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1 the phospholipid requirements of ion channel complexes.
2 grade motor IFT dynein, and the IFT-A and -B complexes.
3 , as well as five crystal structures for JH2 complexes.
4 small ions to nanocrystals and large protein complexes.
5 ion approaches for intact proteins and their complexes.
6 assembly-disassembly cycle of neuronal SNARE complexes.
7 n remodeler family includes the BAF and PBAF complexes.
8 ic and biological functions of specific HDAC complexes.
9 rmed above -15 degrees C, they reform Gd(II) complexes.
10 ation of novel gene products and subcellular complexes.
11 at CytM does not transfer electrons to these complexes.
12 ts of the NURD and BAF chromatin remodelling complexes.
13 ntrolling the energy of the enolate-catalyst complexes.
14 hase stability of the GroEL 7-mer and 14-mer complexes.
15 xtend frustration analysis to protein-ligand complexes.
16 ting distinct modes of interactions in these complexes.
17 actions with PTIP and RIF1/shieldin effector complexes.
18 in only a 74 to 77% identity between the two complexes.
19 ild integrative structural models of protein complexes.
20 inefficient early trafficking of IL10/IL-10R complexes.
21 anticancer activity in tether and nontether complexes.
22 n fluxes from photosynthetic and respiratory complexes.
23 h conserved catalytic subunits in holoenzyme complexes.
24 allosteric signal propagation in multienzyme complexes.
25 , which govern interactions with peptide-MHC complexes.
26 v-SNARE binding to exocyst gain-of-function complexes.
27 fic cellular RNA interactions in RNA-protein complexes.
28 have a multivalent interaction with CYC/CDK complexes.
29 al dynamics of U2AF2 and its splice site RNA complexes.
30 de and form disome, trisome, or higher-order complexes.
31 step affinity enrichment of specific protein complexes.
32 ction of many different proteins and protein complexes.
33 maximise the binding affinity in host-guest complexes.
34 ed the entire suite of SARAH domain-mediated complexes.
35 re gene for type III CRISPR-Cas surveillance complexes.
36 future studies of artificial photosynthetic complexes.
37 ontal cortex in the form of structured event complexes.
38 y reaches near-atomic resolution of isolated complexes.
39 charge-transfer character of these inclusion complexes.
40 acts as a quencher for the light-harvesting complexes.
41 egulated accumulation in these foci of BRCA1 complexes.
42 e level of eIF2-GTP-Met-tRNA(i)(Met) ternary complexes.
43 modes - to be observed in typical host-guest complexes.
44 ormation of metastable [Ni(II)(C(2)H(2))(3)] complexes.
45 sitions and configurations of homeodomain TF complexes.
46 tiating complexes transition into elongation complexes.
47 fusion genes and substantially reduced gene complexes.
48 rom its site of synthesis to the respiratory complexes.
52 pectroscopy has been applied to characterize complexes 2-5, whereas DFT studies have been used to hel
53 tem involves two distinct receptor-G protein complexes, a conventional ternary complex that activates
54 tudies of single WW domain-single PPXY motif complexes abound in the literature, the molecular mechan
56 ssembly be it in proteins or in coordination complexes affords us a better understanding of the assem
58 cluding dendrimers, polyvalent metals, metal complexes, amphiphiles, and alkaloids allow tailoring pr
60 g samples causes formation of enzyme-analyte complexes and a competitive loss of available binding si
61 acitate and copper cyclooctyl iminodiacitate complexes and address whether the complexes can coordina
62 IFITM3 to assemble PIP3-dependent signalling complexes and amplify PI3K signalling for malignant tran
63 y ligands to stabilize late transition metal complexes and are conventionally considered to have litt
64 the reductive elimination reaction from gold complexes and assess their similarity to natural enzymes
65 am images with non-deformable macromolecular complexes and deformable ultrastructures under a unified
66 d ion channel and G protein-coupled receptor complexes and discuss strategies for their pharmacologic
67 eir interaction with blocking omalizumab-IgE complexes and free omalizumab levels in serum (chi(2) =
68 s the dissociation of non-productively bound complexes and inactive synaptic complexes formed by Int.
69 the interactions involved in the host/guest complexes and into the selectivity for acetylcholine ove
70 ting structures do not include CXC subfamily complexes and lack information about the receptor distal
71 many new high-resolution structures of large complexes and membrane proteins are determined regularly
72 fferences and similarities between molecular complexes and metal NPs in their reactivity toward sigma
73 des the capacity to monitor membrane protein complexes and noncovalent binding of ligands and lipids
74 decreased spontaneous premature ventricular complexes and pacing-induced ventricular arrhythmias at
75 orm for studies of large protein and protein complexes and provides a roadmap for extending the perfo
77 erences between the UBE2K-Ub and UBE2K-Ub(2) complexes and show how the UBA domain can alter the posi
78 at KHARON assembles into distinct functional complexes and that the subpellicular complex is essentia
79 the protein-ligand interactions of integrin complexes and the related structure-based drug design of
81 t DC tsMSQ properly identifies heteroprotein complexes and their stoichiometry in the NE by accountin
82 nism that reactivates backtracked elongation complexes and thus helps suppress their interference wit
83 transcription factors, nucleosome remodeling complexes, and histone modifiers to engage chromatin, th
84 ameters that define the stability of p53/DNA complexes, and provide insight into the pathways by whic
85 fine atomic-level structures of virus-glycan complexes, and study these interactions at the single-vi
86 pecific B cells by involvement of gluten-TG2 complexes, and they outline a general mechanism of autoi
88 hetic electron transport, large multiprotein complexes are connected by small diffusible electron car
91 t that silicate-bridging [AlO(2)(OH)(4)](5-) complexes are favored, stabilized by hydroxyl ligands an
92 ligand (MG) exclusively when RNA-RNA kissing complexes are formed, whereas MG does not bind to malasw
95 ures of small organometallic or coordination complexes are often extremely well-defined, with errors
97 inactive state associate with G(s), as these complexes are stabilized by inverse agonists and recepto
98 rtained that five coordinate amide iodine(V) complexes are unreactive toward redox reactions due to t
99 lic cations at alkaline pH, Fe(III)-mimosine complexes are water soluble at alkaline pH, and that mim
100 ubstituted ethynylphosphonates required gold complexes as catalysts to provide the corresponding 2-ar
101 perspectives and significance of using metal complexes as ER stress-inducing agents for the treatment
107 en SWI/SNF chromatin remodeling multiprotein complexes BAF (BRG1/BRM-associated factor) and PBAF (pol
109 hysiology and DFT studies also show that the complexes block the G34E amantadine-resistant mutant des
110 color (DC) tsMSQ to analyze NE heteroprotein complexes built from proteins that carry two spectrally
111 ound in several other electron transfer (ET) complexes, but how this architecture influences activity
112 d the biochemical properties of purified FCP complexes, but limited knowledge is available about thei
113 ticulum (ER) are assembled into multiprotein complexes, but little is known about the mechanisms requ
114 ticals, agrochemicals, and ligands for metal complexes, but strategies to selectively halogenate pyri
116 Cell-specific recruitment of co-regulatory complexes by liganded VDR leads to changes in gene expre
117 y circulating high-density lipoprotein (HDL) complexes called trypanosome lytic factors (TLFs) 1 and
118 odiacitate complexes and address whether the complexes can coordinate with one or more of the His37 i
119 ossibility is that the intermediate alkyl-Pd complexes can undergo a "chain-walking" event, to allow
122 ral basis for active single- and double-ring complexes coexisting in the mHsp60-mHsp10 chaperonin rea
123 itro after activation with zymosan or immune complexes, compared with wild-type (WT) neutrophils.
124 nation mass spectrometry, we recovered known complexes, confirmed complexes predicted to occur in pla
130 ls includes modeling and analysis of protein complexes, delineation of interfaces and the modeling of
131 ial to visualize these molecular-interaction complexes directly within the cell, to show precisely wh
135 beta-1,4-glucan synthase that forms protein complexes displaying similar ultrastructural features to
136 identity and purity of proteins and protein complexes during and after protein purification to ensur
140 ed assembly and disassembly of motor-adaptor complexes ensures that cargoes are loaded at their origi
141 ics of paramagnetic transition metal hydride complexes, especially of the abundant 3d metals, is impo
144 ndensations have produced multinuclear metal complexes exhibiting the shape of tetrahedral containers
145 the extreme disorder in such polyelectrolyte complexes facilitates (i) diffusion-limited binding, (ii
146 y polymerization of molecular Ru(2) [II,III] complexes, featuring unprotected carboxylic acid substit
148 d that the regulatory subunits of these AHAS complexes form a core to which the catalytic subunit dim
154 ew paradigms for how the components of these complexes function, both independently and in concert.
155 (17) O NMR studies suggest that none of the complexes has a single, integral inner-sphere water that
159 raditionally, noble metal particles or metal complexes have been used as catalysts for many reactions
162 that the arrangement of the light-harvesting complexes I (LHCIs) differs substantially in different o
163 erium exchange mass spectrometry (HDX-MS) of complexes I and II on membranes elucidated structural de
164 ncoded subunits in oxidative phosphorylation complexes I and V increased in CLPP2 knockouts, without
167 to obtain atomic models of multiple protein complexes implicated in intraerythrocytic survival of th
168 trinsic flexibility of LHCII pigment-protein complexes in a membrane environment, revealing putative
169 omplicated mixtures of proteoforms and their complexes in both denatured and native modes of operatio
171 of the mobility of individual photosynthetic complexes in grana membranes establishes a foundation th
172 sense RNA viruses assemble their replication complexes in infected cells from a multidomain replicati
173 he conformational dynamics of SNARE/Munc18-1 complexes in multiple intermediate steps towards the SNA
178 increased the amount of alpha2delta-1-GluN1 complexes in the spinal cord and the level of alpha2delt
179 These data point to a role for mSWI/SNF complexes in therapy-related lineage plasticity, which m
180 ion of allergen together with IL-2/alphaIL-2 complexes induced expression of Treg marker molecules CT
181 ellular functions, but how the multi-subunit complexes influence deacetylase activities and site-sele
183 ould be adapted to study the dynamics of the complexes inside intact and photosynthetically functiona
185 capable of preserving biologically relevant complexes into the gas phase as multiply charged ions su
186 have seen an impressive development of iron complexes involving organophosphorus ligands applied in
189 to the exclusive formation of the bis(imido) complexes [((ket)guan)Co(mu-NH)](2) (6) and [((ket)guan)
193 ct with crypt in THF to form the THF-soluble complexes [Ln(III) (crypt)(OTf)(2) ][OTf] with two trifl
194 ally dispersed rhodium in rhodium diethylene complexes, made by the reaction of Rh(eta(2)-C(2)H(4))(2
195 We demonstrate a dynamic equilibrium between complexes, monolayers, and nanocrystals of lead bromide,
199 ethod is shown by synthesizing several metal complexes of 2-(benzo[d]thiazol-2-yl)phenol that can be
203 report the synthesis of PAlP and PBP pincer complexes of Rh with a central bis(N-pyrrolyl)aluminyl o
204 ss A penicillin-binding proteins (aPBPs) and complexes of SEDS proteins and class B PBPs (bPBPs).
205 U2-type or the U12-type spliceosomes, large complexes of small nuclear ribonucleoprotein particles a
206 bility derives from the formation of ternary complexes of the initiator with the single- and double-s
208 s pathway leads to accumulation of SAF-A-RNA complexes on mitotic chromosomes, defects in metaphase c
211 nt of end-to-end-linked troponin-tropomyosin complexes over the thin filament surface, which uncovers
212 ombined, these data indicate that IgG immune complexes potentiate inflammation by human microglia, wh
213 try, we recovered known complexes, confirmed complexes predicted to occur in plants, and identified p
215 of a class of high-spin macrocyclic Fe(III) complexes produces more intense contrast in mice kidneys
216 kinetic studies of a series of new ruthenium complexes provide a platform for understanding how stron
218 ta indicate that often occurring TRP channel complexes regulate diversity in neuronal sensitization a
219 conserved transport protein particle (TRAPP) complexes regulate key trafficking events and are requir
220 the SWI/SNF family of chromatin remodelling complexes - regulate gene expression and developmental p
225 ween the C. gattii and C. neoformans species complexes resulted in only a 74 to 77% identity between
226 The extent to which noncovalent protein complexes retain native structure in the gas phase is hi
227 ent structures of family B GPCR-G(s) protein complexes reveal a disruption in the alpha-helix of tran
228 subunit of the SWI/SNF chromatin-remodeling complexes, serves an indispensable role in cold-induced
230 reveals that the moisture content of CD/CNO complexes significantly decreased, compared to starting
232 n the lung tissue alleviates LPS-/IgG immune complexes-stimulated acute pulmonary damage through redu
233 ries on the native structures of the protein complexes streptavidin, concanavalin A, and C-reactive p
234 decomposition of mCPBA in the presence of Ni complexes suggest that the reaction occurs through free
236 the assembly of integrin-associated adhesome complexes that activate pathways that catalyse actin pol
238 es comprise specialized nucleic acid-protein complexes that help protect chromosome ends from DNA dam
240 s of mRNA genes to form large macromolecular complexes that initiate transcription in a regulated man
241 cription have identified specific, canonical complexes that may promote RNAPII-transcription at these
243 anes scaffold an assortment of large protein complexes that work together to harness the energy of li
244 metal-containing photoactivatable compounds (complexes) that absorb in the visible- and NIR-range to
246 into two functionally distinct nucleoprotein complexes; the maturation complex and the packaging moto
247 view of the structure and function of OXPHOS complexes, their biological functions in cancer, relevan
248 diates, and not kinetically stabilized model complexes, these experiments provide the opportunity to
249 r path to the next generation of two-step VT complexes through incorporation of mixed-valence class I
252 HDACs are commonly found in various protein complexes to confer distinct cellular functions, but how
253 own to wrap DNA must form higher protein-DNA complexes to efficiently work as topological barriers.
254 utoinhibited to allow local regulation, form complexes to jointly coordinate their networks and provi
257 at poly(ADP-ribose) polymerase 1 (PARP1)-DNA complexes trapped by PARP inhibitors, thereby promoting
258 state of existing Env constructs and ligand complexes used for high-resolution structures recently r
260 macromolecules, including proteins and their complexes, very often adopt multiple conformations.
262 mble numerous membrane-bound viral replicase complexes (VRCs) with the help of viral replication prot
267 y comparing crystal structures of paralogous complexes, we provide a rationale for our observations.
268 ize the biological activity of these gold(I) complexes, we used a series of time-kill studies, cytoto
270 8]) hosts in water; resulting supramolecular complexes were characterized by NMR, ESI-MS, UV-vis, ITC
274 the TTFL proteins behave individually and in complexes: whether particular SCN neuronal populations a
276 ns were carried out on the substrate-Fe(III) complexes, which shed light on diastereoselective reduct
277 is indicated a molar ratio of peptide-copper complexes, while a combination of bioinformatics-based s
278 enerating a series of isoskeletal host-guest complexes whose properties can be directly compared.
279 res of 5' and 3' exonuclease oligonucleotide complexes with 5'-(R)- and 5'-(S)-C-methyl substituents
280 ted K(+) channels function in macromolecular complexes with accessory subunits to regulate brain func
281 nergy transfer (BRET), HO-1 formed HO-1*P450 complexes with CYP1A2, CYP1A1, and CYP2D6, but not all P
283 earing takes place in all six dirhodium-gear complexes with different axial ligands and that rotation
284 We also observed plant analogs of animal complexes with distinct molecular assemblies, including
286 MRP are highly conserved, multi-protein/RNA complexes with essential roles in processing ribosomal a
289 at it efficiently crosslinks noncovalent RNA complexes with mimimal sequence bias and establish that
290 talk, and eight structures of its functional complexes with mt-mRNA, mt-tRNAs, recycling factor and a
293 e of the catalytic domain of human MANEA and complexes with substrate-derived inhibitors, which provi
294 esponse to damage, Gal9 displaces USP9X from complexes with TAK1 and promotes K63 ubiquitination of T
295 by the same mechanism: forming RSPO-bridged complexes with the E3 ligases RNF43 and ZNRF3 to inhibit
296 2) macrocycles form square-planar nickel(II) complexes with the R(P)S(P)S(P)R(P) isomer only, in whic
297 RNA virus IBs are important immunomodulatory complexes within infected cells.IMPORTANCE Many viruses