Riley S. Carter

ORCID: 0000-0001-8370-4510
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Research Areas
  • Peptidase Inhibition and Analysis
  • RNA and protein synthesis mechanisms
  • Biochemical and Structural Characterization
  • Plant biochemistry and biosynthesis
  • Microbial Metabolism and Applications
  • Ubiquitin and proteasome pathways
  • Microbial Natural Products and Biosynthesis
  • Chemical Synthesis and Analysis
  • Genomics and Chromatin Dynamics
  • Cancer-related gene regulation

University of Illinois Urbana-Champaign
2024

Mitja M. Zdouc Kai Blin Nico L L Louwen Jorge C. Navarro-Muñoz Catarina Loureiro and 95 more Chantal D. Bader Constance B. Bailey Lena Barra Thomas Booth Kenan A. J. Bozhüyük José D. D. Cediel-Becerra Zachary Charlop–Powers Marc G. Chevrette Yit‐Heng Chooi Paul M. D’Agostino Tristan de Rond Elena Del Pup Katherine Duncan Wenjia Gu Novriyandi Hanif Eric J. N. Helfrich Matthew Jenner Yohei Katsuyama Aleksandra E. Korenskaia Daniel Krug Vincent Libis George Lund Shrikant Mantri Kalindi D. Morgan Charlotte Owen Chin‐Soon Phan Benjamin Philmus Zachary L. Reitz Serina L. Robinson Kumar Saurabh Singh Robin Teufel Yaojun Tong Fidele Tugizimana Dana Ulanová Jaclyn M. Winter César Aguilar Daniel Yuri Akiyama Suhad A. A. Al-Salihi Mohammad Alanjary Fabrizio Alberti Gajender Aleti Shumukh A. Alharthi Manuel Rojo Amr A. Arishi Hannah E. Augustijn Nicole E. Avalon J. Abraham Avelar‐Rivas Kyle K. Axt Hellen Bertoletti Barbieri Júlio César Jerônimo Barbosa Lucas Gabriel Barboza Segato Susanna E. Barrett Martin Baunach Christine Beemelmanns Dardan Beqaj Tim Berger Jordan Bernaldo-Agüero Sandra M Bettenbühl Vincent A. Bielinski Friederike Biermann Ricardo Moraes Borges Rainer Borriss Milena Breitenbach Kevin M. Bretscher Michael W Brigham Larissa Buedenbender Brodie W. Bulcock Carolina Cano‐Prieto João Capela Víctor J. Carrión Riley S. Carter Raquel Castelo‐Branco Gabriel Castro‐Falcón Fernanda O. Chagas Esteban Charria‐Girón Ayesha Ahmed Chaudhri Vasvi Chaudhry Hyukjae Choi Yukyung Choi Roya Choupannejad Jakub Chromy Melinda S Chue Donahey Jérôme Collemare Jack A. Connolly Kaitlin E. Creamer Max Crüsemann Arturo Colín-Cruz Andrés Cumsille Jean‐Félix Dallery Luis Caleb Damas-Ramos Tito Damiani Martinus de Kruijff Belén Martín Gerardo Della Sala Jelle Dillen

Abstract Specialized or secondary metabolites are small molecules of biological origin, often showing potent activities with applications in agriculture, engineering and medicine. Usually, the biosynthesis these natural products is governed by sets co-regulated physically clustered genes known as biosynthetic gene clusters (BGCs). To share information about BGCs a standardized machine-readable way, Minimum Information Biosynthetic Gene cluster (MIBiG) data standard repository was initiated...

10.1093/nar/gkae1115 article EN cc-by Nucleic Acids Research 2024-12-09

Borosins are ribosomally synthesized and post-translationally modified peptides (RiPPs) containing backbone α-N-methylations. These modifications confer favorable pharmacokinetic properties including increased membrane permeability resistance to proteolytic degradation. Previous studies have biochemically bioinformatically explored several borosins, revealing (1) numerous domain architectures (2) diverse core regions lacking conserved sequence elements. Due these characteristics, large-scale...

10.1021/acschembio.4c00066 article EN ACS Chemical Biology 2024-05-02

Cell cycle-regulated gene expression is essential for normal cell growth and development loss of stringent control associated with the acquisition transformed phenotype. The selective synthesis histone proteins during S phase cycle required to render cells competent ordered packaging replicating DNA into chromatin. Regulation H4 transcription requires proliferation-specific promoter binding factor HiNF-D. In diploid cells, HiNF-D activity regulated cycle; nuclear protein extracts prepared...

10.1126/science.247.4949.1454 article EN Science 1990-03-23

Borosins are ribosomally synthesized and post-translationally modified peptides containing backbone α-N-methylations. Identification of borosin precursor is difficult because (1) there no conserved sequence elements among (2) the biosynthetic gene clusters contain numerous domain architectures peptide fusions. To tackle this problem, we updated genome mining tool RODEO to automatically evaluate putative BGCs identify peptides. Enabled by new module, analyzed all found in available data...

10.1101/2024.01.09.574750 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2024-01-10
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