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Crystal structure of vibh, an nrps condensation enzyme

Analyse Crystal structure of vibh, an nrps condensation enzyme in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1L5A
Type
protein
Length
1,272 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Amide synthase
UniProt
Q9KTV9
Pockets
14 · best druggability 0.81

Structure

x-ray diffraction · 1 distinct chain · 42% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CAmide synthaseprotein42442% helix, 21% strandQ9KTV9

Pockets

14 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111690.810.8288empty
211880.800.8282empty
39920.800.8273empty
41120.550.8430empty
52380.530.7739empty

Interfaces

3 interfaces between chains.

  • A–B · 274 Ų buried · 3 hydrogen bonds · protein-protein
  • A–C · 265 Ų buried · 1 hydrogen bond · protein-protein
  • B–C · 58 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 1L5A · Crystal Structure of VibH, an NRPS Condensation Enzyme · the same entry in another collection · chain A against A, TM-score 1.00

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