1 tures for 304 unique protein sequences (2528
crystal structures).
2 at our Rb:hIgG1 model closely matched the co-
crystal structure.
3 materials, in spite of similarities in their
crystal structure.
4 ))(3)N(4) with x = 0 < x < 1 and spinel-type
crystal structure.
5 oxide species, which is observed in the AsqJ
crystal structure.
6 olumab, evaluated with respect to a resolved
crystal structure.
7 gages in extended H-bond interactions in its
crystal structure.
8 orb through the visible, and possess a polar
crystal structure.
9 ntiate internal binding, consistent with the
crystal structure.
10 Ibeta2C2 but had been masked in the previous
crystal structure.
11 n-metallic, with molecular H(2) units in the
crystal structure.
12 e core/P1 domains than suggested in the SurA
crystal structure.
13 is inhibitors has been hampered by a lack of
crystal structures.
14 t motors often have nearly indistinguishable
crystal structures.
15 ions in situ that closely match the in surfo
crystal structures.
16 es described herein are accentuated by their
crystal structures.
17 ated with the solvent-accessible area of the
crystal structures.
18 ctivity of NzeB, we obtained high-resolution
crystal structures (
1.5 angstrom) of the protein in comp
19 mine-bound and substrate analog GlcNAc-bound
crystal structures (
2.33, 2.20, and 2.20 angstrom resolu
20 The
crystal structure also gradually evolved from polytwista
21 Furthermore,
crystal structure analyses of 12 derivatives in complex
22 While our
crystal structure analysis and in vitro binding data ini
23 Unexpectedly, protein
crystal structure analysis and molecular dynamics simula
24 X-ray co-
crystal structure analysis and ultracentrifugation exper
25 Crystal structure analysis of 1 shows a strong pai...pai
26 lly calculated explosive properties, and the
crystal structure analysis of the ETN derivatives are re
27 Detailed
crystal structure analysis suggested that intermolecular
28 point extraction of NPs and their subsequent
crystal structure analysis via SAED is another valuable
29 e X-ray analysis (EDX) elemental mapping and
crystal structure analysis via SAED.
30 face with the DUX4 protein, as determined by
crystal structure analysis.
31 An inward-facing
crystal structure and an outward-facing model of a bacte
32 results provide a direct correlation between
crystal structure and HER activity, thus paving the way
33 rithm allows us to quantify the key roles of
crystal structure and liquid caging length in determinin
34 erated from synthetic NaCl solutions and the
crystal structures and morphologies of manganese oxides,
35 g such freestanding membranes with different
crystal structures and orientations, which is not possib
36 hesized 12 manganese oxides having different
crystal structures and particle sizes and measured the p
37 e these isotopic compounds exhibit identical
crystal structures and solubilities, the trend in derace
38 The electroplated films have cubic
crystal structures and the preferred orientation was fou
39 e-planar intermediate geometry from Cre-loxP
crystal structures and those of other int-superfamily re
40 We determined TCR-peptide-HLA
crystal structures and, using a single-chain peptide-HLA
41 We report the synthesis, X-ray
crystal structure,
and molecular recognition properties
42 GAC RNA tertiary state, corresponding to the
crystal structure,
and that this structure reflects the
43 nd SA chemical structure, nano and mesoscale
crystal structure,
and the oleogel macroscopic character
44 Photophysical studies, single-
crystal structures,
and theoretical calculations indicat
45 These
crystal structures are the first example of human MADS-b
46 secondary structure is equally accurate, but
crystal structures are typically too rigid in loops, whe
47 Here, we present the X-ray
crystal structure at 1.71 angstrom resolution and the bi
48 The
crystal structure at 1.85- angstrom resolution revealed
49 tly, neutralizing SARS-CoV-2, and report the
crystal structure at 2.4 angstrom of the Fab/RBD complex
50 Starting from the OX1R and OX2R
crystal structures bound to suvorexant, we exploited a s
51 e mSAA1 at pH~7.4 agreed in details with the
crystal structures but also showed important differences
52 Due to the complexity of the
crystal structure composed of heavy elements, the report
53 ing colloidal particles in the cubic diamond
crystal structure could potentially be used to make mate
54 rthermore, we solve the sFlaG(2)-sFlaF(2) co-
crystal structure,
define its heterotetrameric complex i
55 omain-swapped Fab dimer from among >3000 Fab
crystal structures determined to date.
56 in boundaries, rather than the change of the
crystal structure,
dominates the reversible and substant
57 Biochemical studies guided by the co-
crystal structures enable the identification of 90 new a
58 ated dataset of ligand-bound and ligand-free
crystal structures for 304 unique protein sequences (252
59 Analysis of reported
crystal structures for carbapenem-derived acyl-enzyme co
60 JH2, and JH2 V617F domains, as well as five
crystal structures for JH2 complexes.
61 In addition, a
crystal structure has been also obtained using single-cr
62 The human OGA X-ray
crystal structure has been recently solved, but bacteria
63 ent of the RNAP active center that, based on
crystal structures,
has been proposed to cycle between a
64 Cs, NH(4), Tl) have been known for decades,
crystal structures have only been reported for CsMoO(2)F
65 though ultra-high-resolution opioid receptor
crystal structures have revealed a specific Na(+) bindin
66 poxide hydrolase A (Mth-EphA) and report its
crystal structure in complex with the inhibitor 1,3-diph
67 allization methods to understand and explore
crystal structure in pharmaceuticals and minimize the ri
68 X-ray
crystal structures in complex with galactose and unhydro
69 mprehensive X-ray crystallographic study (12
crystal structures),
involving both CA II and a soluble
70 lectric polaron in the three-dimensional LHP
crystal structure is a large polaron in two dimensions a
71 revealed that gel strength is enhanced when
crystal structure is isotropically oriented, similar beh
72 Characterization of the experimental
crystal structure matches well with a new theoretical mo
73 An alcove seen in the ACS
crystal structure near the A-cluster, defined by hydroph
74 A
crystal structure of a binary DNA product complex reveal
75 To our knowledge, we present the first
crystal structure of a Co(III) iodosylbenzene complex an
76 Here we report the
crystal structure of a complex between human caspase-1 a
77 s further corroborated by obtaining an X-ray
crystal structure of a derivative.
78 Herein, the
crystal structure of a four-subunit T4CP subcomplex boun
79 Here, we report the
crystal structure of a posttermination Thermus thermophi
80 between AcpP and FabD to elucidate the X-ray
crystal structure of a type II ACP-AT complex.
81 The
crystal structure of an assembled ON-switch shows that t
82 Here we report the
crystal structure of an ATP (ADP:BeF(3)-bound) ground-st
83 The X-ray co-
crystal structure of an early lead (12) revealed a poten
84 The
crystal structure of an EZH2-EED binary complex indicate
85 Here we report the first x-ray
crystal structure of an insect myosin: the D melanogaste
86 (D) of 2 nM), and a 2.6- angstrom-resolution
crystal structure of an RBD-EY6A Fab complex identifies
87 The
crystal structure of AtLEGbeta revealed unrestricted non
88 We present a
crystal structure of BchL in the nucleotide-free form wh
89 A
crystal structure of BRIL in complex with an affinity-ma
90 Here, we report the
crystal structure of CD53 in an open conformation poised
91 Biochemical studies and the co-
crystal structure of CLK1 in complex with AB1 show that
92 Here we provide the x-ray
crystal structure of cone GAFab regulatory domain solved
93 that can provide an atomic-level view of the
crystal structure of copper nanoparticles.
94 We solve the
crystal structure of CxD7L1 in complex with ADP to 1.97
95 To date, no
crystal structure of CYP2J2 is available, and the propos
96 0 Here we report the 1.7 angstrom resolution
crystal structure of CYP73A33.
97 The 3.1 angstrom
crystal structure of DEP1 features a domain swap, simila
98 Finally, we obtained the first
crystal structure of FhTIM at 1.9 angstrom resolution wh
99 Here we report the
crystal structure of FPR2 bound to the potent peptide ag
100 A
crystal structure of full-length BM3 enzyme is not avail
101 Here, we report the first
crystal structure of full-length nsp10 from the arterivi
102 ping the identified KDELR2 variants onto the
crystal structure of G. gallus KDELR2 indicated that the
103 Here we present the
crystal structure of glycoprotein N (G(N)) from the toma
104 Here, we present the
crystal structure of GP38 at a resolution of 2.5 angstro
105 Here, we present the
crystal structure of GP38, which revealed a novel fold w
106 The
crystal structure of H1/PR8 HA in complex with our best
107 Here we present a 2.9- angstrom-resolution
crystal structure of human BRAF(KD) in complex with MEK
108 Here, we report on a
crystal structure of human PSMA in complex with A9g, a 4
109 Here, we report a
crystal structure of human SRD5A2 at 2.8 angstrom, revea
110 Here, we have solved the
crystal structure of HypD from the pathogen Clostridioid
111 osphoprotein is tetrameric, and we solve the
crystal structure of its tetramerization domain.
112 We determined the
crystal structure of LmrP in a ligand-bound outward-open
113 Here, we present the
crystal structure of M(1)AChR in complex with MT7, a sub
114 Determination of the co-
crystal structure of M-808 in complex with menin provide
115 The
crystal structure of mAb397 with an NPNA(4) peptide show
116 degron motif recognized by MAGE-A11 and the
crystal structure of MAGE-A11 bound to the PCF11 substra
117 The first
crystal structure of mammalian ER Glu I will constitute
118 We first report the
crystal structure of mouse DHX36 bound to ADP.
119 We determined the X-ray
crystal structure of N2, combined with monitoring secret
120 The
crystal structure of NfoR in complex with CuSO(4) (1.46
121 The
crystal structure of olmesartan-bound human AT1R (PDB:4Z
122 Here, we report the
crystal structure of PDE5 complexed with the sole second
123 The
crystal structure of pro-myostatin in complex with 29H4-
124 s quorum-sensing signal, SHP3, and the X-ray
crystal structure of Rgg3 alone.
125 The
crystal structure of RgNanOx in complex with the NAD(+)
126 consistent with the first and controversial
crystal structure of SARS-CoV Mpro determined at pH 6.
127 Therefore, we determine the
crystal structure of Sulfolobus acidocaldarius soluble F
128 Here, we report a 1.6- angstrom resolution
crystal structure of TbBILBO1-NTD, which revealed a cons
129 and proteins for food systems, we report the
crystal structure of the (GPO)(10) peptide at 0.89- angs
130 properties of these compounds and channeled
crystal structure of the 1,3,5-tris(pyren-2-yl)adamantan
131 Furthermore, the
crystal structure of the amino analogue reveals an inter
132 We present the
crystal structure of the aptamer domain of this atypical
133 We previously determined the X-ray
crystal structure of the bacterial RNA polymerase engage
134 We have solved the
crystal structure of the BCAP TIG and find that it is mo
135 We report a
crystal structure of the bifunctional FEN/EXO-POL apoenz
136 ct of ATP through a 2.5- angstrom-resolution
crystal structure of the BRAF(KD)-14-3-3 complex, in whi
137 We previously defined and solved the
crystal structure of the C-terminal domain of NP (NP-Ct)
138 The
crystal structure of the C4b:hC4Nb8 complex and a three-
139 The single
crystal structure of the CAM-Ag nanofibers is solved in
140 formation of 6-ACA to HMD, we determined the
crystal structure of the CAR substrate-binding domain in
141 In addition, we report the
crystal structure of the catalytic domain of XOAT1, whic
142 Here, we report the
crystal structure of the central metabolic enzyme pyrido
143 We determined the
crystal structure of the complex at 1.7 angstrom resolut
144 The 1.38 angstrom
crystal structure of the CypA/PreNAC complex displays a
145 Here, we solved the 1.8 angstrom resolution
crystal structure of the cytoplasmic region of RPTPalpha
146 Moreover, the
crystal structure of the disease-mutation-containing seg
147 Here, we report a
crystal structure of the DNA-binding domain of a model A
148 The co-
crystal structure of the DUB (OtDUB) domain with ubiquit
149 The
crystal structure of the ERK7-AC9 complex reveals that A
150 Here, we present the
crystal structure of the Escherichia coli Hfq Core bound
151 Here we present the first
crystal structure of the extracellular domains of human
152 A 2.1 angstrom X-ray
crystal structure of the FigC N-citrylornithine decarbox
153 rt the 3.2 angstrom resolution, peptide-free
crystal structure of the full-length human GLP-1R in an
154 Here we report a
crystal structure of the full-length LCI1 membrane prote
155 We determined the
crystal structure of the HA protein of the avian H7N9 in
156 icular HCV-infected individuals, we solved a
crystal structure of the HCV E2 ectodomain in complex wi
157 Here we present the 1.9- angstrom
crystal structure of the human PD-1H extracellular domai
158 Here, we present the
crystal structure of the LRP6 E1E2-SOST complex with two
159 A 3.0- angstrom
crystal structure of the LRR-RK GSO1/SGN3 regulating Cas
160 nd not just histones, we have determined the
crystal structure of the LSD1/CoREST complex bound to a
161 ) cofactor in catalysis, analyzing the first
crystal structure of the MbtI-Mg(2+)-salicylate ternary
162 of enzymatic activity, we determine here the
crystal structure of the mouse Esco2/CoA complex at 1.8
163 Here, we present the
crystal structure of the N-terminus of TBC1D23 (D23N), w
164 A
crystal structure of the Periphilin-TASOR minimal core c
165 A 1.7 angstrom
crystal structure of the periplasmic domain of the RsbU
166 Here, we report the
crystal structure of the prototypical SEDS protein RodA
167 Here we determined the
crystal structure of the receptor-binding domain (RBD) o
168 Here, we report the
crystal structure of the Reduced Potassium Dependency3/H
169 In this study, we describe the
crystal structure of the RSV surface glycoprotein G in c
170 Here, we determined the
crystal structure of the Saccharomyces cerevisiae Cenp-H
171 Here, we present the X-ray
crystal structure of the TbPRMT1 ENZ-Delta52PRO tetramer
172 Here, we report the
crystal structure of the zebrafish VDR ligand-binding do
173 n of reactive alkyl handles, (iii) the X-ray
crystal structure of TnmH provides the molecular basis t
174 The
crystal structure of two CeD patient-derived TCR in comp
175 on of the 50S-RsfS complex together with the
crystal structure of uL14-RsfS complex solved at 2.3 ang
176 The 1.65- angstrom resolution X-ray
crystal structure of YaaA reveals that the protein posse
177 High-resolution
crystal structures of (Pl)EctA (at 1.2-2.2 angstrom reso
178 The
crystal structures of (Ss)RidA-1 and (Ss)RidA-2 provided
179 physical characterization of 64 designs, and
crystal structures of 5 designs.
180 Models generated based on
crystal structures of 5' and 3' exonuclease oligonucleot
181 Crystal structures of a complex consisting of Prp2-ADP a
182 cular basis for promiscuity, we solved X-ray
crystal structures of a SMR transporter Gdx-Clo in compl
183 Here, Travis et al. report two
crystal structures of a yeast tethering factor, the Dsl1
184 The
crystal structures of AaTPS and FgGS provide insights in
185 Partial or complete
crystal structures of all MSC constituents have been rep
186 In this work, we present
crystal structures of angiotensin II type 1 receptor (AT
187 Crystal structures of arsenic-bound p53 mutants reveal a
188 Here, we report
crystal structures of AvaII alone, in specific complex w
189 Five
crystal structures of B3GNT2 have been determined in the
190 Here, we report the high-resolution X-ray
crystal structures of both PVL and alpha-toxin in their
191 anism for this activity based on a series of
crystal structures of bound complexes.
192 Crystal structures of Ca(2+)-free and Ca(2+)-bound EhAct
193 ROESY and DFT studies, aided by
crystal structures of carboxylic acids bound by the cata
194 Although the
crystal structures of dark- and light-adapted states hav
195 Crystal structures of delta revealed novel pentameric fo
196 Taking inspiration from the
crystal structures of diamine-appended metal-organic fra
197 We report the
crystal structures of equine serum albumin complexed wit
198 High-resolution
crystal structures of ESOC acyl-enzyme complexes with de
199 Here, we present the X-ray
crystal structures of five HDAC6-inhibitor complexes tha
200 Here, we present the
crystal structures of four functionally distinct plant A
201 xed substrate specificity, we determined the
crystal structures of Fpr and that in a novel complex wi
202 Crystal structures of GPCRs provide snapshots of their i
203 X-ray
crystal structures of halide complexes (X(-) =Br(-) , I(
204 We report the
crystal structures of hsNadE and NAD(+) synthetase from
205 We report here
crystal structures of human 8-oxoguanine (oxoG) DNA glyc
206 Crystal structures of human and mouse SCD1 were reported
207 sm of substrate cleavage, we have solved the
crystal structures of human GGT1 (hGGT1) with glutathion
208 and inhibitory mechanism, we report 11 x-ray
crystal structures of human VKOR and pufferfish VKOR-lik
209 High-resolution
crystal structures of inactive MCR lacking the modified
210 one chaperoning activity, we have solved the
crystal structures of its terminal domains and functiona
211 Here, we present four co-
crystal structures of lab-evolved TAR-binding proteins (
212 We then determined
crystal structures of ligase-defective NgrRnl-Ala mutant
213 Crystal structures of Lpg2603 in the apo-form and when b
214 We solved the
crystal structures of mAb HENV-26 in complex with both H
215 The
crystal structures of mammalian DXO with 3'-FADP or CoA
216 Here we report X-ray
crystal structures of MEK bound to the scaffold KSR (kin
217 Here we report the
crystal structures of Metacaspase 4 from Arabidopsis tha
218 Crystal structures of MtmW and its complexes with co-sub
219 We present the first
crystal structures of NRAS and KRAS ITD at 1.65-1.75 ang
220 o obvious sequence similarity to known GEFs,
crystal structures of OtDUB(GEF) alone (3.0 angstrom) an
221 By comparing
crystal structures of paralogous complexes, we provide a
222 We report two
crystal structures of peroxisome proliferator-activated
223 AA-bound
crystal structures of PKM2 displayed distinctive interac
224 nto oxoA-mediated mutagenesis, we determined
crystal structures of poleta bypassing oxoA.
225 tion and synthesis activities, we elucidated
crystal structures of pre- and post-catalytic complexes
226 nsive database containing over 5200 3D X-ray
crystal structures of protein-carbohydrate complexes.
227 tilizing an ionic liquid strategy, we report
crystal structures of salts of free anionic nucleobases
228 Here we present four new
crystal structures of SidA in various redox and ligation
229 Here, we report
crystal structures of substrate mimetic bearing ACPs in
230 Crystal structures of T cell receptors in complex with H
231 Crystal structures of TCR-HLA-C complexes revealed that
232 Here, we present
crystal structures of Teneurin-Latrophilin complexes tha
233 -Lip combine for PAP function, we determined
crystal structures of Tetrahymena thermophila Pah2 (Tt P
234 Crystal structures of tetrameric PfISN1 reveal complex r
235 Molecular docking screens against
crystal structures of the A(2A) adenosine and the D(4) d
236 In this study, x-ray
crystal structures of the Aurora A kinase domain delinea
237 glycoproteins, we determined high-resolution
crystal structures of the binding domains alone and with
238 We present
crystal structures of the butenolide receptor AvaR1 in i
239 Analysis of the
crystal structures of the complexes, NMR titration exper
240 We report
crystal structures of the constitutively expressed PCO4
241 The
crystal structures of the efficient phosphorescent mater
242 report the biochemical characterization and
crystal structures of the founding member of this family
243 forms that inhibit seeding differently, and
crystal structures of the M204-scFv monomer, dimer, and
244 We have solved the
crystal structures of the NTD core and EXO domains of Nb
245 We present X-ray
crystal structures of the peptide-free state of HLA-A*02
246 We report
crystal structures of the POL domain, as apoenzyme and a
247 ation problem' is handled by the HGM; and 3D
crystal structures of the polysaccharide utilisation loc
248 nd bioactivity studies, and solved three new
crystal structures of the RNA duplexes containing these
249 hat predicted from the docking of homologous
crystal structures of the separate transmembrane and deh
250 We present several high-resolution
crystal structures of the UDP-glucuronic acid epimerase
251 Crystal structures of the water-soluble forms of a 12-he
252 Crystal structures of these VHHs bound to their respecti
253 We report
crystal structures of this dual domain in both apo- and
254 Crystal structures of TrtA in apo and holo form were sol
255 Here, we describe the
crystal structures of two distinct isoforms of ligand-fr
256 Co-
crystal structures of two IGHV3-53-neutralizing antibodi
257 Crystal structures of two mAbs in complex with the SARS-
258 Crystal structures of UbVs in complex with three E2 prot
259 X-ray
crystal structures of variously modified ASL(Arg1)(ICG)
260 We also solved the
crystal structures of WT and N53I CaM in complex with th
261 We report two
crystal structures of XoxF1, one with and another withou
262 ally focus on the effects of modifying their
crystal structures or of tuning mobile-ion stoichiometri
263 The copper sulfide
crystal structure plays a key role in the mechanism by w
264 rulence Regulator (PCVR) as indicated by the
crystal structure,
post-translational modifications and
265 We combine state-of-the-art computational
crystal structure prediction (CSP) techniques with a wid
266 by the high-resolution (1.88-1.98 angstrom)
crystal structure presented here.
267 rmation, together with analysis of the x-ray
crystal structures,
provides a starting point for the de
268 ate that this strain effectively changes the
crystal structure,
reduces the bandgap and increases the
269 Despite two
crystal structures reported on fragments of IRBP and dec
270 The
crystal structure revealed an EF domain with two Ca(2+)-
271 methanimido thioate intermediate in the SQOR
crystal structure,
revealing how cyanolysis leads to rev
272 Here, we present the talin2
crystal structure,
revealing that its F0-F1 di-subdomain
273 The
crystal structure reveals key structural features that h
274 th of the charge carriers and is affected by
crystal structure,
scattering from boundaries and defect
275 Here, using an advanced
crystal structure search algorithm in conjunction with f
276 Comparisons of NMR to
crystal structures show that secondary structure is equa
277 X-ray
crystal structures show that the transporter forms a dim
278 In this paper we report the synthesis,
crystal structure,
spectroscopic properties and redox in
279 ich, when aligned with the N-terminal domain
crystal structure,
suggest an N-terminal domain that wra
280 ny similarities to a previous yeast RFC:PCNA
crystal structure,
suggesting that eukaryotic clamp load
281 explored LFHP NCs with an emphasis on their
crystal structures,
synthesis, optical properties, and e
282 We present an LRH-1
crystal structure that illuminates striking mechanistic
283 onstructed from knowledge of either the full
crystal structure -
therefore only applicable to materia
284 Together with previous ultrahigh-resolution
crystal structures,
these findings enable us to follow t
285 es, attributed to the tailored molecular and
crystal structures through molecular design.
286 We solved the DPO-VqmA
crystal structure to 2.0 angstrom resolution and compare
287 The crystallographically refined
crystal structures using single-crystal X-ray diffractio
288 in M2 with the interactions revealed in the
crystal structures,
using the Multiscale Reactive Molecu
289 corporation of TcO(4)(-) into the ettringite
crystal structure via sulfate substitution when synthesi
290 Based on the available FXIII-A2
crystal structure,
we identified 12 amino acid residues
291 From X-ray
crystal structures,
we learn that hydroxyanions dimerize
292 Based on previous X-ray
crystal structures,
we mutated three conserved residues
293 l study of H6 and mH6 shows closely matching
crystal structures,
whereas spectroscopic data and limit
294 f Fe atoms in the tunnels of the W(18) O(49)
crystal structure,
which increases the oxygen vacancies
295 tantially different from the organization in
crystal structures,
which feature flat hexamers.
296 The fabricated silver nanorods show single-
crystal structure with a low resistivity of 8.58 x 10(-5
297 emiconductor Si(2)Te(3) has a unique layered
crystal structure with hexagonal closed-packed Te sublat
298 se insights lay the groundwork for animating
crystal structures with biochemically relevant motions.
299 Complex
crystal structures with subtle atomic-scale details are
300 ials including perovskite, spinel and garnet
crystal structures with varying crystallographic orienta