Riggs, Jennifer R.; Nagy, Mark; Elsner, Jan; Erdman, Paul; Cashion, Dan et al. (2017). The Discovery of a Dual TTK Protein Kinase/CDC2-Like Kinase (CLK2) Inhibitor for the Treatment of Triple Negative Breast Cancer Initiated from a Phenotypic Screen. Journal of Medicinal Chemistry 60(21) , 8989-9002. 10.1021/acs.jmedchem.7b01223. [PDB: 6b4w] |
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Riggs, Jennifer R.; Elsner, Jan; Cashion, Dan; Robinson, Dale; Tehrani, Lida et al. (2019). Design and Optimization Leading to an Orally Active TTK Protein Kinase Inhibitor with Robust Single Agent Efficacy. Journal of Medicinal Chemistry 62(9) , 4401-4410. 10.1021/acs.jmedchem.8b01869. [PDB: 6n6o] |
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Richter, Jeremy M.; Cheney, Daniel L.; Bates, J. Alex; Wei, Anzhi; Luettgen, Joseph M. et al. (2016). Design and Synthesis of Novel Meta-Linked Phenylglycine Macrocyclic FVIIa Inhibitors. ACS Medicinal Chemistry Letters 8(1) , 67-72. 10.1021/acsmedchemlett.6b00375. [PDB: 5tqe] |
CMCF-ID |
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Richardson-Sanchez, Tomas; Chan, Anson C. K.; Sabatino, Brendil; Lin, Helen; Gaynor, Erin C. et al. (2023). Dissecting components of theCampylobacter jejuni fetMP-fetABCDEFgene cluster in iron scavenging. Tribology Letters . 10.1101/2023.07.05.547857. [PDB: 8t4c] |
CMCF-ID |
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Rice, Kyle; Batul, Kissa; Whiteside, Jacqueline; Kelso, Jayne; Papinski, Monica et al. (2019). The predominance of nucleotidyl activation in bacterial phosphonate biosynthesis. Nature Communications 10(1) . 10.1038/s41467-019-11627-6. |
CMCF-ID |
Peer-Reviewed Article |
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Rescourio, Gwenaella; Gonzalez, Ana Z.; Jabri, Salman; Belmontes, Brian; Moody, Gordon et al. (2019). Discovery and in Vivo Evaluation of Macrocyclic Mcl-1 Inhibitors Featuring an α-Hydroxy Phenylacetic Acid Pharmacophore or Bioisostere. Journal of Medicinal Chemistry 62(22) , 10258-10271. 10.1021/acs.jmedchem.9b01310. [PDB: 6ud2, 6udi] |
CMCF-ID |
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Health |
Ren, Li; Grina, Jonas; Moreno, David; Blake, James F.; Gaudino, John J. et al. (2015). Discovery of Highly Potent, Selective, and Efficacious Small Molecule Inhibitors of ERK1/2. Journal of Medicinal Chemistry 58(4) , 1976-1991. 10.1021/jm501921k. [PDB: 4xj0] |
CMCF-ID |
Peer-Reviewed Article |
Health |
Reniere, Michelle L.; Ukpabi, Georgia N.; Harry, S. Reese; Stec, Donald F.; Krull, Robert et al. (2010). The IsdG-family of haem oxygenases degrades haem to a novel chromophore. Molecular Microbiology 75(6) , 1529-1538. 10.1111/j.1365-2958.2010.07076.x. [PDB: 3lgm, 3lgn] |
CMCF-ID |
Peer-Reviewed Article |
Health |
René, Olivier; Fauber, Benjamin P.; Boenig, Gladys de Leon; Burton, Brenda; Eidenschenk, Céline et al. (2014). Minor Structural Change to Tertiary Sulfonamide RORc Ligands Led to Opposite Mechanisms of Action. ACS Medicinal Chemistry Letters 6(3) , 276-281. 10.1021/ml500420y. [PDB: 4wqp] |
CMCF-ID |
Peer-Reviewed Article |
Health |
Reimer, J.M.; Jiang, J.; Harb, I.; Schmeing, T.M. (2018). Crystal structure of the formyltransferase PseJ from Anoxybacillus kamchatkensis. Protein Data Bank: 6ci2. |
CMCF-ID |
PDB Deposition |
Health |
Reimer, J.M.; Harb, I.; Schmeing, T.M. (2018). Crystal structure of the formyltransferase PseJ from Anoxybacillus kamchatkensis in complex with UDP-4,6-dideoxy-4-formamido-L-AltNAc and tetrahydrofolate. Protein Data Bank: 6ci5. |
CMCF-ID |
PDB Deposition |
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Reimer, J.M.; Eivaskhani, M.; Schmeing, T.M. (2019). Crystal structure of a 4-domain construct of LgrA in the substrate donation state. Protein Data Bank: 6mfw. |
CMCF-ID |
PDB Deposition |
Health |
Reimer, J.M.; Eivaskhani, M.; Schmeing, T.M. (2019). Crystal structure of a 4-domain construct of a mutant of LgrA in the substrate donation state. Protein Data Bank: 6mfx. |
CMCF-ID |
PDB Deposition |
Health |
Reimer, J.M.; Eivaskhani, M.; Harb, I.; Schmeing, T.M. (2019). Crystal structure of a 5-domain construct of LgrA in the substrate donation state. Protein Data Bank: 6mfy. |
CMCF-ID |
PDB Deposition |
Health |
Reimer, J.M.; Eivaskhani, M.; Harb, I.; Schmeing, T.M. (2019). Crystal structure of dimodular LgrA in a condensation state. Protein Data Bank: 6mfz. |
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PDB Deposition |
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