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Several cellular DNA binding proteins have been described that bind integration complexes and/or facilitate integration, including BAF, HMGa1, Ku, and LEDGF [4], [14].
Likewise, fatty acid binding proteins have been demonstrated to bind two molecules of the same ligand, oleic acid.
Several XA21 binding proteins have been characterized, however the early events governing XA21 signaling have not been fully elucidated.
To date, several strategies for "reagentless biosensors" based on antibodies and natural and engineered binding proteins have been described.
Extensively redesigned periplasmic binding proteins have been re-introduced into bacteria to function in synthetic signal transduction pathways that respond to extracellular ligands and as biologically active enzymes.
Vanabins (vanadium binding proteins) have been identified in the cytoplasm of such cells.
Similar(21)
Seven chromatin-binding proteins have been isolated by this method.
Many actin-binding proteins have been observed to have a modular architecture.
Due to the roles in telomere length regulation and end protection, telomere-binding proteins have been considered as a good target for drug design.
In addition, naturally occurring ligand-binding proteins have been computationally designed to recognize new ligands while keeping their original biological functions at the same time.
The ease of engineering and robust properties of 10Fn3-based target-binding proteins have been validated by multiple independent academic and industrial groups.
More suggestions(17)
binding constants have been
binding modes have been
binding modules have been
binding interfaces have been
binding proteins have joined
binding templates have been
binding sites have been
binding units have been
binding interactions have been
binding media have been
binding anions have been
binding molecules have been
binding approaches have been
binding sequences have been
binding groups have been
binding affinities have been
binding properties have been
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