Basic side chains play crucial roles in protein–DNA interactions. In this study, using NMR spectroscopy, we investigated the dynamics of Arg and Lys side chains of the fruit fly Antennapedia homeodomain in the free state and in the complex with target DNA. We measured <sup>15</sup>N relaxation for Arg and Lys side chains at two magnetic fields, from which generalized order parameters for the cationic groups were determined. Mobility of the R5 side chain, which makes hydrogen bonds with a thymine base in the DNA minor groove, was greatly dampened. Several Lys and Arg side chains that form intermolecular ion pairs with DNA phosphates were found to retain high mobility with the order parameter being <0.6 in the DNA-bound state. Interestingly, ...
Motions of proteins are essential for the performance of their functions. Aliphatic protein side cha...
The study of protein structure and function is incomplete without an understanding of protein dynami...
Although charged side chains play important roles in protein function, their dynamic properties are ...
An important but poorly characterized contribution to the thermodynamics of protein–DNA interactions...
Due to chemical exchange, the mobility of histidine (His) side chains of proteins is typically diffi...
Nonspecific protein–DNA interactions are inherently dynamic and involve both diffusion of the protei...
ABSTRACT: Intermolecular ion pairs (salt bridges) are crucial for protein−DNA association. For two p...
Ion pairing is one of the most fundamental chemical interactions and is essential for molecular reco...
Protein-nucleic acid interactions are essential in a variety of biological events ranging from the r...
The secondary structure of an N-terminally elongated Antennapedia (Antp) homeodomain (HD) polypeptid...
AbstractDithioation of DNA phosphate is known to enhance binding affinities, at least for some prote...
CONSPECTUS: Many multidomain proteins and ribonucleic acids consist of domains that autonomously fol...
The recognition of specific DNA sequences by proteins and the coupling to signaling events are funda...
15N-1H NMR spectroscopy has been used to probe the dynamic properties of uniformly 15N labeled Esche...
Intermolecular ion pairs (salt bridges) are crucial for protein–DNA association. For two protein–DNA...
Motions of proteins are essential for the performance of their functions. Aliphatic protein side cha...
The study of protein structure and function is incomplete without an understanding of protein dynami...
Although charged side chains play important roles in protein function, their dynamic properties are ...
An important but poorly characterized contribution to the thermodynamics of protein–DNA interactions...
Due to chemical exchange, the mobility of histidine (His) side chains of proteins is typically diffi...
Nonspecific protein–DNA interactions are inherently dynamic and involve both diffusion of the protei...
ABSTRACT: Intermolecular ion pairs (salt bridges) are crucial for protein−DNA association. For two p...
Ion pairing is one of the most fundamental chemical interactions and is essential for molecular reco...
Protein-nucleic acid interactions are essential in a variety of biological events ranging from the r...
The secondary structure of an N-terminally elongated Antennapedia (Antp) homeodomain (HD) polypeptid...
AbstractDithioation of DNA phosphate is known to enhance binding affinities, at least for some prote...
CONSPECTUS: Many multidomain proteins and ribonucleic acids consist of domains that autonomously fol...
The recognition of specific DNA sequences by proteins and the coupling to signaling events are funda...
15N-1H NMR spectroscopy has been used to probe the dynamic properties of uniformly 15N labeled Esche...
Intermolecular ion pairs (salt bridges) are crucial for protein–DNA association. For two protein–DNA...
Motions of proteins are essential for the performance of their functions. Aliphatic protein side cha...
The study of protein structure and function is incomplete without an understanding of protein dynami...
Although charged side chains play important roles in protein function, their dynamic properties are ...