6kdu

X-ray diffraction
2.2Å resolution

Structural basis for domain rotation during adenylation of active site K123 and fragment library screening against NAD+ -dependent DNA ligase from Mycobacterium tuberculosis

Released:

Function and Biology Details

Reaction catalysed:
(1a) NAD(+) + [DNA ligase]-L-lysine = [DNA ligase]-N(6)-(5'-adenylyl)-L-lysine + beta-nicotinamide D-nucleotide
Biochemical function:
Biological process:
  • not assigned
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
monomeric (preferred)
Assembly name:
PDBe Complex ID:
PDB-CPX-161892 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
DNA ligase A Chain: A
Molecule details ›
Chain: A
Length: 327 amino acids
Theoretical weight: 36.85 KDa
Source organism: Mycobacterium tuberculosis H37Rv
Expression system: Escherichia coli 'BL21-Gold(DE3)pLysS AG'
UniProt:
  • Canonical: P9WNV1 (Residues: 8-328; Coverage: 47%)
Gene names: MTV012.28c, Rv3014c, lig, ligA
Sequence domains: NAD-dependent DNA ligase adenylation domain

Ligands and Environments

3 bound ligands:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: ELETTRA BEAMLINE 11.2C
Spacegroup: P6122
Unit cell:
a: 96.168Å b: 96.168Å c: 200.835Å
α: 90° β: 90° γ: 120°
R-values:
R R work R free
0.211 0.21 0.244
Expression system: Escherichia coli 'BL21-Gold(DE3)pLysS AG'