4e4g

X-ray diffraction
2.9Å resolution

Crystal structure of putative Methylmalonate-semialdehyde dehydrogenase from Sinorhizobium meliloti 1021

Released:
Source organism: Sinorhizobium meliloti 1021
Entry authors: Malashkevich VN, Bhosle R, Toro R, Hillerich B, Gizzi A, Garforth S, Kar A, Chan MK, Lafluer J, Patel H, Matikainen B, Chamala S, Lim S, Celikgil A, Villegas G, Evans B, Zenchek W, Love J, Fiser A, Khafizov K, Seidel R, Bonanno JB, Almo SC, New York Structural Genomics Research Consortium (NYSGRC)

Function and Biology Details

Reaction catalysed:
2-methyl-3-oxopropanoate + CoA + H(2)O + NAD(+) = propanoyl-CoA + HCO(3)(-) + NADH
Biological process:
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
homo tetramer (preferred)
PDBe Complex ID:
PDB-CPX-187919 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
methylmalonate-semialdehyde dehydrogenase (CoA acylating) Chains: A, B, C, D, E, F, G, H
Molecule details ›
Chains: A, B, C, D, E, F, G, H
Length: 521 amino acids
Theoretical weight: 57.24 KDa
Source organism: Sinorhizobium meliloti 1021
Expression system: Escherichia coli BL21(DE3)
UniProt:
  • Canonical: Q92RW4 (Residues: 1-498; Coverage: 100%)
Gene names: SMc00781, iolA, mmsA
Sequence domains: Aldehyde dehydrogenase family
Structure domains:

Ligands and Environments

No bound ligands
1 modified residue:

Experiments and Validation Details

Entry percentile scores
X-ray source: NSLS BEAMLINE X29A
Spacegroup: C2
Unit cell:
a: 197.442Å b: 171.285Å c: 159.69Å
α: 90° β: 124.03° γ: 90°
R-values:
R R work R free
0.192 0.188 0.269
Expression system: Escherichia coli BL21(DE3)