ライフサイエンスコーパス: propeller

1 cluster at the top of the seven-bladed beta-propeller.

2 indicate that it is a D3-symmetric molecular propeller.

3 a strongly pitched, C3-symmetric, molecular propeller.

4 BS9 likely results in misfolding of the beta-propeller.

5 -terminal domain reveals a seven-bladed beta-propeller.

6 Rav1, which can be modeled as a double beta-propeller.

7 g site on blades 2-3 of the SEMA domain beta-propeller.

8 ed that Nup37 folds into a seven-bladed beta-propeller.

9 otor and a helical filament, which acts as a propeller.

10 ared by inter-bladed binding grooves of beta-propeller.

11 nto essentially enantiopure, homochiral 9-EP propellers.

12 anded via tandem duplications to form extant propellers.

13 tion to the small family of five-bladed beta-propellers.

14 the hydrophobic core that joins the two beta-propellers.

15 is not shielded from other proteins by beta-propellers.

16 t, modern structural designs such as prisms, propellers, 2-solenoid, super-roll, clam, trefoil and bo

17 ncreasing frequency of a dominant mutant K13-propeller allele correlates with the recent spread of re

18 Mutant K13-propeller alleles cluster in Cambodian provinces where r

19 iled-bundle proteins, and proteins with beta-propeller and alpha-solenoid secondary structures.

20 We test SMURFLite on all propeller and barrel folds in the mainly-beta class of t

21 hat the enzyme folds into the catalytic beta-propeller and beta-sandwich domains characteristic of GH

22 ts platform formed by the alpha-subunit beta-propeller and beta-subunit betaI domains.

23 eracts through a region near the alphaM beta-propeller and beta2 betaI domain with a region of the C3

24 o a pocket at the interface between the beta-propeller and betaI domains.

25 that binds to the interface between the beta propeller and betaI domains.

26 elch13 (PF3D7_1343700) affecting the encoded propeller and BTB/POZ domains, which were associated wit

27 ibrin to multiple sites in the alphaIIb beta-propeller and further indicate that recognition specific

28 er of key structural connections between the propeller and pore domains located close to lipid-bindin

29 We show that Rod's N-terminal beta-propeller and the associated Zwilch subunit bind Spindly

30 The filament functions as a helical propeller and the hook as a flexible universal joint.

31 of the Fab bound to an alpha4 integrin beta-propeller and thigh domain fragment shows that natalizum

32 We propose that the Rrp9 beta-propeller and U3/pre-rRNA binding cooperate in the struc

33 he structure consists of a seven-bladed beta-propeller and, unexpectedly, contains two pseudo-equival

34 des, respectively, show structurally diverse propellers and include a novel fold, highlighting the in

35 ear dictates the rotational direction of the propellers and step-wise rotations can be induced by app

36 eling predicts that WDR-23 folds into a beta-propeller, and we identify the top of this structure and

37 s N-terminal domains of Apaf-1, cognate beta-propellers, and cytochrome c.

38 main architecture consisting of an open beta-propeller appended to an alpha/beta hydrolase domain.

39 l catalytic domain with five-fold alpha/beta-propeller architecture and a C-terminal immunoglobulin-l

40 t is determined by the interplay between the propeller architecture and the intermolecular van der Wa

41 endent metasurface, helicoidal reflector and propeller are applied respectively in this study.

42 ingly, numerous contacts with the Nup37 beta-propeller are located on this extension of the 6D-7A ins

43 , the rotation steps of individual molecular propellers are directly visualized, which confirms the u

44 Propellers are most well known for their ability to act

45 beta-Propellers arise through the amplification of a supersec

46 served surface at the side of the Cdc20 beta propeller as a D-box-binding site.

47 ow that Vps18 indeed has a seven-bladed beta-propeller as its N-terminal domain by revealing its stru

48 disordered surface regions of the Nup37 beta-propeller assume structure when bound to Sp-Nup120.

49 nanomachine and comprises a rotating helical propeller attached to a membrane-embedded motor complex.

50 "K loop," which extends from the N-terminal propeller blade.

51 rotrudes from the intracellular side of the "propeller" blade toward the inner vestibule of the chann

52 The flexible propeller blades can adopt distinct conformations, and c

53 of C. reinhardtii, that the C-terminal beta-propeller but not the N-terminal domain of CrODA16 is re

54 therefore investigated whether such nascent propellers can fold as homo-oligomers before they have b

55 gand's pyridine rings into a left-handed (M) propeller (circular dichroism spectroscopy).

56 ed beta-propeller fold with a rare nonvelcro propeller closure.

57 revalent in sub-Saharan Africa, numerous K13-propeller coding polymorphisms circulate in Africa.

58 of a C-terminal coiled-coil segment and beta-propeller combination (Olfm1(coil-Olf)) that reveals a d

59 Tel 23 maintains a characteristic propeller conformation while binding three gold(I) dicar

60 L/ligand interfaces that tightly constrain a propeller conformer of MG.

61 The catalytic domain was a five-bladed beta-propeller consisting of five radially oriented anti-para

62 17 protruding from one end of the BamB beta-propeller contact the face of the POTRA3 beta-sheet in B

63 action of sclerostin with LRP4 (another beta-propeller containing protein in the LRP family).

64 Three tryptophans in the beta-propeller core are important in maintaining structural s

65 ck residues 537-578 or 897-917 from its beta-propeller core diffused faster on the PM and exhibited r

66 d to be the active state and comprise a beta-propeller core domain and intrinsically disordered N- an

67 de-linked coiled coil with a C-terminal beta-propeller dimer at the tips.

68 , or inserting a linker between NLS and beta-propeller, disrupts specificity for importin alpha3, dem

69 sociate mutations in the PF3D7_1343700 kelch propeller domain ('K13-propeller') with artemisinin resi

70 d a direct interaction between the Rrp9 beta-propeller domain and Rrp36, the strength of which was re

71 apoER2 surprisingly identified the YWTD beta-propeller domain as the Sepp1 binding site.

72 Mutations in the Plasmodium falciparum K13-propeller domain have recently been shown to be importan

73 Trimerization depends on a beta-propeller domain in the carboxy-terminal half of the pro

74 continuous segments within the alphaIIb beta-propeller domain of alphaIIbbeta3 enriched with negative

75 requires an unexpected swiveling of the beta-propeller domain of BBS1, the subunit most frequently im

76 n with the WD40 repeats-based predicted beta-propeller domain of COP1, whereas COP1 activity is regul

77 of Arp2/3 complex, with the N-terminal beta-propeller domain of Coronin positioned near the p35/ARPC

78 The AND-1 trimer uses one beta-propeller domain of its trimerisation region to dock ont

79 that mediates its interaction with the beta-propeller domain of nidogen.

80 Pal is tethered to the OM and binds the beta-propeller domain of periplasmic TolB, which, as recent e

81 Certain point mutations in the propeller domain of PfKelch13 are associated with resist

82 etween the MLL1 SET domain and the WD40 beta-propeller domain of RbBP5, and demonstrate the susceptib

83 17E6 Fab bound exclusively to the Propeller domain of the alphaV subunit.

84 that recognize a defined epitope on the beta-propeller domain of the platelet integrin alphaIIb subun

85 domains of UVR8 interact with COP1: the beta-propeller domain of UVR8 mediates UV-B-dependent interac

86 pfkelch13 propeller domain polymorphisms previously associated wit

87 Its conserved WD40 beta-propeller domain provides attachment sites for other A-C

88 rminal domain and a C-terminal 8-bladed beta-propeller domain that are both required for the associat

89 rom Snc1, or deletion of a beta'-COP subunit propeller domain that binds K63-linked polyubiquitin, di

90 Each monomer contains a five-bladed propeller domain with a cavity that could accommodate a

91 Moreover, replacement of the beta'-COP propeller domain with unrelated ubiquitin-binding domain

92 genotyped the P. falciparum K13 (Pfkelch13) propeller domain, mutations in which can mediate artemis

93 onarily conserved amino acid within the beta-propeller domain, which abrogates almost completely the

94 amples carried the C580Y allele in the PfK13 propeller domain, with flanking microsatellite profiles

95 examining polymorphisms in the Kelch (PfK13) propeller domain.

96 internal cavity through the pore in the beta-propeller domain.

97 differences on the circumference of the beta-propeller domain.

98 omain from its site of insertion in the beta-propeller domain.

99 In another study, Piezo1's N-terminal "propeller" domain was proposed to constitute an intrinsi

100 crystal structure of PorZ revealed two beta-propeller domains and a C-terminal beta-sandwich domain,

101 ns predicted to contain four six-bladed beta-propeller domains and both bind the bone-specific Wnt si

102 of a P. falciparum gene encoding kelch (K13)-propeller domains are the major determinant of resistanc

103 s between the alphaL and alphaX subunit beta-propeller domains concentrate near the binding pocket an

104 brane protein with thioredoxin-like and beta-propeller domains located in the lumen and a haloacid-de

105 h could potentially be useful, including the propeller effect, have therefore not yet been demonstrat

106 s to demonstrate the Baranova and Zel'dovich propeller effect: the separation of a racemic mixture by

107 ed a location for the active site among beta-propeller enzymes cited on the posterior surface of the

108 We found that new propellers evolve continuously by amplification from sin

109 lecular machine that functions as a cellular propeller, exhibits significant structural variability b

110 rod), a universal joint (hook) and a helical propeller (filament).

111 rmational flexibility to wedge the RCC1 beta-propeller flanking the NLS against its lateral surface,

112 es (fanciful ball, puzzle pieces, 3D pixels, propellers, fluidic and multicompartments) with mono-, d

113 ts a classical paramyxoviral six-bladed beta-propeller fold and structurally classifies in close prox

114 find that MojV-G displays a six-bladed beta-propeller fold bearing limited similarity to known param

115 recombinant PLL revealed a seven-bladed beta-propeller fold creating seven putative fucose-binding si

116 wed them to enter the protein vestibule, the propeller fold exceeds the size of the latch region, pro

117 based solution, while it formed the parallel propeller fold in water-depleted potassium-based solutio

118 to recognize blades 2, 3, and 4 of the beta-propeller fold of RON Sema.

119 f62A and PaAbf62A reveals a five-bladed beta-propeller fold that confirms their predicted classificat

120 rotein family, bind via their predicted beta-propeller fold the polyphosphoinositides PtdIns3P and Pt

121 It adopts a seven-bladed beta-propeller fold with a rare nonvelcro propeller closure.

122 trom resolution revealed a seven-bladed beta-propeller fold with an iron cofactor coordinated by four

123 f the OLF domain presents a five-bladed beta-propeller fold with unusual geometric properties.

124 CyRPA has a six-bladed beta-propeller fold, and we identify the region that interact

125 epeat domain, revealing an eight-bladed beta-propeller fold.

126 Sec12 adopts a beta propeller fold.

127 enzyme displayed a type A seven-bladed beta-propeller fold.

128 a G-quadruplex with the parallel-stranded ("propeller") fold, consistent with observations that redu

129 lly related but evolutionarily distinct beta-propeller folds.

130 druplexes, including the hybrid, basket, and propeller folds.

131 dues 70-893), folds into a seven-bladed beta-propeller followed by an alpha-helical domain, which tog

132 ral molecules and active matter, or building propellers for microscale transport.

133 1 and Kir6.2 adjacent to the ATP site in the propeller form and is disrupted in the quatrefoil form.

134 The overall fold is a six-bladed beta-propeller formed by oligomerization as in the Ralstonia

135 se structures, referred to as quatrefoil and propeller forms, were determined by single-particle cryo

136 tivity associated with scaffold protein WD40/Propeller/FYVE (WD40/ProF), which reportedly facilitates

137 ndent FoxO1 phosphorylation occurs on the WD/Propeller/FYVE scaffold in liver and is selectively inhi

138 electron oxidation of dG in chiral hybrid or propeller G-quadruplexes that expose the re or si face t

139 We found two kelch13 propeller gene mutations associated with artemisinin res

140 several polymorphisms in the parasite's K13-propeller gene.

141 rms of suprastructures, collinear chains and propellers, have been achieved with various chiral HgS N

142 een blades 4 and 5 of the hemagglutinin beta-propeller head.

143 5 (beta4-beta5 groove) of the H protein beta-propeller head.

144 the MELT(P) sequence on the side of the beta-propeller in a previously unknown binding mode.

145 llers, which we term a TAPE (tandem atypical propeller in EMLs) domain.

146 alysts in the molecular world and the chiral propellers in the macroscopic world.

147 This revealed four beta propellers, in an assembly markedly similar to those of

148 annel impairments, including: misalignments, propeller-induced airflows, power loss, intermodal cross

149 ain assembly made up of an eight-bladed beta-propeller interrupted by a beta-prism domain.

150 ions of both left and right handed molecular propellers into clockwise and anticlockwise directions r

151 Our propeller is composed of a rotator with three molecular

152 he interaction between RAV1 and the 1st WD40 propeller is conserved with another RAV family member, T

153 r PCSK9 binding, processes in which the beta-propeller is critically involved.

154 One propeller is highly atypical, having a discontinuous sub

155 study, we report that Bub3, a 7-bladed beta-propeller, is the MELT(P) reader.

156 l protein that contains BTB and Kelch-repeat propeller (KREP) domains usually found in E3 ubiquitin l

157 Tectonins are a family of beta-propeller lectins conserved from bacteria to mammals tha

158 subunit of FIPV S protein result in a unique propeller-like conformation, underscoring the importance

159 le domain-domain interactions that lead to a propeller-like construction.

160 SPG11 also has an N-terminal, beta-propeller-like domain, which interacts in vitro with AP-

161 The protein assembles into a propeller-like homotrimer in which each blade contains a

162 ogy, respectively, with AP site located in a propeller-like loop.

163 The identification of short propeller-like motifs (<50 amino acids) in natural genom

164 Propeller-like nanoscale assemblies with exceptionally i

165 Their propeller-like shape leads these molecules to display mu

166 nbonded P...O interaction, hypervalency, and propeller-like shape of the phosphonium groups in 1a(2+)

167 They possess an inherent chirality due to a propeller-like skeleton.

168 WD40 repeats may form the first of two WD40 propellers located on C-terminus of TPL.

169 re formed between the central edgewise loop, propeller loop and 5' flanking terminal.

170 The long lateral-propeller loop is internally very stable but extensively

171 loop region facilitates the formation of the propeller loop.

172 x folding and identify the single-nucleotide propeller loops as the most fragile part of the quadrupl

173 Thus, formation of propeller loops represents a peculiar atomistic aspect o

174 The 1st WD40 propeller mediates interaction with RAV1, and the 2nd WD

175 ates interaction with RAV1, and the 2nd WD40 propeller mediates interaction with VRN5.

176 Fan, spiral, propellers, moonlets and streamer-channels observed by C

177 rotate with the field and act as microscopic propellers; moreover, owing to their opposite handedness

178 K13 propeller mutation alone was a strong risk factor for re

179 h both multiple Pfmdr1 copy number and a K13 propeller mutation were 14 times more likely to fail tre

180 rall, 371 (39%) of 940 samples carried a K13-propeller mutation.

181 o parasite clearance rates indicate that K13-propeller mutations are important determinants of artemi

182 inated initially but were later overtaken by propeller mutations associated with slower parasite clea

183 recorded P falciparum parasites carrying K13-propeller mutations at high prevalence next to the north

184 tudy provides the baseline prevalence of K13-propeller mutations in sub-Saharan Africa.

185 None of the K13-propeller mutations previously reported in Southeast Asi

186 alciparum malaria is associated with kelch13 propeller mutations, reduced ring stage parasite killing

187 21 (47%) of 45 parasite samples carried K13-propeller mutations.

188 lence of P falciparum parasites carrying K13-propeller mutations.

189 ear decline was determined mainly by kelch13 propeller mutations.

190 ur analysis demonstrates that the N-terminal propeller needs to be able to engage the C-terminal tail

191 is work presents a green chiral nanographene propeller (NP), which is built by fusing seven hexabenzo

192 structure identifies blades 4-6 of the beta-propeller of CyRPA as contact sites for Rh5 and Ripr.

193 to bind a similar surface in the third beta-propeller of LRP5/6, sterically interfering with Wnt3/3a

194 th projections clamp to the side of the beta-propeller of Rae1, with the finger also contacting Nup98

195 ions between BCL11A and the side of the beta-propeller of RBBP4 that are not seen with histone H3.

196 urthermore, we demonstrate that the 1st WD40 propeller of TPL can form a complex with RAV1 both in ye

197 We thus conclude that the beta-propeller of Vps18 is required for HOPS stability and fu

198 For example, the beta-propeller olfactomedin domain of myocilin (mOLF) exhibit

199 The two predicted WD40 propellers on TOPLESS function as protein-protein intera

200 Removing the beta-propeller, or inserting a linker between NLS and beta-pr

201 nose, and ribose substitutions stabilize the propeller parallel G-quadruplex form over competing conf

202 arallel lines with enhanced reconstruction ( PROPELLER periodically rotated overlapping parallel line

203 on CT images (3.49), while findings with the PROPELLER periodically rotated overlapping parallel line

204 erated volume acquisition , 2.52 [P = .002]; PROPELLER periodically rotated overlapping parallel line

205 In distant metastases, the PROPELLER periodically rotated overlapping parallel line

206 panied by an increase in phoD, phoX and beta-propeller phytase genes coding for exoenzymes.

207 Beta-propeller phytase genes were most abundant in bare fallo

208 K13-propeller polymorphism constitutes a useful molecular ma

209 his study investigated the prevalence of K13-propeller polymorphisms across sub-Saharan Africa.

210 one distantly related dual seven-bladed beta-propeller protein from a marine bacterium, highlighted k

211 de novo mutations in WDR45, encoding a beta-propeller protein postulated to play a role in autophagy

212 astic cells) domains(7), and WDR41 is a beta-propeller protein that binds to SMCR8 such that the whol

213 TSSC1 is a predicted WD40/beta-propeller protein that coisolates with both GARP and EAR

214 c diseases: EPG5-related Vici syndrome, beta-propeller protein-associated neurodegeneration due to mu

215 Beta-propeller protein-associated neurodegeneration, the only

216 recently been linked to mutations in the K13 propeller protein.

217 he substrate affinity of USP12, the two beta-propeller proteins potentiate the enzyme through differe

218 f these complexes are mLST8 and Raptor, beta-propeller proteins that stabilize the mTOR kinase and re

219 election forces underlying emergence of beta-propeller proteins, a globular and symmetric fold group

220 inase, USP12, which is activated by two beta-propeller proteins, UAF1 and WDR20.

221 mLST8, far from those found for similar beta-propeller proteins.

222 estimated prevalence of mutations of the K13 propeller region across Myanmar.

223 sis that rs688, which is located in the beta-propeller region of LDLR, has effects on LDLR activity b

224 ymous single nucleotide polymorphisms in the propeller region of the kelch 13 gene among isolates cir

225 sociated with single point mutations in the "propeller" region of the P. falciparum kelch protein gen

226 We further proved that the beta-propeller repeat domains of Itgalpha6b are key segments

227 The Propeller residue Asp-150, which normally coordinates Ar

228 aV-Fab interface were interactions involving Propeller residues Lys-203 and Gln-145, with the latter

229 n of an unstructured loop in its second beta-propeller, ruling out models of phosphorylation-dependen

230 structural variation in the six-bladed beta-propeller scaffold of the GhV-G receptor-binding domain,

231 We analyzed the K13-propeller sequence polymorphism in 14,037 samples collec

232 ide a conclusive rationale for worldwide K13-propeller sequencing to identify and eliminate artemisin

233 The Nup82 beta propeller serves as a noncooperative binding platform fo

234 s spanning the sequence of the alphaIIb beta-propeller, several sequences were identified as candidat

235 Here, highly complex propeller shape sensing layers were produced, and the re

236 nt-solubilized complex adopts a three-bladed propeller shape with a curved transmembrane region conta

237 he discovery and optimization of a series of propeller shaped PI3Kdelta inhibitors comprising a novel

238 uted quinolizinone 20 to a novel "four-blade propeller" shaped 1,2,3-trisubstituted quinolizinone 34.

239 systematic transformation of a "three-blade propeller" shaped lead, 2,3-disubstituted quinolizinone

240 The novel hydrocarbon propeller-shaped D3h-symmetric cyclophane (3), "anthraph

241 GM), given the limited conjugation in these propeller-shaped dyes.

242 ivatives create a very intriguing nonplanar, propeller-shaped geometry.

243 volve significantly compared to those of the propeller-shaped hexapole [7]helicene.

244 Piezos oligomerize as propeller-shaped homotrimers that are thought to locally

245 es of Cas1 (Cas2/32:Cas14) into a four-lobed propeller-shaped structure, where the two Cas2 domains f

246 ion pathways, generating compact three-blade propeller-shaped trimers.

247 These compounds are propeller-shaped, and upon precipitation into water, rea

248 This unexpected feature shows how a propeller structure can be assembled from subdomains wit

249 ted CCD4 form, lacking one blade of the beta-propeller structure conserved in all CCDs.

250 Partial opening of the beta-propeller structure due to thermal relaxation of conform

251 lation variation data, we show that the beta-propeller structure of the ubiquitous WD40 domain provid

252 9 is located on the surface of the Rrp9 beta-propeller structure opposite to U3 snoRNA.

253 domain, which potentially folds into a beta-propeller structure resembling the alpha-integrin ligand

254 Lgl2 adopts a double beta-propeller structure that is unchanged by aPKC phosphoryl

255 PfCyRPA adopts a 6-bladed beta-propeller structure with similarity to the classic siali

256 s with each octameric ring adopting a planar propeller structure.

257 ecting loops protruding far beyond the lower propeller surface.

258 the ClpB middle domain (MD) is a coiled-coil propeller that binds Hsp70.

259 and characterize a multi-component molecular propeller that enables unidirectional rotations on a mat

260 la are ultimately constructed from a helical propeller that is attached to a motor embedded in the in

261 beta-propellers that bind polyphosphoinositides (PROPPINs), a

262 PROPPINs (beta-propellers that bind polyphosphoinositides) are a family

263 PROPPINs (beta-propellers that bind polyphosphoinositides) are PtdIns3P

264 Flagella, the helical propellers that extend from the bacterial surface, are a

265 created by the junction of two adjacent beta-propellers that form the core structure of Sro7.

266 ocated near the 2-fold axes, instead of the "propeller tip" as in 135S particles.

267 cause a subtle conformational change in the propeller tips, potentially perturbing an interaction si

268 a long extracellular helical filament like a propeller to push cells through the environment.

269 ide-linked dimeric arrangement with the beta-propeller top faces in an outward exposed orientation.

270 al features (i.e., minor groove width, roll, propeller twist and helix twist) for 739 TF datasets fro

271 l features of DNA (minor groove width, roll, propeller twist and helix twist).

272 itro nucleosome occupancy and high predicted propeller twist DNA shape value.

273 ts four broad and static DNA shape features, Propeller twist, Helical twist, Minor groove width and R

274 tions (GBshape) provides minor groove width, propeller twist, roll, helix twist and hydroxyl radical

275 Our simulations also indicate that the actin propeller twist-angle and nucleotide cleft-angles are in

276 o-8-oxo-2'-deoxyguanosine with a significant propeller twist.

277 two modes are associated with a buckled and propeller-twisted geometry of the basepair.

278 l strands in their structures by stabilizing propeller type loops, shifting the antiparallel htel-22

279 A propeller-type arrangement of the nonchiral ligands arou

280 ution exhibits three G-quartets and flexible propeller-type loops.

281 -quartets, parallel strand orientations, and propeller-type loops.

282 he d(TTGTGGTGGGTGGGTGGGT) sequence reveals a propeller-type parallel-stranded G-quadruplex containing

283 In K(+) solution, this sequence forms a propeller-type parallel-stranded G-quadruplex involving

284 l variability and structural dynamics of the propeller-type topology, we performed molecular dynamics

285 ur repeats can fold into a parallel-stranded propeller-type topology.

286 a large reservoir of naturally occurring K13-propeller variation.

287 ncestral motifs that form five-bladed lectin propellers via oligomeric assembly.

288 Also, the predicted 2nd WD40 propeller was shown in yeast cells to bind Vernalization

289 trad, or located at the top face of the beta-propeller, where 'hotspot' residues affect the binding o

290 for cytochrome c binding to regulatory beta-propellers, which is dependent on shape and charge compl

291 ealing an intimately associated pair of beta-propellers, which we term a TAPE (tandem atypical propel

292 A one-step synthesis of a nanographene propeller with a D3-symmetry was obtained starting from

293 Structurally, PON1 is a six-bladed beta-propeller with a flexible loop (residues 70-81) covering

294 Nup120(1-950) also folds into a seven-bladed propeller with a markedly protruding 6D-7A insert and is

295 N-terminal region and a C-terminal WD40 beta propeller with a preformed KEN-box-binding site at its t

296 Each monomer forms a six-blade beta-propeller with a wide "top" and a narrower "bottom" open

297 The enzyme is a seven-bladed beta-propeller with an iron cofactor coordinated by four hist

298 e PF3D7_1343700 kelch propeller domain ('K13-propeller') with artemisinin resistance in vitro and in

299 ng blocks derived from two seven-bladed WD40 propellers yielded stable homo-oligomers with six to nin

300 nt in vivo and Spindly binding to a Rod beta-propeller-Zwilch complex in vitro.