ライフサイエンスコーパス: biosyntheses

1 y disruption of peptidoglycan and fatty acid biosyntheses.

2 y share parallels with the natural products' biosyntheses.

3 und in bacterial and other fungal polyketide biosyntheses.

4 mmitted step of plastoquinone and tocopherol biosyntheses.

5 yl THF to formate and THF for purine and Gly biosyntheses.

6 rsors in leucine, isoleucine, and coenzyme B biosyntheses.

7 s between aromatic polyketide and fatty acid biosyntheses.

8 lvement in both heme and iron-sulfur cluster biosyntheses.

9 r lipid, cofactor, amino acid, or nucleotide biosyntheses.

10 een recruited for sulfolactate or sulfolipid biosyntheses.

11 at are required for riboflavin and pteridine biosyntheses.

12 principal genes of amino acid and nucleotide biosyntheses.

13 features, biological activity, and proposed biosyntheses.

14 eners" are not derived from enantiodivergent biosyntheses.

15 antipodes arising from separate enantiomeric biosyntheses.

16 gulatory steps in cholesterol and fatty acid biosyntheses, 3-hydroxy-3-methylglutaryl-coenzyme A (HMG

17 These biosyntheses all involve polycyclization via cationic in

18 y of proteins involved in FeMo-co and FeV-co biosyntheses, allows us to define a new family of iron a

19 nsduction, chromatin repair, metabolism, and biosyntheses, among others.

20 gins with a brief discussion of the proposed biosyntheses and biosynthetic connections among the poly

21 depend on NADPH production to feed essential biosyntheses and for oxidative stress defense.

22 oxylipin, glucosinolate, and brassinosteroid biosyntheses and have shown that both P450 and non-P450

23 lipid and glycosylphosphatidylinositol (GPI) biosyntheses and may harbor sterol trafficking defects.

24 ed xanthone, ergochrome, and bianthraquinone biosyntheses are discussed.

25 Yet, the mechanisms of most endoperoxide biosyntheses are not well understood.

26 Their biosyntheses are typically initiated by hydroxylation of

27 and amino acid, sugar, nucleotide and lipid biosyntheses can be reconstituted in high yield under mi

28 ed to deoxyribose triphosphate, and in vitro biosyntheses could be successfully performed with severa

29 carotenoid, brassinosteroid, and gibberellin biosyntheses have been added from the literature.

30 sulfur-containing sugars in nature and their biosyntheses have not been studied.

31 lutathione, F420, folate, and murein peptide biosyntheses illustrate convergent evolution of nonribos

32 e mammals cannot form 24-alkylsterols, their biosyntheses in P. carinii are attractive targets for th

33 s even higher due to inhibition of estrogens biosyntheses in peripheral tissue by the aromatase (CYP1

34 of both peptidoglycan and wall teichoic acid biosyntheses in S. aureus.

35 auxin can reciprocally regulate each other's biosyntheses, influence each other's response pathways,

36 o be involved in cofactor and small molecule biosyntheses, intermediary metabolism, transport, nitrog

37 d in the study of other complex Fe-S cluster biosyntheses is discussed.

38 The structures and biosyntheses of "odd" siderophores can reveal the evolut

39 Therefore, the relatively distinct biosyntheses of cysteine and methionine in E. coli and S

40 ence of LpxC inhibitors, suggesting that the biosyntheses of fatty acids and lipid A are tightly regu

41 Together, the biosyntheses of histidine, purines, and thiamine pyropho

42 ces methylmalonyl-CoA, the substrate for the biosyntheses of multimethyl-branched fatty acids such as

43 finding, which we consider relevant for the biosyntheses of other class III lantibiotics, underlines

44 o-installing di-iron amine oxygenases in the biosyntheses of other natural products.

45 our recent reports describing the bacterial biosyntheses of PBDEs, we predicted the presence of addi

46 efense signalling, transcription regulation, biosyntheses of secondary metabolites, and other biologi

47 In addition, new results indicate that biosyntheses of signal recognition particle RNA and telo

48 in share marked structural similarities, the biosyntheses of their bicyclic nuclei are wholly dissimi

49 enating enzymes postulated to be involved in biosyntheses of these unusual monomers.

50 ere also suggested to play key roles for the biosyntheses of various natural products.

51 These complex biosyntheses, once only in the realm of the biopharmaceu

52 nature, yet the mechanisms underlying their biosyntheses remain largely unknown.

53 inia carotovora, genes common to phosphonate biosyntheses were found in neighboring positions of thos

54 ymes, the ones involved in protein and lipid biosyntheses were observed to be particularly active.