ライフサイエンスコーパス: solenoid

1 erred to as FAT, FATC and N-terminal helical solenoid.

2 he location of the linker DNA in the typical solenoid.

3 em to bend to match the concavity of the VLR solenoid.

4 erature bore of an energized superconducting solenoid.

5 n to be performed within the bore of the MCD solenoid.

6 nsporters, which overwhelmingly fold as beta-solenoids.

7 epeats that assemble into two separate alpha-solenoids.

8 al hinge-an arrangement of interlocked alpha-solenoids-about which it can bend to adapt to cages of v

9 equipped with a stepper motor driven stage, solenoid-actuated pinch valves, miniaturized peristaltic

10 olds into a relatively complex two-rung beta-solenoid amyloid.

11 s, one located near to the N terminus of the solenoid and the other between the C-terminal juxtamembr

12 ovalent salt conditions using both one-start solenoid and two-start zigzag starting configurations.

13 The p115 structures show a novel alpha-solenoid architecture constructed of 12 armadillo-like,

14 1 angstroms reveals a large horseshoe-shaped solenoid assembled from 23 leucine-rich repeats (LRRs).

15 We also constructed beta-solenoid-based insulin fibril models and conducted fiber

16 ure pulse in the sample line by means of the solenoid-based micropump.

17 iserum OC) or antiparallel beta-sheets, beta-solenoids, beta-barrels, and beta-cylindrins (recognized

18 Moreover, solenoids can be degenerated and widely vary in the numb

19 linical-grade microcatheter prototype with a solenoid coil at the distal tip was deflected with a foo

20 the use of a large-diameter radio frequency solenoid coil that permits substantially larger sample v

21 al lobe blocks in a 7T human scanner using a solenoid coil.

22 oduce measured PNS thresholds of two leg/arm solenoid coils with good agreement.

23 ent an irregular folding of an alpha-helical solenoid composed of HEAT-like repeats.

24 structure reveals a triangular beta-helical (solenoid) conformation with conserved residues forming t

25 inner groove spanning the entire ANK repeat solenoid contains multiple target binding sites capable

26 a 28 nm long rod comprising a central alpha-solenoid dimer capped by two beta-propeller domains at e

27 Nup84 forms a U-shaped alpha-helical solenoid domain, topologically similar to two other memb

28 A drawn glass microinjector and solenoid-driven dispenser are utilized to array picolite

29 or homogeneous (seeded with infectious beta-solenoid fibrils) fibrillization.

30 eals that the TcdB CROP domain adopts a beta-solenoid fold consisting of long and short repeats and t

31 dies and bioinformatics shows that the alpha-solenoid fold extends the full length of VPS35, and that

32 dynamics predict a tightly wound left-handed solenoid fold in which the cysteines form a disulfide co

33 It reveals a compressed beta-solenoid fold in which the top and bottom sheets are hel

34 roteins are predicted to have toroidal alpha-solenoid folds composed of 9-11 proteasome/cyclosome rep

35 ld group containing beta-propeller and alpha-solenoid folds, and the peripheral FG group containing p

36 ts of the insulin amyloid fibrils using beta-solenoid folds, namely, the beta-helix and beta-roll.

37 diation source, with cooling effected with a solenoid-gated compressed air source.

38 o have a beta-solenoidal structure; the beta-solenoid has the cross-beta structure characteristic of

39 acteristic for strongly curved alpha-helical solenoids has been constructed and was found to match pr

40 PR65 is the two-layered (alpha-alpha solenoid) HEAT-repeat (Huntingtin, elongation factor 3,

41 hought to be a predominant HEAT repeat alpha-solenoid, implying a role as a facilitator of macromolec

42 concave face of the Toll leucine-rich repeat solenoid in an area delineated by N-linked glycans and i

43 The solenoid is reinforced by intrachain hydrogen bonds, sid

44 lathrin an arrangement of three curved alpha-solenoid legs radiating from a common center, and COPI s

45 Leucine Rich Repeat (LRR) domains and other solenoids like proteins, we show that the automated anal

46 LH condense into zigzag structures and that solenoid-like features are viable only for longer NRLs (

47 Rpn6 consists of an alpha-solenoid-like fold and a proteasome COP9/signalosome eIF

48 a mechanism for the formation of the wrapped solenoid-like segrosome superstructure.

49 Next, the regions of the solenoid-like TRN-SR2 molecule that are involved in the

50 on is largely consistent with that of a beta-solenoid model previously determined by solid-state NMR.

51 The results support the alpha-solenoid model, except that they indicate that the repea

52 the type of linker DNA bending that defines solenoid models may be simultaneously present in a struc

53 solenoid, the packing of nucleosomes in the solenoid must be highly constrained.

54 shown that at low pH, it forms either a beta-solenoid or a stacked beta-sheet structure, depending on

55 ealing an extensive network of alpha-helical solenoids organized into a diamond ring conformation and

56 y of helical HEAT-like repeats, which form a solenoid perfectly shaped to accommodate a DNA duplex on

57 ectromagnetic field, supplied by a wire coil solenoid placed underneath the sample plate.

58 Rpn10 attaches to the central solenoid portion of Rpn1, although this association is s

59 ucleate the formation of the infectious beta-solenoid prions in a process of heterogeneous seeding, b

60 le irregularities of repeat lengths in three solenoid protein families.

61 nsile strength (UTS) for two engineered beta-solenoid protein mutant fibril structures (spruce budwor

62 ovides a fast and accurate tool to recognize solenoid protein structures as a whole and to identify i

63 ing for precise identification of repeats in solenoid protein structures, an important subgroup of pe

64 The alpha-helical solenoid proteins adopt a variety of elongated curved st

65 Solenoid proteins are emerging as a protein class with p

66 Containing repeating structural units, solenoid proteins are expected to share sequence similar

67 Solenoid proteins feature prominently in these pathways.

68 proach to recognize solenoid repeats and non-solenoid proteins using stationary wavelet packet transf

69 cs features that capture repeating motifs of solenoid proteins.

70 ed on the pentapeptide repeat family of beta-solenoid proteins.

71 del for PolyQKd-33 and a model with two beta-solenoid protofibrils for PolyQKd-32.

72 le plumbing design, using a small, low-power solenoid pump and valve, avoids the need for quantitativ

73 kg x soln(-1), n = 242), using low-precision solenoid pumps to introduce sample and titrant.

74 dicted secondary structures containing alpha-solenoids related to those of clathrin heavy chain and C

75 e methods to design a series of closed alpha-solenoid repeat structures (alpha-toroids) in which the

76 ctures as a whole and to identify individual solenoid repeat units from a structure.

77 icle, we propose a new approach to recognize solenoid repeats and non-solenoid proteins using station

78 Recently, several solenoid repeats detection methods have been proposed, s

79 f ConSole analysis, we show how detection of solenoid repeats in structures can be used to improve se

80 essfully designed and validated closed alpha-solenoid repeats with a left-handed helical architecture

81 solic assembly is built on an extended alpha-solenoid scaffold connecting key regulatory domains to t

82 h paired EF-hands originating from the alpha-solenoid scaffold, suggesting a mechanism for channel ga

83 , and proteins with beta-propeller and alpha-solenoid secondary structures.

84 ures that can capture hidden components from solenoid sequence similarities and distinguish them from

85 face to form a large segrosome with an open, solenoid-shaped structure, suggesting a mechanism for Pa

86 bute extensive hydrogen-bonding networks for solenoid stabilization.

87 o Raphael, the only other publicly available solenoid structure detection tool.

88 the leucine-rich repeat concave side of the solenoid structure of NgR.

89 are two loops that protrude from the central solenoid structure of the protein.

90 he concave surface of the LRR modules of the solenoid structure where three key hydrophilic residues,

91 of these features for the formation of beta-solenoid structure, as well as the cumulative effects of

92 rate 35-amino-acid motif which form an alpha-solenoid structure.

93 shows that it folds into a classical curved solenoid structure.

94 tate NMR to be assemblies of a two-rung beta-solenoid structure.

95 chromatin, while non-compact structures and solenoid structures are consistent with open chromatin.

96 ctural designs such as prisms, propellers, 2-solenoid, super-roll, clam, trefoil and box are not wide

97 asic framework of TLRs is a horseshoe-shaped solenoid that contains an extensive beta-sheet on its co

98 rface located in the kink regions of the two solenoids that is reinforced by additional interactions

99 orseshoe-shaped, right-handed, alpha-helical solenoid, the concave face of which completely covers th

100 nd yet forms apparently 'normal' elements of solenoid, the packing of nucleosomes in the solenoid mus

101 th a groove on the surface of the ANK repeat solenoid, thereby regulating the affinities between anky

102 The tandem N-terminal helical solenoid tightly packs against the FAT and kinase domain

103 e plug has been 7-10 times the length of the solenoid to avoid line broadening from volume magnetic s

104 The structure reveals a bent solenoid typical of leucine-rich repeat proteins with an

105 xpiratory-phase TGI was established, using a solenoid valve activated by the ventilator.

106 hanism employing two-beam refraction and one solenoid valve was developed and found to successfully g

107 y modulation experiments are performed using solenoid valves to introduce concentration plugs of a ma

108 nsive components (i.e., peristaltic pump and solenoid valves), which are discretely computer-operated

109 n vitro that are probably several turns of a solenoid with about six nucleosomes per turn.

110 s of Tor form a HEAT repeat-containing alpha-solenoid with four distinct segments: a highly curved 80

111 odel, which envisages axial stacking of beta-solenoids with two coils per subunit, we examined fibril