Related Experiment Video
Updated: Oct 12, 2026

Site Directed Spin Labeling and EPR Spectroscopic Studies of Pentameric Ligand-Gated Ion Channels
Published on: July 4, 2016
Functional characterization of residues in the P-loop motif of the RecA protein ATP binding site
J T Konola1, K M Logan, K L Knight
1Department of Biochemistry and Molecular Biology, University of Massachusetts Medical Center, Worcester 01655.
Abstract:
We have introduced a large number of single amino acid substitutions at six positions that lie within the P-loop motif of the ATP binding site in the Escherichia coli RecA protein. The activity of each recA mutant was determined using genetic assays which assess the catalytic proficiency of the RecA protein for both homologous genetic recombination and recombinational repair of damaged DNA. The six residues displayed unique patterns of allowed versus non-allowed substitutions that define the functional and structural constraints at each position. Our results show that while the restricted mutability of Gly66 and Ser70 conform to expectations based on their positions in the RecA crystal structure, strict constraints are in effect at positions 68 and 69 that are not apparent in the RecA structure but would be compatible with the proximity of these side-chains to bound DNA. Thr74 shows a rather unexpected pattern of allowed substitutions that may reflect two distinct structural solutions to optimal stabilization of bound nucleotide. In addition, specific substitutions at Pro67 result in mutant RecA proteins that appear to discriminate between homologous genetic recombination and recombinational DNA repair.
More Related Videos
12:07Chemical Modification of the Tryptophan Residue in a Recombinant Ca2+-ATPase N-domain for Studying Tryptophan-ANS FRET
Published on: October 9, 2021
06:50Computational Prediction of Amino Acid Preferences of Potentially Multispecific Peptide-Binding Domains Involved in Protein-Protein Interactions
Published on: January 26, 2024
Related Concept Videos
Conserved Binding Sites
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally analyses the...
Ligand Binding and Linkage
Directing Proteins to the Rough Endoplasmic Reticulum
Tail-anchoring of Proteins in the ER Membrane
ATP Driven Pumps II: P-type Pumps
A typical P-type pump has three cytosolic domains: nucleotide-binding (N), phosphorylation (P), and activator (A) domains. These domains are connected to the membrane-spanning helices by short amino acid segments. ATP hydrolysis and covalent phosphoenzyme intermediate formation are crucial parts of the catalytic cycle. At the highly...
Allosteric Proteins-ATCase
Aspartate transcarbamoylase (ATCase) is a cytosolic enzyme that catalyzes the condensation of L-aspartate and carbamoyl phosphate to N-carbamoyl-L-aspartate. This reaction is the first step in pyrimidine biosynthesis. UTP and CTP, the end products of the pyrimidine synthesis pathway,...