Bibliografías temáticas / CP26

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Literatura académica sobre el tema "CP26"

Autor: Grafiati
Publicado: 11 de marzo de 2023

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Artículos de revistas sobre el tema "CP26"

1

Friedrich, Carol, Monisha G. Scott, Nedra Karunaratne, Hong Yan, and Robert E. W. Hancock. "Salt-Resistant Alpha-Helical Cationic Antimicrobial Peptides." Antimicrobial Agents and Chemotherapy 43, no. 7 (1999): 1542–48. http://dx.doi.org/10.1128/aac.43.7.1542.

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ABSTRACT Analogues based on the insect cecropin–bee melittin hybrid peptide (CEME) were studied and analyzed for activity and salt resistance. The new variants were designed to have an increase in amphipathic α-helical content (CP29 and CP26) and in overall positive charge (CP26). The α-helicity of these peptides was demonstrated by circular dichroism spectroscopy in the presence of liposomes. CP29 was shown to have activity against gram-negative bacteria that was similar to or better than those of the parent peptides, and CP26 had similar activity. CP29 had cytoplasmic membrane permeabilizati
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2

Kang, Ho Chul, Ji Hyung Chae, Yeon Ho Lee та ін. "Erythroid Cell-Specific α-Globin Gene Regulation by the CP2 Transcription Factor Family". Molecular and Cellular Biology 25, № 14 (2005): 6005–20. http://dx.doi.org/10.1128/mcb.25.14.6005-6020.2005.

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ABSTRACT We previously demonstrated that ubiquitously expressed CP2c exerts potent erythroid-specific transactivation of α-globin through an unknown mechanism. This mechanism is reported here to involve specific CP2 splice variants and protein inhibitor of activated STAT1 (PIAS1). We identify a novel murine splice isoform of CP2, CP2b, which is identical to CP2a except that it has an additional 36 amino acids encoded by an extra exon. CP2b has an erythroid cell-specific transcriptional activation domain, which requires the extra exon and can form heteromeric complexes with other CP2 isoforms,
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3

Jackowski, Grzegorz, and Stefan Jansson. "Characterization of Photosystem II Antenna Complexes Separated by Non-Denaturing Isoelectric Focusing." Zeitschrift für Naturforschung C 53, no. 9-10 (1998): 841–48. http://dx.doi.org/10.1515/znc-1998-9-1010.

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CP26, CP29 and three different LHC II subcomplexes have been purified from a carnation photosystem II (PSII) preparation using non-denaturing isoelectric focusing in a vertical polyacrylamide slab gel. The identity of the fractions was established by absorption spectroscopy, SDS-PAGE and immunoblotting. CP26 comprised a single apoprotein of 26.6 kDa and CP29 contained two apoproteins of 28.8 and 28.5 kDa. LHC II subcomplex A consisted of Lhcb1 homotrimers, and subcomplexes B and C consisted of Lhcb1/Lhcb2 and Lhcb1/Lhcb3 heterotrimers, respectively. We discuss the data in relation to the organ
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4

Byram, Rebecca, Philip E. Stewart, and Patricia Rosa. "The Essential Nature of the Ubiquitous 26-Kilobase Circular Replicon of Borrelia burgdorferi." Journal of Bacteriology 186, no. 11 (2004): 3561–69. http://dx.doi.org/10.1128/jb.186.11.3561-3569.2004.

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ABSTRACT The genome of the type strain (B31) of Borrelia burgdorferi, the causative agent of Lyme disease, is composed of 12 linear and 9 circular plasmids and a linear chromosome. Plasmid content can vary among strains, but one 26-kb circular plasmid (cp26) is always present. The ubiquitous nature of cp26 suggests that it provides functions required for bacterial viability. We tested this hypothesis by attempting to selectively displace cp26 with an incompatible but replication-proficient vector, pBSV26. While pBSV26 transformants contained this incompatible vector, the vector coexisted with
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5

Marr, K. M., D. N. Mastronarde, and M. K. Lyon. "Two-dimensional crystals of photosystem II: biochemical characterization, cryoelectron microscopy and localization of the D1 and cytochrome b559 polypeptides." Journal of Cell Biology 132, no. 5 (1996): 823–33. http://dx.doi.org/10.1083/jcb.132.5.823.

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Photosystem II (PS II) is a photosynthetic reaction center found in higher plants which has the unique ability to evolve oxygen from water. Several groups have formed two-dimensional PS II crystals or have isolated PS II complexes and studied them by electron microscopy and image analysis. The majority of these specimens have not been well characterized biochemically and have yielded relatively low resolution two-dimensional projection maps with a variety of unit cell sizes. We report the characterization of the polypeptide and lipid content of tubular crystals of PS II. The crystals contain t
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6

Tilly, Kit, Lori Lubke, and Patricia Rosa. "Characterization of Circular Plasmid Dimers inBorrelia burgdorferi." Journal of Bacteriology 180, no. 21 (1998): 5676–81. http://dx.doi.org/10.1128/jb.180.21.5676-5681.1998.

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ABSTRACT We have inactivated the ospC, oppAIV, andguaB genes on the 26-kb circular plasmid of Borrelia burgdorferi (cp26) by allelic exchange. On several occasions following such transformations, the cp26 of transformants had an aberrant mobility through agarose gels. Characterization of these cp26 molecules showed that the plasmid had dimerized. These dimers were quite stable during either selective or nonselective passage. Subsequent transformations with dimer DNA supported the hypothesis that in B. burgdorferi, transforming cp26 DNA most likely does not displace the resident homologous plas
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7

Olszówka, Dorota, Stanisław Krawczyk, and Waldemar Maksymiec. "A study of molecular interactions in light-harvesting complexes LHCIIb, CP29, CP26 and CP24 by Stark effect spectroscopy." Biochimica et Biophysica Acta (BBA) - Bioenergetics 1657, no. 1 (2004): 61–70. http://dx.doi.org/10.1016/j.bbabio.2004.04.004.

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8

Amarie, Sergiu, Laura Wilk, Tiago Barros, Werner Kühlbrandt, Andreas Dreuw, and Josef Wachtveitl. "Properties of zeaxanthin and its radical cation bound to the minor light-harvesting complexes CP24, CP26 and CP29." Biochimica et Biophysica Acta (BBA) - Bioenergetics 1787, no. 6 (2009): 747–52. http://dx.doi.org/10.1016/j.bbabio.2009.02.006.

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9

Branton, Margaret A., Thomas H. MacRae, Fred Lipschultz та Peter G. Wells. "Identification of a small heat shock/α-crystallin protein in the scleractinian coral Madracis mirabilis (Duch. and Mitch.)". Canadian Journal of Zoology 77, № 5 (1999): 675–82. http://dx.doi.org/10.1139/z99-029.

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Immunological evidence is provided for the first time of a small heat shock/α-crystallin protein in the scleractinian coral Madracis mirabilis. The protein, termed cp26, had a molecular weight of 26 000; it reacted with an antibody raised to a small heat shock/α-crystallin protein fromArtemia franciscana and its production in corals was temperature sensitive. Corals collected from seawater at 25.5oC or lower lacked cp26, but the protein was produced in some of these animals when they were heat shocked experimentally. When exposed naturally to high environmental temperatures for relatively shor
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10

Yakushevska, Alevtyna E., Wilko Keegstra, Egbert J. Boekema, et al. "The Structure of Photosystem II inArabidopsis:Localization of the CP26 and CP29 Antenna Complexes†." Biochemistry 42, no. 3 (2003): 608–13. http://dx.doi.org/10.1021/bi027109z.

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