Corrigendum: a two-armed probe for in-cell DEER measurements on proteins (vol 26, pg 17128, 2020)

Autor: Miao, Q., Zurlo, E., Bruin, D. de, Wondergem, J.A.J., Skinner, S.P., Timmer, M., Cramer, A.J., Heinrich, D.M., Overhand, M., Huber, M.I.

Publikováno v: Chemistry-a European Journal, 27(23), 6994-6994

CORRIGENDUM Q. Miao, E. Zurlo, D. de Bruin, J. A. J. Wondergem, S. P. Skinner, M. Timmer, A. Blok, D. Heinrich, M. Overhand, M. Huber,* M. Ubbink* 17128–17133 A Two-Armed Probe for In-Cell DEER Measurements on Proteins Chem. Eur. J., 2020, 26 DOI:

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::665cee9a9262c68a961aa0ec4496006b
http://hdl.handle.net/1887/3254484

Synthesis and structural analysis of a beta-hairpin peptide containing a sugar amino acid

Autor: Aguilera, B., Siegal, G., Overkleeft, H.S., Meeuwenoord, N.J., Rutjes, F.P.J.T., Hest, J.C.M. van, Schoemaker, H.E., Marel, G.A. van der, Boom, J.H. van, Overhand, M.

Publikováno v: European Journal of Organic Chemistry, 2001, 1541-1547. Wiley-v c h verlag gmbh
European Journal of Organic Chemistry, 1541-1547. Wiley-VCH Verlag
STARTPAGE=1541;ENDPAGE=1547;ISSN=1434-193X;TITLE=European Journal of Organic Chemistry
European Journal of Organic Chemistry, 2001, 8, pp. 1541-1547

Item does not contain fulltext

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https://hdl.handle.net/2066/14068

Ring-extended gramicidin S analogs Containing cis δ-sugar amino acid turn mimetics with varying ring size

Autor: Knijnenburg, A.D., Spalburg, E., Neeling, A.J. de, Mars-Groenendijk, R.H., Noort, D., Grotenbreg, G.M., Marel, G.A. van der, Overkleeft, H.S., Overhand, M.

Publikováno v: Helvetica Chimica Acta, 12, 95, 2544-2561

This article presents a series of ring-extended gramicidin S derivatives, 9-14, that have four ornithine residues as polar protonated side chains and one modified turn region containing a mono-functionalized cis-δ-oxetane, δ-furanoid, or δ-pyranoi

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http://resolver.tudelft.nl/uuid:5b1f7a7d-243b-4624-9a73-1ece82d378c5

Exploring the conformational and biological versatility of ß-turn-modified gramicidin s by using sugar amino acid homologues that vary in ring size

Autor: Knijnenburg, A.D., Tuin, A.W., Spalburg, E., Neeling, A.J. de, Mars-Groenendijk, R.H., Noort, D., Otero, J.M., Llamas-Saiz, A.L., Raaij, M.J. van, Marel, G.A. van der, Overkleeft, H.S., Overhand, M.

Publikováno v: Chemistry-A European Journal, 14, 17, 3995-4004

Monobenzylated sugar amino acids (SAAs) that differ in ether ring size (containing an oxetane, furanoid, and pyranoid ring) were synthesized and incorporated in one of the ß-turn regions of the cyclo-decapeptide gramicidin S (GS). CD, NMR spectrosco

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http://resolver.tudelft.nl/uuid:1f6b2e64-5aef-42c9-a9fc-805d3e6fef2f

Evaluation of readily accessible azoles as mimics of the aromatic ring of D-phenylalanine in the turn region of gramicidin S

Autor: Knaap, M. van der, Lageveen, L.T., Busscher, H.J., Mars-Groenendijk, R., Noort, D., Otero, J.M., Llamas-Saiz, A.L., Raaij, M.J. van, Marel, G.A. van der, Overkleeft, H.S., Overhand, M.

Publikováno v: ChemMedChem, 5, 6, 840-847

The influence of replacing the d-phenylalanine residue with substituted and unsubstituted azoles on the structure and biological activity of the antibiotic gramicidinS was investigated against a representative panel of Gram-positive and Gram-negative

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http://resolver.tudelft.nl/uuid:7908424c-fce6-42e2-8f5c-8b06a3004447