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Streptomcyes albus JA3453 oxazolomycin ketosynthase domain ozmh KS7

Analyse Streptomcyes albus JA3453 oxazolomycin ketosynthase domain ozmh KS7 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4OPE
Type
protein
Length
2,284 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NRPS/PKS
UniProt
B2WW42
Ligands
NO3
Pockets
20 · best druggability 0.80

Structure

x-ray diffraction · 4 distinct chains · 35% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANRPS/PKSprotein58035% helix, 20% strandB2WW42
BNRPS/PKSprotein56835% helix, 21% strandB2WW42
CNRPS/PKSprotein57634% helix, 21% strandB2WW42
DNRPS/PKSprotein56035% helix, 21% strandB2WW42

Ligands and binding sites

  • NO3 · Nitrate ion · ion · 2 copies · chains C

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

Pockets

20 pockets found on a 1 Å grid, 12 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12860.800.9155empty
23420.790.9047empty
37120.770.8284empty
46280.770.8378empty
52390.740.8947empty

Interfaces

4 interfaces between chains.

  • A–B · 2718 Ų buried · 41 hydrogen bonds · protein-protein
  • C–D · 2701 Ų buried · 39 hydrogen bonds · protein-protein
  • B–C · 644 Ų buried · 15 hydrogen bonds · protein-protein
  • A–C · 459 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 24 modified (engineered).

Compared structures

  • 4OPE · Streptomcyes albus JA3453 oxazolomycin ketosynthase domain OzmH KS7 · the same entry in another collection · chain A against A, TM-score 1.00

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