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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 e N-terminal domain strongly destabilize the coiled-coil structure.
6 which folds independently into an elongated coiled-coil structure.
7 interact to form an antiparallel tetrameric coiled-coil structure.
8 in gp41, probably by forming a peptide-gp41 coiled-coil structure.
9 protein molecules based on an alpha-helical coiled-coil structure.
10 mately 60 amino acids is predicted to form a coiled-coil structure.
11 have been proposed to form an intramolecular coiled-coil structure.
12 apes of the spectra are characteristic for a coiled-coil structure.
13 assembly into a more stable triple-stranded coiled-coil structure.
14 together by a triple-stranded alpha-helical coiled-coil structure.
15 rical Ub-binding sites on either side of the coiled-coil structure.
16 ated, unprecedented deviation from canonical coiled-coil structure.
17 here we show its ionization destabilizes the coiled-coil structure.
18 residue 139, suggesting a transition out of coiled-coil structure.
19 robably via a domain predicted to be rich in coiled-coil structure.
20 prevent the N-terminal region from forming a coiled-coil structure.
21 hairpin, the tip of which adopts a canonical coiled-coil structure.
22 ossibility that these proteins interact in a coiled-coil structure.
23 re multiple regions which are likely to form coiled-coil structure.
24 lly unfavorable, it is likely to disrupt the coiled-coil structure.
25 led coils that were predicted to disrupt the coiled-coil structure.
26 4-p1d increases the thermal stability of the coiled-coil structure.
27 lt bridges to allow an abnormal extension of coiled-coil structure.
28 have suggested that the LcrG family forms a coiled-coil structure.
29 aligned samples gave patterns indicative of coiled-coil structure.
30 ptad repeat region which might dimerize into coiled-coil structure.
31 ring fusion to form a trimeric alpha-helical coiled-coil structure.
32 (residues 612-756), which contains putative coiled-coil structures.
33 d by generating models for rarer and de novo coiled-coil structures.
34 anisms between dimeric, trimeric, tetrameric coiled-coil structures.
35 fficient and rapid compilation of subsets of coiled-coil structures.
36 nction 622 (DUF622) and is predicted to form coiled-coil structures.
37 ain and a tail domain consisting of extended coiled-coil structures.
38 tides were highly alpha-helical and may form coiled-coil structures.
39 ate their association into stable tetrameric coiled-coil structures.
40 alpha-helical in solution, characteristic of coiled-coil structures.
42 n the Myo J tail domain of both an extensive coiled-coil structure and a large globular domain sugges
43 aperone binding completely disrupts the FliJ coiled-coil structure and alters its interactions with t
44 ues 84 to 112), which is predicted to form a coiled-coil structure and contains a putative leucine zi
45 ite the apparent simplicity of tropomyosin's coiled-coil structure and its well-known periodic associ
46 obic clustering significantly stabilized the coiled-coil structure and may explain how long fibrous p
47 ults indicate that the linker region forms a coiled-coil structure and suggest a mechanism by which a
48 These features are evident in the irregular coiled-coil structure and thermal instability of M prote
49 understanding possibilities in and limits on coiled-coil structures and a basis for future prediction
50 ere able to dimerize and oligomerize through coiled-coil structures and appeared to associate with cy
51 ndogenous, wild-type heavy chains, fold into coiled-coil structures and assemble into higher-order st
53 erminal transmembrane domain (TM), a central coiled-coil structure, and a C-terminal region homologou
55 udies provide evidence that hMPV also uses a coiled-coil structure as a major player in the fusion pr
56 yeast Rad50 does have the same antiparallel coiled-coil structure as SMC proteins, but with no detec
58 R-like repeats are predicted to contain, not coiled coil structures, but rather two closely associate
59 d repeat pattern indicative of alpha-helical coiled-coil structure, but that this heptad repeat patte
60 e hypothesis that the proteins assemble in a coiled-coil structure, but the alignment of alpha helice
61 67) adopt continuous, extended alpha-helical coiled-coil structures, but no experimentally derived in
62 inE-MinD interaction involves formation of a coiled-coil structure by interaction with a complementar
63 hose structure is dominated by alpha-helical coiled-coil structures can undergo unfolding transitions
64 s that reducing the flexibility of native Tm coiled-coil structure decreases the optimum interactions
65 knobs-into-holes packing to produce parallel coiled-coil structures enclosing large tubular cavities.
68 ty of CCBuilder by assembling models for 653 coiled-coil structures from the PDB, which cover >96% of
69 e used SOCKET to gather a set of unambiguous coiled-coil structures from the RCSB Protein Data Bank.
71 Normal mode calculations on models of the coiled-coil structure have been performed to investigate
72 of the dimeric alpha-helical leucine zipper coiled coil structure: (i) length of the leucine zipper,
74 racting with troponin deviate from canonical coiled coil structure in subtle ways, altering the local
75 ary structure prediction of HtrI indicates a coiled coil structure in the cytoplasmic region followin
76 elical c-Myc in its transcriptionally active coiled-coil structure in association with its obligate b
77 t is in addition to the role of the trimeric coiled-coil structure in bringing about apposition of vi
78 tion, CD revealed greater instability of the coiled-coil structure in mutant S2 proteins compared wit
79 Previous work suggested that T21 forms a coiled-coil structure in PBS solution, while T20 is prim
81 inal helices of each subunit form a parallel coiled-coil structure in the interior of the complex whi
82 intermediate (PHI) characterized by extended coiled-coil structure in the region C-terminal of the FP
83 ibria between extended unordered, helix, and coiled-coil structures in solution; when lipid vesicles
85 substantial alpha-helical content and forms coiled coil structures involved in EMILIN-3 homo-oligome
89 lical segments predicted to participate in a coiled-coil structure is essential for oligomerization.
90 We also show that an intact alpha-helical coiled-coil structure is required to provide dimerizatio
92 be important in conferring stability to the coiled-coil structures is found not to have a significan
93 ocalized protein predicted to assume a long, coiled-coil structure, is required for Rab9-dependent re
95 eyi YhcB shows a unique tetrameric a-helical coiled-coil structure likely to be involved in linking t
96 ts of an N-terminal region predicted to form coiled coil structures linked to a C-terminal tail that
99 find that 2 mutants affect the alpha-helical coiled-coil structure of individual molecules, and 2 mut
101 -oligomeric, likely specifically pentameric, coiled-coil structure of Nup358 that may provide the avi
102 mc5 binding by forming a helix bundle with a coiled-coil structure of Smc5; its C-terminal half inclu
105 approximately 20 degrees characterizing the coiled-coil structure of the peptide bundle, the width o
106 minal targeting domain, the overall putative coiled-coil structure of the protein, and the C-terminal
107 esidue repeat appearing in the alpha-helical coiled-coil structure of the rod are critical for such a
108 ons is expected to disrupt the alpha-helical coiled-coil structure of the rod, this region was antici
110 otein has a very high probability of forming coiled-coil structures often associated with oligomeric
111 e enabled by our understanding of ubiquitous coiled-coil structures, opening possibilities for contro
113 n the pre-IQ region predicted to abolish the coiled-coil structure significantly reduces Ca(2+)-depen
114 sidues suggests that the domain forms a long coiled-coil structure, similar to those found in the alp
115 ggest that residues 37-52 adopt a pentameric coiled-coil structure stabilized by a leucine zipper mot
116 ntion signal of GBR1 is not part of the core coiled-coil structure, suggesting that it is sterically
117 esignated as the K domain, and its predicted coiled-coil structure suggests a role in establishing a
118 nd the Jun basic region form a heterodimeric coiled coil structure that stabilizes the complex over 3
119 or NS1 on p85beta is the inter-SH2 domain, a coiled-coil structure that acts as a scaffold for the p1
121 eparated from the GT99 chain terminator by a coiled-coil structure that forms a molecular ruler to de
122 ssociated at the C-terminus by the 4-helical coiled-coil structure that forms the dimer-dimer interfa
123 rily in a parallel arrangement and suggest a coiled-coil structure that is bent rather than fully ext
124 In all, we estimate the space of designable coiled-coil structures to be reduced at least 160-fold r
125 peptides may form nonglobular intramolecular coiled-coil structures under the experimental conditions
126 We analysed and classified a large set of coiled-coil structures using a combination of automated
127 n the d position of a dimeric leucine zipper coiled coil structure was measured by determining the th
128 In contrast to most members of this class a coiled-coil structure was predicted within the LRR regio
129 ing peptides that bind to BZLF1 by forming a coiled-coil structure, we considered both affinity for B
130 ons of the requirements for the formation of coiled-coil structures, we predicted which amino acid di
131 mutations, which are designed to disrupt the coiled-coil structure, weaken or completely abolish the
133 nto the CC+ Database: the 'Periodic Table of Coiled-coil Structures', which presents a graphical path
134 sidue located in the hydrophobic core of its coiled-coil structure, which is unusual in that the resi
137 cture content and they adopt predominantly a coiled-coil structure with an elongated, likely rod-like
138 were able to assemble into a triple-stranded coiled-coil structure with chain-specific interactions.
140 can direct assembly of complex, higher-order coiled-coil structures with rich diversity for close pac
141 r trimerization domain is a highly elongated coiled-coil structure, with a potential break in the coi
142 protein mostly composed of alpha-helical and coiled-coil structures, with domains shared with microtu
143 , while the central large rod probably forms coiled-coil structures, with one large central and sever
144 at regions, denoted HR-N and HR-C, that form coiled-coil structures within the ectodomain of the prot