5G40
Crystal structure of adenylate kinase ancestor 4 with Zn and AMP-ADP bound
Summary for 5G40
Entry DOI | 10.2210/pdb5g40/pdb |
Related | 5G3Y 5G3Z 5G41 |
Descriptor | ADENYLATE KINSE, ZINC ION, ADENOSINE-5'-DIPHOSPHATE, ... (5 entities in total) |
Functional Keywords | adenylate kinase, adp, transferase, phosphoryl transfer, nucleotide-binding |
Biological source | SYNTHETIC CONSTRUCT |
Total number of polymer chains | 1 |
Total formula weight | 25706.45 |
Authors | Nguyen, V.,Kutter, S.,English, J.,Kern, D. (deposition date: 2016-05-03, release date: 2016-12-28, Last modification date: 2024-01-10) |
Primary citation | Nguyen, V.,Wilson, C.,Hoemberger, M.,Stiller, J.B.,Agafonov, R.V.,Kutter, S.,English, J.,Theobald, D.L.,Kern, D. Evolutionary drivers of thermoadaptation in enzyme catalysis. Science, 355:289-294, 2017 Cited by PubMed Abstract: With early life likely to have existed in a hot environment, enzymes had to cope with an inherent drop in catalytic speed caused by lowered temperature. Here we characterize the molecular mechanisms underlying thermoadaptation of enzyme catalysis in adenylate kinase using ancestral sequence reconstruction spanning 3 billion years of evolution. We show that evolution solved the enzyme's key kinetic obstacle-how to maintain catalytic speed on a cooler Earth-by exploiting transition-state heat capacity. Tracing the evolution of enzyme activity and stability from the hot-start toward modern hyperthermophilic, mesophilic, and psychrophilic organisms illustrates active pressure versus passive drift in evolution on a molecular level, refutes the debated activity/stability trade-off, and suggests that the catalytic speed of adenylate kinase is an evolutionary driver for organismal fitness. PubMed: 28008087DOI: 10.1126/science.aah3717 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.69 Å) |
Structure validation
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