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1 ide-involved pathway that is predicted to be endothermic.
2 her parameters was feasible, spontaneous and endothermic.
3 ested that the adsorption is spontaneous and endothermic.
4 hen conventional electron transfer is highly endothermic.
5 s general-base catalysis and the reaction is endothermic.
6         Above 30 degrees C the reactions are endothermic.
7 tions of 1-4d were found to be substantially endothermic.
8 xpansion of 1c to 3c is computed to be quite endothermic.
9 es such that the reaction is predicted to be endothermic.
10 bond, with the enolate addition being highly endothermic.
11 scission with the loss of SO(2) is generally endothermic.
12 on center, rendering attack at that position endothermic.
13 nd cationic heavy metals (Cd, Pb, and Zn) is endothermic.
14 e to an inefficient intersystem crossing, an endothermic 1,5-hydrogen atom transfer (HAT) step, and a
15 ndent, avian-style acclimatization, becoming endothermic.(1)(,)(2) The ability of warm-blooded dinosa
16     Differential scanning calorimetry showed endothermic (123 degrees C) and exothermic peaks (192 de
17 ntities change sign with DeltaHpart becoming endothermic (+70 kJ/mol) and entropically favored (Delta
18                            We found that the endothermic activity of birds within their nests created
19  in the carboxyl-terminal domain so that the endothermic, allosteric activation mechanism of CRP by c
20 xidation by IV(H(2)O), is found to be highly endothermic and cannot occur; this finding is different
21 its constituent monomer, ethylene, is highly endothermic and conventionally accessible only through u
22  Paracoccus cytochrome c-550, the binding is endothermic and driven by a large entropy change, a patt
23 hange suggested that the binding process was endothermic and driven by entropy.
24 reviously, arguments have been made for both endothermic and ectothermic metabolisms on the basis of
25 n the thermodynamics of the reaction that is endothermic and enthalpically driven in PF6- and TF2N-ba
26 es was characterized by a relatively greater endothermic and entropic profile as compared with those
27   The interactions between FasDD and CaM are endothermic and entropically driven, suggesting that hyd
28 he interactions between CaM and myr(+)MA are endothermic and entropically driven, suggesting that hyd
29             The encapsulation of the salt is endothermic and entropically favored by the liberation o
30 hat LA adsorption on OVAn was a spontaneous, endothermic and entropically-driven process, highlightin
31 i and Moab of r-fla S. typhi as spontaneous, endothermic and entropy driven one.
32 The association of halides with [H3L](3+) is endothermic and entropy driven.
33 e organometallic complex in the cavitand was endothermic and exclusively driven by entropy (DeltaH =
34   Relative trends for a significant range of endothermic and exothermic [1,5]-shifts with different i
35 SN2 reactions in three solvents that lead to endothermic and exothermic reaction processes, and we sh
36 al noncovalent ligand makes protonation very endothermic and greatly raises the reduction potential.
37 a a stepwise pathway is 21 kcal mol(-1) less endothermic and has a 12 kcal mol(-1) lower barrier heig
38       For ground state SO2, this reaction is endothermic and has a very high activation barrier; our
39 demonstrated that the dissolution process is endothermic and non-spontaneous and includes an entropy
40 hat the overall photoreduction of Pchlide is endothermic and that rapid dynamic searches are required
41  first tension-generating step may be weakly endothermic and that the rise of tension with temperatur
42  step(s) in the crossbridge cycle was highly endothermic and was therefore itself directly targeted b
43          The binding of LTbetaR to LIGHT was endothermic and, hence, entropy-driven.
44 ies, linking whole-body metabolic control to endothermics and to thyroid function.
45 tep in muscle is both temperature sensitive (endothermic) and strain sensitive.
46 : invertebrate or vertebrate, ectothermic or endothermic, and free-living or parasitic.
47 ) with both P-110 and M-200 was spontaneous, endothermic, and majorly driven by hydrophobic interacti
48                                   Binding is endothermic, and the binding site spans about 12 sacchar
49 eta-sheet aggregates underwent a reversible, endothermic, and very asymmetric thermal transition with
50 advantages of hypothermia risk reduction for endothermic animals and spore spreading enhancement for
51              When food resources are scarce, endothermic animals can lower core body temperature (Tb)
52 rance of various states of dormancy, such as endothermic animals sacrificing high body temperature th
53                Global warming compels larger endothermic animals to adapt either physiologically or b
54 d its corollaries state that pigmentation of endothermic animals will increase from more polar to equ
55 nown about neural control of torpor in other endothermic animals, including the Etruscan shrew.
56  some of the highest body temperatures among endothermic animals.
57 to-volume ratio that is very unfavorable for endothermic animals.
58 al and cellular functions of ectothermic and endothermic animals.
59 scent of thermoregulatory systems in larger, endothermic animals.
60                                         This endothermic approach eliminates runaway reaction hazards
61      Coupling exothermic hydrogenolysis with endothermic aromatization renders the overall transforma
62 s that nonavian dinosaurs were on average as endothermic as extant placental mammals.
63 s substitution of His64 with Gln leads to an endothermic association of CO with the five-coordinate h
64  calorimetry showed the binding was weak and endothermic at 15 degrees C, with a total DeltaH of > or
65 gand from the encounter complex, found to be endothermic at 6 kcal/mol.
66                                   Binding is endothermic at all temperatures examined, with DeltaH va
67 ilamellar EDOPC vesicles and plasmid DNA was endothermic at both physiological and low ionic strength
68  hydrophobic interactions are attractive and endothermic at moderate temperatures.
69                           The association is endothermic at physiologically relevant temperatures, wh
70 atio together with the reaction heat for the endothermic bi-reforming can be conveniently obtained by
71  the case of con-T, a weak (Kd = 410 microM) endothermic binding site is observed for Zn2+.
72  cannot undergo ion-induced folding exhibits endothermic binding.
73 s of environmental temperature fluctuations, endothermic birds and mammals maintain a relatively warm
74 nsfer lays the foundation for explaining how endothermic birds and mammals maintain their high, relat
75 ng (TAP) and class Ia has been documented in endothermic birds and two mammals, lineages of LMP7 are
76 structural changes (free volume collapse and endothermic bond breakage).
77 the dissociation reaction coordinate through endothermic bond breaking and concomitant gain in config
78    At lower temperatures the second phase is endothermic but gradually decreases with increasing temp
79  of 5 to form 6 was, however, computed to be endothermic by 122.0 kcal/mol whereas protonation of 6 t
80 athway for rearrangement of 6 to 8, which is endothermic by 14.5 kcal/mol, involves ring opening to Z
81 ove reactants, while the overall reaction is endothermic by 16.7 kcal/mol.
82  form UO(NO)Cl2(-) and N2 was computed to be endothermic by 169 kJ/mol, which is energetically more f
83 e to form aspirin and benzene is found to be endothermic by 2.7 kcal/mol and provides compelling evid
84  protonation of 6 to form 7 was again highly endothermic by 238.8 kcal/mol.
85 tion of 1 into 5 and N(2) was computed to be endothermic by 25.1 kcal/mol.
86 e formation of phenylaluminum dichloride, is endothermic by 33 kcal/mol.
87 he parent Bergman reaction is computed to be endothermic by 5 kcal/mol) and associated with a signifi
88 /mol, whereas the latter is calculated to be endothermic by 7.4 kcal/mol.
89  a conventional radical ion pair, A*-D*+, is endothermic by approximately 0.6 eV.
90 ecomposition reactions become - on average - endothermic by more than 0.6 eV.
91        The O-O bond homolysis is found to be endothermic by only 15 to 20 kcal/mol due to the fact th
92 ven in nonpolar solvents under isoenergetic (endothermic by ~40 mV) conditions.
93  attachment of other C atoms, which requires endothermic C-H activation and H* desorption steps that
94 othermic herbivore > ectothermic carnivore > endothermic carnivore.
95 ing and that this process is dependent on an endothermic change in SecA conformation.
96           However, in shortening muscle, the endothermic character of force generation becomes more p
97                              Here, we report endothermic charge-transfer-mediated TET as an alternati
98 essures will be substantially limited by the endothermic chemical reactions of the polyatomic species
99 ese systems, thermal energy is used to drive endothermic chemical reactions, which can subsequently r
100               Here, we report high-yielding, endothermic Cl2 photoelimination chemistry from mononucl
101 The first step in H2O oxidation involves the endothermic cleavage of a strong O-H bond (BDFE = 122.7
102                                    Combining endothermic cleavage of the polymer C-C bonds with exoth
103 solvent, bis-guanidinium receptors form more endothermic complexes with dicarboxylates, with a favora
104  salt concentrations were dissected into its endothermic components, yielding the enthalpy change and
105        The enzyme undergoes an ATP-modulated endothermic conformational transition (ECT) believed to
106 nge is different from the well-characterized endothermic conformational transition believed to gate t
107 the lowest temperature of SWCNT growth using endothermic decomposition of CH4 gas on a specially acti
108 alorimetry data indicating that ADT exhibits endothermic decomposition.
109 s suggested that ethanol conversion involves endothermic dehydration step.
110            The lanthanide triflates catalyze endothermic dehydroalkoxylation, while the palladium nan
111 py contribution (DeltaS) and the process was endothermic (DeltaH > 0).
112 t CO photodissociation is associated with an endothermic (DeltaH = 8 +/- 3 kcal mol(-1)) volume expan
113 lpic component stays small and in some cases endothermic (DeltaH degrees >/= -1 kcal/mol).
114 ebound to form a metal-bound amine is highly endothermic (DeltaH(reb)(dtbpe) = +25.1 kcal/mol).
115 drolysis reaction in beta(TP) is found to be endothermic, demonstrating that the catalytic site is ab
116 ing a model in which binding is linked to an endothermic distortion of the DNA in the complex.
117 escence anisotropy experiments to reverse an endothermic domain-dissociation reaction hypothesized to
118 iganded TRPM2, pore opening is intrinsically endothermic, due to ~10-fold larger activation enthalpy
119 iation over this temperature range showed an endothermic effect below 17 degrees C and an exothermic
120 According to the nanoflake based theory, the endothermic effect of glasses is caused by the transitio
121  that these glasses exhibited characteristic endothermic effects in a particular temperature range.
122 on capture is driven by solar thermal heated endothermic electrolyses of concentrated reactants occur
123 , and V(+), intact ligand loss competes with endothermic elimination of purine and of HCN to form MNH
124 ature increments reflected in the associated endothermic energies were determined with differential s
125 enter atoms on SACs for lowering the overall endothermic energy of key intermediates.
126      For both proteins, association involves endothermic enthalpy and positive entropy changes; thus,
127 in entropy and opposed by a relatively small endothermic enthalpy at room temperature.
128 eaker affinity and a less exothermic or even endothermic enthalpy change.
129 acterized by a Kd value of 286 microM and an endothermic enthalpy of binding.
130                                 However, the endothermic enthalpy remained largely unaffected.
131 ein purity, glass transition temperature and endothermic enthalpy.
132                         We suggest that this endothermic, entropically driven adsorption behavior is
133 Because the binding of myosin to actin is an endothermic, entropically driven reaction, work must be
134         For example, Hf(OTf)4 mediates rapid endothermic ether right harpoon over left harpoon alcoho
135 e decomposition of nitrate, if formed, is an endothermic event.
136 omplexes was also exothermic, but additional endothermic events occurred at both lower and higher hos
137 active than that at 700 degrees C due to the endothermic feature of reaction which promotes efficient
138                                              Endothermic fish were the most common predators (n = 13)
139                                           In endothermic fish, niche expansion into cooler waters is
140  physiology, the thermal physiology of large endothermic fishes, reproductive physiology of air breat
141 bining chemical stabilisation with efficient endothermic fission provides a promising avenue towards
142  the DFT calculations, this reaction is more endothermic for 1 due to the reduced stabilization of th
143 f NHC-boryl radicals to alkenes are probably endothermic for alkyl-substituted alkenes, but exothermi
144 ctron transfer was found to be significantly endothermic for all five CuRe(2) complexes: this fact, c
145 This latter reaction is even predicted to be endothermic for substituents with Hammett constant sigma
146 he fast/slow fiber difference in the rate of endothermic force generation (three- to fourfold) is con
147 Q10 approximately 2.7), similar to phase 2b (endothermic force generation) in isometric muscle.
148                     In both fibers, tau(2) ("endothermic force regeneration") became faster with an i
149 cteristics of the force increase on heating (endothermic force) in muscle.
150 nd the basic effects of increased [MgADP] on endothermic force, can be qualitatively simulated using
151 e that the two irreversible high-temperature endothermic HDL transitions involve particle enlargement
152 d that binding of WT apoA-I to SEM generates endothermic heat (DeltaH approximately 30 kcal/mol) in c
153 plex is more stable and unfolds with a lower endothermic heat and lower release of counterion and wat
154 loss around 220 degrees C associated with an endothermic heat effect accompanied by amorphization; an
155 hermal titration calorimetry demonstrates an endothermic heat for the binding of heparin to CLDCs at
156 ately 18 degrees C, and unfolds with a lower endothermic heat of 8.3 kcal/mol.
157 showing that crossbridge force generation is endothermic (heat absorbed) and associated with increase
158  Ca(2+) with G-triplexes is characterized by endothermic heats.
159 t is argued that a commitment to life in the endothermic hepatic portal system favored a filiform bod
160 sed in the sequence: ectothermic herbivore > endothermic herbivore > ectothermic carnivore > endother
161 electron and hole densities, consistent with endothermic hole-transfer-mediated TET.
162 t, growth, fecundity, and development within endothermic hosts and may thus potentially influence tra
163      The DeltaH of binding comprises both an endothermic hydrophobic interaction and exothermic hydro
164 nge in the reaction energetics from strongly endothermic in betaTP to approximately equienergetic in
165                       The reaction is highly endothermic in the gas phase and requires significant ex
166  Both proton-transfer events are found to be endothermic in the oxyferrous state, suggesting that the
167 ding whether O. megalodon was ectothermic or endothermic (including regional endothermy), and whether
168        Thermoregulation of the thorax allows endothermic insects to achieve power outputs during flig
169                                       Flying endothermic insects, including the honeybee Apis mellife
170 es, and this mechanism may occur commonly in endothermic insects.
171 t two-site binding mechanism at pH 7.0 to an endothermic interacting two-site mechanism at pH 5.2, si
172 t two-site binding mechanism at pH 7.0 to an endothermic, interacting two-site binding mechanism at p
173         In contrast, ITC measurements showed endothermic interactions of Cu, Ni, and Rh oxide/hydroxi
174 e of the meso-substituent is able to turn an endothermic interconversion process with a high energy b
175         The titration with Na(+) resulted in endothermic isotherms with (dm(5)C-dG)(4) being more end
176 of evolution pave the way to intelligence in endothermic land vertebrates.
177  identified several genes under selection in endothermic lineages, including carnmt1 (involved in fat
178 gh Cu(+), the primary product corresponds to endothermic loss of the intact adenine molecule, whereas
179                                In all cases, endothermic loss of the intact aromatic amino acid is th
180 ng enthalpy, which partially compensates the endothermic mAb unfolding enthalpy.
181 tical for survival across animals, including endothermic mammals.
182 cardiovascular physiology resembling that of endothermic mammals.
183 ted with the oxygen demands of flying, their endothermic metabolism and unusual pulmonary architectur
184             Stem mammals lacked the elevated endothermic metabolism of living mammals, highlighting t
185 e ability of birds to fly and to maintain an endothermic metabolism.
186 d temperature; the findings indicate that an endothermic molecular step underlies muscle force genera
187 forms ranging from single atom (N) to highly endothermic molecules (N2, N3, N4, N5, N6) and chains (N
188  units, with the ultimate goal of performing endothermic, multielectron transformations that are coup
189 ug molecules throughout the body; how fish's endothermic nature and the varied expression and activit
190 hat nonavian dinosaur metabolism was neither endothermic nor ectothermic but an intermediate physiolo
191 at of reaction of the hydrogenation with the endothermic one of the CO2 release from the capturing re
192            As these materials are formed via endothermic or exothermic equilibria, their thermal resp
193                           By this means, the endothermic oxidation-reduction reaction is pulled such
194 Cd(II) exhibited a characteristic exothermic-endothermic pattern that was used to infer the metal bin
195                                           An endothermic peak at 45-70 degrees C, having enthalpy of
196                                          The endothermic peak at 46.7 degrees C is attributed to a la
197 ons in the differential scanning calorimetry endothermic peak enthalpies and loss of birefringence in
198                            The absence of an endothermic peak for both MPs confirmed all extract solu
199 often appears as splitting of the respective endothermic peak in its thermal (DSC) fingerprint, while
200 ted starch was broadened with a shift of the endothermic peak to higher temperature.
201 tion was observed in the region of the first endothermic peak where the two thermolabile domains melt
202 e inclusion complexes showed the presence of endothermic peaks between 80 degrees C and 150 degrees C
203                                          New endothermic peaks in the calorimetric thermograms of tre
204 d the exothermic phase without affecting the endothermic phase, but it was regained upon addition of
205 ut 6.7 kcal/mol enthalpic advantage over the endothermic phase.
206                          Both exothermic and endothermic phases produce highly negative DeltaC(p) deg
207 inding data conformed to both exothermic and endothermic phases with magnitudes of DeltaG degrees , D
208 rd characteristics such as feathers, flight, endothermic physiology, unique strategies for reproducti
209  shown to be the driving interaction for the endothermic physisorption process of organic vapor parti
210 s were generally higher for ectothermic than endothermic predators, although dietary patterns were si
211              The bent DNA 34-bp mode is most endothermic, presumably because of the cost of HU-induce
212  from state A to state B) was found to be an endothermic process (positive DeltaHswitching) for both
213 e dry reforming of methane (DRM) is a highly endothermic process conducted under harsh conditions; he
214 light alkanes via C-H activation is a highly endothermic process that generally requires high tempera
215 ors is a sequential two-step, entropy-driven endothermic process.
216 emperature (1200 degrees C) of such a highly endothermic process.
217           Adsorption reactions are favorable endothermic processes as evidenced by increased adsorpti
218 ct kinetic and thermodynamic (exothermic and endothermic) properties.
219 hat permits differentiation between exo- and endothermic proton transfer reactions.
220 action, F(-) with dimethyl sulfoxide, and an endothermic proton-transfer reaction with a competing ex
221                               Dynamics of an endothermic proton-transfer reaction, F(-) with dimethyl
222  low catalyst durability, resulting from the endothermic reaction and coke deposition, are two main c
223                         DRM is also a highly endothermic reaction and requires operating temperatures
224                              The competitive endothermic reaction Cl(-) + CH(3)Br --> CH(3) + ClBr(-)
225                              Modeling of the endothermic reaction cross sections yields the 0 K bond
226  force generation step is an entropy driven, endothermic reaction that accompanies a burial of large
227 f 16.4 microM at 25 degrees C, pH 6.0, in an endothermic reaction that is driven by a large entropy c
228             Similarly, Pi binding is also an endothermic reaction with Kb = 167 +/- 17 M(-1), deltaHb
229 he energy barrier as much as possible for an endothermic reaction without yielding a significant conc
230 and free energy of inactivation indicated an endothermic reaction, not spontaneous degradation, where
231 mally hidden in DSC analysis by simultaneous endothermic reactions of soil minerals.
232 xceptional support for highly exothermic and endothermic reactions that operate above 700 degrees C i
233                                           No endothermic reactions were observed.
234 he air-exposed reaction proceeds via slight, endothermic rearrangements of crystalline intermediates
235 iency by using excess fuel-cell heat for the endothermic reforming reaction.
236 of electron transfer is displaced toward the endothermic region by 0.5-0.8 eV.
237                                          The endothermic reverse reaction required as little as 18 mi
238 s the photoluminescent state of CdSe through endothermic reverse triplet-triplet energy transfer.
239                                          The endothermic S(N)2 reaction Cl(-) + CH(3)F --> CH(3)Cl +
240                   The possible advantages of endothermic singlet fission (enhanced use of photon ener
241 es of linear perylene oligomers that undergo endothermic singlet fission and have endothermicities in
242 er of coupled chromophores needed to undergo endothermic singlet fission is three, which provides suf
243 at it plays a critical role in the efficient endothermic singlet fission process.
244 sion, whereas crystalline tetracene displays endothermic singlet fission with near-unity quantum yiel
245 ate warming creates energetic challenges for endothermic species by increasing metabolic and hydric c
246  suggest that adsorption of Sb(III) ions was endothermic, spontaneous and a thermodynamically feasibl
247                        The results showed an endothermic, spontaneous and an entropy-driven dissoluti
248  Gibbs energy and dissolution entropy showed endothermic, spontaneous and entropy-driven dissolution
249 olutionary transitions leading to the modern endothermic state of birds and mammals is incomplete, pa
250 SecA-membrane interaction is regulated by an endothermic step that is azide inhibitable.
251 largely driven by the preceding two strongly endothermic steps of ATP hydrolysis and attachment of M.
252  substrate reveal a binding reaction that is endothermic, suggesting that cobB recognition of substra
253 ergy of electron transfer (DeltaGET) becomes endothermic, syn-anti isomerization is the dominant path
254 eral phenomenon in non-avian ectothermic and endothermic tetrapods.
255 mic isotherms with (dm(5)C-dG)(4) being more endothermic than (dC-dG)(4) by 700 cal/mol basepair.
256 action, is computed to be only slightly more endothermic than the comparable cyclization reaction of
257 0.3 kcal.mol(-1), a value significantly less endothermic than those values suggested from gas-phase m
258         Explicit acetylene loss would be too endothermic to merit consideration.
259 es C, the first DSC heating scan exhibits an endothermic transition at 46.7 degrees C, a small hump n
260   On heating, anhydrous C16:0-SM exhibits an endothermic transition at 75 degrees C (delta H = 4.0 kc
261  71.5 degrees C, followed by a chain-melting endothermic transition at 78 degrees C.
262 exhibited a scan-rate-dependent irreversible endothermic transition at all stages of solubilization.
263 ding site by scanning calorimetry showing an endothermic transition beginning around 725 degrees C ac
264 t 1 deg.C/minute it exhibits an irreversible endothermic transition between 35 and 42 degrees C depen
265 s melt and dissociate reversibly in a second endothermic transition between 60 and 90 degrees C also
266  the low-affinity site strongly inhibits the endothermic transition but does not reduce the rate of A
267 ic binding site on SecA does not perturb the endothermic transition but produces a 10-fold accelerati
268   Data are discussed which indicate that the endothermic transition in the complex is consistent with
269 nd bithiazole-thiophene oligomers display an endothermic transition in their DSC trace below their re
270                                          The endothermic transition of alkali-treated starch was broa
271        By DSC hydrated GM1 undergoes a broad endothermic transition TM = 26 degrees C (delta H = 1.7
272  that polymorph alpha irreversibly undergoes endothermic transition to polymorph beta much before its
273 ed C16:0-LacCer undergoes a complex two-peak endothermic transition with maxima at 69 degrees C and 7
274 y (DSC), anhydrous C16:0-GalSulf exhibits an endothermic transition, T(M) = 93 degrees C (DeltaH = 5.
275 m their consistent effects in inhibiting the endothermic transition.
276 gelation (dynamic rheology); and (3) protein endothermic transitions (differential scanning calorimet
277                                      Protein endothermic transitions (thermal denaturation), rheologi
278 slower heating rate (1.5 degrees C/min), two endothermic transitions are observed at 66 degrees C and
279 y heating curve of the emulsion showed three endothermic transitions at 24.3 degrees C, 33.0 degrees
280 bsequent heating run shows three overlapping endothermic transitions at 66 degrees C, 69 degrees C, a
281 C investigations reveal the presence of four endothermic transitions between 50 and 300 degrees C.
282 reversible melting processes and undergo two endothermic transitions each, at 189/237 and 59/80 degre
283                                              Endothermic transitions showed similar trends to rheolog
284                                     Multiple endothermic unfolding transitions were observed by diffe
285 itation fusion process: this process enables endothermic upconversion and allows efficient upconversi
286 stinct ITC profiles (i.e., exothermic versus endothermic) upon interaction with actinonin.
287 results suggest that the modern dichotomy of endothermic versus ectothermic is overly simplistic.
288     However, lymph nodes are only present in endothermic vertebrates (ie, mammals and possibly some b
289 d plants) is separated from the highest (for endothermic vertebrates) by a factor of about 20.
290  habitats impose severe metabolic demands on endothermic vertebrates, and understanding how high-alti
291 ence thermal stress at each feeding event on endothermic vertebrates.
292 calculations show C-CN bond activation to be endothermic, which contradicts the observation of therma
293 he attachment process was nonspontaneous and endothermic, which may be associated with structural cha
294 gomerization leading to a neutral product is endothermic, while the analogous one-electron reductive
295   We found that the Mg2+ binding reaction is endothermic with a binding constant (Kb) = 142 +/- 4 M(-
296 fully cNMP-ligated CRP-mutant complexes were endothermic with binding constants as high as 6.6 +/- 1.
297 .0 pM, the reaction releases 3.8 protons, is endothermic with DeltaHrxn of +6.4 kcal mol-1, and entro
298                        Complex formation was endothermic with less than 1 kcal absorbed per mole of l
299 nthalpy of the binding reaction changes from endothermic with the wild-type hSBDb to exothermic with
300 eleased upon Zn(II) binding, the reaction is endothermic, with DeltaHrxn of +7.7 kcal mol-1, and entr

 
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