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MolNFT v1 · #32942 · protein

X-ray crystal structure of 5'-fluorodeoxyadenosine synthase from streptomyces cattleya complexed with 2'DEOXY-5'DEOXY- fluoroadenosine.

2C5B · 5'-fluoro-5'-deoxyadenosine synthase: “X-ray crystal structure of 5'-fluorodeoxyadenosine synthase from streptomyces cattleya complexed with…”. X-ray diffraction, 2 ligands (MET, 5F1), 9 pockets (best druggability 0.80). MolNFT v1…

PDB
2C5B
Type
protein
Length
873 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
5'-fluoro-5'-deoxyadenosine synthase
EC
2.5.1.63
UniProt
Q70GK9
Ligands
MET, 5F1
Pockets
9 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 20% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C5'-fluoro-5'-deoxyadenosine synthase (EC 2.5.1.63)protein29120% helix, 30% strandQ70GK9

Ligands and binding sites

  • MET · Methionine · ligand · 3 copies · chains A, B, C
  • 5F1 · 5'-fluoro-2',5'-dideoxyadenosine · ligand · 3 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11310.800.9828MET, 5F1
21200.790.9828MET, 5F1
31280.790.9726MET, 5F1
42510.720.8735empty
53700.710.8351empty

Interfaces

3 interfaces between chains.

  • A–B · 1615 Ų buried · 21 hydrogen bonds · protein-protein
  • A–C · 1605 Ų buried · 23 hydrogen bonds · protein-protein
  • B–C · 1599 Ų buried · 21 hydrogen bonds · protein-protein

Compared structures

  • 2C5B · X-ray crystal structure of 5'-fluorodeoxyadenosine synthase from Streptomyces cattleya… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q70GK9 · AlphaFold monomer V2.0 prediction for 5'-fluoro-5'-deoxy-adenosine synthase (Q70GK9) · a predicted model of the same protein · chain B against A, TM-score 0.99

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