1 A cryo-EM structure of TerS(P76-26) revealed that it forms
2 A cryo-EM structure of the portal protein of thermostable
3 A cryo-EM structure of the spastin-peptide complex at 4.2
4 red flour beetle, Tribolium castaneum, and
a cryo-EM structure of the complex at 3.5 angstrom resolut
5 on-covalent agonist, GNE551, and determine
a cryo-EM structure of the TRPA1-GNE551 complex, revealing
6 omputational pipeline, where the inputs of
a cryo-EM map, the corresponding atomistic structure, and
7 Here, we present
a cryo-EM reconstruction of the native human gamma-TuRC at
8 We present
a cryo-EM structure of an MCU-EMRE-MICU1-MICU2 holocomplex
9 Here we present
a cryo-EM structure of the strain 970 LH1-RC complex at 2.
10 Here, we report
a cryo-EM structure of a B. subtilis transcription activat
11 We report
a cryo-EM structure of a complex between the Mycobacterium
12 We also report
a cryo-EM structure of DNA-PK at 3.5- angstrom resolution
13 Here we report
a cryo-EM structure of FPR2-G(i) signaling complex with a
14 Here, we report
a cryo-EM structure of human NKCC1 captured in a partially
15 Here, we report
a cryo-EM structure of human NPC1 bound to itraconazole, w
16 We report
a cryo-EM structure of the S. cerevisiae RNase MRP holoenz
17 Herein, we used
a cryo-EM single-particle approach, revealing that full-le
18 image data using two-fold symmetry yielded
a cryo-EM map in which both DNA ends appeared well ordered
19 His-tag that binds 5-nm Ni-nanogold
allowed cryo-EM tomography mapping of the C terminus of protein
20 determined by both x-ray crystallography
and cryo-EM.
21 bunits, site-specific photocrosslinking,
and cryo-EM reconstruction.
22 vitro biochemistry, ribosome profiling,
and cryo-EM to define molecular mechanisms that lead to thes
23 is work, we used both negative stain TEM
and cryo-EM to determine 3D maps of the full-length Aquifex
24 Here, we present a ~3.0-
angstrom cryo-EM structure of trimeric human STEAP1 bound to thre
25 Here, we describe the 3.2
angstrom cryo-EM structure of human DEC-205, thereby illuminating
26 Here we report the 3.2-
angstrom cryo-EM structure of S.c. Pol delta in complex with prim
27 Our ~3.5
angstrom cryo-EM structure of the E. coli MCE protein LetB reveal
28 A 2.5-
angstrom cryo-EM structure of a 1-18-BG505(SOSIP.664) Env complex
29 ivated Gi protein and from the 3.5-
angstrom cryo-EM structure of muOR-Gi complex after replacing the
30 We show here a 3.5-
angstrom cryo-EM structure of yeast Pol epsilon revealing that th
31 Here, we present a 3.67
angstrom cryo-EM structure of the RSV polymerase (L:P) complex.
32 (+)/H(+) symporter and report a 3.7
angstrom cryo-EM structure of the KimA homodimer in an inward-occ
33 iques and ultimately solved the 4.9
angstrom cryo-EM structure of the DEC-205 tetramer to identify th
34 Here we present the 2.68-3.96
angstrom cryo-EM structures of the human 55S mitoribosome in comp
35 red with a structure derived from
asymmetric cryo-EM reconstructions.
36 We report both closed- and open-state
atomic cryo-EM structures of a full-length Caenorhabditis elega
37 les, which increases throughput in
automated cryo-EM without degrading data quality.
38 sue of Cell, two papers report agonist-
bound cryo-EM structures of the cannabinoid receptor, CB2, in
39 by constructing deletion proteins guided
by cryo EM structural knowledge.
40 We have compared the two capsids
by cryo-EM at 3.5 angstrom resolution.
41 ned the structure of the PG16-Env complex
by cryo-EM to an overall resolution of 4.6 angstrom.
42 btained reconstructions of mCF and CstF77
by cryo-EM, assembled around the mPSF core.
43 ucture of human SOAT1 (hSOAT1) determined
by cryo-EM.
44 (KCC) KCC4, in lipid nanodiscs determined
by cryo-EM.
45 nd CHMP1B + IST1, and IST1-only filaments
by cryo-EM.
46 We have identified
by cryo-EM a segment in CPSF100 that tethers mCF to mPSF, a
47 e human type-3 IP(3)R (IP(3)R-3) obtained
by cryo-EM (at an overall resolution of 3.8 angstrom), reve
48 ve been captured at increasing resolution
by cryo-EM.
49 article was visualized at high resolution
by cryo-EM.
50 ex from Anoxybacillus flavithermus solved
by cryo-EM at 3.0 angstrom resolution.
51 interest in extending structural studies
by cryo-EM into the cell, where biological structures and p
52 zation of amyloids for structural studies
by cryo-EM, but also pave the way to elucidate the structur
53 tructural properties of AAVv66 visualized
by cryo-EM at 2.5- angstrom resolution, suggest that critic
54 n open spiral to a closed ring visualized
by cryo-EM.
55 most of the N-glycans could be visualized
by cryo-EM.
56 Here, we use two
complementary cryo-EM strategies to determine structures of the major
57 ram can be easily used on any RNA-
containing cryo-EM structure, and an associated Coot plugin allows
58 In
contrast,
cryo-EM structures of ribosomes from mutant cells lackin
59 Electron
cryomicroscopy (
cryo-EM) structures of apo and acyldepsipeptide-bound Mt
60 We report the electron
cryomicroscopy (
cryo-EM) structures of the native bovine BBSome in inact
61 of single-particle electron
cryomicroscopy (
cryo-EM), computational modeling, and site-specific mass
62 Using electron
cryomicroscopy (
cryo-EM), we imaged an in vitro initiation reaction whic
63 Here we
determine cryo-EM structures of Escherichia coli MlaFEDB in an apo
64 We also
determined cryo-EM structures of major and minor native states of t
65 d pleomorphic assemblies, we have
determined cryo-EM structures of apo-CA hexamers and in complex wit
66 d-TW sub-module to the previously
determined cryo-EM map of the S. cerevisiae CCAN-Cenp-ANuc complex.
67 We
determined cryo-EM structures for RaTG13 S and for both furin-cleav
68 rget recognition and cleavage, we
determined cryo-EM structures of Cas12i in multiple functional stat
69 By
devising cryo-EM methodologies for exceedingly flexible and pleom
70 of allostery, protein quality control
during cryo-EM construct optimization, and in the study of prot
71 Here, yeast and human
EMC cryo-EM structures reveal conserved intricate assemblies
72 To interpret the
experimental cryo-EM maps, we present molecular-dynamics-based method
73 graphene-water interface, which
facilitates cryo-EM 3D reconstruction of archaea 20S proteasomes at
74 ee method that, starting only from the
final cryo-EM map, decomposes local resolution into the differ
75 The
first cryo-EM structure of an HCN1 channel revealed that a nov
76 ) subunit in liver, thus reporting the
first cryo-EM structure of any PKA holoenzyme.
77 Herein, we report
five cryo-EM structures of nanodisc-embedded Ca(v) 1.1 in the
78 Here, we report
five cryo-EM structures, at resolutions of 3.0-3.3 angstrom,
79 We design a fully automated approach
for cryo-EM 3D density maps reconstruction (Auto3DCryoMap).
80 soluble domains, lays out the foundation
for cryo-EM analysis of integral or peripheral MPs whose fun
81 and aid the development of robust tools
for cryo-EM structure modeling and refinement.
82 l, here we present a convenient workflow
for cryo-EM structural analysis of MPs embedded in liposomes
83 toms, using models fitted to or derived
from cryo-EM maps.
84 Furthermore,
cryo-EM reveals a range of partially full, condensed DNA
85 we describe a method for preparing
graphene cryo-EM grids with up to 99% monolayer graphene coverage
86 Here,
cryo-EM data were derived from filaments reconstituted w
87 Here,
cryo-EM of myelin-like proteolipid multilayers revealed
88 pressed in different cell lines revealed
how cryo-EM can detect subtle changes in glycan occupancy, c
89 are verified by electron microcopy
imaging,
cryo-EM tomography and in-situ X-ray scattering methods.
90 Here, we report a series of human
IMPDH2 cryo-EM structures in both active and inactive conformat
91 ography but in both phases and amplitudes
in cryo-EM, and that half-maps with independent errors are
92 ize the resolvability of individual atoms
in cryo-EM maps, the map Q-score.
93 aps with independent errors are available
in cryo-EM.
94 computational models reveal that features
in cryo-EM images result from a complex interplay between t
95 have contributed to the principal methods
in cryo-EM and identify persisting challenges and bottlenec
96 s an effective approach to pick particles
in cryo-EM images automatically and accurately.
97 can be used as a measure of resolvability
in cryo-EM maps at various scales, from entire macromolecul
98 tures from Single Particle Analysis (SPA)
in cryo-EM and subtomogram averaging (SA) in electron cryot
99 Individual cryo-EM particles can be aligned to reconstruct a 3D den
100 capping strategy can be used on full-
length cryo-EM fibril structures.
101 nded to isolated mammalian plasma
membranes,
cryo-EM reveals similar nanoscale lateral heterogeneitie
102 ith existing cryogenic electron
microscopic (
cryo-EM) maps, limit binding to incoming monomers, and f
103 ve determined the cryo-electron
microscopic (
cryo-EM) structures of two archaeal type IV pili (T4P),
104 g a combination of electron cryo-
microscopy (
cryo-EM) and reconstituted translation initiation assays
105 Electron cryo-
microscopy (
cryo-EM) reveals that the HIV stem-loop docks into the A
106 Electron cryo-
microscopy (
cryo-EM) single-particle analysis has yielded protein st
107 Recent cryoelectron
microscopy (
cryo-EM) of nodavirus RNA replication complexes revealed
108 Cryoelectron
microscopy (
cryo-EM) showed that engagement of both eIF2B regulatory
109 ent a 5.8- angstrom cryoelectron
microscopy (
cryo-EM) structure of EEEV complexed with the HS analog
110 angstrom resolution cryoelectron
microscopy (
cryo-EM) structure of gammaTuRC, combined with crosslink
111 , we determined the cryoelectron
microscopy (
cryo-EM) structure of Streptococcus thermophilus Rgg3 bo
112 us to determine the cryoelectron
microscopy (
cryo-EM) structure of the channel functionally arrested
113 A cryoelectron
microscopy (
cryo-EM) structure of the IRP2-FBXL5-SKP1 complex reveal
114 ort a 3.3- angstrom cryoelectron
microscopy (
cryo-EM) structure of the serotype I FIPV spike (S) prot
115 Here, we present cryoelectron
microscopy (
cryo-EM) structures of Bacillus subtilis RQC complexes r
116 , we determined the cryoelectron
microscopy (
cryo-EM) structures of chromatosomes containing 197 bp D
117 Here, we report the cryoelectron
microscopy (
cryo-EM) structures of DNA-PKcs (DNA-PK catalytic subuni
118 ere, we present the cryoelectron
microscopy (
cryo-EM) structures of nanodisc-reconstituted ligand-fre
119 Here, we report the cryoelectron
microscopy (
cryo-EM) structures of two termination process intermedi
120 ere, we present two cryoelectron
microscopy (
cryo-EM) structures of UCN1-bound CRF1R and CRF2R with t
121 High-resolution cryoelectron
microscopy (
cryo-EM) structures reveal that the binding sites for PF
122 Cryoelectron
microscopy (
cryo-EM) structures reveal the essential tubulin tail gl
123 Recent cryoelectron
microscopy (
cryo-EM) studies of TRPM8 have shown distinct structural
124 ical approaches and cryoelectron
microscopy (
cryo-EM) to visualize a cohesin loading intermediate in
125 me, generated using cryoelectron
microscopy (
cryo-EM), cross-linking mass spectrometry, and homology
126 A) as visualized by cryoelectron
microscopy (
cryo-EM), cryoelectron tomography (cryo-ET), and scannin
127 very low-resolution cryoelectron
microscopy (
cryo-EM), that C. jejuni accommodated these mutations by
128 Using cryoelectron
microscopy (
cryo-EM), we resolved the first three-dimensional (3D) s
129 Using cryoelectron
microscopy (
cryo-EM), we show that KCNE3 tucks its single-membrane-s
130 1-GFRP complexes by cryoelectron
microscopy (
cryo-EM).
131 ure in the field of cryoelectron
microscopy (
cryo-EM).
132 tomic resolution by cryoelectron
microscopy (
cryo-EM).
133 haq heterotrimer by cryoelectron
microscopy (
cryo-EM).
134 ngle-particle electron cryogenic
microscopy (
cryo-EM) is presented.
135 Cryogenic electron
microscopy (
cryo-EM) analysis confirms that incubation of spike with
136 Using cryo-electron
microscopy (
cryo-EM) and biochemical approaches, we show that PF846
137 analyzing filament cryo-electron
microscopy (
cryo-EM) data at the single subunit level to directly in
138 tion is present in cryo-electron
microscopy (
cryo-EM) density maps and it has not been utilized yet f
139 Cryo-electron
microscopy (
cryo-EM) has become a leading technology for determining
140 Cryogenic electron
microscopy (
cryo-EM) has become one of the most powerful techniques
141 Cryo-electron
microscopy (
cryo-EM) images show that new aggregates protrude from t
142 rapid progress of cryo-electron
microscopy (
cryo-EM) in structural biology has raised an urgent need
143 ntly reported cryogenic electron
microscopy (
cryo-EM) open-state channel structure, multiple microsec
144 Here, we present a cryo-electron
microscopy (
cryo-EM) reconstruction of a human SMG1-8-9 kinase compl
145 ith the results of cryo-electron
microscopy (
cryo-EM) reconstruction of multiple 3D DNA origami objec
146 cular structure by cryo-electron
microscopy (
cryo-EM) relies on accurate determination of the orienta
147 Cryo-electron
microscopy (
cryo-EM) revealed that one nanobody, Nb6, binds Spike in
148 Cryo-electron
microscopy (
cryo-EM) showed that the design is accurate and can simu
149 provements in cryogenic electron
microscopy (
cryo-EM) single-particle analysis have enabled routine h
150 al single-particle cryo-electron
microscopy (
cryo-EM) snapshots of ryanodine receptor type 1 (RyR1),
151 ation loss in cryogenic electron
microscopy (
cryo-EM) stems from particle movement during imaging, wh
152 er, a 3.4 angstrom cryo-electron
microscopy (
cryo-EM) structure of a neutralizing monoclonal Fab-spik
153 ore determined the cryo-electron
microscopy (
cryo-EM) structure of alpha-synuclein fibrils containing
154 is a 3.8- angstrom cryo-electron
microscopy (
cryo-EM) structure of CDT, a bipartite toxin comprised o
155 ere, we report the cryo-electron
microscopy (
cryo-EM) structure of Homo sapiens CHD4 engaged with a n
156 om-resolution cryogenic electron
microscopy (
cryo-EM) structure of M1214_N1 complexed with CH505 SOSI
157 om resolution cryogenic electron
microscopy (
cryo-EM) structure of palmitoleated human WNT8A in compl
158 Here, we present a cryo-electron
microscopy (
cryo-EM) structure of the Escherichia coli 50S subunit a
159 ent low-resolution cryo-electron
microscopy (
cryo-EM) structure of this large membrane-bound protein
160 Here, we report cryo-electron
microscopy (
cryo-EM) structures of an intact Escherichia coli class-
161 he high-resolution cryo-electron
microscopy (
cryo-EM) structures of cucumber leaf spot virus and red
162 Here, we report cryo-electron
microscopy (
cryo-EM) structures of DNA-bound Drosophila ORC with and
163 Here, we present cryo-electron
microscopy (
cryo-EM) structures of translationally inactive yeast an
164 the advent of cryogenic electron
microscopy (
cryo-EM) techniques.
165 Here, we use cryo-electron
microscopy (
cryo-EM) to characterize J-C bound to RIIbeta, the major
166 Here, we use cryo-electron
microscopy (
cryo-EM) to determine the structures of tau filaments fr
167 biochemistry, and cryo-electron
microscopy (
cryo-EM) to investigate the functions of two NPET-associ
168 We have used cryo-electron
microscopy (
cryo-EM) to solve the atomic structures of two filamento
169 e use genetics and cryo-electron
microscopy (
cryo-EM) to study the high-resolution solution structure
170 Cryo electron
microscopy (
cryo-EM), a key method for structure determination invol
171 Using cryo-electron
microscopy (
cryo-EM), we determined the structure of human cohesin b
172 nd single-particle cryo-electron
microscopy (
cryo-EM), we present evidence for extensive interactions
173 ng single particle cryo-electron
microscopy (
cryo-EM), we report reconstructions of the core complex
174 by single-particle cryo-electron
microscopy (
cryo-EM), which show novel assembly of the four transmem
175 m a combination of cryo-electron
microscopy (
cryo-EM), x-ray crystallography, and computational predi
176 ctural analysis by cryo-electron
microscopy (
cryo-EM).
177 rystallography and cryo-electron
microscopy (
cryo-EM).
178 by single-particle cryo-electron
microscopy (
cryo-EM).
179 om resolution from cryo-electron
microscopy (
cryo-EM).
180 cryogenic transmission electron
microscopy (
cryo-EM).
181 ir structure using cryo-electron
microscopy (
cryo-EM).
182 imaging, and cryogenic electron
microscopy (
cryo-EM).
183 Analysis of
multiple cryo EM maps, further modelling and mutagenesis provide
184 Q-score analysis of
multiple cryo-EM maps of the same proteins derived from different
185 We report
multiple cryo-EM and X-ray structures in four different states, i
186 Here we present
nine cryo-EM structures of E. coli ATP synthase to 3.1-3.4 an
187 on-optimized spectroscopy (TROSY)-based
NMR,
cryo-EM, and biochemical assays show that, on binding Bz
188 However, it has proved difficult to
obtain cryo-EM reconstructions with sufficient resolution to vi
189 ovide a route towards routine application
of cryo-EM in high-throughput screening of small molecule m
190 Using a combined approach
of cryo-EM and atomistic molecular dynamics simulation, we
191 ed, we developed a program for assessment
of cryo-EM map quality.
192 Based on asymmetric features
of cryo-EM structures and a sequential hand-over-hand model
193 d by the sub-nanometer resolution imaging
of cryo-EM.
194 esolution evaluation in experimental maps
of cryo-EM.
195 e very well with the estimated resolution
of cryo-EM maps for both protein and RNA.
196 n has enormously helped the understanding
of cryo-EM maps.
197 Here we report
optimizing cryo-EM tomography and image processing to improve crown
198 microscopy with use of the negative stain
or cryo-EM imaging.
199 Our cryo-EM structure of the Nsp1-40S ribosome complex shows
200 Our cryo-EM, biochemical, and functional analyses reveal the
201 Using
our cryo-EM structure as a testbed, we developed a program f
202 A single
particle cryo-EM reconstruction of an ~160-kD N-terminal fragment
203 o paroxetine analogues using single-
particle cryo-EM and x-ray crystallography, respectively.
204 ded human Fzd5 determined by single-
particle cryo-EM at 3.7 angstrom resolution, with the aid of an a
205 Here we present single-
particle cryo-EM studies of ABCG2 in the apo state, and bound to
206 termined its structure using single-
particle cryo-EM to 3.1- angstrom resolution, revealing a flat, n
207 Here, we used single-
particle cryo-EM to analyze the three-dimensional structure of th
208 We used single-
particle cryo-EM to reveal the organisation and architecture of t
209 Single-
particle cryo-EM unveils that ArfB employs two modes of function
210 of a protein molecule using single-
particle cryo-EM.
211 NH domain was not visible in a
postcatalytic cryo-EM structure.
212 Here, we
present cryo-EM maps of SARM1 at 2.9 and 2.7 angstrom resolution
213 Here, we
present cryo-EM structures of ClpXP bound to the ssrA degron.
214 Here we
present cryo-EM structures of human TMEM175 in open and closed c
215 We
present cryo-EM structures of piggyBac transpososomes: a synapti
216 We
present cryo-EM structures of the Saccharomyces cerevisiae Polze
217 Here, we
present cryo-EM structures of the substrate-bound ClpXP complex
218 We
present cryo-EM studies of the E. coli enzyme that show how asym
219 hod, we built a database involving
published cryo-EM protein structures and a server to be able to co
220 3D modeling using the
published cryo-EM structure of human Nav1.7 showed that introducti
221 Recent cryo-EM analyses have produced near-complete models of t
222 Recent cryo-EM analyses of mammalian and yeast complex I have r
223 Combined with the analysis of a
recent cryo-EM structure, we suggest that p44/p62 acts as a nov
224 However,
recent cryo-EM studies of CENP-A NCP complexes comprising prima
225 Our results, together with
recent cryo-EM structures of ClpXP bound to substrates, support
226 Here we
report cryo-EM data for the substrate, creatine kinase (CKB) bo
227 Here, we
report cryo-EM reconstructions of a core complex lacking Cag3 a
228 Here we
report cryo-EM structures of bovine bestrophin-2 (bBest2) bound
229 Here, we
report cryo-EM structures of E. coli sigma(28) -dependent trans
230 Here, we
report cryo-EM structures of Thermococcus gammatolerans McrB an
231 Here we
report cryo-EM structures of TRPC6 in both antagonist-bound and
232 d camera to obtain a 1.7 angstrom
resolution cryo-EM reconstruction for a human membrane protein, the
233 ubunit and present a 3.2 angstrom
resolution cryo-EM reconstruction of the 50S-RsfS complex together
234 Here we report a ~3.9 angstrom
resolution cryo-EM structure of activated Schizosaccharomyces pombe
235 re, we describe the 3.0- angstrom
resolution cryo-EM structure of complex I from mouse heart mitochon
236 Here, we present a 3.1 angstrom
resolution cryo-EM structure of the Desulfovibrio vulgaris type I-C
237 Here, we report the 2.9 angstrom
resolution cryo-EM structure of the TEN2-LPHN3 complex, and describ
238 lar filament from a 3.5- angstrom-
resolution cryo-EM reconstruction, and show that it has 11 protofil
239 Here, we present a 3.3- angstrom-
resolution cryo-EM structure of yeast Maf1 bound to Pol III, establ
240 We developed a high-
resolution cryo-EM refinement method that divides an imaged microtu
241 We present the high-
resolution cryo-EM structure of the human processive Pol delta-DNA-
242 Here, we present high-
resolution cryo-EM structures of full-length 5-HT(3A)R in complex w
243 Furthermore, we present high-
resolution cryo-EM structures of the Leishmania tarentolae proteaso
244 methods, including TEM, AFM, high-
resolution cryo-EM, and SAXS/WAXS measurements, reveals that the sh
245 Higher-
resolution cryo-EM of filaments bound to helical bicelles confirms
246 avenue that is ready to use for large-
scale cryo-EM-based structure modeling and atomic-level densit
247 Using real and
simulated cryo-EM data, we show that FTIP could be applied in the
248 le 3 D classes that co-exist within a
single cryo-EM image dataset.
249 Using multiple recently
solved cryo-EM structures, we show that observed cross-links re
250 To address this question, we
solved cryo-EM structures of Msp1-substrate complexes at near-a
251 (TYGRESS) that is a hybrid of cryo-ET and
SP-
cryo-EM, and is able to achieve close-to-nanometer resol
252 single-particle cryo-electron microscopy (
SP-
cryo-EM) routinely reaches near-atomic resolution of iso
253 TYGRESS combines the advantages of
SP-
cryo-EM (images with good signal-to-noise ratio and cont
254 agnetic resonance (NMR) and H1 tail-
swapping cryo-EM experiments revealed that the C-terminal tails o
255 f varying chain lengths, we demonstrate
that cryo-EM can distinguish bilayer thickness differences as
256 The cryo-EM structure, combined with small-angle X-ray scatt
257 ent and visualize the protein just above
the cryo-EM grid surface.
258 14)-(mHsp10(7))(2) football complex, and
the cryo-EM structures of the ADP-bound successor mHsp60(14)
259 Here, we determine
the cryo-EM structures of DOCK2-ELMO1 alone, and as a ternar
260 We determined
the cryo-EM structure of nanodisc-reconstituted human ABCB4
261 We report here
the cryo-EM structure of a six-protein core COMPASS subcompl
262 Here,
the cryo-EM structure of PRC2 on dinucleosomes reveals how b
263 s strikingly similar to that observed in
the cryo-EM structure of the bovine CLC-K channel, though th
264 ch a substrate path was then resolved in
the cryo-EM structure of the FtsH hexamer.
265 rlying AAV Rep function, we investigated
the cryo-EM and X-ray structures of Rep68-ssDNA complexes.
266 New designs of
the cryo-EM grids-aimed at preserving thin, uniform vitrifie
267 improvement remain in various aspects of
the cryo-EM single-particle analysis workflow (e.g., sample
268 Here we present
the cryo-EM structure of a denaturant- and protease-resistan
269 Here, we present
the cryo-EM structure of a frog pannexin 1 (Panx1) channel a
270 Here we present
the cryo-EM structure of an early ancestor in the evolution
271 Here, we present
the cryo-EM structure of mouse RNF213.
272 s issue, Malik et al. (2020) (1) present
the cryo-EM structure of polymerase zeta and show how it cat
273 Here, we present
the cryo-EM structure of the full-length SNX-BAR Mvp1, which
274 Here, we present
the cryo-EM structure of the UMOD filament core at 3.5 angst
275 We present
the cryo-EM structures of Rags in complex with their lysosom
276 Here we present
the cryo-EM structures of the III(2)-IV(1) and III(2)-IV(2)
277 Here, we report
the cryo-EM and crystal structures of human STAT2 (hSTAT2) i
278 Here we report
the cryo-EM structure of CMG on forked DNA at 3.9 angstrom,
279 Here we report
the cryo-EM structure of recombinant full-length hIAPP fibri
280 Here we report
the cryo-EM structure of the Campylobacter jejuni cap comple
281 Here, we report
the cryo-EM structure of the CENP-A 601 NCP determined by Vo
282 Three recent papers report
the cryo-EM structure of the complete ASFV virion, comprisin
283 Here we report
the cryo-EM structure of the complete EC* that contains RTF1
284 Here we report
the cryo-EM structure of the human CB2-G(i) signaling comple
285 Here, we report
the cryo-EM structure of VopQ bound to the V(o) subcomplex o
286 Here, we report
the cryo-EM structures of heptameric PA channels with partia
287 Here, we report
the cryo-EM structures of human NatE and NatE/HYPK complexes
288 Here, we report
the cryo-EM structures of human ZnT8 (HsZnT8) in both outwar
289 Our approach, which can be widely applied
to cryo-EM analysis of MPs with distinctive soluble domains
290 cessing and storage of biopharmaceuticals
to cryo-EM analysis of protein complexes.
291 accurate image orientation using
traditional cryo-EM.
292 Here, we report
two cryo-EM structures of endogenously produced group II int
293 Here, we report
two cryo-EM structures of the intact V-ATPase from bovine br
294 We
used cryo-EM to investigate the nucleotide-driven reaction cy
295 Here,
using cryo-EM single particle analysis we describe the equilib
296 Here,
using cryo-EM, we determine the structures of human SERINC5 an
297 mitochondrial ribosome (mitoribosome)
using cryo-EM.
298 Immunoblotting along
with cryo-EM showed gingipain expression in W83 but not Delta
299 e complex (NPC) continues to be refined
with cryo-EM and x-ray crystallography, in vivo conformationa
300 l validation of DNA objects in solution
with cryo-EM based methodologies.