› 6qe3

X-ray diffraction
1.75Å resolution

Re-refinement of 6ESR human IBA57 at 1.75 A resolution

Released:
DOI: 10.2210/pdb6qe3/pdb
PDB entry 6qe3 coloured by chain, front view.
PDB entry 6qe3 coloured by chain, side view.
PDB entry 6qe3 coloured by chain, top view.
Source organism: Homo sapiens
Primary publication:
In-house high-energy-remote SAD phasing using the magic triangle: how to tackle the P1 low symmetry using multiple orientations of the same crystal of human IBA57 to increase the multiplicity.
Gourdoupis S, Nasta V, Ciofi-Baffoni S, Banci L, Calderone V
Acta Crystallogr D Struct Biol 75 317-324 (2019)
PMID: 30950402

Function and Biology Details

Biochemical function:
  • not assigned
Biological process:
  • not assigned
Cellular component:
  • not assigned
Sequence domains:

Structure analysis Details

Assembly composition:
monomeric (preferred)
Assembly name:
PDBe Complex ID:
PDB-CPX-178301 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Putative transferase CAF17, mitochondrial Chain: A
Molecule details ›
Chain: A
Length: 309 amino acids
Theoretical weight: 33.28 KDa
Source organism: Homo sapiens
Expression system: Escherichia coli
UniProt:
  • Canonical: Q5T440 (Residues: 44-352; Coverage: 87%)
Gene names: C1orf69, IBA57

Ligands and Environments

No bound ligands
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: ESRF BEAMLINE ID30B
Spacegroup: P1
Unit cell:
a: 37.28Å b: 43.25Å c: 55.3Å
α: 94.88° β: 93.25° γ: 108.18°
R-values:
R R work R free
0.176 0.175 0.197
Expression system: Escherichia coli

Quick links

Citations

1 review citation

Molecular Basis of Rare Diseases Associated to the Maturation of Mitochondrial [4Fe-4S]-Containing Proteins.
Camponeschi et al. (2022)

2 mentions without citation

Multiple Mitochondrial Dysfunction Syndrome Type 3: A Likely Pathogenic Homozygous Variant Affecting a Patient of Cuban Descent and Literature Review.
Lang et al. (2022)
1 more