Sequentielle α-Ketosäurehydroxylamin(KAHA)-Ligationen: Synthese C-terminaler Varianten des Modifikationsproteins UFM1.
- Published in:
- Angewandte Chemie, 2012, v. 124, n. 38, p. 9831, doi. 10.1002/ange.201204144
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Works matching AU Pattabiraman, Vijaya R.
Results: 22
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Titelbild: Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline (Angew. Chem. 21/2012).
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- Angewandte Chemie, 2012, v. 124, n. 21, p. 5101, doi. 10.1002/ange.201202064
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- Publication type:
- Article
3
Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline.
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- Angewandte Chemie, 2012, v. 124, n. 21, p. 5204, doi. 10.1002/ange.201200907
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- Publication type:
- Article
4
Introduction of d‐Amino Acids in Minimalistic Peptide Substrates by an S‐Adenosyl‐l‐Methionine Radical Epimerase.
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- Angewandte Chemie, 2019, v. 131, n. 8, p. 2268, doi. 10.1002/ange.201809508
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- Article
5
Sequential α-Ketoacid-Hydroxylamine (KAHA) Ligations: Synthesis of C-Terminal Variants of the Modifier Protein UFM1.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 38, p. 9693, doi. 10.1002/anie.201204144
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- Article
6
Cover Picture: Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline (Angew. Chem. Int. Ed. 21/2012).
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- Angewandte Chemie International Edition, 2012, v. 51, n. 21, p. 5015, doi. 10.1002/anie.201202064
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- Publication type:
- Article
7
Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline.
- Published in:
- Angewandte Chemie International Edition, 2012, v. 51, n. 21, p. 5114, doi. 10.1002/anie.201200907
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- Publication type:
- Article
8
Cover Picture: Solid-Supported Synthesis and Biological Evaluation of the Lantibiotic Peptide Bis(desmethyl) Lacticin 3147 A2 (Angew. Chem. Int. Ed. 49/2008).
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- Angewandte Chemie International Edition, 2008, v. 47, n. 49, p. 9357, doi. 10.1002/anie.200890251
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9
Solid-Supported Synthesis and Biological Evaluation of the Lantibiotic Peptide Bis(desmethyl) Lacticin 3147 A2.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 49, p. 9472, doi. 10.1002/anie.200802919
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- Article
10
Introduction of d‐Amino Acids in Minimalistic Peptide Substrates by an S‐Adenosyl‐l‐Methionine Radical Epimerase.
- Published in:
- Angewandte Chemie International Edition, 2019, v. 58, n. 8, p. 2246, doi. 10.1002/anie.201809508
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- Publication type:
- Article
11
Chemical Synthesis of the Highly Hydrophobic Antiviral Membrane-Associated Protein IFITM3 and Modified Variants.
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- Angewandte Chemie, 2017, v. 129, n. 41, p. 12813, doi. 10.1002/ange.201707554
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- Publication type:
- Article
12
Spurlose Herstellung C-terminaler α-Ketosäuren zur chemischen Proteinsynthese mittels α-Ketoäure-Hydroxylamin-Ligation: Synthese von SUMO2/3.
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- Angewandte Chemie, 2014, v. 126, n. 45, p. 12445, doi. 10.1002/ange.201407014
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- Article
13
Berichtigung: Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline.
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- Angewandte Chemie, 2014, v. 126, n. 45, p. 12200, doi. 10.1002/ange.201406880
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- Publication type:
- Article
14
Berichtigung: Sequentielle α-Ketosäurehydroxylamin(KAHA)-Ligationen: Synthese C-terminaler Varianten des Modifikationsproteins UFM1.
- Published in:
- Angewandte Chemie, 2014, v. 126, n. 45, p. 12200, doi. 10.1002/ange.201406882
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- Publication type:
- Article
15
Bildung und Umlagerung von Homoserin-Depsipeptiden und -proteinen durch α-Ketosäure-Hydroxylamin-Ligation mit 5-Oxaprolin.
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- Angewandte Chemie, 2014, v. 126, n. 45, p. 12441, doi. 10.1002/ange.201406097
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- Publication type:
- Article
16
Myotubularin-related protein 7 activates peroxisome proliferator-activated receptor-gamma.
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- Oncogenesis, 2020, v. 9, n. 6, p. 1, doi. 10.1038/s41389-020-0238-8
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- Article
17
Rethinking amide bond synthesis.
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- Nature, 2011, v. 480, n. 7378, p. 471, doi. 10.1038/nature10702
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- Publication type:
- Article
18
Chemical Synthesis of the Highly Hydrophobic Antiviral Membrane-Associated Protein IFITM3 and Modified Variants.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 41, p. 12639, doi. 10.1002/anie.201707554
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- Publication type:
- Article
19
Traceless Preparation of C-Terminal α-Ketoacids for Chemical Protein Synthesis by α-Ketoacid-Hydroxylamine Ligation: Synthesis of SUMO2/3.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 45, p. 12248, doi. 10.1002/anie.201407014
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- Publication type:
- Article
20
Corrigendum: Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 45, p. 12005, doi. 10.1002/anie.201406880
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- Publication type:
- Article
21
Corrigendum: Sequential α-Ketoacid-Hydroxylamine (KAHA) Ligations: Synthesis of C-Terminal Variants of the Modifier Protein UFM1.
- Published in:
- Angewandte Chemie International Edition, 2014, v. 53, n. 45, p. 12005, doi. 10.1002/anie.201406882
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- Publication type:
- Article
22
Formation and Rearrangement of Homoserine Depsipeptides and Depsiproteins in the α-Ketoacid-Hydroxylamine Ligation with 5-Oxaproline.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 45, p. 12244, doi. 10.1002/anie.201406097
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- Publication type:
- Article