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8CO7

Crystal structure of human soluble adenylyl cyclase (sAC) in complex with inhibitor TDI-09066

Summary for 8CO7
Entry DOI10.2210/pdb8co7/pdb
DescriptorAdenylate cyclase type 10, 4-chloranyl-6-[1-methyl-4-(thiophen-2-ylmethyl)pyrazol-3-yl]pyrimidin-2-amine, DIMETHYL SULFOXIDE, ... (9 entities in total)
Functional Keywordscamp, adenylyl cyclase, inhibitor, catalytic domain, signaling protein
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight55970.92
Authors
Steegborn, C. (deposition date: 2023-02-27, release date: 2024-01-03)
Primary citationSun, S.,Fushimi, M.,Rossetti, T.,Kaur, N.,Ferreira, J.,Miller, M.,Quast, J.,van den Heuvel, J.,Steegborn, C.,Levin, L.R.,Buck, J.,Myers, R.W.,Kargman, S.,Liverton, N.,Meinke, P.T.,Huggins, D.J.
Scaffold Hopping and Optimization of Small Molecule Soluble Adenyl Cyclase Inhibitors Led by Free Energy Perturbation.
J.Chem.Inf.Model., 63:2828-2841, 2023
Cited by
PubMed: 37060320
DOI: 10.1021/acs.jcim.2c01577
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

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