ライフサイエンスコーパス: operativity

1 iple molecular targets, amplification and co-operativity.

2 ly explaining the reduced protein-protein co-operativity.

3 keletal muscle sodium channel may exhibit co-operativity.

4 positions 68 and 83 is required for this co-operativity.

5 eness relative to other species, but high co-operativity.

6 ering degrees of selectivity and positive co-operativity.

7 vidual domains for PPG6, thus precluding co- operativity, although they may interact simultaneously w

8 es DHFR.TMP.NADPH (large positive binding co-operativity) and DHFR.folinic acid.NADPH (large negative

9 ichia coli phospholipids increased enzyme co-operativity, and in vitro cross-linking demonstrated tha

10 preceding the puffs, suggesting that this co-operativity arises through binding of multiple InsP3 mol

11 A model involving co-operativity between the binding of Ca2+ and myosin to th

12 In this study we demonstrate positive co-operativity between the binding of MelR and CRP at the m

13 suggest that there is cross-talk/negative co-operativity between the cannabinoid CB(2) receptor and t

14 we showed that there is at least 3.4-fold co-operativity between them at korApin vivo.

15 on of ATP with both positive and negative co-operativity both in the absence and in the presence of v

16 tivity of the FliI ATPase showed positive co-operativity, establishing that oligomerization and enzym

17 imerization with the AraC hybrid provides co-operativity for operator binding and repression by the L

18 A high degree of co-operativity has been determined for the NBDs of the huma

19 e of calcium extrusion indicated a strong co-operativity (Hill coefficient, 3).

20 idual calcium hypothesis with the calcium co-operativity hypothesis of non-facilitated release.

21 ave found unique evidence of atomic level co-operativity in an inorganic material.

22 Chloride ions lack binding co-operativity in facilitating ligand binding.

23 cadmium selenide exhibits strong positive co-operativity in its reaction with copper ions.

24 play an important role in determining the co-operativity in the ligand binding.

25 Protein-protein co-operativity in the mutant is reduced relative to the wil

26 Movement, and co-operativity, in the sense of formation of a single patch

27 Co-operativity is a remarkable phenomenon mostly seen in bi

28 The co-operativity is consistent with observations from equilib

29 olinic acid.NADPH (large negative binding co-operativity) mirror the co-operative effects seen in the

30 ciation by RAF inhibitors, as well as the co-operativity observed between RAS activity and RAF kinase

31 that is consistent with both the apparent co-operativity of binding and the anti-competitive effects.

32 ament structural changes suggest that the co-operativity of calcium activation in physiological condi

33 ain at the 84 position is crucial for the co-operativity of camphor and cation binding, and that the

34 lent agreement, demonstrating the overall co-operativity of folding and the robustness of the Phi-ana

35 nd CPX coregulate the kinetics and Ca(2+) co-operativity of neurotransmitter release.

36 this side chain are shown to disrupt the co-operativity of potassium and camphor binding by P450cam,

37 of specific residues to the stability and co-operativity of the intact protein.

38 may influence the cross-bridge-dependent co-operativity of thin filament Ca(2+) activation.

39 rties, has raised the issue of functional co-operativity of this system with the classical opioid sys

40 We examined the co-operativity of ultra-fast folding of a protein and wheth

41 These results indicate that co-operativity, previously observed between TrbA and KorB,

42 a high affinity and a pronounced positive co-operativity such that tetramers become the receptor's pr

43 lges can bind Rev with a higher degree of co-operativity than the native structure.

44 re complex and displays apparent positive co-operativity that is associated with the formation of lar

45 Movement, but not co-operativity, was also shown to be dependent, directly or

46 The change in apparent co-operativity with ionic species suggests the presence of

47 onserved region may provide the basis for co-operativity with KorB either indirectly, by modulating D

48 etion of 5 or 10 residues of XerC reduces co-operativity with XerD some 20-fold.