ライフサイエンスコーパス: PMSF

コーパス検索結果 (left1)

通し番号をクリックするとPubMedの該当ページを表示します

1 its both mouse and Torpedo californica AChE, PMSF does not react measurably with the T. californica e

2 nd mouse AChE and mutants of both by BSF and PMSF both in the presence and absence of substrate.

3 ports that this enzyme is not inactivated by PMSF.

4 the increased sensitivity to inactivation by PMSF of butyrylcholinesterase.

5 b, R15.7, and also by protease inhibition by PMSF.

6 n 330 is not responsible for their differing PMSF sensitivities.

7 resence of p-phenylmethanesulfonyl fluoride (PMSF) and investigated by X-ray diffraction analysis.

8 d absence of phenylmethanesulfonyl fluoride (PMSF), a serine protease blocker and inhibitor of ananda

9 activation by phenylmethylsulfonyl fluoride (PMSF) and benzenesulfonyl fluoride (BSF).

10 ying reagents phenylmethylsulfonyl fluoride (PMSF) and diisopropylfluorophosphate.

11 activity with phenylmethylsulfonyl fluoride (PMSF) or heat treatment.

12 honate (DFP), phenylmethylsulfonyl fluoride (PMSF), and Z-Pro-Proaldehyde-dimethyl acetate, but not b

13 se inhibitor, phenylmethylsulfonyl fluoride (PMSF), forms a covalent complex with MIF and inhibits th

14 proteinase 3, phenylmethylsulfonyl fluoride (PMSF)-inactivated HLE, or PMSF-inactivated CG inhibited

15 hibited by phenyl methyl sulphonyl fluoride (PMSF) (100%), N-alpha-p-tosyl-l-lysine chloromethyl keto

16 rmation of a stable, novel covalent bond for PMSF between the catalytic nitrogen of the N-terminal pr

17 ssays in the absence of the enzyme inhibitor PMSF.

18 be inhibited by a serine protease inhibitor, PMSF, but could be inhibited by a cocktail of protease i

19 with the general serine protease inhibitor, PMSF, prevented proenzyme cleavage and permitted its pur

20 itive to the protease active site inhibitors PMSF, Z-AAPF-CMK, and Z-AAPL-CMK.

21 as suppressed by serine protease inhibitors (PMSF, Pefabloc SC), but not by metallo- or thiol-proteas

22 lsullonyl phenylalanyl chloromethyl ketone), PMSF (phenylmethylsulfonyl fluoride), and dichloroisocou

23 for the reactivity of PPT1 with HDSF but not PMSF.

24 in PPT1 is modified by a substrate analog of PMSF, hexadecylsulfonylfluoride (HDSF) in a specific and

25 though this could be due to the presence of PMSF at the active site.

26 of the N-terminal proline and the sulfur of PMSF with complete, well-defined electron density in all

27 ne nucleophile (which has been the target of PMSF inhibition in earlier studies) is dispensible for M

28 monocyte chemotactic activity, since DFP- or PMSF-inactivated cathepsin G no longer induced monocyte

29 sulfonyl fluoride (PMSF)-inactivated HLE, or PMSF-inactivated CG inhibited binding of radiolabeled li

30 the H157A mutant is also in complex with the PMSF inhibitor.

31 nactivation or pre-exposure of the lysate to PMSF.

32 anamycin A, and this killing is sensitive to PMSF inhibition, suggesting that killing was mediated ex

33 had similar inactivation rate constants with PMSF, implying that the difference between mouse and T.

34 activity was eliminated when inhibited with PMSF, suggesting that its proteolytic activity is requir

35 Cells treated with PMSF accumulate DBP vs time with over 90% of the protein

WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。