ChemInform Abstract: Peptidic Ring Expansion. Synthesis of Ring-Expanded Macrocyclic Lactams by Amino Acid Insertion.

ChemInform ◽  
2010 ◽  
Vol 26 (39) ◽  
pp. no-no
Author(s):  
A. BORCHARDT ◽  
W. C. STILL
Author(s):  
Jing Shang ◽  
Varsha J. Thombare ◽  
Carlie L. Charron ◽  
Uta Wille ◽  
Craig A. Hutton

Synlett ◽  
1995 ◽  
Vol 1995 (SI) ◽  
pp. 539-540 ◽  
Author(s):  
Allen Borchardt ◽  
W. Clark Still

Author(s):  
João Pereira‐Vaz ◽  
Pedro Crespo ◽  
Luísa Mocho ◽  
Patrícia Martinho ◽  
Teresa Fidalgo ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Clare S. K. Lee ◽  
Ming Fung Cheung ◽  
Jinsen Li ◽  
Yongqian Zhao ◽  
Wai Hei Lam ◽  
...  

AbstractThe Origin Recognition Complex (ORC) is an evolutionarily conserved six-subunit protein complex that binds specific sites at many locations to coordinately replicate the entire eukaryote genome. Though highly conserved in structure, ORC’s selectivity for replication origins has diverged tremendously between yeasts and humans to adapt to vastly different life cycles. In this work, we demonstrate that the selectivity determinant of ORC for DNA binding lies in a 19-amino acid insertion helix in the Orc4 subunit, which is present in yeast but absent in human. Removal of this motif from Orc4 transforms the yeast ORC, which selects origins based on base-specific binding at defined locations, into one whose selectivity is dictated by chromatin landscape and afforded with plasticity, as reported for human. Notably, the altered yeast ORC has acquired an affinity for regions near transcriptional start sites (TSSs), which the human ORC also favors.


1999 ◽  
Vol 274 (4) ◽  
pp. 2093-2096 ◽  
Author(s):  
Kunihiko Tanaka ◽  
Gregorio D. Chazenbalk ◽  
Sandra M. McLachlan ◽  
Basil Rapoport

2009 ◽  
Vol 392 (4) ◽  
pp. 1074-1086 ◽  
Author(s):  
Stuart E. Knowling ◽  
Angelo Miguel Figueiredo ◽  
Sara B.-M. Whittaker ◽  
Geoffrey R. Moore ◽  
Sheena E. Radford

2020 ◽  
Vol 64 (8) ◽  
Author(s):  
Laurent Poirel ◽  
Xavier Vuillemin ◽  
Mario Juhas ◽  
Amandine Masseron ◽  
Ursina Bechtel-Grosch ◽  
...  

ABSTRACT KPC-50 is a KPC-3 variant identified from a Klebsiella pneumoniae clinical isolate recovered in Switzerland in 2019. Compared to KPC-3, KPC-50 shows (i) a three-amino-acid insertion (Glu-Ala-Val) between amino acids 276 and 277, (ii) an increased affinity to ceftazidime, (iii) a decreased sensitivity to avibactam, explaining the ceftazidime-avibactam resistance, and (iv) an association with a sharp reduction of its carbapenemase activity.


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