Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Lars G J Hammarström"'
Autor:
Ömer Poyraz, Katharina Brunner, Bernhard Lohkamp, Hanna Axelsson, Lars G J Hammarström, Robert Schnell, Gunter Schneider
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0121494 (2015)
In Mycobacterium tuberculosis the sulfate activating complex provides a key branching point in sulfate assimilation. The complex consists of two polypeptide chains, CysD and CysN. CysD is an ATP sulfurylase that, with the energy provided by the GTPas
Externí odkaz:
https://doaj.org/article/bab1d0b6fc6b4ba293bab66fdfbd0176
Autor:
Helge, Gad, Tobias, Koolmeister, Ann-Sofie, Jemth, Saeed, Eshtad, Sylvain A, Jacques, Cecilia E, Ström, Linda M, Svensson, Niklas, Schultz, Thomas, Lundbäck, Berglind Osk, Einarsdottir, Aljona, Saleh, Camilla, Göktürk, Pawel, Baranczewski, Richard, Svensson, Ronnie P-A, Berntsson, Robert, Gustafsson, Kia, Strömberg, Kumar, Sanjiv, Marie-Caroline, Jacques-Cordonnier, Matthieu, Desroses, Anna-Lena, Gustavsson, Roger, Olofsson, Fredrik, Johansson, Evert J, Homan, Olga, Loseva, Lars, Bräutigam, Lars, Johansson, Andreas, Höglund, Anna, Hagenkort, Therese, Pham, Mikael, Altun, Fabienne Z, Gaugaz, Svante, Vikingsson, Bastiaan, Evers, Martin, Henriksson, Karl S A, Vallin, Olov A, Wallner, Lars G J, Hammarström, Elisee, Wiita, Ingrid, Almlöf, Christina, Kalderén, Hanna, Axelsson, Tatjana, Djureinovic, Jordi, Carreras Puigvert, Maria, Häggblad, Fredrik, Jeppsson, Ulf, Martens, Cecilia, Lundin, Bo, Lundgren, Ingrid, Granelli, Annika, Jenmalm Jensen, Per, Artursson, Jonas A, Nilsson, Pål, Stenmark, Martin, Scobie
Publikováno v:
Nature. 544(7651)
Autor:
Mark L. McLaughlin, Yanwen Fu, Tod J. Miller, Lars G. J. Hammarström, Robert P. Hammer, Frank R. Fronczek
Publikováno v:
The Journal of Organic Chemistry. 66:7118-7124
The preparation of sterically hindered and polyfunctional Cα,α-disubstituted α-amino acids (ααAAs) via alkylation of ethyl nitroacetate and transformation into derivatives ready for incorporation into peptides are described. Treatment of ethyl n
Publikováno v:
The Journal of Peptide Research. 58:108-116
A series of short, amphipathic peptides incorporating 80% C(alpha),C(alpha)-disubstituted glycines has been prepared to investigate amphipathicity as a helix-stabilizing effect. The peptides were designed to adopt 3(10)- or alpha-helices based on amp
Autor:
Damon R. Billodeaux, Lars G. J. Hammarström, Tao Zhang, Frank R. Fronczek, Mark L. McLaughlin, José Giraldés
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 56:1484-1486
The carboxy group of 2-methyl-N-[(2-nitrophenyl)sulfonyl]alanine, C10H12N2O6S, forms centrosymmetric hydrogen-bonded dimers with an O⋯O distance of 2.629 (2) A and an intramolecular N—H⋯O(nitro) hydrogen bond N⋯O distance of 2.823 (2) A. 1-
Publikováno v:
Peptides for the New Millennium ISBN: 0792364457
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6db3e4f0483ca50589ce3976dc6d5c8
https://doi.org/10.1007/0-306-46881-6_109
https://doi.org/10.1007/0-306-46881-6_109
Publikováno v:
Organic Syntheses
DMAP(4-Dimethylamino)pyridine 1-tert-Butoxycarbonylpiperidine-4-spiro-5′-(1′,3′-bis(tert-butoxycarbonyl)hydantoin 4-Amino1-tert-butoxycarbonylpiperidine-4-carboxylic acid 1-tert-Butyloxycarbonyl-4-(9-fluorenylmethyloxyamino)piperidine-4-carboxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfd5bf7232fb65f4ec3667cb8c846aba
https://doi.org/10.1002/0471264229.os081.23
https://doi.org/10.1002/0471264229.os081.23
Publikováno v:
Peptides: The Wave of the Future ISBN: 9789401039055
The efficacy of current antibiotics is declining at an alarming rate due to the proliferation of multi-drug resistant bacteria [1]. Synthetic antimicrobial peptides are currently being investigated as potential agents to address the increased need of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ede793c40bb93f1a54c0c120a7d04e4f
https://doi.org/10.1007/978-94-010-0464-0_354
https://doi.org/10.1007/978-94-010-0464-0_354
Publikováno v:
Peptides: The Wave of the Future ISBN: 9789401039055
The discovery of Cα, α-disubstituted amino acids (ααAAs) and their propensity to induce secondary structure even into short peptides has resulted in an increased interest in novel methods for their synthesis [1, 2]. Herein ethyl nitroacetate, a u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d8d16d396e7d661fcf1934499500b55
https://doi.org/10.1007/978-94-010-0464-0_11
https://doi.org/10.1007/978-94-010-0464-0_11
Publikováno v:
Peptides: The Wave of the Future ISBN: 9789401039055
The ability to design desired secondary peptide structure a priori from specific amino acid sequence is a major goal in peptide studies. In particular, influences on the 310-/α-helical equilibrium have gained considerable recent interest [1]. The ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b84d9d18103359d408fad56dc28dfd32
https://doi.org/10.1007/978-94-010-0464-0_205
https://doi.org/10.1007/978-94-010-0464-0_205