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We observed two such apparent co-occurrences: in Cox4A and Cox7R - both components of Complex IV of the respiratory chain.
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CKIδ/ε destabilizes the β-catenin degradation complex [8], and Dpr and Dsh are both components of this complex, so CKIδ may disrupt the interaction between Dpr and Dsh as well.
The analysis of the frontier orbitals shows that the LUMOs of the complexes mainly reside on the CNT, while the HOMOs spread over both components of each complex.
(1) Given that there has been no high-resolution study of any of the 2-oxo acid dehydrogenase complexes, the HDX-MS studies accomplish a remarkable feat: they produce peptide-level resolution on both components of a complex, one partner of which, PDK1 or PDK2, has a dimer mass of 90 kDa, while the other partner, the intact E2·E3BP core of PDC, has a mass exceeding 3 MDa (as many as 60 subunits).
Strong electrostatic interactions are present between charged residues from both components of the complex.
Strong electrostatic interactions are observed between charged residues from both components of the complex.
Therefore, the template structures for both components of nitrogenase complex were the A. vinelandii subunits.
Thus both components of the CREB/CBP/p300 complex are necessary for an optimal induction by PGE2 of IL-6.
Hpr1 and Tho2 are both components of the THO complex that couples transcription elongation to recombinational repair and defects in these genes exhibit hyper-recombination phenotypes in haploids.
Therefore, we examined the influence of SPL expression on both components of this kinase complex.
Of these women, 20/34 (59%) had persistent caseness for both components of the illness complex over the next two years, 10/34 (29%) subsequently reported fatigue only, and in 4/34 (12%) all symptoms resolved.
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