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The crystal structure of gilr, an oxidoreductase that catalyzes the terminal step of gilvocarcin biosynthesis

Analyse The crystal structure of gilr, an oxidoreductase that catalyzes the terminal… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3POP
Type
protein
Length
1,972 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Gilr oxidase
UniProt
Q7X2G7
Ligands
FAD
Pockets
20 · best druggability 0.87

Structure

x-ray diffraction · 1 distinct chain · 33% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DGilr oxidaseprotein49333% helix, 23% strandQ7X2G7

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17940.870.90118FAD
26070.870.9291FAD
36290.870.9189FAD
46510.860.9189FAD
57790.850.8886empty

Interfaces

3 interfaces between chains.

  • B–C · 1746 Ų buried · 34 hydrogen bonds · protein-protein
  • A–D · 1731 Ų buried · 34 hydrogen bonds · protein-protein
  • B–D · 355 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 8 cofactor (flavinylation).

Compared structures

  • 3POP · The crystal structure of GilR, an oxidoreductase that catalyzes the terminal step of… · the same entry in another collection · chain A against A, TM-score 1.00

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