6C9R
Mycobacterium tuberculosis adenosine kinase bound to (2R,3S,4R,5R)-2-(hydroxymethyl)-5-(6-(thiophen-3-yl)-9H-purin-9-yl)tetrahydrofuran-3,4-diol
Summary for 6C9R
Entry DOI | 10.2210/pdb6c9r/pdb |
Descriptor | Adenosine kinase, 9-beta-D-ribofuranosyl-6-(thiophen-3-yl)-9H-purine, SODIUM ION, ... (5 entities in total) |
Functional Keywords | nucleoside analog, complex, inhibitor, structural genomics, psi-2, protein structure initiative, tb structural genomics consortium, tbsgc, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Mycobacterium tuberculosis |
Total number of polymer chains | 2 |
Total formula weight | 73436.51 |
Authors | Crespo, R.A.,TB Structural Genomics Consortium (TBSGC) (deposition date: 2018-01-28, release date: 2019-05-01, Last modification date: 2023-10-04) |
Primary citation | Crespo, R.A.,Dang, Q.,Zhou, N.E.,Guthrie, L.M.,Snavely, T.C.,Dong, W.,Loesch, K.A.,Suzuki, T.,You, L.,Wang, W.,O'Malley, T.,Parish, T.,Olsen, D.B.,Sacchettini, J.C. Structure-Guided Drug Design of 6-Substituted Adenosine Analogues as Potent Inhibitors of Mycobacterium tuberculosis Adenosine Kinase. J.Med.Chem., 62:4483-4499, 2019 Cited by PubMed: 31002508DOI: 10.1021/acs.jmedchem.9b00020 PDB entries with the same primary citation |
Experimental method |
Structure validation
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