1U7Z
Phosphopantothenoylcysteine synthetase from E. coli, 4'-phosphopantothenoyl-CMP complex
Summary for 1U7Z
Entry DOI | 10.2210/pdb1u7z/pdb |
Related | 1U7U 1U7W 1U80 |
Descriptor | Coenzyme A biosynthesis bifunctional protein coaBC, PHOSPHORIC ACID MONO-[3-(3-{[5-(4-AMINO-2-OXO-2H-PYRIMIDIN-1-YL)-3,4- DIHYDROXY-TETRAHYDRO-FURAN-2- YLMETHOXY]-HYDROXY-PHOSPHORYLOXY}-3-OXO-PROPYLCARBAMOYL)-3-HYDROXY-2,2- DIMETHYL-PROPYL] ESTER (3 entities in total) |
Functional Keywords | coenzyme a biosynthesis, ligase |
Biological source | Escherichia coli |
Total number of polymer chains | 3 |
Total formula weight | 76313.23 |
Authors | Stanitzek, S.,Augustin, M.A.,Huber, R.,Kupke, T.,Steinbacher, S. (deposition date: 2004-08-04, release date: 2004-11-30, Last modification date: 2023-10-25) |
Primary citation | Stanitzek, S.,Augustin, M.A.,Huber, R.,Kupke, T.,Steinbacher, S. Structural Basis of CTP-Dependent Peptide Bond Formation in Coenzyme A Biosynthesis Catalyzed by Escherichia coli PPC Synthetase STRUCTURE, 12:1977-1988, 2004 Cited by PubMed Abstract: Phosphopantothenoylcysteine (PPC) synthetase forms a peptide bond between 4'-phosphopantothenate and cysteine in coenzyme A biosynthesis. PPC synthetases fall into two classes: eukaryotic, ATP-dependent and eubacterial, CTP-dependent enzymes. We describe the first crystal structure of E. coli PPC synthetase as a prototype of bacterial, CTP-dependent PPC synthetases. Structures of the apo-form and the synthetase complexed with CTP, the activated acyl-intermediate, 4'-phosphopantothenoyl-CMP, and with the reaction product CMP provide snapshots along the reaction pathway and detailed insight into substrate binding and the reaction mechanism of peptide bond formation. Binding of the phosphopantothenate moiety of the acyl-intermediate in a cleft at the C-terminal end of the central beta sheet of the dinucleotide binding fold is accomplished by an otherwise flexible flap. A second disordered loop may control access of cysteine to the active site. The conservation of functionalities involved in substrate binding and catalysis provides insight into similarities and differences of prokaryotic and eukaryotic PPC synthetases. PubMed: 15530362DOI: 10.1016/j.str.2004.08.007 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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