Abstract Protein functional constraints are manifest as superfamily and functional-subgroup conserved residues, and as pairwise correlations. Deep Analysis of Residue Constraints (DARC) aids the visualization of these constraints, characterizes how they correlate with each other and with structure, and estimates statistical significance. This can identify determinants of protein functional specificity, as we illustrate for bacterial DNA clamp loader ATPases. These load ring-shaped sliding clamps onto DNA to keep polymerase attached during replication and contain one δ, three γ, and one δ’ AAA+ subunits semi-circularly arranged in the order δ-γ1-γ2-γ3-δ’. Only γ is active, though both γ and δ’ functionally influence an adjacent γ subunit. DARC identifies, as functionally-congruent features linking allosterically the ATP, DNA, and clamp binding sites: residues distinctive of γ and of γ/δ’ that mutually interact in trans, centered on the catalytic base; several γ/δ’-residues and six γ/δ’-covariant residue pairs within the DNA binding N-termini of helices α2 and α3; and γ/δ’-residues associated with the α2 C-terminus and the clamp-binding loop. Most notable is a trans-acting γ/δ’ hydroxyl group that 99% of other AAA+ proteins lack. Mutation of this hydroxyl to a methyl group impedes clamp binding and opening, DNA binding, and ATP hydrolysis—implying a remarkably clamp-loader-specific function.
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Floquet isospectrality of the zero potential for discrete periodic Schrödinger operators
Let Γ=q1Z⊕q2Z⊕⋯⊕qdZ, with qj∈Z+ for each j ∈ {1, …, d}, and denote by Δ the discrete Laplacian on ℓ2Zd. Using Macaulay2, we first numerically find complex-valued Γ-periodic potentials V:Zd→C such that the operators Δ + V and Δ are Floquet isospectral. We then use combinatorial methods to validate these numerical solutions.
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- PAR ID:
- 10521204
- Publisher / Repository:
- AIP
- Date Published:
- Journal Name:
- Journal of Mathematical Physics
- Volume:
- 65
- Issue:
- 7
- ISSN:
- 0022-2488
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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