ライフサイエンスコーパス: phosphate donor

1 ly, by using either GTP, dGTP or dTTP as the phosphate donor.

2 de 2'-phosphotransferases utilize GTP as the phosphate donor.

3 treated with CK2 and [gamma-(32)P]GTP as the phosphate donor.

4 cleotide alone indicating that GTP acts as a phosphate donor.

5 rmation of JH diol phosphate with GTP as the phosphate donor.

6 osphate using inorganic pyrophosphate as the phosphate donor.

7 microM when CMP is the other substrate) as a phosphate donor.

8 used nicotinamide mononucleotide as a ribose phosphate donor.

9 osphoenzyme and only when ATP is used as the phosphate donor.

10 and mild reaction conditions using ATP as a phosphate donor.

11 that PKM2 is a protein kinase using PEP as a phosphate donor.

12 and dGDP, respectively, in the presence of a phosphate donor.

13 e controlled by phosphorylation by different phosphate donors.

14 hown by chase experiments with GTP or ATP as phosphate donors.

15 alent cation and can use both GTP and ATP as phosphate donors.

16 lly relevant modifications using inexpensive phosphate donors.

17 ATP, PSTK utilizes GTP, CTP, UTP and dATP as phosphate-donors.

18 phosphate over adenosine triphosphate as the phosphate donor, a unique observation among all characte

19 letely eliminates phosphorylation by a small phosphate donor, acetyl phosphate, but not phosphorylati

20 on opposite sides of the protein for the NTP phosphate donor and a 5'-OH single-stranded oligonucleot

21 Studies suggest two functions of dTTP, as a phosphate donor and a positive effector of the dTMP kina

22 specifically utilize N(6)-(benzyl)-ATP as a phosphate donor and for its selective inhibition by 1NA-

23 e triphosphate synthesis required PEP as the phosphate donor and pyruvate kinase as the catalyst.

24 lel lines, initial velocity plots with other phosphate donors and product inhibition studies indicate

25 nosine 5'-O-(thiotriphosphate) was used as a phosphate donor, and (iii) no change in reaction velocit

26 ATP or inorganic polyphosphate (poly(P)) as phosphate donor, and is regarded as the only enzyme resp

27 The phosphate donors are dTTP, dGTP, and ribo-GTP as well as

28 tween ATP and GTP, that GTP is the exclusive phosphate donor at intracellular nucleotide levels.

29 m Archaeoglobus fulgidus in complex with its phosphate donor ATP at 1.7 A resolution, with its substr

30 go mineralization on addition of the organic phosphate donor, beta-glycerophosphate (betaGP).

31 The enzyme was most active with ATP as the phosphate donor, but slight activity was observed with I

32 been shown to serve as a low molecular mass phosphate donor for certain response regulators.

33 relative to Mg(2+) and could not use GTP as phosphate donor for either substrate phosphorylation or

34 Ni2+ and UO2(2+), and glycerol 2-phosphate (phosphate donor for phosphate release and metal biopreci

35 that poly(P), rather than ATP, is the major phosphate donor for poly(P)-glucokinase in M. tuberculos

36 re of Trl1 is its preferential use of GTP as phosphate donor for the RNA kinase reaction.

37 ridine triphosphate (UTP) is the physiologic phosphate donor for this enzyme, a study of the kinetic

38 sphate or potassium phosphate, which are not phosphate donors, fully substitutes for Ac~P.

39 ady-state kinetic characterization using the phosphate donor GTP demonstrates that AAC(6')-Ie/APH(2''

40 ed adenosine triphosphate ((18)O-ATP) as the phosphate donor in a RIKA, then quantified the ratio of

41 the accepted dogma that ATP is the canonical phosphate donor in aminoglycoside kinases and protein ki

42 e for pyruvate kinase in cells, can act as a phosphate donor in mammalian cells because PEP participa

43 and each of these substrates can serve as a phosphate donor in the phosphorylation of ATX.

44 ethod involving the activation of a glycosyl phosphate donor in the presence of a thioglycoside accep

45 enzyme utilizes CTP, instead of ATP, as the phosphate donor in the reaction.

46 ATP, the phosphate donor in these reactions, must first cross the

47 ATP was a good phosphate donor (Km = 1100 +/- 140 microM); however, the

48 e ability of casein kinase 2 to use GTP as a phosphate donor, may be a source of differences between

49 leoside triphosphate was based on ATP as the phosphate donor, nucleoside diphosphate kinase as the ca

50 o functions in most signaling pathways, as a phosphate donor or a precursor for cyclic adenosine mono

51 ponents of the genetic material, function as phosphate donors, participate in cellular signaling, are

52 Phosphorylation of NarLN by a small-molecule phosphate donor, phosphoramidate, decreases this interac

53 group of the ribose are important for gamma-phosphate donor recognition, and GTP is the only nucleot

54 Phosphate donor specificity within the PFK-A family coul

55 to accumulate phosphates from small-molecule phosphate donors, such as acetyl phosphate, while the Vi

56 our strategy obviates the need for ATP as a phosphate donor that complicates NTP isolation using exi

57 bi-bi reaction sequence, but with UTP as the phosphate donor, the addition of nucleotide prior to dCy

58 gE, which transfers maltose from a maltose-1-phosphate donor to alpha-glucan/maltooligosaccharide cha

59 ndoplasmic reticulum, where it uses GTP as a phosphate donor to phosphorylate INSIG1 at Ser207 and IN

60 lyze the phosphoryl transfer reaction from a phosphate donor (usually ATP) to a receptor substrate.

61 UTP was the preferred phosphate donor with a true Km value of 1 microM compare

62 dic linkage was installed using a galactosyl phosphate donor with high selectivity.

63 gamma-32P]ATP or [gamma-32P]GTP were used as phosphate donors with the same cells.

64 ential preferences between ATP or GTP as the phosphate donor, with aminoglycoside 2''-phosphotransfer

65 or Mn2+, and utilized either ATP or GTP as a phosphate donor, with Kms of 2 and 4 microM, respectivel

66 used all of the nucleoside triphosphates as phosphate donors, with ATP and dATP being the best donor