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1 o 13-fold, indicating that different SUR can coassemble.
2  associated in distinct complexes and do not coassemble.
3 essed with sigma3, with which it is known to coassemble.
4 te that HIV-1 and HIV-2 Gag can interact and coassemble.
5 t with conventional actin and found it could coassemble.
6 ent isotypes within the Kv1 or Kv3 subfamily coassemble.
7 resulting segregated beta-sheets can further coassemble.
8 we show that TREK1, TREK2, and TRAAK readily coassemble.
9 amer-forming peptides and determine how they coassemble.
10 gly suggested that alpha7 and beta2 subunits coassemble.
11 n, the amorphous imine polymer and F127 form coassembled 3D-printable hydrogels with suitable shear t
12                                Being able to coassemble a large dataset does not preclude one from mu
13              The hybrid JVs were produced by coassembling a mixture of hydrophobic MNPs, free amphiph
14  shown that the alpha 2 and gamma 1 subunits coassemble and are incorporated into GABAA receptors whi
15 us expression systems, these subunits avidly coassemble and exhibit biophysical and pharmacological p
16           Four alpha-subunits are thought to coassemble and form a voltage-dependent potassium (Kv) c
17 te that HIV-1 and HIV-2 Gag polyproteins can coassemble and functionally complement each other during
18 eficiency virus type 1 (HIV-1) and HIV-2 can coassemble and functionally complement each other.
19 ned whether HIV-1 and HIV-2 Gag proteins can coassemble and functionally complement each other.
20 tion velocity that the ATDs of GluR6 and KA2 coassemble as a heterodimer of K(d) 11 nM, 32,000-fold l
21 ombinations of two or more DEG/ENaC subunits coassemble as heteromultimers to generate transient H(+)
22 on it is likely that different TRPC subunits coassemble as heterotetrameric structures to form smooth
23 terminal residue, phosphotyrosine vs lysine, coassemble as stacks of antiparallel beta-sheets with pr
24 er these data argue that UNC-49B and UNC-49C coassemble at the C. elegans neuromuscular junction.
25 pressed septins (Spn1, Spn2, Spn3, and Spn4) coassemble at the fusion site and are necessary for its
26 ies of terabyte datasets that could never be coassembled before, demonstrating MetaHipMer's scaling p
27 rel oligomers are also suggested to occur in coassembled beta-strand peptide systems.
28  predict that CATCH(+) and CATCH(-) peptides coassemble but do not self-assemble.
29                                     However, coassembled capsids are more fragile, with disassembly o
30 ng lipopolysaccharide release that activated coassembled caspase-4.
31  arrangements of beta-strands predominate in coassembled CATCH structures, but deviations from perfec
32 d thereby confer functional sensitivity upon coassembled channel subunits that are themselves not bou
33 tivated potassium channels (SK channels) are coassembled complexes of pore-forming SK alpha subunits
34                                           By coassembling dilysine (+2) and carboxylate (-1) amphiphi
35                     UNC-49B and UNC-49C also coassemble efficiently in Xenopus oocytes and HEK-293 ce
36 However, FtsZ1 increased FtsZ2 exchange into coassembled filaments.
37 nally, the polyglutamine amyloid fibrils are coassembled from differently structured monomers, which
38   Synthetic vesicles have been assembled and coassembled from phospholipids, their modified versions,
39 o export from the endoplasmic reticulum (ER) coassembled from purified cargo adaptor Sec23-24 and Sec
40 genomes (SAGs) from a single human donor and coassembling genomes of almost 100 bacterial species, in
41 ls explaining why certain subunits prefer to coassemble has been lacking in our understanding of glut
42  ribosomal RNA and ribosomal proteins, which coassemble hierarchically during a process termed riboso
43 tubulin-like proteins BtubA and BtubB, which coassemble in a strict 1:1 stoichiometry.
44 aggregate in kinetic simulations selectively coassemble in biophysical experiments, with four forming
45 e homodimer subunits, but the two homodimers coassemble in forming the heterotetramer.
46 5 freely exchange between dimers but fail to coassemble in vitro with dodecameric plant cytosolic sHS
47 forming cationic semiconducting polymers can coassemble in water with cationic fullerene derivatives
48 s suggest that Cx43alpha1 and N-cadherin are coassembled in a multiprotein complex containing various
49 ments established that the two subunits were coassembled in the cerebellum along with the beta2 subun
50             Relative to wild type, filaments coassembled in vitro from purified K5-1649delG and K14 p
51 nd graphene oxide sheets can be conveniently coassembled in water to yield a stable colloidal dispers
52 h chemically distinct monomers spontaneously coassemble into a dynamic, functional structure.
53 n pearl cells, the delta and sigma3 subunits coassemble into a heterodimer, whereas mu3 gets destroye
54   In mocha cells, the beta3 and mu3 subunits coassemble into a heterodimer, whereas the sigma3 subuni
55 st seven distinct beta-tubulin isotypes that coassemble into all cellular microtubules.
56 ulin isotypes are freely interchangeable and coassemble into all classes of microtubules.
57 ode two CPs (P2 and P4, respectively), which coassemble into approximately 450-A-diameter capsids.
58 arge-complementary peptides that selectively coassemble into B-sheet nanofibers when mixed together b
59  cytosol in which proteins and nucleic acids coassemble into compartments.
60 e an intrinsic capacity of RNP components to coassemble into either large semiliquids or solid lattic
61 that overexpressed Drosophila Sas-6 and Ana2 coassemble into extended tubules (SAStubules) that bear
62 osed of all-l and all-d peptides, but rather coassemble into fibrils that contain alternating L- and
63                When mixed, 3R tau and 4R tau coassemble into heterogeneous filaments.
64                  We show that NM II isoforms coassemble into heterotypic filaments in a variety of se
65  conditions, smitin and smooth muscle myosin coassemble into irregular aggregates containing large si
66        Therefore, different SUR subtypes can coassemble into K(ATP) channels with distinct metabolic
67           On stimulation, Dyn2 and cortactin coassemble into large, circular structures on the dorsal
68         In vitro, MinC and MinD are known to coassemble into linear polymers; therefore, we monitored
69 r CA proteins from two different viruses can coassemble into mature cores of infectious viruses, we e
70 isotypes of alpha- and beta-tubulin that can coassemble into MTs.
71                             The proteins can coassemble into particles together with full-length, wil
72  (v) the UL26.5 and UL80.5 proteins will not coassemble into scaffold structures.
73       All dendritic dipeptides were shown to coassemble into single columns regardless of their stere
74 d cationic amphiphiles of unequal charge can coassemble into small buckled vesicles and present a phy
75              Ribonucleoproteins (RNPs) often coassemble into supramolecular bodies with regulated dyn
76 nvestigate how GluN1 and GluN2 type subunits coassemble into tetramers.
77                  However, if hCA and sCA can coassemble into the same core structure to form a mixed
78                        If hCA and sCA cannot coassemble into the same core when equal amounts of sCA
79    Our results indicate that hCA and sCA can coassemble into the same mature core to produce infectio
80 e this, HIV-1 and HIV-2 Gag polyproteins can coassemble into the same particle and their genomes can
81 amily of six alpha-chains (alpha1 to alpha6) coassemble into three distinct protomers that form supra
82       Meanwhile, NR1, NR2, and NR3 appear to coassemble into triheteromeric receptors in neurons, but
83 enin, and beta-catenin, but not plakoglobin, coassemble into Triton X-100 insoluble (TX-insoluble) st
84 troscopy indicate that CATCH(+) and CATCH(-) coassemble into two-component nanofibers instead of self
85 Finally, we show that ESCRT-II and ESCRT-III coassemble into ~65 nm diameter rings indicative of a ca
86     The colloidal nanodisks and nanorods are coassembled into AB-, AB2-, and AB6-type binary arrays d
87  blocks and functional coronal segments were coassembled into low-dispersity, one-dimensional archite
88                                     beta3 is coassembled into microtubules with beta1, the sole beta-
89 o P22 assembly assay where portal protein is coassembled into procapsid-like particles (PLPs).
90 n CE cell nuclei, ferritin and ferritoid are coassembled into stable complex(es) present in embryonic
91 egulated cytoskeleton-associated protein are coassembled into the same RNA granules and targeted to d
92 cated that adherens junction components were coassembled into these structures along with desmosomal
93  and chimeric CP-TMOF (20:1 ratio) that were coassembled into virus particles in infected Nicotiana t
94                              Peripherin also coassembles into a single network of filaments containin
95 dent increases in cell surface expression of coassembled Kv1.1 and Kv1.2, while coassembly with Kv1.1
96 ed shape, morphology, and surface pattern by coassembling MAMs of block copolymers (BCPs) and NPAMs c
97                      In vivo, CARM1 and BRG1 coassemble on an estrogen receptor (ER)-target gene to c
98                                   HIF and GR coassembled on the BRK promoter in response to either hy
99 faceted polyhedra with diverse symmetries by coassembling oppositely charged molecules of different s
100 nts self-assembles, the molecules can either coassemble, or self-sort, where a preference for like-li
101 c engineering of M13 viruses can allow us to coassemble other functional materials (e.g., catalysts a
102 lls identified a class of genes that rapidly coassemble p300 and RNA polymerase II (pol II) following
103 te NMR, which is applied to characterize the coassembling pairs, suggests that the in silico peptides
104 rotein under optical control provided by the coassembled PCS.
105  an optoelectronic cardiac biomaterial where coassembled peptide nanostructures are molecularly desig
106 PepCAD) algorithm that searches for pairs of coassembling peptides.
107 zero to two or even up to four KCNE subunits coassembling per KCNQ1 tetramer.
108                                              Coassembling polyhedral and spherical NPs with complemen
109 lar chirality to a preferred helicity of the coassembled polymers.
110 in which crystalline lamellae made up of the coassembled proteorhodopsin and charged lipid molecules
111                                              Coassembled SeFtsZ-AtFtsZ2 protofilaments began disassem
112 or inhomogeneous shells, we demonstrate that coassembled shells with two elastic components buckle in
113                     The FtsZ1:FtsZ2 ratio in coassembled structures mirrors their input ratio, sugges
114 ones containing a free C-terminus results in coassembled structures, as demonstrated by circular dich
115 act cell irrespective of the identity of the coassembled SUR subunit.
116                              (ii) L(i) could coassemble the unmodified L and the small delta protein,
117  poor monomers are prepared that kinetically coassemble through a temperature-controlled protocol int
118                          E4-ORF3 dimer units coassemble through reciprocal and nonreciprocal exchange
119 Multiple copies of the six proteins involved coassemble to form a 34-40S ring-like "MGM" holocomplex
120 wo bifunctional protein building blocks that coassemble to form a bioelectrocatalytic hydrogel that c
121 ransmembrane proteins in which five subunits coassemble to form a central ion channel pore.
122          Mixtures of the two building blocks coassemble to form a continuous supramolecular hydrogel
123  and KCNQ3 ion channel pore-forming subunits coassemble to form a heteromeric voltage-gated potassium
124 are coordinately rescued and therefore might coassemble to form a heteromultimeric GABA receptor.
125 n some auditory neurons, Kv3.1 and Kv3.3 may coassemble to form functional channels.
126 indicating that WT TRESK and TREK-2 subunits coassemble to form functional heterodimeric channels als
127 nown to encode K(+) channel monomers and can coassemble to form hetero-tetrameric K(+) channels.
128 l data imply that different HCN isoforms may coassemble to form heteromeric channel complexes, but li
129 have now found that Slick and Slack subunits coassemble to form heteromeric channels that differ from
130 ucts reveals that the family of polypeptides coassemble to form heteromeric IMPDH complexes, suggesti
131       We conclude that Shaker and eag do not coassemble to form heteromultimers in Xenopus oocytes.
132 HCN channels, and that HCN1 and HCN2 readily coassemble to form heterotetrameric complexes.
133 r Cx isoforms found in the cochlea, and they coassemble to form hybrid (heteromeric and heterotypic)
134 hy reveals that the enantiomeric macrocycles coassemble to form racemic fibril-like assemblies of unp
135 A) receptor alpha4 and delta subunits, which coassemble to form receptors mediating tonic inhibition,
136 e limiting components of gamma-secretase and coassemble to form the active enzyme in mammalian cells.
137 tural proteins, L1 and L2, can spontaneously coassemble to form virus-like particles, currently avail
138  the alpha4, beta2, and alpha5 gene products coassemble to produce epibatidine-binding receptors.
139 of the KCNQ channel family, KCNQ2 and KCNQ3, coassemble to underlie the M current in the nervous syst
140 nition using aptamers and peptide substrates coassembled to a central semiconductor quantum dot (QD).
141 n contain terabytes of reads, too many to be coassembled together on a single shared-memory computer;
142  native subunits, the native subunit and PCS coassemble, traffic to the plasma membrane, and place th
143                              alpha5 subunits coassembled very efficiently with alpha3beta2 or alpha3b
144 ed whether ASCs would cooperate with EPCs to coassemble vessels in in vivo implants.
145 dylanthracene and meta-N-dipyridylanthracene coassemble with 1,2,4,5-tetracyanobenzene (TCNB) into co
146   This is the first evidence that Aalpha can coassemble with Abeta and alter its biological effects a
147                 Beta subunits are thought to coassemble with alpha subunits in a 1:1 stoichiometry, s
148  that although the auxiliary subunits do not coassemble with alpha(1) and aid trafficking, they are r
149 ed, indicating that Cav1.3 channels normally coassemble with alpha2delta2 at IHC presynapses.
150  defective in GTP binding and hydrolysis can coassemble with and stimulate GTP hydrolysis by wild-typ
151            We considered that K(V)LQT1 might coassemble with another subunit to form functional chann
152           Voltage-gated calcium channels can coassemble with auxiliary subunit alpha2delta isoforms 1
153 a7 subunits are coexpressed, colocalize, and coassemble with beta2 subunit(s).
154  amounts of partially processed Gag subunits coassemble with CA during virion maturation, resulting i
155 ment of Cav2 channels in the brain, directly coassemble with Cav2.2 channels upon heterologous coexpr
156 ith age in monkey prefrontal cortex, and can coassemble with delta subunits to form functional GABA(A
157                    Although Kir6.1 or Kir6.2 coassemble with different SUR isoforms to form heteromul
158 heir role in Drp1 membrane recruitment, MiDs coassemble with Drp1 in vitro.
159 foci at mitochondrial constriction sites and coassemble with Drp1 to drive fission.
160 s, it is not known whether Kir6.1 and Kir6.2 coassemble with each other.
161 ests to determine whether these subunits can coassemble with each other.
162 ysiological evidence that the pi subunit can coassemble with either alpha5beta3 or alpha5beta3gamma3
163 sly introduced into hippocampal neurons, can coassemble with endogenous NR1 and NR2A and can reduce t
164 , in which four channel-tethered RCK domains coassemble with four soluble (untethered) RCK domains.
165                              These filaments coassemble with FtsZ polymers but are destabilized by un
166 ays reduced binding to Gbetagamma and cannot coassemble with GIRK1.
167  mossy fiber synapses where they most likely coassemble with GluR6 subunits to form functional hetero
168  Gag proteins of endogenous retroviruses can coassemble with HIV-1 Gag and modulate the late phase of
169    Furthermore, HERV-K(CON) Gag was found to coassemble with HIV-1 Gag, as demonstrated by (i) proces
170    Multiple K(+) channel alpha-subunits that coassemble with Hk, including Shaker, Ether-a-go-go, and
171 g template, Pluronic F127, was introduced to coassemble with imine polymers in an aqueous environment
172 norganic-containing molecular additives that coassemble with ionomer, enabling pure water-fed AEMWEs
173  to therapeutically target ion channels that coassemble with KCNE beta-subunits.
174                         KCNQ1 alpha-subunits coassemble with KCNE1 beta-subunits to form channels tha
175 eart, KCNQ1 voltage-gated potassium channels coassemble with KCNE1 beta-subunits to generate the IKs
176 nificantly, we show that Kir2.6 subunits can coassemble with Kir2.1 and Kir2.2 in vitro and in vivo.
177 either Kvbeta1.2 or Kvbeta1.3, both of which coassemble with Kv1.5 and induce fast inactivation.
178 ted double-ring structures that bind ATP and coassemble with LIP5/Vta1.
179 isoform does not by itself form OAPs but can coassemble with M23 in OAPs as heterotetramers.
180                                        IAJDs coassemble with mRNA into predictable-size vesicles, nam
181 ypical rapid desensitization, and they could coassemble with native P2X2 subunits in pheochromocytoma
182           Neto1 and Neto2 auxiliary subunits coassemble with NMDA receptors (NMDARs) and kainate rece
183 and the need for the synthesized proteins to coassemble with nuclear-encoded subunits have had substa
184 PARs) is observed when pore-forming subunits coassemble with or without auxiliary subunits, respectiv
185 ked inactivation, suggesting that Kv3.1b may coassemble with other members of the Kv3 subfamily.
186 that NF180 could not self-assemble but could coassemble with rat NFL, suggesting the existence of add
187 ased amphiphiles at increased concentrations coassemble with RGG-RGG into multiphasic structures.
188 py and microscopy, we found that surfactants coassemble with the supramolecular polymers to change fi
189                       However, Cp-Y132A will coassemble with the wild-type protein on the basis of li
190 ostsynaptic density, however, AMPA receptors coassemble with transmembrane AMPA receptor regulatory p
191  in Xenopus laevis oocytes, two NR3 subunits coassemble with two NR1 subunits to form a glycine-gated
192 UNC-2 in the ER, indicating that they do not coassemble with UNC-2 in the ER.
193 two-hybrid assay, since these same molecules coassemble with wild-type Gag into Ty1 virus-like partic
194 gnated dominant negative (DN), were found to coassemble with wild-type PA and generate defective hept
195 suggested a mechanism by which the fragments coassembled with Abeta42 to form heterooligomers.
196               The hybrid RHF Janus dendrimer coassembled with both RF and RH.
197 ctenophore Shaker subfamily channel subunits coassembled with cnidarian and mouse Shaker subunits, bu
198                         The chimeric GFP-NFH coassembled with endogenous neurofilaments.
199                                         When coassembled with FtsZ on lipid monolayers, these FtsA mi
200 tors require two copies of the GluN1 subunit coassembled with GluN2 (and/or GluN3) subunits into a he
201  domain adopts a more open conformation when coassembled with GluN2A than with GluN2B.
202                      Phospholipids were also coassembled with hybrid RHF Janus dendrimers.
203                                         When coassembled with kainate receptors, NETO proteins are kn
204 ng associated with channel inactivation when coassembled with KvLQT1.
205 rehybridized with a thiolated short DNA) was coassembled with mercaptohexanol onto the gold surface o
206                                    MIIA(F46) coassembled with MIIB(alpha)(F47)-wt and -CK-5D and alte
207 A virus, referred to as a virophage, that is coassembled with Mimivirus in the host amoeba.
208 e demonstrate that droplets of poly-arginine coassembled with mono/polynucleotides have approximately
209 -phenylene tetramer has been synthesized and coassembled with monotopic and ditopic, achiral and chir
210 celerated modular-orthogonal methodology and coassembled with mRNA into dendrimersome nanoparticles (
211 nst a 70-kDa human ELP and showed that ELP70 coassembled with MTs in HeLa cell extracts and colocaliz
212 ecific and isoform-redundant functions while coassembled with other NM II isoforms.
213 he QD was used as a central nanoplatform and coassembled with peptides or oligonucleotides that were
214 AtFtsZ1 did not alter disassembly onset when coassembled with SeFtsZ, but fluorescence recovery after
215 nvelope proteins (E1 or E2) were efficiently coassembled with the wild-type HBV S protein into subvir
216 eas irreversible binding results when tau is coassembled with tubulin into a tau-microtubule copolyme
217 ortant aspects of effector secretion: (i) It coassembles with a second regulator (Pcr1) on the inner
218                        Alpha-internexin also coassembles with all three neurofilament proteins into a
219              We conclude that the pi subunit coassembles with alpha, beta, and gamma subunits to form
220        Within the rat striatum, this subunit coassembles with alpha2, beta1, and gamma1, suggesting t
221 CN1b, an integral subunit of Na(V) channels, coassembles with and modulates the biophysical propertie
222 rotrimer, [alpha1(V)]2alpha2(V), and it both coassembles with and regulates type I collagen-fibril di
223                                          DCX coassembles with brain microtubules, and recombinant DCX
224 raphy experiments demonstrated that Caskin 1 coassembles with CASK on the immobilized cytoplasmic tai
225  LEM2 condenses into a liquid-like phase and coassembles with CHMP7 to form a macromolecular O-ring s
226 y that beta-filagenin is a core protein that coassembles with either myosin or paramyosin in C. elega
227 ich synthesize Pol as a Gag-Pol protein that coassembles with Gag.
228                                  GluClalpha2 coassembles with GluClbeta to form heteromeric channels
229 KCNE1 encoding a transmembrane protein which coassembles with K+ channels mediating slow K+, I(Ks), c
230 s from the colon, stomach, and kidney, KCNE3 coassembles with KCNQ1 to form K(+) channels that are vo
231 t that a splice variant of the Kv3.4 subunit coassembles with Kv3.1 subunits in rat brain FS neurons.
232            In cocultures, alpha4(V) collagen coassembles with laminin on the surface of polarized Sch
233                                       Merg1b coassembles with Merg1a to form channels with deactivati
234      Therefore, K(V)LQT1 is the subunit that coassembles with minK to form I(Ks) channels and I(Ks) d
235 e-cell imaging data argue strongly that M18A coassembles with NM2 into mixed bipolar filaments.
236                       Here we show that NR3A coassembles with NR1-1a and NR2A to form a receptor comp
237 ed rectifier K+ channel Kv1.1 (Kv1.1N206Tag) coassembles with other K+ channels of the Kv1 subfamily
238 quitously expressed cytoplasmic protein that coassembles with pallidin and the muted protein in the B
239     In the colon, stomach, and kidney, KCNE3 coassembles with the alpha-subunit KCNQ1 to form K(+) ch
240                  The KCNE1 auxiliary subunit coassembles with the Kv7.1 channel and modulates its pro
241  heart, has rapid deactivation kinetics, and coassembles with the longer isoform in Xenopus oocytes.
242                                     When tau coassembles with tubulin to form unstable microtubules,
243 he intermediate filament (IF) protein nestin coassembles with vimentin and promotes the disassembly o
244 s a single-transmembrane domain protein that coassembles with voltage-gated K+ channel KVS-1 in the n
245         When expressed in trans, TubZ(D269A) coassembles with wild-type TubZ and significantly reduce
246  functionally distinct potassium channels by coassembling with KCNE ancillary subunits MinK and MiRP2
247  can also form slower activating channels by coassembling with MinK-related peptide 2 (MiRP2), a sing
248 elical states, two of which are triggered by coassembling with monomeric water that is codissolved in
249  in division by specifically interacting and coassembling with the guanosine triphosphate-bound form
250 beta2 subunits confirmed that these subunits coassemble within functional receptors.

 
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