ライフサイエンスコーパス: magnesium-dependent

1 cating that actin and ADP binding linkage is magnesium-dependent.

2 Although protein phosphatase magnesium-dependent 1 delta (PPM1D) was initially charac

3 Protein phosphatase magnesium dependent 1A (PPM1A) has been implicated in fi

4 Loss of expression of protein phosphatase magnesium-dependent 1A during kidney injury promotes fib

5 Protein phosphatase magnesium-dependent-1A (PPM1A) dephosphorylates SMAD2/3,

6 RNase P, which catalyzes the magnesium-dependent 5'-end maturation of tRNAs in all th

7 The recombinant enzyme showed magnesium-dependent acid phosphatase activity comparable

8 MDP-1 is a eukaryotic magnesium-dependent acid phosphatase with little sequenc

9 HAD) superfamily, which contains a number of magnesium-dependent acid phosphatases.

10 FBN1-RZ1 cleavage is magnesium dependent and efficient at both 37 and 50 degr

11 This activity is magnesium dependent and is inhibited by phosphate ions,

12 QueE is also magnesium-dependent and exhibits a K(app) for the divale

13 The RNA triphosphatase activity of Cet1p is magnesium-dependent and has a turnover number of 1 s-1.

14 tic enzymes) are structurally homologous and magnesium-dependent, and all perform similar chemical pe

15 Nocturnin nuclease activity is magnesium dependent, as the addition of EDTA or mutation

16 ve, relaxing negatively supercoiled DNA in a magnesium-dependent, ATP-independent reaction.

17 protein JFC1 is an ATP-binding protein with magnesium-dependent ATPase activity.

18 ere we show that Lef4 possesses an intrinsic magnesium-dependent ATPase with a distinctive alkaline p

19 e and recombinant protein harbored intrinsic magnesium-dependent bisphosphate nucleotidase activity (

20 n magnesium utilization in vivo also display magnesium-dependent changes in vitro.

21 de priming required tyrosine kinase(s) and a magnesium-dependent conformational change of the I-domai

22 horibosyltransferase (OPRTase) catalyzes the magnesium-dependent conversion of alpha-D-phosphoribosyl

23 and thermodynamic framework for defining the magnesium-dependent coupling between the actin and nucle

24 additive, and microcystin did not block the magnesium-dependent desensitization, the targets for the

25 haracterized previously) is an RNase H1-type magnesium-dependent endonuclease with stringent specific

26 nd with EhUba1 (E1) in vitro, in an ATP- and magnesium-dependent fashion.

27 Tissue transglutaminase (tTG) exhibits a magnesium-dependent GTP/ATPase activity that is involved

28 yotic, and viral organisms are thought to be magnesium dependent in vivo, and therefore these mutant

29 h we termed mifA and mifB, respectively, for magnesium-dependent induction of flagellation.

30 Magnesium-dependent induction of Vibrio fischeri flagell

31 atellite (VS) ribozyme is the formation of a magnesium-dependent loop/loop interaction between the te

32 can form dimeric and trimeric multimers in a magnesium-dependent manner, with dissociation constants

33 d that the protein dephosphorylates PAP in a magnesium-dependent manner, with optimal activity observ

34 s found in the human U6 coding sequence in a magnesium-dependent manner.

35 In this study, we show that the magnesium-dependent, neutral pH-optimum and membrane-ass

36 uclease is an important member of a class of magnesium dependent nucleases that are widely distribute

37 tructures of a member of the third subclass, magnesium-dependent phosphatase-1 (MDP-1) both in its un

38 rvations, the enzyme has been given the name magnesium-dependent phosphatase-1 (MDP-1).

39 tive double-stranded replication region in a magnesium-dependent reaction and made this fragment sens

40 In this ATP- and magnesium-dependent reaction, nitrate elicited a greater

41 ge with rates only 13-20-fold lower than the magnesium-dependent reaction.

42 t hairpin cleavage with rates similar to the magnesium-dependent reaction.

43 the membrane bound, neutral pH optimal, and magnesium-dependent SMase (N-SMase) from rat brain.

44 One of these, a magnesium-dependent species of 18.6 kDa, was purified to

45 ted that GSH inhibits, in vitro, the neutral magnesium-dependent sphingomyelinase (N-SMase) from Molt

46 A high throughput screen for neutral, magnesium-dependent sphingomyelinase (SMase) was perform

47 Acetate kinase catalyzes the reversible magnesium-dependent synthesis of acetyl phosphate by tra

48 ed in the structural model are important for magnesium-dependent tertiary structure formation.

49 Acetate kinase catalyzes the magnesium-dependent transfer of the gamma-phosphate of A

50 rvative mutations E9D and E183D abrogate the magnesium-dependent triphosphatase activities of Lef4 an

51 The lipin family is a magnesium-dependent type I PA phosphatase involved in de

52 First, telomerase binding to short DNAs is magnesium-dependent, while binding to long DNAs is magne