about
Total synthesis of glycosylated proteinsApplication of the protein semisynthesis strategy to the generation of modified chromatinSynthesis of homogeneous MUC1 oligomers via a bi-directional ligation strategy.Total synthesis of homogeneous variants of hirudin P6: a post-translationally modified anti-thrombotic leech-derived protein.Histones: at the crossroads of peptide and protein chemistry.A PEGylated photocleavable auxiliary mediates the sequential enzymatic glycosylation and native chemical ligation of peptides.The winding pathway to erythropoietin along the chemistry-biology frontier: a success at last.Peptide ligation chemistry at selenol amino acids.Intramolecular acyl transfer in peptide and protein ligation and synthesis.Developments and recent advancements in the field of endogenous amino acid selective bond forming reactions for bioconjugation.Chemical and semisynthesis of modified histones.Modern tools for the chemical ligation and synthesis of modified peptides and proteins.Oxidative Deselenization of Selenocysteine: Applications for Programmed Ligation at Serine.Chemoselective peptide ligation-desulfurization at aspartate.A molecular engineering toolbox for the structural biologist.Thirteen decades of peptide synthesis: key developments in solid phase peptide synthesis and amide bond formation utilized in peptide ligation.Aziridine-Mediated Ligation at Phenylalanine and Tryptophan Sites.Traceless reductive ligation at a tryptophan site: a facile access to β-hydroxytryptophan appended peptides.Synthesis of l- and d-Ubiquitin by One-Pot Ligation and Metal-Free Desulfurization.Convergent synthesis of MUC1 glycopeptides via serine ligation.Chemoselective fragment condensation between peptide and peptidomimetic oligomers.A Type of Auxiliary for Native Chemical Peptide Ligation beyond Cysteine and Glycine Junctions.Mosquito-Derived Anophelin Sulfoproteins Are Potent Antithrombotics.
P2860
Q28083496-BE3EB21A-9B5B-4B11-B6D3-AAB8EF5B9E7CQ28831322-B759640F-3A93-472D-AC14-C9E1B2E2F42DQ34901076-733BF71A-6BB5-49CF-BC58-5556A0196BFEQ35116875-9C310E23-DE1A-4B66-9196-EF33C6059CB1Q35229609-E3D85A21-0FED-4514-9C77-8C8DE96C1B64Q35915524-B609F25F-D340-4957-A522-3B3F765370CBQ36508946-56736E49-915F-4071-A4BB-376D79261787Q38166998-6C2C426A-C002-435B-BE28-C77FF073B5C6Q38340077-D50E6EB4-9EA5-4E11-B4C7-BB244314D4E1Q38497871-2DFC10DC-8CF5-4E98-B37F-FEF595F4F5B5Q38700270-D6E31785-0BE1-4559-8AF5-3A3B6E741AAFQ38792098-7B5D10E5-2966-4A28-A864-ACD7AA7F16EEQ40524884-46840EFC-E14B-48B9-AF97-C0CD6B8B2CBFQ45892251-A1BF5372-E1D0-4DC5-80E4-526546D1639EQ47256792-098CDC46-6B2C-41E2-866F-2A61A909C727Q47353754-ACBF1430-BD20-489D-AF56-F374A4DD75D4Q48793448-391ED700-D73F-456D-9CFC-66B0A7C87885Q48987240-D5FE1D1E-51CC-40CB-89E9-BD3B8F7CB8AEQ50861673-72DF6150-2C52-4701-9527-7F6F8524EB70Q50940828-B109001C-A369-43D3-907A-D29C5CD869E6Q50954669-36C3F7B6-D804-402B-8533-0B454D1451C5Q52860657-06E6E842-F2F1-412F-B1C5-D8006FDBB051Q55045502-D5143E6D-7710-4AB6-8FAE-FE58F77F96CC
P2860
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Peptide ligation-desulfurization chemistry at arginine.
@en
Peptide ligation-desulfurization chemistry at arginine.
@nl
type
label
Peptide ligation-desulfurization chemistry at arginine.
@en
Peptide ligation-desulfurization chemistry at arginine.
@nl
prefLabel
Peptide ligation-desulfurization chemistry at arginine.
@en
Peptide ligation-desulfurization chemistry at arginine.
@nl
P2860
P356
P1433
P1476
Peptide ligation-desulfurization chemistry at arginine
@en
P2093
Katie M Cergol
Richard J Payne
P2860
P304
P356
10.1002/CBIC.201300049
P577
2013-02-20T00:00:00Z