4lng

X-ray diffraction
1.9Å resolution

Aspergillus fumigatus protein farnesyltransferase complex with farnesyldiphosphate and tipifarnib

Released:

Function and Biology Details

Reactions catalysed:
Farnesyl diphosphate + protein-cysteine = S-farnesyl protein + diphosphate
Geranylgeranyl diphosphate + protein-cysteine = S-geranylgeranyl-protein + diphosphate
Biochemical function:
Biological process:

Structure analysis Details

Assembly composition:
hetero dimer (preferred)
PDBe Complex ID:
PDB-CPX-175834 (preferred)
Entry contents:
2 distinct polypeptide molecules
Macromolecules (2 distinct):
Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha Chain: A
Molecule details ›
Chain: A
Length: 367 amino acids
Theoretical weight: 42.39 KDa
Source organism: Aspergillus fumigatus Af293
Expression system: Escherichia coli
UniProt:
  • Canonical: Q4WP27 (Residues: 1-353; Coverage: 100%)
Gene name: AFUA_4G07800
Sequence domains: Protein prenyltransferase alpha subunit repeat
Structure domains: Protein prenylyltransferase
Protein farnesyltransferase subunit beta Chain: B
Molecule details ›
Chain: B
Length: 519 amino acids
Theoretical weight: 56.64 KDa
Source organism: Aspergillus fumigatus Af293
Expression system: Escherichia coli
UniProt:
  • Canonical: Q4WPS9 (Residues: 1-519; Coverage: 100%)
Gene name: AFUA_4G10330
Sequence domains: Prenyltransferase and squalene oxidase repeat
Structure domains: Glycosyltransferase

Ligands and Environments

No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: APS BEAMLINE 22-BM
Spacegroup: P21
Unit cell:
a: 63.537Å b: 90.658Å c: 83.163Å
α: 90° β: 111.09° γ: 90°
R-values:
R R work R free
0.156 0.155 0.184
Expression system: Escherichia coli