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MolNFT v1 · #99707 · protein

Crystal structure of aspergillus fumigatus protein farnesyltransferase binary complex with farnesyldiphosphate

4MBG · Caax farnesyltransferase alpha subunit RAM2: “Crystal structure of aspergillus fumigatus protein farnesyltransferase binary complex with farnesyldiphosphate”. X-ray diffraction, 3 ligands (FPP, ZN, K), 8 pockets (best druggability…

PDB
4MBG
Type
protein
Length
780 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Caax farnesyltransferase alpha subunit RAM2; Caax farnesyltransferase beta subunit RAM1
EC
2.5.1.-, 2.5.1.58
UniProt
Q4WP27, Q4WPS9
Ligands
FPP, ZN, K
Pockets
8 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 54% helix, 4% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACaax farnesyltransferase alpha subunit RAM2 (EC 2.5.1.-)protein33565% helix, 0% strandQ4WP27
BCaax farnesyltransferase beta subunit RAM1 (EC 2.5.1.58)protein44546% helix, 7% strandQ4WPS9

Ligands and binding sites

  • FPP · Farnesyl diphosphate · ligand · chains A, B
  • ZN · Zinc ion · metal · chains B
  • K · Potassium ion · metal · chains B
  • EDO · 1,2-ethanediol · additive · 6 copies · chains A, B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

8 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15060.800.8755EDO
210670.790.8184EDO, FPP, K
33240.690.8341empty
4710.590.8926EDO
5930.520.8422empty

Interfaces

1 interface between chains.

  • A–B · 3672 Ų buried · 71 hydrogen bonds · protein-protein

Compared structures

  • 4MBG · Crystal structure of Aspergillus fumigatus protein farnesyltransferase binary complex… · the same entry in another collection · chain A against A, TM-score 1.00

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