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Crystal structure of a novel cyclase (PFAM04199).

Analyse Crystal structure of a novel cyclase (PFAM04199). in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5IBZ
Type
protein
Length
1,215 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Uncharacterized protein
UniProt
A0A0G3FEK2
Ligands
UVW
Pockets
9 · best druggability 0.80

Structure

x-ray diffraction · 4 distinct chains · 30% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUncharacterized proteinprotein30630% helix, 23% strandA0A0G3FEK2
BUncharacterized proteinprotein30828% helix, 23% strandA0A0G3FEK2
CUncharacterized proteinprotein30131% helix, 24% strandA0A0G3FEK2
DUncharacterized proteinprotein30031% helix, 23% strandA0A0G3FEK2

Ligands and binding sites

  • UVW · Acetylphosphate · ligand · 4 copies · chains A, C, B, D
  • PGE · Triethylene glycol · additive · chains A, 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, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19160.800.8273UVW
25730.760.8334empty
32380.680.8442UVW
42610.670.8339UVW
53820.640.7945UVW

Interfaces

6 interfaces between chains.

  • B–D · 3501 Ų buried · 69 hydrogen bonds · protein-protein
  • A–C · 3441 Ų buried · 63 hydrogen bonds · protein-protein
  • C–D · 1111 Ų buried · 15 hydrogen bonds · protein-protein
  • A–B · 1106 Ų buried · 15 hydrogen bonds · protein-protein
  • B–C · 457 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 12 modified (engineered).

Compared structures

  • 5IBZ · Crystal structure of a novel cyclase (pfam04199). · the same entry in another collection · chain A against A, TM-score 1.00

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