1 ned from a polarized XAS model and the 1.9-A
high resolution crystal structure.
2 ta-sheet structure of Fn modules seen in the
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 es observed in a benchmark data set of 2,304
high-resolution crystal structures.
7 l7B is a cellobiohydrolase and obtained four
high-resolution crystal structures.
8 ic desymmetrization mechanism as observed in
high-resolution crystal structures.
9 evidenced by alternate conformations in very
high-resolution crystal structures.
10 resent tools to compare a given structure to
high-resolution crystal structures.
11 itative comparison of the given structure to
high-resolution crystal structures.
12 l, large, and leaving group pockets based on
high-resolution crystal structures.
13 ment to biophysical studies and to obtaining
high-resolution crystal structures.
14 ith the experimental B-factors obtained from
high-resolution crystal structures.
15 ct a complete X-ray diffraction data set for
high-resolution crystal structures.
16 solution differ from its recently determined
high-resolution crystal structures.
17 ity for the determination of lipid-dependent
high-resolution crystal structures.
18 and binding and compare the PELDOR data with
high-resolution crystal structures.
19 High resolution crystal structures (
1.3-1.5 A) of three
20 y, and chemoselectivity of NzeB, we obtained
high-resolution crystal structures (
1.5 angstrom) of the
21 Here, we report three
high-resolution crystal structures (
1.50-1.55 A) of hKAT
22 Two
high-resolution crystal structures (
1.65 and 1.11 A) of
23 High-resolution crystal structure analysis confirmed tha
24 Building on
high-resolution crystal-structure analysis, pore vestibu
25 A
high resolution crystal structure and solution NMR struc
26 Here we present 10
high resolution crystal structures and enzyme kinetic an
27 nomeric transmembrane beta-barrel of a known
high-resolution crystal structure and displays three dis
28 Here, we describe the
high-resolution crystal structure and solution NMR struc
29 High-resolution crystal structures and biophysical analy
30 relevant glycans in this epitope by fitting
high-resolution crystal structures and by performing neu
31 We present
high-resolution crystal structures and functional analys
32 Together, the new SAM analog and the
high-resolution crystal structure are a step towards the
33 Data from NMR mapping and
high-resolution crystal structures are congruent with th
34 meters, particularly in cases where reliable
high-resolution crystal structures are not available.
35 In contrast,
high-resolution crystal structures are only available fo
36 Here, we present a
high-resolution crystal structure at 2.1 A of the biotin
37 We report here the
high-resolution crystal structures,
at 1.9 and 2.35 A, r
38 e and protein/drug-bound) was 'mapped' using
high resolution crystal structures cataloged in the Nucl
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 Here, we report a
high-resolution crystal structure for the Serratia sp. A
47 an apparent disagreement between two sets of
high-resolution crystal structures for MbCO and deoxyMb.
48 We describe here
high-resolution crystal structures for the GluR5 ligand-
49 ailability of extensive mutagenesis data and
high-resolution crystal structures for the TEM-1/BLIP an
50 sis by 2 orders of magnitude, we have solved
high-resolution crystal structures for the W354F YopH in
51 l basis of this potency, we determined eight
high-resolution crystal structures:
four each of the wil
52 Analysis of aligned RNA sequences and
high-resolution crystal structures has revealed a new RN
53 Recent analysis of
high-resolution crystal structures has suggested a new m
54 High resolution crystal structures have provided snapsho
55 ligand-gated ion channels for which multiple
high-resolution crystal structures have been solved.
56 High-resolution crystal structures have highlighted func
57 Recent biochemical reconstitution and
high-resolution crystal structures have provided proof t
58 Recent
high-resolution crystal structures have revealed that rh
59 ed rhomboids and, most recently, a flurry of
high-resolution crystal structures,
have led to real ins
60 ubjected to crystal structure analysis and a
high resolution crystal structure in complex with PTR1 w
61 For this compound, a
high-resolution crystal structure in complex with E. col
62 Herein, we present five
high-resolution crystal structures including one first-t
63 /U wobble basepairs in the ribosome based on
high-resolution crystal structures,
including the recent
64 A
high-resolution crystal structure is reported for d(TpA)
65 Four
high resolution crystal structures,
namely complexes wit
66 High-resolution crystal structures obtained in two confo
67 We report the
high resolution crystal structure of a competent fragmen
68 In a
high resolution crystal structure of fascin, molecules o
69 activities of the two enzymes, we report the
high resolution crystal structure of human NPP4 and expl
70 Here we report a
high resolution crystal structure of MC159, a v-FLIP der
71 Here we present the
high resolution crystal structure of murine SMPDL3B, whi
72 This
high resolution crystal structure of NKX2.5 protein prov
73 The
high resolution crystal structure of PTHrP bound to the
74 In light of the
high resolution crystal structure of the DAF four-CCP fu
75 We present the first
high resolution crystal structure of the kinase domain o
76 he dual role of HR23, we have determined the
high resolution crystal structure of the mouse peptide N
77 chanism of these enzymes, we report here the
high resolution crystal structure of wild-type murine ca
78 The
high resolution crystal structures of a recombinant frag
79 High resolution crystal structures of apoGilR and GilR i
80 Four
high resolution crystal structures of B. cereus PPM reve
81 High resolution crystal structures of complexes with dif
82 cificity and selectivity, we have determined
high resolution crystal structures of each of the two CB
83 We also determined
high resolution crystal structures of HRAS-like tumor su
84 Here we present
high resolution crystal structures of human AChE, alone
85 To investigate this question, we solved
high resolution crystal structures of human SUN2 in comp
86 The
high resolution crystal structures of isatin hydrolase f
87 esolution images from electron microscopy or
high resolution crystal structures of isolated component
88 Here, we present
high resolution crystal structures of murine and yeast C
89 The
high resolution crystal structures of N-domain ACE in co
90 This study reports the first
high resolution crystal structures of periplasmic glucos
91 Here we report the
high resolution crystal structures of PitB and SrtG1 and
92 Only minimal differences are observed in
high resolution crystal structures of PR(D25N) complexed
93 High resolution crystal structures of PR20-inhibitor com
94 High resolution crystal structures of seven selected SL9
95 We also solved the
high resolution crystal structures of SlAMADH1 and ZmAMA
96 In this study, we present a series of
high resolution crystal structures of Spa47 and use the
97 We have presented here the
high resolution crystal structures of the beta-lactamase
98 High resolution crystal structures of the E120H mutant i
99 Here, we report
high resolution crystal structures of the RsrR dimer, re
100 kallikrein, along with the purification and
high resolution crystal structures of the two recombinan
101 Here we present the
high resolution crystal structures of Tom71 and the prot
102 We report
high resolution crystal structures of yCT-H9 complexed w
103 difference between the derived model and the
high-resolution crystal structure of a 54% homologous ga
104 Here we provide a
high-resolution crystal structure of a full-length T-box
105 In this study, we first solved the
high-resolution crystal structure of a Hat1p/Hat2p/CoA/H
106 We have determined the
high-resolution crystal structure of a human-type ACA fr
107 Herein we report a
high-resolution crystal structure of a Lys73-ligated cyt
108 The
high-resolution crystal structure of a PNK-FHA-XRCC1 pho
109 The
high-resolution crystal structure of a ternary complex o
110 We solved the
high-resolution crystal structure of ACDH-11 and establi
111 Here we report the first
high-resolution crystal structure of ACMSD from Pseudomo
112 The
high-resolution crystal structure of all-trans-retinal b
113 dditionally, we provide for the first time a
high-resolution crystal structure of an active exoribonu
114 We report the first, to our knowledge,
high-resolution crystal structure of an antiviral compou
115 ere, we present, to our knowledge, the first
high-resolution crystal structure of an erythrocyte-bind
116 Considering the
high-resolution crystal structure of bacteriorhodopsin,
117 cedure by comparing its predictions with the
high-resolution crystal structure of bovine rhodopsin.
118 Here, we determined the
high-resolution crystal structure of C. reinhardtii ODA1
119 Here, we describe the solution of the
high-resolution crystal structure of CDP-D-glucose 4,6-d
120 A
high-resolution crystal structure of compound 16 in comp
121 Using the
high-resolution crystal structure of cPLA2-C2 as a start
122 basis of 3' repair activity, we determined a
high-resolution crystal structure of E. coli Nfo-H69A mu
123 Although the
high-resolution crystal structure of FluPol(A) of bat in
124 Recent emergence of a
high-resolution crystal structure of GLIC captured in a
125 estral variant of GR as a tool to generate a
high-resolution crystal structure of GR in complex with
126 We report the
high-resolution crystal structure of Hje from Sulfolobus
127 We report a
high-resolution crystal structure of HTLV-1 PR complexed
128 In the present study, we reveal the first
high-resolution crystal structure of human menin in comp
129 Recently, a
high-resolution crystal structure of human mPGES-1 was p
130 this study, we focus on the recently solved
high-resolution crystal structure of Ig-like repeats 19-
131 the function of occludin, we determined the
high-resolution crystal structure of its C-terminal dist
132 The
high-resolution crystal structure of kexin (Kex2) in com
133 he combination of a dehydratase assay with a
high-resolution crystal structure of MAB_4780 opens the
134 Here we report the
high-resolution crystal structure of Myo7b CMF in comple
135 We have determined the
high-resolution crystal structure of NovP from Streptomy
136 The
high-resolution crystal structure of P. falciparum GK, t
137 The
high-resolution crystal structure of p38alpha has led to
138 We sought to determine the
high-resolution crystal structure of Phl p 4 and to eval
139 We present the
high-resolution crystal structure of Sso2452, which reve
140 A
high-resolution crystal structure of the 5-bromouridine-
141 The published
high-resolution crystal structure of the ACA from Lactob
142 The recent
high-resolution crystal structure of the beta2-adrenergi
143 Here we determined the
high-resolution crystal structure of the BoNT/A receptor
144 We have solved the
high-resolution crystal structure of the C-terminal MA3
145 Here we report the
high-resolution crystal structure of the carboxy-termina
146 Here, we present the
high-resolution crystal structure of the coiled-coil dom
147 Here, we determined the
high-resolution crystal structure of the complex between
148 The
high-resolution crystal structure of the complex formed
149 n that could be verified a posteriori by the
high-resolution crystal structure of the CREBBP bromodom
150 L (called GNY), binds to H-2K(b), and a very
high-resolution crystal structure of the GNY-K(b) comple
151 ting activity of Bmp2 were obtained from the
high-resolution crystal structure of the halogenase cont
152 A
high-resolution crystal structure of the hit compound in
153 Examination of the
high-resolution crystal structure of the hPOT1-TTAGGGTTA
154 Here we present the 1.8 A
high-resolution crystal structure of the human delta-opi
155 The
high-resolution crystal structure of the mouse RAG2 PHD
156 Here, we present the
high-resolution crystal structure of the N-terminal two
157 d the variant features of p73, we solved the
high-resolution crystal structure of the p73 DBD as well
158 anism of plant SOTs, we determined the first
high-resolution crystal structure of the plant ds-Gl SOT
159 known messenger RNA structures and with the
high-resolution crystal structure of the Saccharomyces c
160 accurate compared with a recently determined
high-resolution crystal structure of the same complex.
161 Here we report the
high-resolution crystal structure of the SWIRM domain fr
162 an initial series of these inhibitors and a
high-resolution crystal structure of the ternary complex
163 Furthermore, the
high-resolution crystal structure of this D-amino acid-c
164 High-resolution crystal structure of TIPE3 shows a large
165 We present here the
high-resolution crystal structure of ToxA in two differe
166 We determined the
high-resolution crystal structure of unbound Brag2 conta
167 High-resolution crystal structures of (Pl)EctA (at 1.2-2
168 Despite the availability of
high-resolution crystal structures of a bacterial homolo
169 We report
high-resolution crystal structures of a four-domain alph
170 By representing the
high-resolution crystal structures of a number of enzyme
171 ystematically analyzed for 68 non-redundant,
high-resolution crystal structures of adenylate-binding
172 We have obtained
high-resolution crystal structures of AKR4C8 (1.4 A) and
173 We present three
high-resolution crystal structures of an octamer RNA dup
174 The comparison of the
high-resolution crystal structures of arrestin2, visual
175 We determined the
high-resolution crystal structures of both enzymes, deri
176 High-resolution crystal structures of CARM1 in complex w
177 High-resolution crystal structures of caspase-3 and casp
178 We further present
high-resolution crystal structures of CD0873, at 1.35-2.
179 In a previous work, we presented
high-resolution crystal structures of CheY in complex wi
180 We have determined the
high-resolution crystal structures of chicken villin hea
181 The
high-resolution crystal structures of ColG-CBD (s3b) and
182 Biochemical experiments and
high-resolution crystal structures of covalent and nonco
183 Seven new
high-resolution crystal structures of CypD-inhibitor com
184 rk is observed above the hemes in all of the
high-resolution crystal structures of cytochrome oxidase
185 High-resolution crystal structures of ESOC acyl-enzyme c
186 The availability of
high-resolution crystal structures of five prototypical
187 We have determined for the first time the
high-resolution crystal structures of GluK3 and GluK5 AT
188 Here, we present seven
high-resolution crystal structures of Gmm from the enter
189 We present here two
high-resolution crystal structures of heptamer RNA duple
190 High-resolution crystal structures of HMGS alone and in
191 Here we describe several
high-resolution crystal structures of human LPLA2 and a
192 Here we report
high-resolution crystal structures of human Poleta at fo
193 Furthermore, we present
high-resolution crystal structures of human Poleta with
194 have determined the first three-dimensional
high-resolution crystal structures of human SQLE catalyt
195 High-resolution crystal structures of inactive MCR lacki
196 High-resolution crystal structures of isolated actin and
197 Here, we report biochemical studies and
high-resolution crystal structures of KsgA from Thermus
198 We analyze
high-resolution crystal structures of ligand bound (holo
199 High-resolution crystal structures of ligand complexes o
200 Here, we present two
high-resolution crystal structures of LipA from Mycobact
201 Four
high-resolution crystal structures of Loktanella ALDH16
202 High-resolution crystal structures of LoopA and LoopB ha
203 using biochemical experiments combined with
high-resolution crystal structures of LptB pre- and post
204 Here, we describe
high-resolution crystal structures of LTA4H complexed wi
205 tons are not available in current medium and
high-resolution crystal structures of multidrug and toxi
206 the use of disulphide crosslinking to obtain
high-resolution crystal structures of MutY-DNA lesion-re
207 r a south sugar pucker in agreement with the
high-resolution crystal structures of other CDA inhibito
208 pyrazole template and supported by dozens of
high-resolution crystal structures of p38alpha inhibitor
209 High-resolution crystal structures of parental 3B4 and o
210 ogen-bonding geometries that are observed in
high-resolution crystal structures of protein-DNA and pr
211 M-Score, has been developed based upon 2331
high-resolution crystal structures of protein-ligand com
212 Using atomic B-factors from
high-resolution crystal structures of proteins and prote
213 Here we describe
high-resolution crystal structures of pY53-actin and unp
214 High-resolution crystal structures of reconstructed homo
215 Surprisingly, no
high-resolution crystal structures of s(2)U-containing R
216 Here,
high-resolution crystal structures of Salmonella typhi T
217 The structure, along with additional
high-resolution crystal structures of several analogs in
218 e basis of the steady-state spectroscopy and
high-resolution crystal structures of several variants d
219 High-resolution crystal structures of six fragments bind
220 We report
high-resolution crystal structures of six new alpha/beta
221 e overall catalytic mechanism, we report the
high-resolution crystal structures of substrate-loaded A
222 High-resolution crystal structures of TgAMA4 in the apo
223 Our
high-resolution crystal structures of the aldehyde dehyd
224 ted glycans and glycoproteins, we determined
high-resolution crystal structures of the binding domain
225 Here, we report the
high-resolution crystal structures of the Ca(V)beta2a co
226 High-resolution crystal structures of the catalytic doma
227 High-resolution crystal structures of the CCA enzymes re
228 Structural information has been provided by
high-resolution crystal structures of the complex RNase
229 number of fluorine atoms, and we determined
high-resolution crystal structures of the complexes with
230 High-resolution crystal structures of the dark and light
231 We report the
high-resolution crystal structures of the Did2- and Vps6
232 High-resolution crystal structures of the DNA duplex seq
233 High-resolution crystal structures of the enzyme from mo
234 In this study, we provide
high-resolution crystal structures of the Epa1A domain i
235 Here, we describe the
high-resolution crystal structures of the eubacterial la
236 High-resolution crystal structures of the EvdO1 and EvdO
237 We determined the
high-resolution crystal structures of the GAO(V), Cl(2)-
238 In the present study,
high-resolution crystal structures of the H-NOX protein
239 High-resolution crystal structures of the headpiece of l
240 Here, we report
high-resolution crystal structures of the human cytosoli
241 Here, we report
high-resolution crystal structures of the human JMJD5 ca
242 Here we report
high-resolution crystal structures of the human NK(1) re
243 The previously reported
high-resolution crystal structures of the iminoarginine
244 kinetic data are interpreted in view of the
high-resolution crystal structures of the iminoarginine-
245 e dual role of TlpA was documented best with
high-resolution crystal structures of the kinetically tr
246 Here, we report several
high-resolution crystal structures of the nicotinamidase
247 We report herein
high-resolution crystal structures of the nocardicin thi
248 Here, we present the
high-resolution crystal structures of the ORC interactio
249 Here, we present
high-resolution crystal structures of the p53 core domai
250 Using
high-resolution crystal structures of the PcrA-DNA compl
251 Here, we address this question by solving
high-resolution crystal structures of the pivotal Arabid
252 erved to bind cholesterol in several recent,
high-resolution crystal structures of the protein, and i
253 Here, we report
high-resolution crystal structures of the RET1 catalytic
254 Herein, we present two additional
high-resolution crystal structures of the same RNA duple
255 High-resolution crystal structures of the set of P4s all
256 Here, we present
high-resolution crystal structures of the Thermus thermo
257 types and conformations in the rRNAs in the
high-resolution crystal structures of the Thermus thermo
258 We present several
high-resolution crystal structures of the UDP-glucuronic
259 We report
high-resolution crystal structures of the wild-type sequ
260 Seven
high-resolution crystal structures of these proteins in
261 High-resolution crystal structures of this GT-1a3a bound
262 Furthermore, we solved
high-resolution crystal structures of three macrocyclic
263 ructure-based drug design, we determined the
high-resolution crystal structures of three MetX protein
264 ainst a large variety of MCPs, combined with
high-resolution crystal structures of three selected can
265 We report here five
high-resolution crystal structures of TtgR from the solv
266 Optimization was further guided by
high-resolution crystal structures of two of the macrocy
267 We also report
high-resolution crystal structures of two of these D-pep
268 We have determined the
high-resolution crystal structures of UIC-94017 in compl
269 al base in the reaction has been observed in
high-resolution crystal structures of various reaction s
270 We report two
high-resolution crystal structures of wild-type PR (PRWT
271 High-resolution crystal structures of Zn(2+)-bound ERp44
272 ed for many years, the recent discovery of a
high-resolution crystal structure opens up new avenues o
273 Overall, these
high resolution crystal structures provide a framework f
274 The publication of five
high-resolution crystal structures provides a comprehens
275 t attractive fragments were determined using
high resolution crystal structures providing chemical st
276 High-resolution crystal structures reveal that the CASK
277 A combination of solution data and
high-resolution crystal structures revealed that a singl
278 High-resolution crystal structures revealed that the mut
279 nd to the Ras effector domain as dimers, and
high-resolution crystal structures revealed that these m
280 Its
high-resolution crystal structure reveals an iron-oxygen
281 A
high-resolution crystal structure reveals the presence o
282 A survey of
high-resolution crystal structures reveals that unconven
283 High-resolution crystal structures show that designed pe
284 Three
high-resolution crystal structures show that DncV and hu
285 Their
high-resolution crystal structures show that the designe
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 backbone and side-chain conformations in the
high-resolution crystal structures upon which the model
294 coli and biochemically characterized, and a
high-resolution crystal structure was determined.
295 of diffraction quality crystals for which a
high-resolution crystal structure was obtained.
296 idues involved in hydrogen bonds in a set of
high resolution crystal structures were analyzed and thi
297 High resolution crystal structures were determined for t
298 ptors, and structures for intact antibodies,
high-resolution crystal structures were not reported for
299 and channels are reviewed, emphasizing those
high-resolution crystal structures,
which reveal water m
300 In this study, a set of 83 ultra-
high resolution crystal structures with experimentally d