Examples of 'd-amino acids' in a sentence
Meaning of "d-amino acids"
d-amino acids ~ a term used in biochemistry to refer to a specific type of amino acids that have a distinctive structural configuration. Unlike the more commonly occurring l-amino acids, d-amino acids have a different arrangement of atoms
How to use "d-amino acids" in a sentence
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d-amino acids
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 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.
Peptides may also be prepared with D-amino acids.
D-amino acids are highly resistant to protease mediated degradation and have a low immunogenic response.
The polypeptides may also be produced using D-amino acids.
Plants can not therefore use D-amino acids as a source of nitrogen.
A peptidic component of the compound is comprised entirely of D-amino acids.
D-amino acids may be used in MTS molecules having features of the invention.
Figure 2 shows examples of potential metabolic conversions of D-amino acids in organisms.
Compositions containing exclusively D-amino acids have the advantage of decreased enzymatic degradation.
See also
Lower case letters are used to designate the corresponding 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.
These peptides have one or more D-amino acids in their amino acid sequences.
These sequences are preferably inverted sequences ; more preferably comprising D-amino acids.
Fmoc derivatives of many non-trivial as well as D-amino acids are commercially available.
In some embodiments, such reverse sequences will preferably be produced using D-amino acids.
The additional amino acids may be D-amino acids or L-amino acids or combinations thereof.
In still further embodiments employing amino acid groups, D-amino acids can be used.
Identification of L - and D-amino acids was based on retention time and mass selective detection.
These results demonstrate the herbicidal properties of D-amino acids on wild-type plants.
D-amino acids can be used.
Nevertheless, there has been no case of using only D-amino acids industrially as bioactive substances.
First and second domains can include or consist of one or more D-amino acids.
The substance is a peptide consisting mostly of D-amino acids instead of the common L-amino acids.
Polypeptides for use in the invention may also be produced using D-amino acids.
Said enzyme catalyzes the conversion of D-amino acids into the corresponding a-keto acids.
In this embodiment, it is preferred that ADNF polypeptides comprising all D-amino acids are used.
Peptidic molecules may also be synthesized with D-amino acids to increase resistance to enzymatic degradation.
The enzyme has a very broad specificity and can act on most D-amino acids.
These molecules may also be synthesized with D-amino acids to increase resistance to enzymatic degradation.
The effect of single amino acid substitutions may also be probed using D-amino acids.
Polypeptides containing either L - or D-amino acids may be synthesized in this manner.
A peptide analogue may have none or one or more of these derivatives, and D-amino acids.
However, D-amino acids are also found in nature.
In still further compounds employing amino acid groups, D-amino acids can be used.
D-amino acids altered by DAO act similarly to D-Asp.
In a presently preferred embodiment, the invention provides ADNF polypeptides comprising all D-amino acids.
In some embodiments, D-amino acids may be used as selection markers.
DAO is an enzyme which catalyze oxidative deamination of D-amino acids.
However, D-amino acids may be present as may amino acid analogs.
The JNK inhibitor sequence as used herein is composed of D-amino acids.
Where D-amino acids are included, however, it is preferred to use chemical synthesis.
A D-protein has an amino acid residue sequence consisting essentially of D-amino acids.
Other D-amino acids have a similar conformation as peptide 14 in the docked models.
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