, the aromatic amino acid residue is a D-amino acid residue.
Compositions containing exclusively D-amino acids have the advantage of decreased enzymatic degradation.
Protein variants also include peptides having at least one D-amino acid.
No germination was observed for D-amino oxidase expressing plants, indicating a total inhibition of growth.
Chemokine peptide variants include peptides having at least one D-amino acid.
Decarboxylases convert a D-amino acid into a Y-amino acid which can be metabolised by plants.
In still further embodiments employing amino acid groups, D-amino acids can be used.
The D-amino acid oxidase encoding sequences characterising the selected clones are determined.
These peptides have one or more D-amino acids in their amino acid sequences.
The D-amino acid residue can be located at any position of the proteinaceous compound.
The additional amino acids may be D-amino acids or L-amino acids or combinations thereof.
Purification of the total fraction of mRNA specific for said D-amino acid oxidase ;.
The D-amino acid oxidase enzymes are able to convert amino acids into imino acids.
Nevertheless, there has been no case of using only D-amino acids industrially as bioactive substances.
