ライフサイエンスコーパス: proteinogenic

1 ed to measure alpha-helix propensities among proteinogenic alpha-amino acid residues, and quantitativ

2 no acids can be biosynthesized directly from proteinogenic alpha-amino acids by the action of MIO (4-

3 l for the preparation of unsaturated and non-proteinogenic alpha-amino acids, directly usable for the

4 for eight cases) for quaternizing a range of proteinogenic alpha-amino acids.

5 fficiently exploited to synthesize novel non-proteinogenic alpha-amino esters.

6 acilitate the multicomponent assembly of non-proteinogenic alpha-amino esters.

7 nce, defining the biosynthetic route of this proteinogenic amino acid as a potential antifungal targe

8 Selenocysteine is the only proteinogenic amino acid encoded by a recoded in-frame U

9 involved in the biosynthesis of the rare non-proteinogenic amino acid residue L-4-methylproline from

10 Proteinogenic amino acid residues that promote beta-shee

11 misincorporated into protein in place of the proteinogenic amino acid threonine.

12 Aptamers selected to bind the non-proteinogenic amino acid, p-amino phenylalanine (pAF), a

13 eference toward phosphinothricin over the 20 proteinogenic amino acids (1) , indirect effects of BAR-

14 iazepine-2,5-diones derived from enantiopure proteinogenic amino acids allows retentive replacement o

15 cids derived from 19 out of the 20 canonical proteinogenic amino acids and demonstrate their use in t

16 tor interaction based on linear sequences of proteinogenic amino acids and for the design of chemical

17 e PheATE adenylation domain with a number of proteinogenic amino acids and observed that three additi

18 ilyl-N-methyltrifluoroacetamide)-derivatized proteinogenic amino acids by removing background noise.

19 In grains, several proteinogenic amino acids concentrations were increased,

20 ibution of ionic currents for each of the 20 proteinogenic amino acids encoded by eukaryotic genes is

21 We analyzed the labeling patterns of proteinogenic amino acids in individual deletions of all

22 n reported for 19 of the 20 directly encoded proteinogenic amino acids in their natural (enantiomeric

23 Moreover, the incorporation of many non-proteinogenic amino acids into ribosomal peptides in con

24 hyllaceae-type cyclic peptides (CPs) of 5-12 proteinogenic amino acids occur in 10 plant families.

25 The isotopomer patterns of proteinogenic amino acids revealed an alternate pathway

26 All proteinogenic amino acids were converted to their alpha-

27 ic transport of proteinogenic as well as non-proteinogenic amino acids with moderate affinity.

28 te balancing, biosynthetic (13)C labeling of proteinogenic amino acids, and isotopomer balancing all

29 the full range of functionality found in the proteinogenic amino acids, and it is demonstrated that t

30 es, where the central X residue is one of 19 proteinogenic amino acids, and water-soluble X5 and X10

31 Among the proteinogenic amino acids, only proline is a secondary a

32 ein amino acids, particularly isomers of the proteinogenic amino acids, present a threat to proteome

33 Despite being flanked by non-proteinogenic amino acids, proteolysis of this pentapept

34 mercapto-acetaldehyde, and the corresponding proteinogenic amino acids, serine and cysteine, led us t

35 ncorporate multiple tandem mutations and non-proteinogenic amino acids, using eight heterologous comp

36 reparation of proteins containing unmodified proteinogenic amino acids, which can be altered readily

37 ctionalities present in both natural and non-proteinogenic amino acids.

38 ts of each position with one of the other 19 proteinogenic amino acids.

39 ph, labeling analysis provided enrichment of proteinogenic amino acids.

40 amino acids or by one-carbon homologation of proteinogenic amino acids.

41 provides a potential route for preparing non-proteinogenic amino acids.

42 proved lacticin 481 analogues containing non-proteinogenic amino acids.

43 It transports 18 of the 20 proteinogenic amino acids.

44 re typically limited to the 20 most abundant proteinogenic amino acids.

45 ng biosynthetic fractional (13)C labeling of proteinogenic amino acids.

46 Indospicine, a non-proteinogenic analogue of arginine, occurs only in Indig

47 For most proteinogenic and all studied unproteinogenic alpha-amin

48 e have analyzed the quantum chemistry of all proteinogenic and various prebiotic amino acids.

49 s, AtCAT6 mediated electrogenic transport of proteinogenic as well as non-proteinogenic amino acids w

50 ilizing force places limitations on nature's proteinogenic building blocks.

51 n protecting groups, and are tolerant of all proteinogenic functional groups.

52 The molecular shape of proteinogenic glutamic acid has been determined for the

53 ymeric peptides comprising lysine or the non-proteinogenic lysine analogues ornithine or, to a lesser

54 Hundreds of non-proteinogenic (np) amino acids (AA) are found in plants

55 nstrated to be highly regiospecific, forming proteinogenic para-Tyr (p-Tyr) exclusively.

56 This approach, and the resulting linear and proteinogenic polypeptides, represents a new route for c

57 Proline, the only proteinogenic secondary amino acid, is metabolized by it

58 ino-2-carboxyethyl)-l-homocysteine) is a non-proteinogenic thioether containing amino acid.