5BPH
Crystal structure of AMP complexed D-alanine-D-alanine ligase(DDL) from Yersinia pestis
Summary for 5BPH
Entry DOI | 10.2210/pdb5bph/pdb |
Related | 5BPF |
Descriptor | D-alanine--D-alanine ligase, ADENOSINE MONOPHOSPHATE, SODIUM ION, ... (6 entities in total) |
Functional Keywords | d-alanine-d-alanine ligase (ddl), drug target; bacterial cell wall synthesis, ligase |
Biological source | Yersinia pestis |
Cellular location | Cytoplasm : Q8ZIE7 |
Total number of polymer chains | 4 |
Total formula weight | 135221.91 |
Authors | Tran, H.T.,Kang, L.W.,Hong, M.K. (deposition date: 2015-05-28, release date: 2016-03-02, Last modification date: 2024-03-20) |
Primary citation | Tran, H.T.,Hong, M.K.,Ngo, H.P.,Huynh, K.H.,Ahn, Y.J.,Wang, Z.,Kang, L.W. Structure of D-alanine-D-alanine ligase from Yersinia pestis: nucleotide phosphate recognition by the serine loop. Acta Crystallogr D Struct Biol, 72:12-21, 2016 Cited by PubMed Abstract: D-Alanyl-D-alanine is an essential precursor of bacterial peptidoglycan and is synthesized by D-alanine-D-alanine ligase (DDL) with hydrolysis of ATP; this reaction makes DDL an important drug target for the development of antibacterial agents. Five crystal structures of DDL from Yersinia pestis (YpDDL) were determined at 1.7-2.5 Å resolution: apo, AMP-bound, ADP-bound, adenosine 5'-(β,γ-imido)triphosphate-bound, and D-alanyl-D-alanine- and ADP-bound structures. YpDDL consists of three domains, in which four loops, loop 1, loop 2 (the serine loop), loop 3 (the ω-loop) and loop 4, constitute the binding sites for two D-alanine molecules and one ATP molecule. Some of them, especially the serine loop and the ω-loop, show flexible conformations, and the serine loop is mainly responsible for the conformational change in substrate nucleotide phosphates. Enzyme-kinetics assays were carried out for both the D-alanine and ATP substrates and a substrate-binding mechanism was proposed for YpDDL involving conformational changes of the loops. PubMed: 26894530DOI: 10.1107/S2059798315021671 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.7 Å) |
Structure validation
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