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1  which assemble as a soluble, tightly packed coiled coil structure.
2 lasses that define different elements of the coiled coil structure.
3 nus are predicted to form an alpha-helix for coiled coil structure.
4 e to partial retention of the solution-phase coiled coil structure.
5  interact to form an antiparallel tetrameric coiled-coil structure.
6  in gp41, probably by forming a peptide-gp41 coiled-coil structure.
7  protein molecules based on an alpha-helical coiled-coil structure.
8 mately 60 amino acids is predicted to form a coiled-coil structure.
9 have been proposed to form an intramolecular coiled-coil structure.
10 apes of the spectra are characteristic for a coiled-coil structure.
11  assembly into a more stable triple-stranded coiled-coil structure.
12  together by a triple-stranded alpha-helical coiled-coil structure.
13 ated, unprecedented deviation from canonical coiled-coil structure.
14 hairpin, the tip of which adopts a canonical coiled-coil structure.
15 here we show its ionization destabilizes the coiled-coil structure.
16  residue 139, suggesting a transition out of coiled-coil structure.
17 robably via a domain predicted to be rich in coiled-coil structure.
18  have suggested that the LcrG family forms a coiled-coil structure.
19 prevent the N-terminal region from forming a coiled-coil structure.
20 ossibility that these proteins interact in a coiled-coil structure.
21 re multiple regions which are likely to form coiled-coil structure.
22 lly unfavorable, it is likely to disrupt the coiled-coil structure.
23 led coils that were predicted to disrupt the coiled-coil structure.
24 4-p1d increases the thermal stability of the coiled-coil structure.
25 lt bridges to allow an abnormal extension of coiled-coil structure.
26  aligned samples gave patterns indicative of coiled-coil structure.
27 ptad repeat region which might dimerize into coiled-coil structure.
28 ring fusion to form a trimeric alpha-helical coiled-coil structure.
29 d by generating models for rarer and de novo coiled-coil structures.
30 anisms between dimeric, trimeric, tetrameric coiled-coil structures.
31 fficient and rapid compilation of subsets of coiled-coil structures.
32 nction 622 (DUF622) and is predicted to form coiled-coil structures.
33 ain and a tail domain consisting of extended coiled-coil structures.
34 tides were highly alpha-helical and may form coiled-coil structures.
35 ate their association into stable tetrameric coiled-coil structures.
36 alpha-helical in solution, characteristic of coiled-coil structures.
37  (residues 612-756), which contains putative coiled-coil structures.
38 other contains a putative 3,4 heptad repeat (coiled-coil) structure (amino acids 441 to 483).
39 n the Myo J tail domain of both an extensive coiled-coil structure and a large globular domain sugges
40 ues 84 to 112), which is predicted to form a coiled-coil structure and contains a putative leucine zi
41 ite the apparent simplicity of tropomyosin's coiled-coil structure and its well-known periodic associ
42 obic clustering significantly stabilized the coiled-coil structure and may explain how long fibrous p
43 ults indicate that the linker region forms a coiled-coil structure and suggest a mechanism by which a
44  These features are evident in the irregular coiled-coil structure and thermal instability of M prote
45 understanding possibilities in and limits on coiled-coil structures and a basis for future prediction
46 ere able to dimerize and oligomerize through coiled-coil structures and appeared to associate with cy
47 ndogenous, wild-type heavy chains, fold into coiled-coil structures and assemble into higher-order st
48 erminal transmembrane domain (TM), a central coiled-coil structure, and a C-terminal region homologou
49               We show that over 95% of known coiled-coil structures are within 1-A C(alpha) root mean
50 udies provide evidence that hMPV also uses a coiled-coil structure as a major player in the fusion pr
51  yeast Rad50 does have the same antiparallel coiled-coil structure as SMC proteins, but with no detec
52        Spectroscopy data prove alpha-helical coiled-coil structures at individual amino acids 316-336
53 R-like repeats are predicted to contain, not coiled coil structures, but rather two closely associate
54 d repeat pattern indicative of alpha-helical coiled-coil structure, but that this heptad repeat patte
55 e hypothesis that the proteins assemble in a coiled-coil structure, but the alignment of alpha helice
56 67) adopt continuous, extended alpha-helical coiled-coil structures, but no experimentally derived in
57 inE-MinD interaction involves formation of a coiled-coil structure by interaction with a complementar
58 hose structure is dominated by alpha-helical coiled-coil structures can undergo unfolding transitions
59 s that reducing the flexibility of native Tm coiled-coil structure decreases the optimum interactions
60 knobs-into-holes packing to produce parallel coiled-coil structures enclosing large tubular cavities.
61                       Mechanisms for how the coiled-coil structures facilitate annealing are discusse
62  of kinectin cDNA indicated an alpha-helical coiled-coil structure from amino acid 320 to 1310.
63 ty of CCBuilder by assembling models for 653 coiled-coil structures from the PDB, which cover >96% of
64 e used SOCKET to gather a set of unambiguous coiled-coil structures from the RCSB Protein Data Bank.
65 ax=320A) than predicted for a fully extended coiled-coil structure (>500A).
66    Normal mode calculations on models of the coiled-coil structure have been performed to investigate
67  of the dimeric alpha-helical leucine zipper coiled coil structure: (i) length of the leucine zipper,
68 racting with troponin deviate from canonical coiled coil structure in subtle ways, altering the local
69 ary structure prediction of HtrI indicates a coiled coil structure in the cytoplasmic region followin
70 elical c-Myc in its transcriptionally active coiled-coil structure in association with its obligate b
71 t is in addition to the role of the trimeric coiled-coil structure in bringing about apposition of vi
72     Previous work suggested that T21 forms a coiled-coil structure in PBS solution, while T20 is prim
73 ate filaments, as well as direct evidence of coiled-coil structure in rod 1A.
74 inal helices of each subunit form a parallel coiled-coil structure in the interior of the complex whi
75 intermediate (PHI) characterized by extended coiled-coil structure in the region C-terminal of the FP
76 ibria between extended unordered, helix, and coiled-coil structures in solution; when lipid vesicles
77 tructure, we developed a new method to probe coiled-coil structures in vivo.
78  substantial alpha-helical content and forms coiled coil structures involved in EMILIN-3 homo-oligome
79                                            A coiled-coil structure involving alpha-helical segments a
80             Furthermore, it appears that the coiled coil structure is maintained up to residue 259 of
81 l evidence that this functional region forms coiled coil structures is under investigation.
82 lical segments predicted to participate in a coiled-coil structure is essential for oligomerization.
83    We also show that an intact alpha-helical coiled-coil structure is required to provide dimerizatio
84                                 The trimeric coiled-coil structure is therefore a prerequisite for in
85  be important in conferring stability to the coiled-coil structures is found not to have a significan
86 ocalized protein predicted to assume a long, coiled-coil structure, is required for Rab9-dependent re
87 ts of an N-terminal region predicted to form coiled coil structures linked to a C-terminal tail that
88                By covering >90% of the known coiled-coil structures, LOGICOIL is a net improvement co
89                             The unfolding of coiled-coil structures occurs much later during the atom
90 find that 2 mutants affect the alpha-helical coiled-coil structure of individual molecules, and 2 mut
91                                     From the coiled-coil structure of kinectin and the coiled-coil ta
92 mc5 binding by forming a helix bundle with a coiled-coil structure of Smc5; its C-terminal half inclu
93 e of these same substitutions on the helical coiled-coil structure of synthetic peptide models.
94           Mutations predicted to disrupt the coiled-coil structure of the BST2 ectodomain impaired bo
95  approximately 20 degrees characterizing the coiled-coil structure of the peptide bundle, the width o
96 minal targeting domain, the overall putative coiled-coil structure of the protein, and the C-terminal
97 esidue repeat appearing in the alpha-helical coiled-coil structure of the rod are critical for such a
98 ons is expected to disrupt the alpha-helical coiled-coil structure of the rod, this region was antici
99     MS analysis of H-D exchange supports the coiled-coil structure of the substituted peptides.
100 otein has a very high probability of forming coiled-coil structures often associated with oligomeric
101 n the pre-IQ region predicted to abolish the coiled-coil structure significantly reduces Ca(2+)-depen
102 sidues suggests that the domain forms a long coiled-coil structure, similar to those found in the alp
103 ggest that residues 37-52 adopt a pentameric coiled-coil structure stabilized by a leucine zipper mot
104 ntion signal of GBR1 is not part of the core coiled-coil structure, suggesting that it is sterically
105 esignated as the K domain, and its predicted coiled-coil structure suggests a role in establishing a
106 nd the Jun basic region form a heterodimeric coiled coil structure that stabilizes the complex over 3
107 or NS1 on p85beta is the inter-SH2 domain, a coiled-coil structure that acts as a scaffold for the p1
108 eparated from the GT99 chain terminator by a coiled-coil structure that forms a molecular ruler to de
109 ssociated at the C-terminus by the 4-helical coiled-coil structure that forms the dimer-dimer interfa
110 rily in a parallel arrangement and suggest a coiled-coil structure that is bent rather than fully ext
111  In all, we estimate the space of designable coiled-coil structures to be reduced at least 160-fold r
112 peptides may form nonglobular intramolecular coiled-coil structures under the experimental conditions
113    We analysed and classified a large set of coiled-coil structures using a combination of automated
114 n the d position of a dimeric leucine zipper coiled coil structure was measured by determining the th
115  In contrast to most members of this class a coiled-coil structure was predicted within the LRR regio
116 ing peptides that bind to BZLF1 by forming a coiled-coil structure, we considered both affinity for B
117 ons of the requirements for the formation of coiled-coil structures, we predicted which amino acid di
118 mutations, which are designed to disrupt the coiled-coil structure, weaken or completely abolish the
119 ce, so that parallel and antiparallel heptad coiled-coil structures were formed.
120 nto the CC+ Database: the 'Periodic Table of Coiled-coil Structures', which presents a graphical path
121 sidue located in the hydrophobic core of its coiled-coil structure, which is unusual in that the resi
122                 The acidic extension forms a coiled coil structure with the VBP basic region in the V
123 eveals a parallel two-stranded alpha-helical coiled-coil structure with a remarkable core.
124 cture content and they adopt predominantly a coiled-coil structure with an elongated, likely rod-like
125 were able to assemble into a triple-stranded coiled-coil structure with chain-specific interactions.
126                       Overall, this extended coiled-coil structure with inherent plasticity is undoub
127 can direct assembly of complex, higher-order coiled-coil structures with rich diversity for close pac
128 r trimerization domain is a highly elongated coiled-coil structure, with a potential break in the coi
129 protein mostly composed of alpha-helical and coiled-coil structures, with domains shared with microtu
130 , while the central large rod probably forms coiled-coil structures, with one large central and sever
131 at regions, denoted HR-N and HR-C, that form coiled-coil structures within the ectodomain of the prot

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