6UDX
X-ray co-crystal structure of compound 7 with Mcl-1
Summary for 6UDX
Entry DOI | 10.2210/pdb6udx/pdb |
Related | 6UD2 6UDI 6UDT 6UDU 6UDV |
Descriptor | Induced myeloid leukemia cell differentiation protein Mcl-1, (2R)-[(3S)-6'-chloro-5-(cyclobutylmethyl)-3',4,4',5-tetrahydro-2H,2'H-spiro[1,5-benzoxazepine-3,1'-naphthalen]-7-yl](hydroxy)acetic acid (3 entities in total) |
Functional Keywords | protein-protein interaction, apoptosis, inhibitor, apoptosis-inhibitor complex, apoptosis/inhibitor |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 2 |
Total formula weight | 36728.58 |
Authors | Huang, X. (deposition date: 2019-09-19, release date: 2019-12-11, Last modification date: 2024-03-13) |
Primary citation | Rescourio, G.,Gonzalez, A.Z.,Jabri, S.,Belmontes, B.,Moody, G.,Whittington, D.,Huang, X.,Caenepeel, S.,Cardozo, M.,Cheng, A.C.,Chow, D.,Dou, H.,Jones, A.,Kelly, R.C.,Li, Y.,Lizarzaburu, M.,Lo, M.C.,Mallari, R.,Meleza, C.,Rew, Y.,Simonovich, S.,Sun, D.,Turcotte, S.,Yan, X.,Wong, S.G.,Yanez, E.,Zancanella, M.,Houze, J.,Medina, J.C.,Hughes, P.E.,Brown, S.P. Discovery and in Vivo Evaluation of Macrocyclic Mcl-1 Inhibitors Featuring an alpha-Hydroxy Phenylacetic Acid Pharmacophore or Bioisostere. J.Med.Chem., 62:10258-10271, 2019 Cited by PubMed: 31736296DOI: 10.1021/acs.jmedchem.9b01310 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.7 Å) |
Structure validation
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