4PLY: Crystal Structure Of Ancestral Apicomplexan Malate Dehydrogenase With Malate

Citation:
Abstract
Malate and lactate dehydrogenases (MDH and LDH) are homologous, core metabolic enzymes that share a fold and catalytic mechanism yet possess strict specificity for their substrates. In the Apicomplexa, convergent evolution of an unusual LDH from MDH produced a difference in specificity exceeding 12 orders of magnitude. The mechanisms responsible for this extraordinary functional shift are currently unknown. Using ancestral protein resurrection, we find that specificity evolved in apicomplexan LDHs by classic neofunctionalization characterized by long-range epistasis, a promiscuous intermediate, and few gain-of-function mutations of large effect. In canonical MDHs and LDHs, a single residue in the active-site loop governs substrate specificity: Arg102 in MDHs and Gln102 in LDHs. During the evolution of the apicomplexan LDH, however, specificity switched via an insertion that shifted the position and identity of this 'specificity residue' to Trp107f. Residues far from the active site also determine specificity, as shown by the crystal structures of three ancestral proteins bracketing the key duplication event. This work provides an unprecedented atomic-resolution view of evolutionary trajectories creating a nascent enzymatic function.
PDB ID: 4PLYDownload
MMDB ID: 121220
PDB Deposition Date: 2014/5/19
Updated in MMDB: 2017/10
Experimental Method:
x-ray diffraction
Resolution: 1.9  Å
Source Organism:
Similar Structures:
Biological Unit for 4PLY: tetrameric; determined by author and by software (PISA)
Molecular Components in 4PLY
Label Count Molecule
Proteins (4 molecules)
4
Malate Dehydrogenase
Molecule annotation
Chemicals (7 molecules)
1
4
2
3
* Click molecule labels to explore molecular sequence information.

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