ライフサイエンスコーパス: tyrosine radical

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1 he CcP W191G mutant which is known to form a tyrosine radical.

2 th a sharp maximum at 405 nm assigned to the tyrosine radical.

3 ution pH diagram are described for a protein tyrosine radical.

4 l-tryptophan radicals as has been done for l-tyrosine radicals.

5 e (comprising Cu(II) with a unique cysteinyl-tyrosine radical) and a reduced state (comprising Cu(I)

6 gation and is available as a phototrigger of tyrosine radical at position 356 in the beta2 subunit; t

7 Heterolytic cleavage of this tyrosine radical at the Calpha-Cbeta bond forms a transi

8 at an N-terminal 4Fe-4S cluster, generates a tyrosine radical bound to a C-terminal 4Fe-4S cluster.

9 th low overpotential, akin to the use of the tyrosine radical by Photosystem II to oxidize the CaMn4

10 otosystem II contains two well-characterized tyrosine radicals, D(.) and Z(.).

11 n catalytic features, including the use of a tyrosine radical during catalysis, little is known about

12 Fo, cytochrome a donates an electron to the tyrosine radical, forming tyrosinate.

13 he same radical spectrum, but no significant tyrosine radical forms in mutant Y193H, implicating Y193

14 A tyrosine radical has been proposed as the species respon

15 Tyrosine radicals have been observed and quantified by E

16 potential to a value similar to that of the tyrosine radical in class Ia RNR, and the OH(-) terminal

17 atom radical abstraction by the active site tyrosine radical in the rate-determining step, in agreem

18 e, which is identified as the formation of a tyrosine radical in the UV-vis.

19 eement with previously reported g-tensors of tyrosine radicals in photosystem II.

20 k of an activated copper-oxygen species on a tyrosine radical intermediate, is proposed for TPQ forma

21 A tryptophan and a tyrosine radical maquette, denoted alpha(3)W(1) and alph

22 Therefore, the formation of an alternative tyrosine radical on Tyr504 probably accounts for the tra

23 This work required a de novo designed tyrosine-radical protein displaying a unique combination

24 ficantly narrowed and is characteristic of a tyrosine radical signal.

25 ligand, and cysteine 228 provides a modified tyrosine radical site believed to act as a one-electron

26 This illustrates the range of tyrosine-radical stabilization that a structured protein

27 fold and assembly, implicates Tyr370 as the tyrosine radical, suggests the structural basis for redo

28 roperties and reactivity of the redox-active tyrosine radical; the Y272 tyrosyl radicals in both the

29 fficient electron donor to the photooxidized tyrosine radical, TyrZ+, than is the mononuclear Mn cent

30 Lys-Tyr-Lys, the reactivity of the DNA-bound tyrosine radical was found to differ considerably from t

31 uctively activating O(2) to produce a stable tyrosine radical (Y122*), which is essential for product

32 ce relaxation enhancement of the dark-stable tyrosine radical, YD., by the S2 state of the O2-evolvin

33 Mn4-Ca cluster to the oxidized redox active tyrosine radical, YZ*, generated by photosynthetic charg

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