Examples of 'amino acids having' in a sentence
Meaning of "amino acids having"
amino acids having: This phrase denotes the presence or possession of amino acids, which are the building blocks of proteins and essential for various biological processes
How to use "amino acids having" in a sentence
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amino acids having
Amino acids having similar properties are well known in the prior art.
This enumeration does not exclude the use of other amino acids having a similar effect.
Amino acids having additional nitrogen atoms on side chains are especially preferred.
Endothelins are peptides of 21 amino acids having very potent vasoconstrictor activity.
The amino acids having the same properties are known to one skilled in the art.
In embodiments, suitable cationic constituents contain amino acids having a positive charge.
It is preferred that all amino acids having a free amino group are chemically modified.
Amino acids having an acidic side chain include glutamic acid and aspartic acid.
In general, a peptide comprises amino acids having an order of magnitude with the tens.
Amino acids having similar properties are well-known by a person skilled in the art.
In general, a protein comprises amino acids having an order of magnitude within the hundreds.
Amino acids having a basic side chain include arginine, lysine and histidine.
The term " polypeptide " means herein a polymer of amino acids having no specific length.
Examples of acidic amino acids having a negative charge include aspartic acid and glutamic acid.
The non-natural amino acids are selected from amino acids having aromatic amine sidechains.
See also
The natural amino acids having a carboxyl group on the side chain are Asp or Glu.
Non-natural amino acids also include amino acids having derivatized side groups.
Exemplary amino acids having reactive functional groups include, but are not limited to, cysteine.
Preferred derivatives include amino acids having a C-terminal amide group.
Amino acids having a small side chain include glycine, serine, alanine and threonine.
Substitutions can be performed with amino acids having hydrophilicity values within ± 2 of each other.
Amino acids having two basic grouping, lysine, arginine and histidine ;.
Substitutions may be performed with amino acids having hydrophilicity values within ± 2 of each other.
Amino acids having two basic groupings, lysine, argine and histidine ;.
Preferred examples of the neutral amino acids having a linear alkyl group at a side chain include,.
Amino acids having a neutral / polar side chain include asparagine, glutamine, cysteine, histidine, serine and threonine.
Ammo acid is also meant to include amino acids having L or D stereochemistry at the a-carbon.
Amino acids having a hydrophobic side chain include tyrosine, valine, isoleucine, leucine, methionine, phenylalanine and tryptophan.
Natural human wildtype alpha-synuclein is a peptide of 140 amino acids having the following amino acid sequence,.
Examples of basic amino acids having a positive charge include arginine, histidine, and lysine.
A human placenta derived heparin-binding growth factor of 168 amino acids having the following amino acid sequence,.
Exemplary amino acids having planar side chains include arginine, aspartate, and glutamine.
The term " oligopeptide " refers to a polymer of amino acids having a length of from 5 to 49 aa.
In one aspect, amino acids having hydropathic indexes of ± 2 are substituted.
Human alpha-synuclein is a peptide of 140 amino acids having the following amino acid sequence,.
However, amino acids having non-polar side chains can also be used.
The domain antibody comprises amino acids having the sequence set forth in SEQ ID NO, 543.
In addition, amino acids having the structure of Formula ( XXXXXVIII ) are included, wherein,.
Preferred values for A ² include all amino acids having a D-configuration, most preferably ( D ) Phe.
Vi Amino acids having acidic side chains ( Asp, Glu ).
Fig . 4A shows identification of amino acids having a binding nucleotide specifying capacity in the PPR motif.
Ix Amino acids having hydroxy side chains ( Ser, Thr ).
In addition, the following amino acids having the structure of Formula ( XXXXVIII ) are included,.
In addition, amino acids having the structure of Formula ( XX ) are included, wherein,.
In another embodiment, amino acids having a pKa above 9.0 are preferred.
Viii Amino acids having amide side chains ( Asn, Gin ).
Such amino acids include amino acids having the structure of Formula ( IV ), wherein,.
When using amino acids having functional groups, such as e . g.
Examples of groups of amino acids having such similar properties are provided in Table 1.
In addition, amino acids having the structure of Formula ( XXXXXIX ) are included, wherein,.
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