1 ation of O as necessary stabilization of the
crystal structure.
2 nly to the NC host material, but also to its
crystal structure.
3 N-connected ligands was characterized by its
crystal structure.
4 r with no permanent voids or channels in its
crystal structure.
5 d is partly occluded by the bound Fab in the
crystal structure.
6 this stabilization with an atomic resolution
crystal structure.
7 nodes are a consequence of the orthorhombic
crystal structure.
8 deprotonated closely resembles the available
crystal structure.
9 Dirac cone for the ideal, perfectly ordered
crystal structure.
10 easured distances were compared to available
crystal structures.
11 s, and so enables the determination of their
crystal structures.
12 parison with NLPB calculations for available
crystal structures.
13 o enables assignment of tautomeric states in
crystal structures.
14 software (e.g. SQUEEZE) to obtain acceptable
crystal structures.
15 espectively, possibly due to their different
crystal structures.
16 ermophilum RIOK-2 protein kinase (Ct-RIOK-2)
crystal structure 4GYG as a template.
17 sized perovskite NPLs exhibit a single cubic
crystal structure,
a 1.6-fold enhanced photoluminescence
18 Theory, which can predict the change of the
crystal structure across the MIT at finite temperature.
19 etic and orbital degrees of freedom with the
crystal structure across the MIT in rare-earth nickelate
20 X-ray
crystal structures also revealed "pre-bound" molecular o
21 The comparison of the two ternary
crystal structures,
AmbP3-DMSPP/hapalindole U and AmbP3-
22 While its biological role remains unclear,
crystal structure analyses and biochemical approaches ha
23 X-ray
crystal structure analysis of both Rh complexes formed f
24 Co-
crystal structure analysis revealed a dual active site-d
25 Crystal structure analysis revealed that FePYR1 recogniz
26 e ORAI1 gene, modeling of mutations on ORAI1
crystal structure,
analysis of ORAI1 mRNA and protein ex
27 razing incident X-ray diffraction to observe
crystal structure and chemical transition of perovskites
28 A recent
crystal structure and in vitro experiments highlighted p
29 range of applications owing to their unique
crystal structure and optoelectronic properties.
30 used to demonstrate correlation between the
crystal structure and supramolecular nanostructures.
31 Both the high-temperature average
crystal structure and the low-temperature incommensurate
32 Crystal structures and accompanying solution data confir
33 d design studies based on chemokine receptor
crystal structures and homology models illustrates the p
34 The
crystal structures and mass spectrometry also show that
35 However, their range of stability,
crystal structures and the thermodynamic conditions of t
36 Crystal structures and TPS dynamics of native and F159Y
37 ed in either cubic or hexagonal (metastable)
crystal structures and used as the host material in cati
38 solving the high-resolution channelrhodopsin
crystal structure,
and by structural model-guided redesi
39 heory computed electronic structures, single
crystal structures,
and experimental lattice cohesion me
40 ssess different melting points, NMR spectra,
crystal structures,
and stacking patterns in the solid s
41 , the new SAM analog and the high-resolution
crystal structure are a step towards the development of
42 The majority of macromolecular
crystal structures are determined using the method of mo
43 piens and Chaetomium thermophilum, for which
crystal structures are known.
44 res is 8.2 K, a twofold increase in the same
crystal structure as in compression.
45 m(5)rC into the SRL motif resulted in an RNA
crystal structure at 0.85 A resolution.
46 The
crystal structure at 1.9 A resolution deciphered that S1
47 The
crystal structure at 2.19 A resolution shows a large dis
48 Here we report
crystal structures at up to 2.6 A resolution of the yeas
49 ypeptides has remained challenging, with few
crystal structures available to show their overall struc
50 ent accessibility-related parameters both by
crystal structure-
based calculations of solvent-accessib
51 The morphology,
crystal structures,
chemical, and optical properties of
52 terin synthase association pathways and near-
crystal structure complexes from protein-protein associa
53 Surface morphology with elemental mapping,
crystal structure,
composition and oxidation states, and
54 Its
crystal structure consists of planar ribbon-like molecul
55 egulatory mechanisms in SHIP2, we determined
crystal structures containing the 5-phosphatase and a pr
56 property, kinetic analysis was coupled with
crystal structure determination of these WoA variants.
57 onal accuracy associated with each atom in a
crystal structure determined by NMR crystallography.
58 Its
crystal structure,
determined as a novel zinc-free hexam
59 cs (CVSMD) simulations starting with the two
crystal structures embedded in model lipid bilayers, and
60 tionships among composition, morphology, and
crystal structure for copper sulfide-based nanocrystals,
61 Additionally, we solved a
crystal structure for the apo form of AgmNAT with an ato
62 Crystal structures for the B-subunits of Polalpha and Po
63 e low-temperature incommensurately modulated
crystal structure (
for Sm2Ru3Ge5 as a representative) ha
64 lculations of structures consistent with the
crystal structure gave calculated values of J incompatib
65 Docking studies using available
crystal structures have been used for structure-based op
66 X-ray
crystal structures have played an important role in the
67 Crystal structures have shown a mono- or dinuclear Cu si
68 lysis confirmed several features seen in the
crystal structure,
including the importance of a hydroge
69 A
crystal structure is reported for 3.DQ(PF6)2.
70 Analysis of the co-
crystal structure led to the identification of a contami
71 Crystal structures,
MANT-GTPgammaS binding, thermal dena
72 for bioenergy production, were deduced from
crystal structures,
molecular docking, site-directed mut
73 , providing a functional significance to the
crystal structure NS5 dimer.
74 s described and rationalized using the X-ray
crystal structure of 6 bound to human IDO-1, which shows
75 Here we present the
crystal structure of a CD23/IgE-Fc complex and conduct i
76 250-550, we report here the 2.3A resolution
crystal structure of a complex containing Sac3 residues
77 Here we present the
crystal structure of a complex of a cytidine deaminase w
78 Here, we determined the
crystal structure of a complex of the HAstV capsid prote
79 A
crystal structure of a Complexin-I fragment bearing a so
80 ...H-C interaction was observed in the X-ray
crystal structure of a fluorinated triterpenoid.
81 This first
crystal structure of a monocot CAD combined with enzyme
82 We determined a 2.76 A-resolution
crystal structure of a mycobacterial transcription initi
83 The
crystal structure of a PH-START complex revealed that th
84 Our recent
crystal structure of a pre-catalytic state of this RNA s
85 Here, we present the
crystal structure of a prokaryotic TMEM175 channel from
86 Here, the authors present the
crystal structure of a Pseudomonas MDC and give insights
87 We report a 3.4-A resolution X-ray
crystal structure of a sigma(N) fragment in complex with
88 We present a high resolution (1.95 A) co-
crystal structure of a small molecule bound to the catal
89 A
crystal structure of an AcrIIC1-Cas9 HNH domain complex
90 Here, we determined the
crystal structure of an amino-terminally truncated EHD4
91 Here, we determined the
crystal structure of an apo-PRC2 from the fungus Chaetom
92 Here, we have solved the X-ray
crystal structure of an EBNA1 DNA-binding domain (DBD) a
93 Here, we present the
crystal structure of an N-terminal fragment of Saccharom
94 Here we present the
crystal structure of an NST, the GDP-mannose transporter
95 We recently published the
crystal structure of an unusual (S)P species [(MeAN)2Cu(
96 cteristics are discussed in the light of the
crystal structure of AnCDA, providing insight into how t
97 The
crystal structure of Bacillus subtilis NrnA reveals a dy
98 We determined a
crystal structure of CaM bound to a peptide encompassing
99 An X-ray
crystal structure of caspase-7 bound to a fragment hit a
100 Furthermore, we determined the
crystal structure of ciA-C2 in complex with the receptor
101 A
crystal structure of CYP2C9 in complex with a TCA1 analo
102 nt increment of glycogen content in vivo The
crystal structure of EcAGPase-R130A revealed unprecedent
103 The NhaA
crystal structure of Escherichia coli has become the par
104 Here, we report the 2.6-A
crystal structure of Escherichia coli Lnt.
105 We illustrate how the
crystal structure of Fe14 Pd17 Al69 provides an example
106 part in Streptomyces griseus We obtained the
crystal structure of FNO in complex with NADP(+) at 1.8
107 The
crystal structure of GLIC shows R-ketamine bound to an e
108 Here we describe the
crystal structure of GS-5745.MMP9 complex and biochemica
109 A
crystal structure of HA with bound Fab6649 shows the con
110 Here, we report the
crystal structure of hRSV NS1 protein, which suggests th
111 We determined a
crystal structure of human IL-23 in complex with its cog
112 We determine the
crystal structure of human TRIP13, and identify function
113 Here, we report the
crystal structure of human XPNPEP3 with bound apstatin p
114 We have determined the
crystal structure of inactive mutant (D88N) of RecU from
115 Here we report the
crystal structure of kinesin-6 Zen4 in a nucleotide-free
116 We investigated the small molecule
crystal structure of lead molecule 7 and hypothesized th
117 insight and experimental explorations of the
crystal structure of lead-free perovskite, thin film dep
118 A third
crystal structure of LmFBPase complexed with its alloste
119 The
crystal structure of M. burtonii Rubisco (MbR) presented
120 using sulfur-SAD phasing, we determined the
crystal structure of m4-1BB to 2.2-A resolution.
121 Here, we present the
crystal structure of MacB at 3.4-A resolution.
122 Here we report the 2.7-A X-ray
crystal structure of MazF-mt6.
123 Here we report the
crystal structure of MyRF DBD.
124 The
crystal structure of NCS-1 bound to FD44 and the structu
125 Here, we report the first
crystal structure of ObgE at 1.85-A resolution in the GD
126 ghts into its mode of action and present the
crystal structure of OM bound to bovine cardiac myosin,
127 Here, we report the
crystal structure of one of the allergens from Blo t, re
128 tallization properties, we obtained a 2.24-A
crystal structure of pig-tailed macaque APOBEC3H with bo
129 Here, we describe the
crystal structure of PRL-1 in complex with the Bateman m
130 ed the first and high resolution (at 1.25 A)
crystal structure of proMPO and its solution structure o
131 A co-
crystal structure of PvPKG bound to ML10, reveals intima
132 The
crystal structure of the [CYP121(cYY)CN] ternary complex
133 We present here the X-ray
crystal structure of the ADAM10 ectodomain, which, toget
134 A recently published
crystal structure of the AT1R was used to guide site-dir
135 Here we present the
crystal structure of the C-terminal portion of human POT
136 We determined the
crystal structure of the capsid protein spike domain fro
137 The X-ray
crystal structure of the catalytic domain was determined
138 Here, we present the
crystal structure of the CBP catalytic core encompassing
139 Here, we present the
crystal structure of the CdiA-CT/CdiIYkris complex from
140 We further reveal that the
crystal structure of the CdSe shell (cubic zinc-blende o
141 on cross-linking-coupled mass spectrometry,
crystal structure of the CPSF160-WDR33 subcomplex and bi
142 Solving the
crystal structure of the DEKK Fc region at a resolution
143 The
crystal structure of the EBD dimer was solved to 2.2 A r
144 Here, we report the
crystal structure of the fission yeast Tpz1(475-508)-Poz
145 Here we present the
crystal structure of the functionally essential ICP4 DNA
146 uranyl(VI) ions as elucidated by the single-
crystal structure of the gamma-ray irradiated material,
147 Here, we report the 2.25 A resolution
crystal structure of the GAPDH1 holoenzyme in a quaterna
148 Here, we describe the
crystal structure of the Gn glycoprotein ectodomain from
149 was screened in silico against the available
crystal structure of the GtfC catalytic domain.
150 To this end, we determined the X-ray
crystal structure of the HLA-DQ2.5.
151 We report the
crystal structure of the human Chk1 KA1 domain, demonstr
152 By solving the
crystal structure of the IL-1alpha/aptamer, we provide a
153 We have determined the
crystal structure of the interacting domains of Saccharo
154 Here, we report the
crystal structure of the IntS9-IntS11 CTD complex at 2.1
155 linking data were compared directly with the
crystal structure of the isolated N-terminal extracellul
156 Here we report the 2.2 A
crystal structure of the kinase domain of Trl1 from the
157 The
crystal structure of the leptospiral PerR revealed an as
158 We present the first
crystal structure of the LRH-1-PGC1alpha complex, which
159 We solve the
crystal structure of the LZ:CM2 complex, revealing that
160 The
crystal structure of the metal-ion dependent esterase MG
161 A
crystal structure of the mitochondrial Hsp90, TRAP1, rev
162 Here, we report the
crystal structure of the MOB1/NDR2 complex and define ke
163 Here, we present the
crystal structure of the Mtb DnaE1 polymerase.
164 On the basis of the active state
crystal structure of the muscarinic M2 receptor in compl
165 The
crystal structure of the N-terminal domain of pyoS2 (pyo
166 Here, we determined the
crystal structure of the N-terminal half of a conserved
167 Here we report the
crystal structure of the N-terminal IMS domain of Toc75
168 A
crystal structure of the p107 CTD bound to E2F5 and its
169 ed at the interface between protomers in the
crystal structure of the PCNA-K20ac ring.
170 In this study, we determined the X-ray
crystal structure of the PEAK1 pseudokinase domain to 2.
171 OTs, we determined the first high-resolution
crystal structure of the plant ds-Gl SOT AtSOT18 in comp
172 We have determined the
crystal structure of the PPARgamma ligand-binding domain
173 crystals to elastically deform, the inherent
crystal structure of the principal molecular component o
174 A co-
crystal structure of the rabbit family 4 enzyme CYP4B1 w
175 Here the authors present the
crystal structure of the retinoic acid receptor beta-ret
176 Here, we present the
crystal structure of the SNX5-PX:IncE complex, showing I
177 alt PbSe nanocrystals, we show here that the
crystal structure of the starting nanocrystals has a str
178 e panel and allowed us to obtain an X-ray co-
crystal structure of the synthetic secondary metabolite
179 We present a comprehensive study of the
crystal structure of the thin-film, ferromagnetic topolo
180 The
crystal structure of the TRF2-NBS1 complex at 3.0 A reso
181 Here we present the
crystal structure of the trimeric, prefusion ectodomain
182 The
crystal structure of this ANbP in complex with human HGP
183 The
crystal structure of this inactivated assembly provides
184 The
crystal structure of trans-[Pd(IPr)2(OOH)(OH)] is report
185 A
crystal structure of two PA50 Fabs bound to a segment of
186 We solved the
crystal structure of UbV.7.2 and rationalized the molecu
187 In addition, we determined the
crystal structure of yeast ChaC2 homologue, GCG1, at 1.3
188 The 2.85 A-resolution
crystal structure of zebrafish HDAC10 complexed with a t
189 The
crystal structures of 1 and 3a reveal stair-step infinit
190 ogeneous backbones, we recently reported two
crystal structures of a decamer RNA duplex containing tw
191 X-ray co-
crystal structures of AACs further allowed for a detaile
192 Crystal structures of affimers bound to their cognate ch
193 Crystal structures of alphaIIbbeta3 and alphaVbeta3 have
194 We determined
crystal structures of an anaerobically prepared fragment
195 The
crystal structures of apo PllA and complexes with three
196 We determined
crystal structures of Arbidol in complex with influenza
197 Crystal structures of AspRedAm in complex with NADP(H) a
198 Here, we report
crystal structures of B. multivorans HpnN, revealing a d
199 By solving the
crystal structures of Btk inhibitors bound to the enzyme
200 High-resolution
crystal structures of CARM1 in complex with these compou
201 In this paper, we describe the
crystal structures of CCT5 and the CCT5-H147R mutant, wh
202 The approach is demonstrated on the
crystal structures of cocaine, flutamide, flufenamic aci
203 The
crystal structures of CusB, CusC, CusF, and the CusBA co
204 Previous
crystal structures of cytochrome P450cam complexed with
205 Here we present
crystal structures of engineered human MFN1 containing t
206 Crystal structures of enzymes are indispensable to under
207 This questions whether the available x-ray
crystal structures of EPOR truly represent active or ina
208 X-ray
crystal structures of example compounds from this series
209 om Arabidopsis thaliana We observed that the
crystal structures of free, Mg(2+)-bound, and berylloflu
210 Here, we report the
crystal structures of full length Escherichia coli RapZ
211 Presented are 2.1-A-resolution
crystal structures of GusRs from Escherichia coli and Sa
212 n and propagation of dislocations within the
crystal structures of HOIPs and IP.
213 in other studies, the pre-catalytic ternary
crystal structures of hPolbeta, DNA and L-dCTP or the tr
214 vity between these receptors, here we report
crystal structures of human AT2R bound to an AT2R-select
215 Two
crystal structures of Japanin, an 18 kDa immune-modulato
216 CYP126A1 dimers were observed in
crystal structures of ligand-free CYP126A1 and for CYP12
217 ed with PG-binding assays and fitting of the
crystal structures of MotB fragments to the small angle
218 hibit Mtb RNAP and Mtb growth, and we report
crystal structures of Mtb RNAP in complex with AAPs.
219 Previous X-ray
crystal structures of Nef in complex with key host cell
220 Crystal structures of P- and E-selectin suggest a two-st
221 Finally, we present the co-
crystal structures of PCNA with two specific motifs in Z
222 Furthermore, using
crystal structures of PDZ1 and PDZ3 bound to beta-PIX, w
223 We report six
crystal structures of Pfs25 in complex with antibodies e
224 Here, we report the
crystal structures of PopP2, a YopJ effector produced by
225 X-ray
crystal structures of prototypical RRNPP members have pr
226 High-resolution
crystal structures of reconstructed homodimeric receptor
227 Here we present the
crystal structures of S. hematobium and S. japonicum SUL
228 Here we report the
crystal structures of SETD2 SET domain in complex with a
229 Here, we report
crystal structures of tandem-SH3 domains of different ST
230 Our high-resolution
crystal structures of the aldehyde dehydrogenase lead to
231 Here, we present
crystal structures of the apo enzyme and a binary Ago-gu
232 Crystal structures of the BAF component BAF45C indicate
233 We describe the atomic
crystal structures of the catalytic flavin adenine dinuc
234 We have determined
crystal structures of the Cdk2-Spy1 and p27-Cdk2-Spy1 co
235 ction, and ligand recognition, we determined
crystal structures of the D4 dopamine receptor in its in
236 Here, we report
crystal structures of the founding members of the ATP-de
237 Co-
crystal structures of the highest affinity binder reveal
238 We present
crystal structures of the human LARP1 DM15 region in com
239 Here we present
crystal structures of the inward-facing, intermediate, a
240 Here, we determined the
crystal structures of the isolated dimeric globin domain
241 Crystal structures of the large terminase nuclease from
242 Crystal structures of the muPA:nanobody complexes and hy
243 Here we solve the
crystal structures of the N-terminal domains of PHF1 and
244 re we present the syntheses, activities, and
crystal structures of the p53-MDM2/MDMX inhibitors based
245 Here we determine
crystal structures of the primed pre-fusion SNARE-comple
246 n, we present two additional high-resolution
crystal structures of the same RNA duplex containing fou
247 Furthermore, we present the
crystal structures of the Seb1 CTD- and RNA-binding modu
248 Here, we present the
crystal structures of the SHR-SCR binary and JACKDAW (JK
249 Crystal structures of the SNX5 phox-homology (PX) domain
250 2) kinase, is still unknown, as the numerous
crystal structures of the unphosphorylated and phosphory
251 olecular docking and comparisons between the
crystal structures of the Vitis vinifera dihydroflavonol
252 We also determined
crystal structures of these compounds bound to PARP1 or
253 Crystal structures of these three factors revealed an al
254 Crystal structures of these VHHs in complex with prefusi
255 human anti-D8 antibodies and determined the
crystal structures of three VACV-mAb variants, VACV-66,
256 The X-ray
crystal structures of two active complexes are reported,
257 zation was further guided by high-resolution
crystal structures of two of the macrocyclized peptides
258 ghts into reaction mechanisms, we determined
crystal structures of two relevant complexes: a THO hete
259 mined electron cryo-microscopy (cryo-EM) and
crystal structures of unbound and H1-bound nucleosomes a
260 The entropy engineering using multicomponent
crystal structures or other possible techniques provides
261 te this importance and the existence of NS5B
crystal structures,
our understanding of the conformatio
262 G-Dock reproduces accurately (<1-A rmsd) the
crystal structure poses for four known heparin-protein s
263 These maps fuse
crystal-structure prediction with the computation of phy
264 e Corynebacterium ammoniagenes FADS (CaFADS)
crystal structure predicts a dimer of trimers organizati
265 A series of
crystal structures reveal unique features that distingui
266 A
crystal structure revealed that HO-2 binds myristate via
267 Its
crystal structure revealed the self-assembly of two Pt-c
268 The Axl
crystal structure revealed two distinct conformational s
269 Crystal structures revealed pi-pi intramolecular interac
270 fector domain as dimers, and high-resolution
crystal structures revealed that these miniprotein dimer
271 Here we present
crystal structures revealing the MCR-1 periplasmic, cata
272 The
crystal structure reveals that YbAnbu subunits form tigh
273 modulate pump activity, and, as observed in
crystal structures,
several lipids are bound within the
274 Two
crystal structures show that Csm1 interacts with Ulp2 an
275 High-resolution
crystal structures show that designed peptide FS2 binds
276 Crystal structures showed that pT1471 binds the canonica
277 Although the
crystal structure shows a hydrogen bond between the iron
278 The
crystal structure shows a remarkably short Pd-Cu bond an
279 The
crystal structure shows that the hydrogen bonding intera
280 y a templated clipping reaction and an X-ray
crystal structure shows that the squaraine gem-dimethyl
281 Trans pairs occurring in high-resolution RNA
crystal structures shows that they are found in 14 diffe
282 erations in highly conserved residues, using
crystal structures solved in the absence of tRNA as a gu
283 med between the materials with diamond cubic
crystal structures studied in this work, the presence of
284 ntation of the clusters is not random in the
crystal structure,
such that the side-by-side aligned po
285 nction that can be calculated from predicted
crystal structures,
such as electronic structure or mech
286 n fuels in various DCFC systems, in terms of
crystal structure,
surface properties, impurities and pa
287 Based on its
crystal structure,
the RNA polymerase domain contains tw
288 A new
crystal structure,
together with molecular dynamics and
289 hey are typically based on a small subset of
crystal structures using measurements biased towards the
290 n intermediates agree well with the relevant
crystal structures,
validating the computational protoco
291 ther, by comparing solution binding data and
crystal structure,
we gained insight on how the probe se
292 Using the recently resolved hCB1 receptor
crystal structures,
we also performed a modeling study t
293 ie2 dimers in solution and modeling based on
crystal structures,
we suggest that Ang1 binding may cro
294 X-ray
crystal structures were obtained for five of the designs
295 ghly organized capsules is shown by an X-ray
crystal structure which features the assembly of two XB
296 leaving only a small number of protein-ssNA
crystal structures,
while forcing solution investigation
297 on to form MV(+*) radical cations within the
crystal structure with half-lives of several hours in ai
298 The combination of our
crystal structure with solution state analysis of recomb
299 , based on fitting experimental PDF to known
crystal structure,
with a controversy.
300 itions and predicting compositions for known
crystal structures,
with notable successes.