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 d loop samples multiple conformations in the unliganded state.
2 ylated HIV-1 Env trimer in its uncleaved and unliganded state.
3 ut maintain the extended conformation in the unliganded state.
4 presents the first structure of HDAC8 in the unliganded state.
5 --> close" conformational equilibrium in the unliganded state.
6 s dynamic nucleocytoplasmic shuttling in the unliganded state.
7 the efficiency with which Env moved from the unliganded state.
8 ace (high-affinity conformation) even in the unliganded state.
9 +) complex with bound ADP-ribose, and in the unliganded state.
10 re potent repressors of transcription in the unliganded state.
11 f the extent of salt bridge formation in the unliganded state.
12  rationally designed GP muc trimers in their unliganded state.
13 h SCP-2 being monomeric in both liganded and unliganded states.
14                          Comparison with its unliganded state (3.0 angstrom) reveals conformational r
15  or Asp markedly reduced dimerization in the unliganded state, albeit with apparent retention of the
16 arently affect the relative stability of the unliganded state and CD4-induced conformations.
17 nuclear magnetic resonance techniques in the unliganded state and in complex with beryllofluoride.
18  microscopy structures of human CD163 in its unliganded state and in its complex with HpHb.
19 tibility to tryptic cleavage at Arg-8 in the unliganded state and in the pH dependence of peptide bin
20 age in any hydrogen bond interactions in the unliganded state and it donates a hydrogen bond to only
21  Env proteins are kinetically trapped in the unliganded state and require the drug to negotiate CD4-i
22 T) has been determined by SADa phasing in an unliganded state and several ligand-bound states.
23                            Comparison of the unliganded state and substrate-bound state of the enzyme
24 ontribute to gp120-trimer association in the unliganded state and to CD4 binding.
25 ith the introduced cysteines in the resting (unliganded) state and compared them with rates determine
26  in decreased gp120-gp41 association (in the unliganded state) and decreased chemokine receptor bindi
27 epressors to nuclear receptors occurs in the unliganded state, and can be stabilized by antagonists.
28 diverse conformations that make up the gp120 unliganded state are reasonably ordered.
29 nooxygenase, stachydrine demethylase, in the unliganded state (at 1.6 A resolution) and in the produc
30 g cavity of CD1a is largely preserved in the unliganded state because of persistent electrostatic int
31 ontribute to gp120-trimer association in the unliganded state but also help secure CD4 binding.
32 tein domains, is more stable than the native unliganded state by approximately 1 kcal/mol in this sys
33 ane envelope glycoprotein that stabilize the unliganded state by modulating the transitions from the
34                                       In the unliganded state, CD163 can also form a trimer, but in a
35                                       In the unliganded state, comparison of the 15N and proton NMR s
36  or to which the environment of Arg-8 in the unliganded state differs in monomers and dimers, is rele
37                   A conformationally dynamic unliganded state for the binding pocket is stabilized fi
38 ated form of EpsE in nucleotide-liganded and unliganded state has been determined, and reveals a two-
39 v to change conformation from the metastable unliganded state in response to the binding of ligands (
40 romoting assembly of the gating ring from an unliganded state in which the four subunits interact as
41 rimeric Env displayed on native HIV-1 in the unliganded state, in complex with the broadly neutralizi
42  the overall shape of ct-AChBP in the apo or unliganded state is similar to that of homologues with k
43 uct state with the intermediate state and an unliganded state of MurA, we propose that dissociation o
44 tine has minimal interaction with the closed-unliganded state of the channel.
45 ciency virus (SIV) must be maintained in the unliganded state of the envelope glycoprotein trimer.
46 nce of agonist but can become trapped in the unliganded state of the receptor by prior washout of ago
47 stration of an effect of dimerization in the unliganded state on neurophysin's hormone-binding site,
48 1 has the ability to pass through its GDP or unliganded state prior to being GTP-loaded.
49 istic insights into the metastability of the unliganded state, receptor-induced conformational change
50   Both TR homodimers and heterodimers in the unliganded state selectively associated with glutathione
51 d roughly 20-fold more rapid exchange in the unliganded state than regions of low diversity (outer do
52           Two structures were solved for the unliganded state, the ERRgamma LBD alone, and in complex
53 tes HIV-1 entry by rearranging from a mature unliganded state, through receptor-bound intermediates,
54 gp120 and regulates Env transitions from the unliganded state to downstream conformations.IMPORTANCE
55 state by modulating the transitions from the unliganded state to the CD4-bound state.
56 v conformational changes from the metastable unliganded state to the fusion-active state.
57 nding sites, such as the transition from the unliganded state to the low-affinity agonist-bound confo
58 tential of the AF-1 activation domain in the unliganded state; upon ligand activation, a conformation
59 urophysin-II derivatives in the liganded and unliganded states, with the notable exception of the ext