戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

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 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 dation of the copper, consists of a cysteine-tyrosine radical (Cys-Tyr(*)) as a copper ligand.
11 otosystem II contains two well-characterized tyrosine radicals, D(.) and Z(.).
12 n catalytic features, including the use of a tyrosine radical during catalysis, little is known about
13  Fo, cytochrome a donates an electron to the tyrosine radical, forming tyrosinate.
14 he same radical spectrum, but no significant tyrosine radical forms in mutant Y193H, implicating Y193
15                                            A tyrosine radical has been proposed as the species respon
16                                              Tyrosine radicals have been observed and quantified by E
17  potential to a value similar to that of the tyrosine radical in class Ia RNR, and the OH(-) terminal
18  atom radical abstraction by the active site tyrosine radical in the rate-determining step, in agreem
19 e, which is identified as the formation of a tyrosine radical in the UV-vis.
20 eement with previously reported g-tensors of tyrosine radicals in photosystem II.
21 k of an activated copper-oxygen species on a tyrosine radical intermediate, is proposed for TPQ forma
22                           A tryptophan and a tyrosine radical maquette, denoted alpha(3)W(1) and alph
23   Therefore, the formation of an alternative tyrosine radical on Tyr504 probably accounts for the tra
24        This work required a de novo designed tyrosine-radical protein displaying a unique combination
25 ficantly narrowed and is characteristic of a tyrosine radical signal.
26 ligand, and cysteine 228 provides a modified tyrosine radical site believed to act as a one-electron
27                This illustrates the range of tyrosine-radical stabilization that a structured protein
28  fold and assembly, implicates Tyr370 as the tyrosine radical, suggests the structural basis for redo
29 roperties and reactivity of the redox-active tyrosine radical; the Y272 tyrosyl radicals in both the
30 fficient electron donor to the photooxidized tyrosine radical, TyrZ+, than is the mononuclear Mn cent
31 Lys-Tyr-Lys, the reactivity of the DNA-bound tyrosine radical was found to differ considerably from t
32 uctively activating O(2) to produce a stable tyrosine radical (Y122*), which is essential for product
33 ce relaxation enhancement of the dark-stable tyrosine radical, YD., by the S2 state of the O2-evolvin
34  Mn4-Ca cluster to the oxidized redox active tyrosine radical, YZ*, generated by photosynthetic charg