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 screening and identified protein phosphatase magnesium-dependent 1A (PPM1A/PP2Ca) as the bona fide an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

27 ating increased requirement for thiamine and magnesium dependent enzyme activity during SIR.

28 en acute changes in the SIR and thiamine and magnesium dependent enzyme activity in patients undergoi

29 ine dinucleotide-, thiamine diphosphate- and magnesium-dependent enzyme that catalyses the first step

30 ydroxy-2-butanone 4-phosphate synthase) is a magnesium-dependent enzyme that excises the C4 of d-ribu

31 ofluorescence experiments confirmed NIPAL1's magnesium-dependent expression and that it specifically

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

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

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

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

36 Magnesium-dependent induction of Vibrio fischeri flagell

37 otidase 2 (BPNT2) is a member of a family of magnesium-dependent, lithium-inhibited phosphatases that

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

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

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

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

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

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

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

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

46 Integrase catalyzes two successive magnesium-dependent polynucleotidyl transferase reaction

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

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

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

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

51 We showed that PP2Calpha, a prototypical magnesium-dependent serine/threonine phosphatase, is sus

52 uced Phosphatase 1 (WIP1) is a member of the magnesium-dependent serine/threonine protein phosphatase

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

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

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

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

57 ions are consistent with previously observed magnesium-dependent structures of trinucleosomes with sh

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

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

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

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

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

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