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1 oxocalix[4]arene adopts in the crystal a 1,2-alternate conformation.
2 studied superhelical transitions to a single alternate conformation.
3 ne-like conformation, and HC6.Cs has a 1,2,3-alternate conformation.
4 formers, but in the crystal both adopt a 1,2-alternate conformation.
5 ying simulation where the simulation samples alternate conformations.
6 otein pocket, allowing for rapid sampling of alternate conformations.
7  state among a vast ensemble of unfolded and alternate conformations.
8 tain the phospho-accepting His45 do not have alternate conformations.
9 r in the identity of side-chains that occupy alternate conformations.
10 posal that OmpA can fold into one of the two alternate conformations.
11 molecules hydrating the oligonucleotide have alternate conformations.
12 cture, the hemiphthaloyl ring occupies three alternate conformations.
13                     Four side-chains display alternate conformations.
14 eal previously hidden, biologically relevant alternate conformations.
15 anipulation will enable Alphafold2 to sample alternate conformations.
16 te the deposited model, 16% confidently find alternate conformations, 22% have ambiguous density wher
17 he ES enzyme, a mutated Omega loop adopts an alternate conformation allowing the side chain to be muc
18        Calix[4]arenes constrained to the 1,3-alternate conformation and functionalized at the upper r
19           Cys side chains of (CSL9C)(3) show alternate conformations and are partially preorganized f
20 mer, which is typically less stable than the alternated conformation and is a rare phenomenon in orga
21  A) was studied as a function of resolution, alternate conformations, and temperature factor (B), lea
22                                          The alternate conformations are most likely the result of th
23  For the C-terminal domain of protein IX two alternate conformations are proposed, either binding on
24 hosphorylation of DNA-bound CREB promotes an alternate conformation characterized by an apparent incr
25  that the Asp318 side chain exhibits a minor alternate conformation, compared to that in the wild typ
26 n, as a disease-causing mutation leads to an alternate conformation completely incapable of hydrolyzi
27                               The accessible alternate conformations depend on base sequence and comp
28 icated that Trp104 is capable of undertaking alternate conformations depending on the length of the B
29                                          The alternate conformation, described by Kuriyan and co-work
30 of dimers, the helicase domain exists in two alternate conformations, each of which can form symmetri
31                    Thus, there must exist an alternate conformation for LeuT in which the substrate i
32  Mn(2+).UDP.phosphoglyceric acid revealed an alternate conformation for the nucleotide sugar beta-pho
33 lectron density maps has enabled modeling of alternate conformations for 83 residues in the enzyme, m
34 idges, which are stable in the cone or 1,2,3-alternate conformation, form pseudorotaxanes with dialky
35 ed structure-activity relationships and used alternate conformations from a crystallographic structur
36 the cytoplasmic accessibility pathway of the alternate conformation in a mammalian serotonin transpor
37 x[6]arene P6(H)(2)(2+), which adopts a 1,3,5-alternate conformation in the presence of chloride anion
38 ation in the ER membranes changes SCAP to an alternate conformation in which it binds ER retention pr
39 petitive behavior of transitions to multiple alternate conformations in a negatively supercoiled DNA
40 ecognized, the overall significance of these alternate conformations in biology has only recently bec
41 the inherent ability of the H3 tail to adopt alternate conformations in complex with chromatin regula
42 133 and AppA1-126 contain Trp104 in distinct alternate conformations in solution and that light absor
43                                Resolving the alternate conformations in the active site residues prov
44               Two of the metal ligands adopt alternate conformations in the crystal structure, both c
45 hydroxylase, caused by the occurrence of two alternate conformations in the hinge region that leads t
46 ransmembrane (TM) domain of EphA2 adopts two alternate conformations in the ligand-dependent and the
47 ate sidechain rotamer jumps, as evidenced by alternate conformations in very high-resolution crystal
48   In the unbound state, DtpA adopts two main alternate conformations in which transmembrane alpha-hel
49 ts show that recombinant alpha-chain assumes alternating conformations in the absence of beta-chain a
50  calix[4]arene, neither the cone nor the 1,2-alternate conformation is computed to be a ground-state
51  considerable importance, but distinguishing alternate conformations is a challenge.
52  are discussed within the context of a C1/C2 alternating conformation model in which lactose transloc
53 models for other P2XR subtypes, and a second alternate conformation not previously observed.
54                                         This alternate conformation now causes a steric hindrance to
55  E256Q mutant with putrescine added shows an alternate conformation of His243, Glu11, Lys80, and Ser2
56                The C319Y protein exhibits an alternate conformation of the flap, explaining its lack
57 partner monomer is incompletely occupied, an alternate conformation of the loop involving residues 12
58                   These structures reveal an alternate conformation of the microtubule binding region
59 rphyrin, prepared in 91% yield, shows an 1,3-alternate conformation of the molecule with partial over
60 tinguished by a projecting beta-shelf and an alternate conformation of the N-terminal polypeptide.
61                          The pincer-like 1,3-alternate conformation of the oxacalix[4]arene scaffold,
62  domain, whereas arachidonic acid prompts an alternate conformation of the TPR domain, destabilising
63                                              Alternate conformations of Asn214 near the active site a
64       SCOR also presents the predominant and alternate conformations of hairpin loops, as shown in th
65 ee energy differences between at least a few alternate conformations of many proteins are not large.
66 acting NAD(H)-NADPH pairs are observed where alternate conformations of the NAD(H) phosphodiester and
67                                              Alternate conformations of the putative PE-PPE binding s
68 nts displayed small local perturbations with alternate conformations of the Ser side chains.
69 n contrast to the wild-type protein, several alternate conformations of the substrate, confirming tha
70  and to obtain more accurate descriptions of alternate conformations of the two proteins, we first pe
71 t is suggested that these signals arise from alternate conformations of Trp191 having different degre
72 main of this group of enzymes, exists in two alternate conformations, only one of which makes the enz
73 es would not be analyzed for residues in 'b' alternate conformations or with B-factors of 40 or above
74 ermined and if no atom had a B factor >/=40, alternate conformation, or severe clash; that selection
75    Thus, both TCR V-domains can switch among alternate conformations, perhaps extending their ability
76 l group, 4.4 A from the heme Fe, whereas the alternate conformation positions the second, infrequent
77 , it is unique in that NADP+ is bound in two alternate conformations, probably because of the lack of
78 6 symmetry, the C-terminal domains adopt two alternating conformations, producing a symmetry-broken h
79 n the dengue virus family, with the reported alternate conformation resulting from a unique metal-bin
80                              In addition, an alternate conformation similar to the omega-helix forms
81 th data from the reactivation kinetics, this alternate conformation suggests a key interaction betwee
82 in (NBD1) of CFTR can spontaneously adopt an alternate conformation that departs from the canonical N
83 he inactive state is a biologically relevant alternate conformation that regulates ribosome function
84 lements confer unique phenotypes by adopting alternate conformations that specify new traits.
85 e resistant, supporting a transition from an alternate conformation to a well packed triple helix.
86  molecules, resulting in the formation of an alternate conformation to standard B-DNA known as B'-DNA
87 is specific for cytochrome c550 and utilizes alternate conformations to recognize redox partners.
88 s 1 and 2, possessing either a cone or a 1,3-alternate conformation, to NO(2)/N(2)O(4), both in chlor
89 he possibility that this region may adopt an alternate conformation upon DNA binding.
90                                          The alternate conformation was correlated with protonation o
91  of DADH in complex with iminohistidine, two alternate conformations were observed for iminohistidine
92 binding is required for stabilization of the alternate conformation, which catalyzes the 4-CBA-CoA th
93   For five cases where our approach finds an alternate conformation with high confidence, high-resolu
94 cture of reduced P94A amicyanin exhibits two alternate conformations with the positions of the copper
95      The reduced P94A amicyanin exhibits two alternate conformations with the positions of the copper
96     Each DNA helix is quite anisotropic, and alternate conformations, with motion in the direction of