5VRP
Crystal Structure of Human Renin in Complex with a biphenylpipderidinylcarbinol
Summary for 5VRP
Entry DOI | 10.2210/pdb5vrp/pdb |
Related | 5V8V 5VPM |
Descriptor | Renin, 2-acetamido-2-deoxy-beta-D-glucopyranose, SULFATE ION, ... (5 entities in total) |
Functional Keywords | renin inhibitor, biphenyl, hypertension, cyp 3a4, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Homo sapiens (Human) |
Cellular location | Secreted: P00797 |
Total number of polymer chains | 2 |
Total formula weight | 76536.24 |
Authors | Concha, N.,Zhao, B. (deposition date: 2017-05-11, release date: 2017-10-18, Last modification date: 2024-10-30) |
Primary citation | Lawhorn, B.G.,Tran, T.,Hong, V.S.,Morgan, L.A.,Le, B.T.,Harpel, M.R.,Jolivette, L.,Diaz, E.,Schwartz, B.,Gross, J.W.,Tomaszek, T.,Semus, S.,Concha, N.,Smallwood, A.,Holt, D.A.,Kallander, L.S. Discovery of renin inhibitors containing a simple aspartate binding moiety that imparts reduced P450 inhibition. Bioorg. Med. Chem. Lett., 27:4838-4843, 2017 Cited by PubMed Abstract: Discovery of potent renin inhibitors which contain a simplified alkylamino Asp-binding group and exhibit improved selectivity for renin over Cyp3A4 is described. Structure-function results in this series are rationalized based on analysis of selected compounds bound to renin, and the contribution of each molecular feature leading to the reduced P450 inhibition is quantified. PubMed: 28985999DOI: 10.1016/j.bmcl.2017.09.046 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.22 Å) |
Structure validation
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