ライフサイエンスコーパス: imino acid

1 ize the triple helix compared to the P and O imino acids.

2 d profile of BSG showed a high percentage of imino acids.

3 r step represents cis-trans isomerization of imino acids.

4 and other D-amino acids to the corresponding imino acids.

5 always flanked by a specific distribution of imino acids.

6 The non-canonical imino acid, (2S,4S)-4-aminoproline (amp), was used to sp

7 ritical for the function of the channel, two imino acids and an alpha-hydroxy acid were incorporated

8 itions show the highly stabilizing nature of imino acids and the destabilizing effects of Gly and aro

9 ly as every third residue, a high content of imino acids, and interchain hydrogen bonds.

10 Anionic amino acids, cationic amino acids, imino acids, and N-methylated amino acids are excluded b

11 Thus, rigid imino acids are unfavorable within a break, despite thei

12 ace of collagen molecules, it is likely that imino acid-aromatic CH...pi interactions are important i

13 gnetic resonance was used to assign the free imino acid as (3S,5S)-5-chloropiperazate, distinct from

14 In the unfolded state, imino acids both restrict conformational space and prese

15 explains the apparent Na + dependence of the imino acid carrier in studies with mammalian intestine.

16 hPAT1 is the high-capacity imino acid carrier localized at the small intestinal lum

17 ificity of hPAT1 is identical to that of the imino acid carrier.

18 ), or solute carrier SLC36A1, represents the imino acid carrier; the Na(+) -dependent imino acid tran

19 1032) structure reveals that the central non-imino acid-containing region adopts 10/3 superhelical pr

20 d not be readily explained by differences in imino acid content, or in numbers of charged or hydropho

21 ryptophan for effective hydride transfer and imino acid decarboxylation.

22 Unique properties of this imino acid have led to speculations of structural and pe

23 roscopy are used to characterize the role of imino acids in a triple-helical peptide, T1-892, which c

24 een to complement the stabilizing effects of imino acids in modulating stability and may become domin

25 The structure shows that the multiple non-imino acids make several types of direct intrahelical as

26 ht serve in relaying a H(+) from the product imino acid =NH(2)(+) group bound on the flavin Re-side t

27 an opportunity to characterize the impact of imino acids on the unfolded state and folding kinetics.

28 evant sequence and was designed to model the imino acid-poor 785-796 region of human type III collage

29 u or a Gly-Ile bond that is upstream from an imino acid-poor region.

30 reduced enzyme prior to dissociation of the imino acid product.

31 th E(red).P prior to the dissociation of the imino acid product.

32 ro-tRNAPhe and Phe-tRNAPro, we show that the imino acid proline and not tRNAPro imposes the primary e

33 The imino acid proline is a poor donor and acceptor for pept

34 tide bond synthesis by most amino acids, the imino acid proline is a poor substrate for protein synth

35 ically pre-treated bone gelatines had higher imino acids (proline and hydroxyproline) contents compar

36 ntained glycine as the major amino acid with imino acids (proline and hydroxyproline) of 194-195 resi

37 The looser superhelical structure of the non-imino acid region of collagen triple helices combined wi

38 Since collagen has a high content of imino acid residues, the cumulative effects of cis-trans

39 ts 10/3 superhelical properties, whereas the imino acid rich N- and C-terminal regions adhere to a 7/

40 th those of collagen-like peptides with more imino acid-rich sequences indicates the sequence depende

41 pus oocytes, rat SIT1 mediated the uptake of imino acids such as proline (K0.5 approximately 0.2 mM)

42 Yaa triplets support the favorable nature of imino acids, the importance of hydroxyproline, the varyi

43 the imino acid carrier; the Na(+) -dependent imino acid transport function measured at the brush-bord

44 ular identity of the classic Na(+)-dependent imino acid transporter (identified functionally in the 1

45 cteristics and tissue distribution of Sodium/Imino-acid Transporter 1 (SIT1), which exhibits the prop

46 interaction between aromatic amino acids and imino acids within the triple helix is also supported by

47 terms of interchain interactions between non-imino acid X and Y residues, through the use of host-gue