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1 Aug 2000: 9 62 ( :1 $; ) :&1 $; ) :. $; )) ' ( 9 --./ --8+#9 ' <1=.1 $; $ &=>1 $; )? @. :11 ' $ ) #-8-# 62 ) ' ( ---# 9 $ ( ' ' # 62 4 A77 )( $ 7 ' )B # --&/ B( C' --8+ ... B( ;#R# A# D #C## R## ;9##C'2## #9# )--- 6 7 # 3 81&=8&#.

10 Mar 2014: Venn Diagram:. A B. B ={ four, five,six}. one. two, three six four five. ... Set Notation. Venn Diagram:. A B. A B ={two,three}. one. two, three six four five.

16 Jul 2023: Email: andela.saric@ist.ac.at (A.Š.); r.vlijm@rug.nl (R.V.);bbaum@mrc-lmb.cam.ac.uk (B.B.). Hurtig et al., Sci. Adv. ... B) Quantification of preferred ESCRT-III homolog localization from imageslike those presented in (A).

10 Mar 2014: Venn Diagram:. A B. B ={ four, five,six}. one. two, three six four five. ... Set Notation. Venn Diagram:. A B. A B ={two,three}. one. two, three six four five.

1 Mar 2021: The Coot User Manual

4 Mar 2019: b, Identification of the elbow. Long-distance cross-link midpoint density (see Fig. ... HeadN HeadCJointN JointCElbowN ElbowCHinge. Sm. c5–S. mc6. Sm. c–S. cpA. B.

24 Sep 2015: Biol. Chem. 273, 19554–1955916. Liu, X., Singh, B. B., and Ambudkar, I. ... 93–10419. Singh, B. B., Liu, X., Tang, J., Zhu, M. X., and Ambudkar, I.

3 Nov 2001: interaction, in comparison with the longitudi-nal contact, has an important ionic contribution,both for a-a and b-b contacts. ... Lateral contacts. Lateral contacts between protolaments in thezinc sheets entail extensive interactions betweenhomologous

30 Aug 2001: b,. pH optimum. MreB was incubated under standard conditions (see Methods) with 100 mM. ... After washing with 5% buffer B the protein waseluted with 30% buffer B.

28 Apr 2024: 3B). Dimer–dimer interactions between the two strands are primarily along the lateral direction, including type 4 (pair B- B’, antiparallel) and type 5 (pairs B- D’ and B’- D, parallel) ... D’. A-C or A’-C’. B-B’. D-B’ orD’-B.

13 Jun 2022: 7A, B). Structuralmodels of these Heimdallarchaeotal proteins were generatedusing AlphaFold 274,75 (Supplementary Fig. ... Ubiquitin. I44V45. Heim Ubiquitin(model). (ii). (i). B. A CVPS28UEV. 469 aaSB SB.

3 Mar 2014: y-a)/(b-a) = 1-exp(-lambda x)  y = b – (b-a) exp(-lambda x), if we see exponential function then we may have this particular relationship. ... y = a bx and a = 3, b=10. Conclusions. Average and variance are usual measures for location and spread of

29 Dec 2017: Along three proto-filament interfaces, lateral contacts form a B-lattice with A-Aand B-B contacts (Fig. ... The view shown highlights theseam (A lattice, A-B lateral contacts). (B, Right) Rotated by 180, showing the B lattice (A-A and B-B lateral contacts

14 Nov 2021: grids. The dark lines are the edges of GO flakes. (B) Representative 2D class averages. ... K33-linked polyubiquitin. Mol Cell 58, 95–109.22 Monika B-B, Martin TG, Naylor CE, Basak AK,.

31 Mar 2014: y=f(x,b,e). ipipiii xxxy εβββ =. 2211. ipipiii. xxxy ebbb =. 2211. ... E(β̂)= β. E(. ˆ. b)=b. V(β̂)=σ 2(XTX)1. V(. ˆ. b)=s. 2.

7 May 2013: ruvw = u a v b w c where u, v, w are integers. ... b.b = 1 b.c = 0. c.c = 1 c.a = 0.

29 May 2019: B) GFP-PrP from wild type and DTMED10 cells was affinity purified under non-denaturing. ... B. B. B. Y B. BNb. APEX2. surface. Nb. total. lysate.

4 Mar 2008: The topology of thea-domain is b-a-a-b-b, where the third b-strand is packedin between the first and the second strands. ... coli FtsQ (green) on the b-domain of DivIB from G. stearothermophilus (blue).

16 Oct 2009: B. B. Zhou, S. J. Elledge, Nature 408, 433 (2000).2. J. ... 13, 2665 (2004).29. We thank B. Davletov for the provision of synaptotagmin.

16 Jul 1998: These membranes were then included during fully translocated into the lumen suggests that additionaltranslation reactions of prolactin (B), b-lactamase (C), wild-type PrP. ... Eachmembrane preparation was also included intranslation reactions of