Insights into the mechanism of peptide cyclodehydrations achieved through the chemoenzymatic generation of amide derivatives.
about
Cyclisation mechanisms in the biosynthesis of ribosomally synthesised and post-translationally modified peptidesThe Cyanobactin Heterocyclase Enzyme: A Processive Adenylase That Operates with a Defined Order of ReactionDiscovery of a new ATP-binding motif involved in peptidic azoline biosynthesis.Nucleophilic 1,4-additions for natural product discovery.HIV protease inhibitors block streptolysin S productionIdentification of an Auxiliary Leader Peptide-Binding Protein Required for Azoline Formation in Ribosomal Natural Products.Structural analysis of leader peptide binding enables leader-free cyanobactin processingRecognition sequences and substrate evolution in cyanobactin biosynthesisIn Vitro Biosynthesis of the Core Scaffold of the Thiopeptide ThiomuracinEngineering unnatural variants of plantazolicin through codon reprogramming.Orchestration of enzymatic processing by thiazole/oxazole-modified microcin dehydrogenases.α,β-Dehydroamino acids in naturally occurring peptides.The structural biology of patellamide biosynthesisYcaO-Dependent Posttranslational Amide Activation: Biosynthesis, Structure, and Function.Employing the promiscuity of lantibiotic biosynthetic machineries to produce novel antimicrobials.Mechanisms of cyanobactin biosynthesisIn Vitro Biosynthesis and Substrate Tolerance of the Plantazolicin Family of Natural Products.Cysteine Isocyanide in Multicomponent Reaction: Synthesis of Peptido-Mimetic 1,3-Azoles.Dissecting Bottromycin Biosynthesis Using Comparative Untargeted Metabolomics.
P2860
Q26738949-53329CFD-C8F6-400D-9B15-CF9B971CDC56Q27680570-ABB201AE-D3AC-4492-AAA8-9BA7D067916DQ34207315-B68AEBCC-1022-4A61-9C2B-AE482ED203F2Q34211690-059596A2-E469-4E8F-A0FB-1E3BA8D2AE39Q34462102-6EE02C26-96D0-4E8E-B498-D59030D4F5E7Q34478499-12727A8B-DBB8-4853-93D4-A32A7A7E9611Q34481795-72DCA9DA-4B69-4164-A761-181010CC720CQ35262723-7A9599B5-6B1A-4013-B3B2-E3341D9DDFE2Q36761831-4AF387A5-FB55-486A-9875-F580AA3F100AQ37198599-1ECF39C7-C1F2-4CB5-9FF4-AF3200571C43Q37592315-825294E2-9B2A-4AFD-AADA-5D1F696DEB07Q38260920-225F12A8-55A8-4BF3-8FDD-5671CFB4AC16Q38280503-ABE8FDE0-6899-415A-B7C7-210DA6BD89F5Q38751212-4820923E-71CF-452F-BC24-A4F30802B06CQ38945513-8BEB73E1-A644-4944-8A29-A8CD8C4CE790Q38957421-140D9791-0A09-4DC0-9924-4F6349AEC509Q41492401-EA8647EF-09AF-4CF9-B78E-3167588B9A19Q41707652-B8ED03A8-BBF9-486D-85D4-E53780CEFEB1Q41920228-942B8CCC-8258-43AB-B801-4FB770CB07C9
P2860
Insights into the mechanism of peptide cyclodehydrations achieved through the chemoenzymatic generation of amide derivatives.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Insights into the mechanism of ...... neration of amide derivatives.
@en
type
label
Insights into the mechanism of ...... neration of amide derivatives.
@en
prefLabel
Insights into the mechanism of ...... neration of amide derivatives.
@en
P2860
P356
P1476
Insights into the mechanism of ...... neration of amide derivatives.
@en
P2093
Douglas A Mitchell
Kyle L Dunbar
P2860
P304
P356
10.1021/JA4029507
P407
P577
2013-05-30T00:00:00Z