scholarly article | Q13442814 |
P50 | author | Masafumi Yanase | Q92278148 |
Akimitsu Okamoto | Q56557586 | ||
Gosuke Hayashi | Q90328608 | ||
P2093 | author name string | Koki Nakatsu | |
Charlane Joy Cardos | |||
Yoshiki Konda | |||
P2860 | cites work | Synthesis of proteins by native chemical ligation | Q29616750 |
Recent extensions to native chemical ligation for the chemical synthesis of peptides and proteins. | Q30367477 | ||
Expanding the chemical toolbox for the synthesis of large and uniquely modified proteins | Q30387202 | ||
Fmoc solid-phase synthesis of peptide thioesters using an intramolecularn,S-acyl shift | Q33217181 | ||
Peptidyl N,N-bis(2-mercaptoethyl)-amides as thioester precursors for native chemical ligation | Q34156008 | ||
Histones: at the crossroads of peptide and protein chemistry | Q35229609 | ||
From protein total synthesis to peptide transamidation and metathesis: playing with the reversibility of N,S-acyl or N,Se-acyl migration reactions. | Q35464860 | ||
Shifting Native Chemical Ligation into Reverse through N→S Acyl Transfer | Q35752105 | ||
Chemical Synthesis of Phosphorylated Histone H2A at Tyr57 Reveals Insight into the Inhibition Mode of the SAGA Deubiquitinating Module. | Q37093722 | ||
One-pot multi-segment condensation strategies for chemical protein synthesis | Q90633240 | ||
Chemistry-Driven Epigenetic Investigation of Histone and DNA Modifications | Q90708022 | ||
Examination of the Deubiquitylation Site Selectivity of USP51 by Using Chemically Synthesized Ubiquitylated Histones | Q91327571 | ||
Native chemical ligation in protein synthesis and semi-synthesis | Q93002062 | ||
Affibody molecules: engineered proteins for therapeutic, diagnostic and biotechnological applications. | Q37730252 | ||
Sequential native peptide ligation strategies for total chemical protein synthesis. | Q38039308 | ||
Recent progress in the chemical synthesis of proteins | Q38200443 | ||
Peptide Thioester Formation via an Intramolecular N to S Acyl Shift for Peptide Ligation | Q38265067 | ||
Intramolecular acyl transfer in peptide and protein ligation and synthesis | Q38340077 | ||
Histone exchange, chromatin structure and the regulation of transcription | Q38343838 | ||
An efficient Fmoc-SPPS approach for the generation of thioester peptide precursors for use in native chemical ligation | Q38589907 | ||
N-methylcysteine-mediated total chemical synthesis of ubiquitin thioester | Q38599572 | ||
Chemical and semisynthesis of modified histones. | Q38700270 | ||
A statistical view of protein chemical synthesis using NCL and extended methodologies. | Q38746019 | ||
A one-pot three-segment ligation strategy for protein chemical synthesis | Q39440953 | ||
Chemical Protein Synthesis Using a Second-Generation N-Acylurea Linker for the Preparation of Peptide-Thioester Precursors. | Q40935294 | ||
Peptide o-aminoanilides as crypto-thioesters for protein chemical synthesis | Q41726421 | ||
3-Mercaptopropionic acid-mediated synthesis of peptide and protein thioesters. | Q41790279 | ||
Serine promoted synthesis of peptide thioester-precursor on solid support for native chemical ligation | Q41845807 | ||
Bis(2-sulfanylethyl)amino native peptide ligation | Q42851853 | ||
Fmoc solid-phase synthesis of C-terminal peptide thioesters by formation of a backbone pyroglutamyl imide moiety | Q43280904 | ||
Free-radical-based, specific desulfurization of cysteine: a powerful advance in the synthesis of polypeptides and glycopolypeptides | Q46875940 | ||
Total chemical synthesis of histones and their analogs, assisted by native chemical ligation and palladium complexes | Q47693387 | ||
P-B Desulfurization: An Enabling Method for Protein Chemical Synthesis and Site-Specific Deuteration. | Q47710669 | ||
Regulation of the Stability of the Histone H2A-H2B Dimer by H2A Tyr57 Phosphorylation. | Q47789073 | ||
A Facile N-Mercaptoethoxyglycinamide (MEGA) Linker Approach to Peptide Thioesterification and Cyclization | Q48202682 | ||
Chemically synthesized histone H2A Lys13 di-ubiquitination promotes binding of 53BP1 to nucleosomes | Q49829381 | ||
Chemical chromatin ubiquitylation | Q49833767 | ||
Total Chemical Synthesis of Modified Histones | Q50280774 | ||
New t-butyl based aspartate protecting groups preventing aspartimide formation in Fmoc SPPS. | Q50963132 | ||
Development of new thioester equivalents for protein chemical synthesis. | Q50967300 | ||
Benchmarking and validating algorithms that estimate pK(a) values of drugs based on their molecular structures. | Q51908993 | ||
Acyl donors for native chemical ligation. | Q52588662 | ||
Peptide and protein thioester synthesis via N-->S acyl transfer. | Q52599877 | ||
Efficient Palladium-Assisted One-Pot Deprotection of (Acetamidomethyl)Cysteine Following Native Chemical Ligation and/or Desulfurization To Expedite Chemical Protein Synthesis. | Q53111970 | ||
Fmoc synthesis of peptide thioesters without post-chain-assembly manipulation. | Q53237060 | ||
Chemical synthesis of proteins using peptide hydrazides as thioester surrogates. | Q53671255 | ||
A thioethylalkylamido (TEA) thioester surrogate in the synthesis of a cyclic peptide via a tandem acyl shift. | Q54481958 | ||
A straightforward method for automated Fmoc-based synthesis of bio-inspired peptide crypto-thioesters. | Q55315084 | ||
Expedient synthesis of pseudo-Pro-containing peptides: towards constrained peptidomimetics and foldamers | Q56982244 | ||
Tandem Thiol Switch Synthesis of Peptide Thioesters via N–S Acyl Shift on Thiazolidine | Q57236365 | ||
Peptide ligations using aryloxycarbonyl-o-methylaminoanilides: chemical synthesis of palmitoylated-Sonic Hedgehog | Q57279603 | ||
Triple Function of 4-Mercaptophenylacetic Acid Promotes One-Pot Multiple Peptide Ligation | Q57800803 | ||
Novel Protein Science Enabled by Total Chemical Synthesis | Q57807007 | ||
Palladium prompted on-demand cysteine chemistry for the synthesis of challenging and uniquely modified proteins | Q58375316 | ||
Allyl-based groups for side-chain protection of amino-acids | Q72618461 | ||
Efficient microwave-assisted tandem N- to S-acyl transfer and thioester exchange for the preparation of a glycosylated peptide thioester | Q80302079 | ||
Cysteine-derived s-protected oxazolidinones: potential chemical devices for the preparation of peptide thioesters | Q82369093 | ||
N-->S acyl-transfer-mediated synthesis of peptide thioesters using anilide derivatives | Q83221169 | ||
Insights into the mechanism and catalysis of the native chemical ligation reaction | Q83355026 | ||
Protein chemical synthesis by ligation of peptide hydrazides | Q84291313 | ||
Synthetic procedure for N-Fmoc amino acyl-N-sulfanylethylaniline linker as crypto-peptide thioester precursor with application to native chemical ligation | Q84592366 | ||
One-pot/sequential native chemical ligation using N-sulfanylethylanilide peptide | Q84883119 | ||
Convergent chemical synthesis of proteins by ligation of peptide hydrazides | Q84962712 | ||
A new method for synthesis of peptide thioesters via irreversible N-to-S acyl transfer | Q85250855 | ||
An efficient one-pot four-segment condensation method for protein chemical synthesis | Q86932433 | ||
One-Pot/Sequential Native Chemical Ligation Using Photocaged Crypto-thioester | Q87053427 | ||
In vitro and in cell analysis of chemically synthesized histone H2A with multiple modifications | Q87468905 | ||
Development of an Anilide-Type Scaffold for the Thioester Precursor N-Sulfanylethylcoumarinyl Amide | Q88137587 | ||
N-Sulfanylethylaminooxybutyramide (SEAoxy): A Crypto-Thioester Compatible with Fmoc Solid-Phase Peptide Synthesis | Q88672642 | ||
Peptide Weinreb amide derivatives as thioester precursors for native chemical ligation | Q89221490 | ||
Advances in Native Chemical Ligation-Desulfurization: A Powerful Strategy for Peptide and Protein Synthesis | Q89278273 | ||
P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 23 | |
P304 | page(s) | 5967-5975 | |
P577 | publication date | 2019-05-09 | |
P1433 | published in | Chemical Science | Q2962267 |
P1476 | title | Cysteinylprolyl imide (CPI) peptide: a highly reactive and easily accessible crypto-thioester for chemical protein synthesis | |
P478 | volume | 10 |
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