181 - 181 |
Coiled-coils and fibrous proteins Parry DAD, Squire JM |
182 - 183 |
A tribute to the memory of Tom MacRae In Memorium Fraser B |
184 - 191 |
50 years of fiber diffraction Holmes KC |
192 - 201 |
The many types of interhelical ionic interactions in coiled coils - An overview Meier M, Stetefeld J, Burkhard P |
202 - 215 |
A novel coiled-coil repeat variant in a class of bacterial cytoskeletal proteins Walshaw J, Gillespie MD, Kelemen GH |
216 - 225 |
12 Arylstibonic acids that inhibit the DNA binding of five B-ZIP dimers Rishi V, Oh WJ, Heyerdahl SL, Zhao JF, Scudiero D, Shoemaker RH, Vinson C |
226 - 235 |
Measuring the conformational space of square four-helical bundles with the program samCC Dunin-Horkawicz S, Lupas AN |
236 - 245 |
A transition from strong right-handed to canonical left-handed supercoiling in a conserved coiled-coil segment of trimeric autotransporter adhesins Alvarez BH, Gruber M, Ursinus A, Dunin-Horkawicz S, Lupas AN, Zeth K |
246 - 256 |
Specific coiled-coil interactions contribute to a global model of the structure of the spindle pole body Zizlsperger N, Keating AE |
257 - 265 |
Cryo-electron tomography of microtubule-kinesin motor complexes Cope J, Gilbert S, Rayment I, Mastronarde D, Hoenger A |
266 - 269 |
Cytoplasmic dynein is not a conventional processive motor Walter WJ, Brenner B, Steffen W |
270 - 277 |
The effects of PKC alpha phosphorylation on the extensibility of titin's PEVK element Anderson BR, Bogomolovas J, Labeit S, Granzier H |
278 - 285 |
A novel approach to the structural analysis of partially decorated actin based filaments Paul DM, Squire JM, Morris EP |
286 - 293 |
Alternatively spliced N-terminal exons in tropomyosin isoforms do not act as autonomous targeting signals Martin C, Schevzov G, Gunning P |
294 - 306 |
Critical interactions in the stability control region of tropomyosin Kirwan JP, Hodges RS |
307 - 312 |
Curvature variation along the tropomyosin molecule Li XC, Lehman W, Fischer S, Holmes KC |
313 - 318 |
The relationship between curvature, flexibility and persistence length in the tropomyosin coiled-coil Li XC, Lehman W, Fischer S |
319 - 324 |
What makes tropomyosin an actin binding protein? A perspective Hitchcock-DeGregori SE, Singh A |
325 - 333 |
Differential splicing of the large sarcomeric protein nebulin during skeletal muscle development Buck D, Hudson BD, Ottenheijm CAC, Labeit S, Granzier H |
334 - 343 |
Altered myofilament function depresses force generation in patients with nebulin-based nemaline myopathy (NEM2) Ottenheijm CAC, Hooijman P, DeChene ET, Stienen GJ, Beggs AH, Granzier H |
344 - 353 |
MuRF1 is a muscle fiber-type II associated factor and together with MuRF2 regulates type-II fiber trophicity and maintenance Moriscot AS, Baptista IL, Bogomolovas J, Witt C, Hirner S, Granzier H, Labeit S |
354 - 363 |
Insights into the domain and repeat architecture of target of rapamycin Knutson BA |
364 - 368 |
A different conformation for linker L12 in IF molecules in the molecular and filamentous forms: An hypothesis Parry DAD, Smith TA |
369 - 376 |
Atomic structure of vimentin coil 2 Nicolet S, Herrmann H, Aebi U, Strelkov SV |
377 - 391 |
A new method for describing the helical conformation of collagen: Dependence of the triple helical twist on amino acid sequence Bella J |
392 - 397 |
Three-dimensional reconstruction of collagen-proteoglycan interactions in the mouse corneal stroma by electron tomography Parfitt GJ, Pinali C, Young RD, Quantock AJ, Knupp C |
398 - 405 |
Laminin chain assembly is regulated by specific coiled-coil interactions Macdonald PR, Lustig A, Steinmetz MO, Kammerer RA |
406 - 412 |
Non-equilibrium silk fibroin adhesives Yucel T, Kojic N, Leisk GG, Lo TJ, Kaplan DL |
413 - 419 |
The role of salt and shear on the storage and assembly of spider silk proteins Eisoldt L, Hardy JG, Heim M, Scheibel TR |
420 - 425 |
Characterization of recombinantly produced spider flagelliform silk domains Heim M, Ackerschott CB, Scheibel T |