Thiamin-Diphosphate Enzymes Are an Ancient Family of Repeat Proteins
Merski, M.; Gorna, M.
Show abstract
A repeating sequence and structure pattern that is highly similar to the canonical cofactor binding motif has been identified in the thiamin-diphosphate dependent (ThDP) enzyme family. We have identified more than a thousand of these repeats in a non-redundant set (N = 58) of ThDP enzyme structures. The repeating element has a helix-turn-strand secondary structure which typically begins with an [G/A]{X(1,2)}[G/A] sequence motif with a typical length of 29 residues. The catalytically important diphosphate and aminopyrimidine interacting domains are comprised of a set of six of these repeats in a conserved architecture with a flavodoxin-like 213465 strand order. The canonical ThDP binding motif is the fourth repeat in the ThDP binding domain, while the conserved aminopyrimidine interacting glutamate is part of the second repeat in its domain. The third and fourth repeats form a contact between the functional domains, while the fifth repeat in the N-terminal domain forms an inter-chain contact. The conservation of these functional properties highlights the role of these repeats in the function and structure of this well-studied enzyme family and agrees with the principle of modular assembly in protein ancestry.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- The Structural Basis of the Genetic Code: Amino Acid Recognition by Aminoacyl-tRNA Synthetases 95%
- Two sequence- and two structure-based ML models have learned different aspects of protein biochemistry 93%
- Structure and mechanism of potent bifunctional β-lactam- and homoserine lactone-degrading enzymes from marine microorganisms 93%
Similar papers in this journal
- Archaeal S-adenosyl-L-homocysteine hydrolases: structure, function and substrate preferences 95%
- Differences in the regulation mechanisms of the glutamine synthetase from methanogenic archaea unveiled by structural investigations 95%
- Cryo-EM structure of the transcription termination factor Rho from Mycobacterium tuberculosis reveals mechanism of resistance to bicyclomycin 94%
Similar papers in this journal
- Insertions and deletions mediated functional divergence of Rossmann fold enzymes 96%
- Integrated evolutionary and structural analysis reveals xenobiotics and pathogens as the major drivers of mammalian adaptation 96%
- Actinobacteria challenge the paradigm: a unique protein architecture for a well-known central metabolic complex 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.