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1 degrade specific protein pools depending on assembly state.
2 -GlcNAc sites and show that they regulate NF assembly state.
3 idual pigment sites as a function of protein assembly state.
4 ertoire of Lon substrates to be tuned by its assembly state.
5 latory mechanisms in controlling kinetochore assembly state.
6 ative electrophoresis (BNE) to study GluA1-3 assembly state.
7 eptors shows a strong dependence on the TMVP assembly state.
8 f NMIIB to mechanorespond by influencing its assembly state.
9 the coupling of molecular interactions with assembly state.
10 ciliogenesis, tubulin synthesis, and tubulin assembly state.
11 d structures but lacks temporal control over assembly state.
12 ein refolding activities enabled by distinct assembly states.
13 substrate that likely represent intermediate assembly states.
14 basis of aggregation of Abeta into distinct assembly states.
15 neurodegenerative diseases exist in diverse assembly states.
16 does not induce the formation of additional assembly states.
17 pping thousands of phosphopeptides and their assembly states.
18 or simultaneous characterization of PTMs and assembly states.
23 iate filaments (IF) is known to affect their assembly state and organization; however, little is know
24 ely freely through a large space of possible assembly states and demonstrates the power of characteri
25 tionships between phosphorylation events and assembly states and generates testable hypotheses for fo
26 a systematic method to simultaneously study assembly states and PTMs from the same sample is critica
27 ng the transition from dimeric to tetrameric assembly states and, second, at a postassembly trafficki
28 exhibited purification behavior, CD spectra, assembly state, and inducer binding properties similar t
29 examined the equilibrium folding properties, assembly states, and stabilities of the early folding st
30 valence of intermediate and large oligomeric assembly states are associated with both ageing and Alzh
32 sitions through different conformational and assembly states as it matures into a functional helicase
33 gulation is morphogenetically coupled to the assembly state by control of the anti-sigma factor FlgM.
34 tamer is a physiological, stable, and active assembly state capable of forming lethal toxins that may
36 abeled MNP monitored non-invasively based on assembly state-dependent changes in the emission spectru
37 ors that arrest SNARE complexes in different assembly states differentially modulate a-syn(FL)'s abil
38 ch represent the features of an intermediate assembly state during maturation, the SP1 peptide exists
42 ons was performed to compare the microtubule assembly state in neurons of diseased and control cases
45 rototypical SPI-1 NC in four distinct needle assembly states, including near-atomic resolution, and l
46 onassociating species or as a combination of assembly states independent of protein concentration.
47 osterically regulated by the transmission of assembly-state information from the C-terminal domain, w
48 strate that multiple inputs to the myosin II assembly state integrate at the level of myosin II to go
49 iological alpha-syn conformers into compact, assembly-state intermediates by glucosylceramide (GluCer
51 ore dynamic than previously reported and its assembly state is sensitive to stimuli that alter cellul
52 ly, the relative population of the different assembly states is determined via a Bayesian-based Monte
53 st, a basis set comprising a small number of assembly states is generated from extensive CG simulatio
54 s in terms of their sizes, interactions, and assembly states is key to understanding their biological
55 We demonstrate wide tunability of transient assembly state lifetimes over two orders of magnitude by
56 ows that resistin circulates in two distinct assembly states, likely corresponding to hexamers and tr
62 cate that, in addition to lipid content, the assembly state of apoE influences Abeta binding and rece
63 t studies have shown that the lipidation and assembly state of apolipoprotein E (apoE) determine rece
64 otide analogues, we have also correlated the assembly state of ClpA in the presence of these nucleoti
65 lytical ultracentrifugation to determine the assembly state of CVX in solution and surface plasmon re
67 es of these mice showed, besides an abnormal assembly state of endocytic factors at synapses, the pre
69 r spatiotemporal expression and the physical assembly state of fibronectin (FN) matrix play key roles
72 nction as a dynamic, polymerized GTPase, the assembly state of its partner, FtsA, and the role of ATP
73 larity of migrating cells by controlling the assembly state of NMII-A, its cellular localization, and
74 en together, these data demonstrate that the assembly state of peroxisomal proteins and the chaperone
77 self and foreign epitopes regardless of the assembly state of the antigen, suggesting that conjugati
81 ochemical studies conflict on the oligomeric assembly state of the protease complex, and its detailed
83 ontrol cardiolipin metabolism and affect the assembly state of TIM23 and its association with PAM in
85 mine the effects of nestin expression on the assembly state of vimentin IFs in nestin-free cells.
90 heir GTP- and GDP-bound states, intermediate assembly states of GTP-tubulin, and final assembly stage
91 simulations is developed to characterize the assembly states of Hck, a member of the Src-family kinas
92 spectrometry experiments characterizing the assembly states of intact NtrC4 (a sigma(54) activator f
94 rogress has been achieved in quantifying the assembly states of NE proteins in their native environme
95 how that smMDS is effective in resolving the assembly states of protein oligomers and in characterizi
100 ternary structure occurs via changes in self-assembly state or through the gain or loss of protein su
102 pramolecular structures were compared to the assembly states predicted by packing constraints that we
104 tinct catalytic site coordination sphere and assembly state relative to QueD and possesses a dynamic
105 rbed, whereby a decrease in the III(2)-IV(2) assembly state relative to the III(2)-IV form is observe
106 sting state and the CymA-induced alternative assembly state rely on interactions between the ClpC1 co
111 IM21) degrades antibody-bound proteins in an assembly state-specific manner due to the requirement of
112 resist the effects of O-GlcNAcylation on NF assembly state, suggesting a potential link between dysr
114 ion of the full repertoire of conformers and assembly states that can be accessed by PrP under specif
115 otides in the bI3 group I intron RNP in four assembly states: the free RNA, maturase-bound RNA, Mrs1-
116 nance biosensor analysis to characterize the assembly state, thermodynamics, and kinetics of the CD4-
119 and Abeta42 have different conformations and assembly states upon refolding from their unfolded ensem
120 rent shifts in the equilibrium population of assembly states upon the binding of different signaling
121 , stability, and dynamics of P8 in different assembly states using time-resolved Raman spectroscopy a
122 nting all viable individual or combinatorial assembly states, we dissect the basic organizational pri
123 dynamics as well as relative populations of assembly states, we here employ a combination of native