1 ta-sheet structure of Fn modules seen in the
high resolution crystal structure.
2 ned from a polarized XAS model and the 1.9-A
high resolution crystal structure.
3 imers, and this was confirmed for Spc42 by a
high-resolution crystal structure.
4 ith 1 A rms deviation to the backbone of the
high-resolution crystal structure.
5 hydrogen bonds with the nitrogenous bases in
high resolution crystal structures.
6 evidenced by alternate conformations in very
high-resolution crystal structures.
7 resent tools to compare a given structure to
high-resolution crystal structures.
8 itative comparison of the given structure to
high-resolution crystal structures.
9 l, large, and leaving group pockets based on
high-resolution crystal structures.
10 ment to biophysical studies and to obtaining
high-resolution crystal structures.
11 ith the experimental B-factors obtained from
high-resolution crystal structures.
12 solution differ from its recently determined
high-resolution crystal structures.
13 and binding and compare the PELDOR data with
high-resolution crystal structures.
14 lts were found to agree very well with known
high-resolution crystal structures.
15 es observed in a benchmark data set of 2,304
high-resolution crystal structures.
16 l7B is a cellobiohydrolase and obtained four
high-resolution crystal structures.
17 High resolution crystal structures (
1.3-1.5 A) of three
18 Here, we report three
high-resolution crystal structures (
1.50-1.55 A) of hKAT
19 Two
high-resolution crystal structures (
1.65 and 1.11 A) of
20 High-resolution crystal structure analysis confirmed tha
21 Building on
high-resolution crystal-structure analysis, pore vestibu
22 A
high resolution crystal structure and solution NMR struc
23 Here we present 10
high resolution crystal structures and enzyme kinetic an
24 Determination of
high resolution crystal structures and molecular modelin
25 nomeric transmembrane beta-barrel of a known
high-resolution crystal structure and displays three dis
26 Here, we describe the
high-resolution crystal structure and solution NMR struc
27 High-resolution crystal structures and biophysical analy
28 relevant glycans in this epitope by fitting
high-resolution crystal structures and by performing neu
29 We present
high-resolution crystal structures and functional analys
30 Together, the new SAM analog and the
high-resolution crystal structure are a step towards the
31 Data from NMR mapping and
high-resolution crystal structures are congruent with th
32 meters, particularly in cases where reliable
high-resolution crystal structures are not available.
33 In contrast,
high-resolution crystal structures are only available fo
34 The
high resolution crystal structures at 1.75-2.1 A of the
35 Here, we present a
high-resolution crystal structure at 2.1 A of the biotin
36 We report here the
high-resolution crystal structures,
at 1.9 and 2.35 A, r
37 e and protein/drug-bound) was 'mapped' using
high resolution crystal structures cataloged in the Nucl
38 The
high-resolution crystal structure clearly revealed the e
39 A
high-resolution crystal structure confirmed the mode of
40 Here, we present 29
high-resolution crystal structures,
covering all BRD fam
41 Its
high-resolution crystal structure defines the molecular
42 meters for the above measures, obtained from
high-resolution crystal structures enable us to provide
43 se SecA can also form functional dimers, and
high-resolution crystal structures exist for both the mo
44 A
high resolution crystal structure for the monoamine tran
45 Here we describe
high resolution crystal structures for the N(2)-guanine
46 Although a
high-resolution crystal structure for the ground state o
47 Here, we report a
high-resolution crystal structure for the Serratia sp. A
48 an apparent disagreement between two sets of
high-resolution crystal structures for MbCO and deoxyMb.
49 We describe here
high-resolution crystal structures for the GluR5 ligand-
50 ailability of extensive mutagenesis data and
high-resolution crystal structures for the TEM-1/BLIP an
51 sis by 2 orders of magnitude, we have solved
high-resolution crystal structures for the W354F YopH in
52 l basis of this potency, we determined eight
high-resolution crystal structures:
four each of the wil
53 Analysis of aligned RNA sequences and
high-resolution crystal structures has revealed a new RN
54 Recent analysis of
high-resolution crystal structures has suggested a new m
55 High resolution crystal structures have provided snapsho
56 ligand-gated ion channels for which multiple
high-resolution crystal structures have been solved.
57 High-resolution crystal structures have highlighted func
58 Recent biochemical reconstitution and
high-resolution crystal structures have provided proof t
59 Recent
high-resolution crystal structures have revealed that rh
60 ed rhomboids and, most recently, a flurry of
high-resolution crystal structures,
have led to real ins
61 ubjected to crystal structure analysis and a
high resolution crystal structure in complex with PTR1 w
62 For this compound, a
high-resolution crystal structure in complex with E. col
63 Herein, we present five
high-resolution crystal structures including one first-t
64 /U wobble basepairs in the ribosome based on
high-resolution crystal structures,
including the recent
65 y other peroxidase in this group for which a
high-resolution crystal structure is available, cytochro
66 A
high-resolution crystal structure is reported for d(TpA)
67 Four
high resolution crystal structures,
namely complexes wit
68 High-resolution crystal structures obtained in two confo
69 We report the
high resolution crystal structure of a competent fragmen
70 In a
high resolution crystal structure of fascin, molecules o
71 activities of the two enzymes, we report the
high resolution crystal structure of human NPP4 and expl
72 Here we report a
high resolution crystal structure of MC159, a v-FLIP der
73 Here we present the
high resolution crystal structure of murine SMPDL3B, whi
74 This
high resolution crystal structure of NKX2.5 protein prov
75 The
high resolution crystal structure of PTHrP bound to the
76 In light of the
high resolution crystal structure of the DAF four-CCP fu
77 We present the first
high resolution crystal structure of the kinase domain o
78 he dual role of HR23, we have determined the
high resolution crystal structure of the mouse peptide N
79 chanism of these enzymes, we report here the
high resolution crystal structure of wild-type murine ca
80 The
high resolution crystal structures of a recombinant frag
81 High resolution crystal structures of apoGilR and GilR i
82 Four
high resolution crystal structures of B. cereus PPM reve
83 High resolution crystal structures of complexes with dif
84 cificity and selectivity, we have determined
high resolution crystal structures of each of the two CB
85 We also determined
high resolution crystal structures of HRAS-like tumor su
86 Here we present
high resolution crystal structures of human AChE, alone
87 The
high resolution crystal structures of isatin hydrolase f
88 esolution images from electron microscopy or
high resolution crystal structures of isolated component
89 The
high resolution crystal structures of maltose-bound rfhS
90 Here, we present
high resolution crystal structures of murine and yeast C
91 The
high resolution crystal structures of N-domain ACE in co
92 A molecular model of Bla g 2, based on the
high resolution crystal structures of pepsin and chymosi
93 This study reports the first
high resolution crystal structures of periplasmic glucos
94 Here we report the
high resolution crystal structures of PitB and SrtG1 and
95 Only minimal differences are observed in
high resolution crystal structures of PR(D25N) complexed
96 High resolution crystal structures of PR20-inhibitor com
97 High resolution crystal structures of seven selected SL9
98 We also solved the
high resolution crystal structures of SlAMADH1 and ZmAMA
99 In this study, we present a series of
high resolution crystal structures of Spa47 and use the
100 We have presented here the
high resolution crystal structures of the beta-lactamase
101 High resolution crystal structures of the E120H mutant i
102 The
high resolution crystal structures of the protozoan para
103 kallikrein, along with the purification and
high resolution crystal structures of the two recombinan
104 Here we present the
high resolution crystal structures of Tom71 and the prot
105 We report
high resolution crystal structures of yCT-H9 complexed w
106 difference between the derived model and the
high-resolution crystal structure of a 54% homologous ga
107 In this study, we first solved the
high-resolution crystal structure of a Hat1p/Hat2p/CoA/H
108 We have determined the
high-resolution crystal structure of a human-type ACA fr
109 Herein we report a
high-resolution crystal structure of a Lys73-ligated cyt
110 The
high-resolution crystal structure of a PNK-FHA-XRCC1 pho
111 The
high-resolution crystal structure of a ternary complex o
112 This is the first
high-resolution crystal structure of a TSR domain that p
113 We solved the
high-resolution crystal structure of ACDH-11 and establi
114 Here we report the first
high-resolution crystal structure of ACMSD from Pseudomo
115 The
high-resolution crystal structure of all-trans-retinal b
116 dditionally, we provide for the first time a
high-resolution crystal structure of an active exoribonu
117 We report the first, to our knowledge,
high-resolution crystal structure of an antiviral compou
118 ere, we present, to our knowledge, the first
high-resolution crystal structure of an erythrocyte-bind
119 Considering the
high-resolution crystal structure of bacteriorhodopsin,
120 f the isolated loop A and loop B stems and a
high-resolution crystal structure of both loops in a doc
121 cedure by comparing its predictions with the
high-resolution crystal structure of bovine rhodopsin.
122 Here, we determined the
high-resolution crystal structure of C. reinhardtii ODA1
123 Here, we describe the solution of the
high-resolution crystal structure of CDP-D-glucose 4,6-d
124 A
high-resolution crystal structure of compound 16 in comp
125 Using the
high-resolution crystal structure of cPLA2-C2 as a start
126 basis of 3' repair activity, we determined a
high-resolution crystal structure of E. coli Nfo-H69A mu
127 Recent emergence of a
high-resolution crystal structure of GLIC captured in a
128 estral variant of GR as a tool to generate a
high-resolution crystal structure of GR in complex with
129 We report the
high-resolution crystal structure of Hje from Sulfolobus
130 We report a
high-resolution crystal structure of HTLV-1 PR complexed
131 We have determined the
high-resolution crystal structure of human ATTP with (2R
132 In the present study, we reveal the first
high-resolution crystal structure of human menin in comp
133 Recently, a
high-resolution crystal structure of human mPGES-1 was p
134 this study, we focus on the recently solved
high-resolution crystal structure of Ig-like repeats 19-
135 the function of occludin, we determined the
high-resolution crystal structure of its C-terminal dist
136 The
high-resolution crystal structure of kexin (Kex2) in com
137 he combination of a dehydratase assay with a
high-resolution crystal structure of MAB_4780 opens the
138 Here we report the
high-resolution crystal structure of Myo7b CMF in comple
139 We have determined the
high-resolution crystal structure of NovP from Streptomy
140 The
high-resolution crystal structure of P. falciparum GK, t
141 The
high-resolution crystal structure of p38alpha has led to
142 We sought to determine the
high-resolution crystal structure of Phl p 4 and to eval
143 The
high-resolution crystal structure of PPAT complexed with
144 have been placed on a firm foundation by the
high-resolution crystal structure of recombinant, wild t
145 Here we report the
high-resolution crystal structure of Smac/DIABLO complex
146 We present the
high-resolution crystal structure of Sso2452, which reve
147 A
high-resolution crystal structure of the 5-bromouridine-
148 The published
high-resolution crystal structure of the ACA from Lactob
149 The recent
high-resolution crystal structure of the beta2-adrenergi
150 Here we determined the
high-resolution crystal structure of the BoNT/A receptor
151 We have solved the
high-resolution crystal structure of the C-terminal MA3
152 Here we report the
high-resolution crystal structure of the carboxy-termina
153 Here, we present the
high-resolution crystal structure of the coiled-coil dom
154 Here, we determined the
high-resolution crystal structure of the complex between
155 The
high-resolution crystal structure of the complex formed
156 n that could be verified a posteriori by the
high-resolution crystal structure of the CREBBP bromodom
157 L (called GNY), binds to H-2K(b), and a very
high-resolution crystal structure of the GNY-K(b) comple
158 ting activity of Bmp2 were obtained from the
high-resolution crystal structure of the halogenase cont
159 A
high-resolution crystal structure of the hit compound in
160 Examination of the
high-resolution crystal structure of the hPOT1-TTAGGGTTA
161 Here we present the 1.8 A
high-resolution crystal structure of the human delta-opi
162 The
high-resolution crystal structure of the mouse RAG2 PHD
163 Here, we present the
high-resolution crystal structure of the N-terminal two
164 d the variant features of p73, we solved the
high-resolution crystal structure of the p73 DBD as well
165 anism of plant SOTs, we determined the first
high-resolution crystal structure of the plant ds-Gl SOT
166 Previously, the
high-resolution crystal structure of the product form of
167 We report here the
high-resolution crystal structure of the ribosomal prote
168 known messenger RNA structures and with the
high-resolution crystal structure of the Saccharomyces c
169 accurate compared with a recently determined
high-resolution crystal structure of the same complex.
170 Here we report the
high-resolution crystal structure of the SWIRM domain fr
171 an initial series of these inhibitors and a
high-resolution crystal structure of the ternary complex
172 Furthermore, the
high-resolution crystal structure of this D-amino acid-c
173 High-resolution crystal structure of TIPE3 shows a large
174 We present here the
high-resolution crystal structure of ToxA in two differe
175 We determined the
high-resolution crystal structure of unbound Brag2 conta
176 Despite the availability of
high-resolution crystal structures of a bacterial homolo
177 We report
high-resolution crystal structures of a four-domain alph
178 By representing the
high-resolution crystal structures of a number of enzyme
179 ystematically analyzed for 68 non-redundant,
high-resolution crystal structures of adenylate-binding
180 We have obtained
high-resolution crystal structures of AKR4C8 (1.4 A) and
181 We present three
high-resolution crystal structures of an octamer RNA dup
182 The comparison of the
high-resolution crystal structures of arrestin2, visual
183 High-resolution crystal structures of CARM1 in complex w
184 High-resolution crystal structures of caspase-3 and casp
185 In a previous work, we presented
high-resolution crystal structures of CheY in complex wi
186 We have determined the
high-resolution crystal structures of chicken villin hea
187 The
high-resolution crystal structures of ColG-CBD (s3b) and
188 Seven new
high-resolution crystal structures of CypD-inhibitor com
189 rk is observed above the hemes in all of the
high-resolution crystal structures of cytochrome oxidase
190 The availability of
high-resolution crystal structures of five prototypical
191 The
high-resolution crystal structures of four different com
192 We have determined for the first time the
high-resolution crystal structures of GluK3 and GluK5 AT
193 Here, we present seven
high-resolution crystal structures of Gmm from the enter
194 We present here two
high-resolution crystal structures of heptamer RNA duple
195 High-resolution crystal structures of HMGS alone and in
196 We present here the first
high-resolution crystal structures of HSA complexed with
197 Here we describe several
high-resolution crystal structures of human LPLA2 and a
198 Here we report
high-resolution crystal structures of human Poleta at fo
199 have an arrangement similar to that seen in
high-resolution crystal structures of IGF-I and insulin,
200 High-resolution crystal structures of isolated actin and
201 Here, we report biochemical studies and
high-resolution crystal structures of KsgA from Thermus
202 We analyze
high-resolution crystal structures of ligand bound (holo
203 High-resolution crystal structures of ligand complexes o
204 Here, we present two
high-resolution crystal structures of LipA from Mycobact
205 High-resolution crystal structures of LoopA and LoopB ha
206 using biochemical experiments combined with
high-resolution crystal structures of LptB pre- and post
207 Here, we describe
high-resolution crystal structures of LTA4H complexed wi
208 tons are not available in current medium and
high-resolution crystal structures of multidrug and toxi
209 the use of disulphide crosslinking to obtain
high-resolution crystal structures of MutY-DNA lesion-re
210 r a south sugar pucker in agreement with the
high-resolution crystal structures of other CDA inhibito
211 pyrazole template and supported by dozens of
high-resolution crystal structures of p38alpha inhibitor
212 High-resolution crystal structures of P450cam bound to r
213 High-resolution crystal structures of parental 3B4 and o
214 ogen-bonding geometries that are observed in
high-resolution crystal structures of protein-DNA and pr
215 M-Score, has been developed based upon 2331
high-resolution crystal structures of protein-ligand com
216 Using atomic B-factors from
high-resolution crystal structures of proteins and prote
217 Here we describe
high-resolution crystal structures of pY53-actin and unp
218 High-resolution crystal structures of reconstructed homo
219 Surprisingly, no
high-resolution crystal structures of s(2)U-containing R
220 Here,
high-resolution crystal structures of Salmonella typhi T
221 e basis of the steady-state spectroscopy and
high-resolution crystal structures of several variants d
222 High-resolution crystal structures of six fragments bind
223 We report
high-resolution crystal structures of six new alpha/beta
224 e overall catalytic mechanism, we report the
high-resolution crystal structures of substrate-loaded A
225 High-resolution crystal structures of TgAMA4 in the apo
226 Our
high-resolution crystal structures of the aldehyde dehyd
227 Here, we report the
high-resolution crystal structures of the Ca(V)beta2a co
228 High-resolution crystal structures of the catalytic doma
229 High-resolution crystal structures of the CCA enzymes re
230 Structural information has been provided by
high-resolution crystal structures of the complex RNase
231 number of fluorine atoms, and we determined
high-resolution crystal structures of the complexes with
232 High-resolution crystal structures of the dark and light
233 on, the base-pair and backbone geometry from
high-resolution crystal structures of the Dickerson-Drew
234 We report the
high-resolution crystal structures of the Did2- and Vps6
235 High-resolution crystal structures of the DNA duplex seq
236 High-resolution crystal structures of the enzyme from mo
237 In this study, we provide
high-resolution crystal structures of the Epa1A domain i
238 To investigate the reaction mechanism, the
high-resolution crystal structures of the Escherichia co
239 Here, we describe the
high-resolution crystal structures of the eubacterial la
240 High-resolution crystal structures of the EvdO1 and EvdO
241 In the present study,
high-resolution crystal structures of the H-NOX protein
242 High-resolution crystal structures of the headpiece of l
243 Here, we report
high-resolution crystal structures of the human cytosoli
244 Here, we report
high-resolution crystal structures of the human JMJD5 ca
245 The previously reported
high-resolution crystal structures of the iminoarginine
246 kinetic data are interpreted in view of the
high-resolution crystal structures of the iminoarginine-
247 e dual role of TlpA was documented best with
high-resolution crystal structures of the kinetically tr
248 Presented here are
high-resolution crystal structures of the m3A DNA glycos
249 Here, we report the very
high-resolution crystal structures of the mutant and wil
250 Here, we report several
high-resolution crystal structures of the nicotinamidase
251 Here, we present the
high-resolution crystal structures of the ORC interactio
252 Here, we present
high-resolution crystal structures of the p53 core domai
253 Using
high-resolution crystal structures of the PcrA-DNA compl
254 Here, we address this question by solving
high-resolution crystal structures of the pivotal Arabid
255 erved to bind cholesterol in several recent,
high-resolution crystal structures of the protein, and i
256 Here, we report
high-resolution crystal structures of the RET1 catalytic
257 Herein, we present two additional
high-resolution crystal structures of the same RNA duple
258 High-resolution crystal structures of the set of P4s all
259 Here, we present
high-resolution crystal structures of the Thermus thermo
260 types and conformations in the rRNAs in the
high-resolution crystal structures of the Thermus thermo
261 We report
high-resolution crystal structures of the wild-type sequ
262 Seven
high-resolution crystal structures of these proteins in
263 High-resolution crystal structures of this GT-1a3a bound
264 We report here five
high-resolution crystal structures of TtgR from the solv
265 Optimization was further guided by
high-resolution crystal structures of two of the macrocy
266 We also report
high-resolution crystal structures of two of these D-pep
267 We have determined the
high-resolution crystal structures of UIC-94017 in compl
268 al base in the reaction has been observed in
high-resolution crystal structures of various reaction s
269 We report two
high-resolution crystal structures of wild-type PR (PRWT
270 ed for many years, the recent discovery of a
high-resolution crystal structure opens up new avenues o
271 Overall, these
high resolution crystal structures provide a framework f
272 The publication of five
high-resolution crystal structures provides a comprehens
273 t attractive fragments were determined using
high resolution crystal structures providing chemical st
274 High-resolution crystal structures reveal that the CASK
275 A combination of solution data and
high-resolution crystal structures revealed that a singl
276 High-resolution crystal structures revealed that the bin
277 High-resolution crystal structures revealed that the mut
278 nd to the Ras effector domain as dimers, and
high-resolution crystal structures revealed that these m
279 Its
high-resolution crystal structure reveals an iron-oxygen
280 A
high-resolution crystal structure reveals the presence o
281 A survey of
high-resolution crystal structures reveals that unconven
282 High-resolution crystal structures show that designed pe
283 Three
high-resolution crystal structures show that DncV and hu
284 Their
high-resolution crystal structures show that the designe
285 A
high-resolution crystal structure shows the homotetramer
286 computationally designed active sites, and a
high-resolution crystal structure suggests that the desi
287 en made in the past few years as a result of
high-resolution crystal structures that capture various
288 Here, we present a series of
high-resolution crystal structures that illustrate key s
289 In light of the
high resolution crystal structures,
the biochemical resu
290 delta virus (HDV) ribozyme, there are three
high-resolution crystal structures,
the product state of
291 We have also determined five
high-resolution crystal structures:
the structures of wi
292 High resolution crystal structures,
thermodynamic bindin
293 e enzyme are presented, and coupled with the
high-resolution crystal structures,
they will serve as a
294 backbone and side-chain conformations in the
high-resolution crystal structures upon which the model
295 coli and biochemically characterized, and a
high-resolution crystal structure was determined.
296 of diffraction quality crystals for which a
high-resolution crystal structure was obtained.
297 idues involved in hydrogen bonds in a set of
high resolution crystal structures were analyzed and thi
298 High resolution crystal structures were determined for t
299 ptors, and structures for intact antibodies,
high-resolution crystal structures were not reported for
300 In this study, a set of 83 ultra-
high resolution crystal structures with experimentally d