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1  the plasmid DNA molecule indirectly via two noncovalent bonds.
2 bunits of approximately 15 kDa associated by noncovalent bonds.
3  ions only if these are not held together by noncovalent bonds.
4  two identical 28-kDa subunits associated by noncovalent bonds.
5  12-kDa subunits (alpha(2)beta(2)) linked by noncovalent bonds.
6 ble but weak in strength due to formation of noncovalent bonds.
7 s with axial ligands is a sensitive test for noncovalent bonding.
8 e 5+ ions completely destroys their tertiary noncovalent bonding.
9 ons are one of the most important classes of noncovalent bonding, and are seen throughout biology, ch
10 tures, such as strand length, entanglements, noncovalent bonds, and chemical reactions, govern crack
11 ks-based assembly, suprastructures formed by noncovalent bonds are more influenced by specific bond f
12  of positively cooperative binding, in which noncovalent bonds are reduced in length and thereby incr
13 ly a few results have been reported based on noncovalent bond-based building block multistage assembl
14                  The basis for unprecedented noncovalent bonding between anions and the aryl centroid
15 alled expansins that nonenzymatically loosen noncovalent bonding between cellulose microfibrils.
16 therwise been realized from the formation of noncovalent bonds between the ligand and repressor monom
17 , are stabilized by longitudinal and lateral noncovalent bonds between the tubulin subunits.
18 nzyme katanin uses ATP hydrolysis to disrupt noncovalent bonds between tubulin dimers within the micr
19  was consistent with the formation of weaker noncovalent bonds between uranium and the carbonyl oxyge
20 we simulate the weakening or dilution of the noncovalent bonds during protein unfolding, and identify
21 less inclined to donate their electrons into noncovalent bonds, e.g., (CDCl2)2, and when relatively b
22 adily donate their nonbonding electrons into noncovalent bonds, e.g., DMF, and when spacer units that
23 The second wheel of Cy3R can form additional noncovalent bonds, e.g., salt bridges, cation-pi interac
24             Some recently studied biological noncovalent bonds have shown increased lifetime when str
25 he biotin-streptavidin bond is the strongest noncovalent bond in nature and is thus used extensively
26 nding affinity is described as the strongest noncovalent bond in nature, and is ~10(6) - 10(8) times
27                        Finally, we show that noncovalent bonding in a DNA duplex can be preserved fol
28                 However, the ECD data on the noncovalent bonding in the 5+ to 13+ ions, determined ov
29                          The exploitation of noncovalent bonding in the solid state is attractive to
30 ent bonds in aptazyme ligases (as opposed to noncovalent bonds in antibodies) potentiated stringent w
31 directed protocols--which rely on the use of noncovalent bonding interactions between molecular build
32 halogen substituents and the strength of the noncovalent bonding interactions between the analyte and
33 override the influence of all other possible noncovalent bonding interactions between them and the tu
34 ting their formation using various different noncovalent bonding interactions have been introduced an
35 ents that can be tuned through the extensive noncovalent bonding interactions in these interfaces.
36                                              Noncovalent bonding interactions of nitric oxide (NO) wi
37 ective recognition of these dianions through noncovalent bonding interactions on the outer surface of
38 ycol chain length has on the strength of the noncovalent bonding interactions taking place between cy
39 y using redox energy and precisely organized noncovalent bonding interactions to pump positively char
40 yzed by other antibodies or proteins through noncovalent bonding interactions with the substrates.
41 ding and unfolding, investigate covalent and noncovalent bonding interactions, and probe enzyme kinet
42 iffusion pathways, effected entirely through noncovalent bonding interactions, has inspired chemists
43 g affinities as a result of a combination of noncovalent bonding interactions, including face-to-face
44                      The subtle interplay of noncovalent bonding interactions, resulting from the tin
45 ted by threadlike precursors, as a result of noncovalent bonding interactions, to produce [2]pseudoro
46 tem relies solely on reversible, yet stable, noncovalent bonding interactions.
47 r than fragile supermolecules resulting from noncovalent bonding interactions.
48 t with one another by means of programmable, noncovalent bonding interactions.
49 single crystals as a consequence of multiple noncovalent-bonding interactions between each of the inc
50 e solid state, it has been demonstrated that noncovalent-bonding interactions with a variety of molec
51 ike materials through the utilization of the noncovalent bond, is a developing area of research.
52 lts with the P378L carboxylase indicate that noncovalent bonds maintain the two-chain structure even
53 02B on the fibril surface through an intense noncovalent bonding network via inter-ligand interaction
54 h polymers (systems integrating covalent and noncovalent bonding of structural units) consisting of p
55  product ions and by denaturing the tertiary noncovalent bonding of the molecular ions under a variet
56 ly this ion activation breaks intramolecular noncovalent bonds of the ion's secondary and tertiary st
57  to promote underwater adhesion via covalent/noncovalent bonds, or through micro/macro-interlock mech
58                             We highlight how noncovalent bonds, particularly hydrogen and halogen bon
59                                          The noncovalent bonding patterns indicate higher fitness cos
60 rk provides an intriguing example where weak noncovalent bonds serve as the determining factor of the
61 Our results suggest that interplay involving noncovalent bonds subjected to mechanochemical condition
62       In model A, the proton involved in the noncovalent bond suffers a smaller downfield shift becau
63       In model B, the proton involved in the noncovalent bond suffers a smaller downfield shift becau
64 itive-strand genomic RNAs linked together by noncovalent bonds that can be dissociated under mild con
65 by the strengths as well as lifetimes of the noncovalent bonds that lead to the formation of the stru
66  efficient capture, dissociation of tertiary noncovalent bonds that prevent product separation, and m
67 o 9+, not the 10+ to 13+ ions, have tertiary noncovalent bonding; this is indicated as hydrogen bondi
68 lating a metal center by way of covalent and noncovalent bonding, thus preserving its unsaturated val
69 bone bond, but with negligible excitation of noncovalent bonds; thus ECD of a linear protein ion prod
70 and possibly CO) result from anesthetic-like noncovalent bonding to sites within protein or other tis
71     This could easily give rise to dozens of noncovalent bond types.
72        The second is the presence of CN...Se noncovalent bonds which show similarities to the more co
73  I atom play a dual role: forming additional noncovalent bonds with the ligated substrate and increas
74 n swapping, a domain of a protein breaks its noncovalent bonds with the protein core and its place is
75 nd induce extension by reversibly disrupting noncovalent bonds within this polymeric network.