6C67
Mycobacterium tuberculosis adenosine kinase bound to iodotubercidin
Summary for 6C67
Entry DOI | 10.2210/pdb6c67/pdb |
Related | 2PKF 2PKK 2PKM 2PKN |
Descriptor | Adenosine kinase, (2R,3R,4S,5R)-2-(4-AMINO-5-IODO-7H-PYRROLO[2,3-D]PYRIMIDIN-7-YL)-5-(HYDROXYMETHYL)TETRAHYDROFURAN-3,4-DIOL, SODIUM ION, ... (6 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 (strain ATCC 25618 / H37Rv) |
Total number of polymer chains | 2 |
Total formula weight | 70906.71 |
Authors | Crespo, R.A.,TB Structural Genomics Consortium (TBSGC) (deposition date: 2018-01-17, 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 | X-RAY DIFFRACTION (2.11 Å) |
Structure validation
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