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Structure of farnesyl protein transferase bound to pb-93

Analyse Structure of farnesyl protein transferase bound to pb-93 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2R2L
Type
protein
Length
716 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Farnesyltransferase subunit alpha; Farnesyltransferase subunit beta
EC
2.5.1.58
UniProt
Q5RKJ4, Q02293
Ligands
FPP, PB9, ZN
Pockets
11 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 59% helix, 4% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFarnesyltransferase subunit alphaprotein31568% helix, 1% strandQ5RKJ4
BFarnesyltransferase subunit beta (EC 2.5.1.58)protein40152% helix, 6% strandQ02293

Ligands and binding sites

  • FPP · Farnesyl diphosphate · ligand · chains A, B
  • PB9 · methyl 4-{[{(3S)-6-cyano-1-[(1-methyl-1H-imidazol-5-yl)methyl]-1,2,3,4-tetrahydroquinolin-3-yl}(pyridin-2-ylsulfonyl)amino]methyl}piperidine-1-carboxylate · ligand · chains A, B
  • ZN · Zinc ion · metal · chains B

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

Pockets

11 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18570.760.7953FPP, PB9
2840.740.9724empty
33660.730.8458empty
42190.620.8226empty
53100.590.7836empty

Interfaces

1 interface between chains.

  • A–B · 3474 Ų buried · 70 hydrogen bonds · protein-protein

Compared structures

  • 2R2L · Structure of Farnesyl Protein Transferase bound to PB-93 · the same entry in another collection · chain A against A, TM-score 1.00
  • Q02293 · AlphaFold monomer V2.0 prediction for protein farnesyltransferase subunit beta (Q02293) · a predicted model of the same protein · chain B against A, TM-score 0.99

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