... A- and P-loops, 25 56–7 and 22 54–5, respectively, can be superimposed on each other with no apparent deviations, whereas noticeable differences are found between their neighbors, 25 54–5 and 22 52 3 ... A-site tRNA and G2553 [41], can be formed in the symmetryrelated region While rotating, the RM interacts with the rear-wall bases belonging to nucleotides C2573, A2451, and C24 52, and slides along ... of L 22; on the conservation of the L 22 double-hook; and on the finding that sequence related translational arrest could be suppressed by mutations localized in the L 22 double-hook region [ 72] We...
... Acad Sci USA 91, 22 60– 22 64 34 Welcker M, Singer J, Loeb KR, Grim J & Bloecher A (20 03) Multisite phosphorylation by Cdk2 and GSK3 controls cyclin E degradation Mol Cell 12, 381–3 92 35 Kim SY, Song ... signaling network Science 29 7, 1018–1 023 24 Heinrich R, Neel BG & Rapoport TA (20 02) Mathematical models of protein kinase signal transduction Mol Cell 9, 957–970 25 Roach PJ (1991) Multisite and hierarchal ... Hill coefficient ranges between and (Fig 3E) For random and mixed FEBS Journal 27 4 (20 07) 1046–1061 ª 20 07 The Authors Journal compilation ª 20 07 FEBS C Salazar and T Hofer ¨ Kinetic models of...
... Biophys Acta 1387, 22 6 23 8 30 Ryan, M., Carlson, B.M & Ohlendieck, K (20 00) Oligomeric status of the dihydropyridine receptor in aged skeletal muscle Mol Cell Biol Res Commun 4, 22 4 22 9 31 He, Z., ... SDS/PAGE under reducing conditions was carried out by standard methodology [21 ] using 7% gels and 20 lg protein per lane [22 ] Protein band patterns were visualized by Coomassie Brilliant Blue ... calcium-handling proteins in native sarcoplasmic reticulum membranes from rabbit skeletal muscle Biochim Biophys Acta 1515, 120 –1 32 Ó FEBS 20 02 Supramolecular calsequestrin complex (Eur J Biochem 26 9)...
... 13 and 16) Truncations of IRF-3 to amino acids 328 , 26 4 or 24 1 resulted in much stronger binding to the ISRE (lanes 19, 22 and 25 ) In the presence of GST-CBP-N a doublet of supershifted bands ... Wathelet, M.G (1998) Structure and Function of Ó FEBS 20 02 10 11 12 13 14 15 16 17 18 19 20 21 22 Mechanism of IRF-3 virus-dependent activation (Eur J Biochem 26 9) 6151 the Interferon-b Enhanceosome ... -p300-N, -M and -C were described previously [24 ], GST-CBP-N1, -N2, -N3, -C1, -C2, -C3 and GST-p300-C1, -C2, -C3 were generated by subcloning PCR products and verified by sequencing GST and GST fusions...
... M., and Draper, D E (1991) Recognition of the highly conserved GTPase center of 23 S ribosomal RNA by ribosomal protein L11 and the antibiotic thiostrepton J Mol Biol 22 1, 125 7 126 8 Wyman, J and ... Curtis A Machida, 20 00 125 Glycoprotein Methods and Protocols: The Mucins, edited by Anthony P Corfield, 20 00 124 Protein Kinase Protocols, edited by Alastair D Reith, 20 01 123 In Situ Hybridization ... Hybridization Protocols (2nd ed.), edited by Ian A Darby, 20 00 122 Confocal Microscopy Methods and Protocols, edited by Stephen W Paddock, 1999 121 Natural Killer Cell Protocols: Cellular and Molecular...
... Biochem Biophys 20 06, 453:108- 122 Page 10 of 11 (page number not for citation purposes) Virology Journal 20 08, 5:61 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 Shepherd DN, ... PstI and partially digested with NcoI Fragments of both plasmids approximately 0.33 kbp, 0.69 kbp, and 4.4 kbp in size (respectively referred to as K1, K2, and K3 for pKNco and S1, S2, and S3 ... purified fragments from pKNco and pSNco, using the following combinations of fragments: 1) S1, K2, K3; 2) K1, S2, K3; 3) S1, S2, K3; 4) K1, S2, S3; 5) S1, K2, S3; 6) K1, K2, S3 These six ligations...