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Amino-transferase (AMT) Domain - Arg Complex of Hybrid Polyketide/Non-Ribosomal Peptide Synthetase

Analyse Amino-transferase (AMT) Domain - Arg Complex of Hybrid Polyketide/Non-Ribosomal… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6KFR
Type
protein
Length
898 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
3.1
Source
Bacillus subtilis
Molecule
Mycosubtilin synthase subunit A
EC
2.3.1.-
UniProt
Q9R9J1
Ligands
PLP, ARG
Pockets
7 · best druggability 0.80

Structure

x-ray diffraction · resolution 3.1 · 1 distinct chain · 43% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BMycosubtilin synthase subunit A (EC 2.3.1.-)protein44943% helix, 17% strandQ9R9J1

Ligands and binding sites

  • PLP · Pyridoxal-5'-phosphate · ligand · 2 copies · chains A, B
  • ARG · Arginine · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11460.800.9728empty
21600.790.9530empty
35060.720.8168PLP, ARG
45070.720.8175ARG, PLP
5560.680.9718empty

Interfaces

1 interface between chains.

  • A–B · 5291 Ų buried · 77 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 cofactor (pyridoxal phosphate Schiff base).

Compared structures

  • 6KFR · Amino-transferase (amt) domain - arg complex of hybrid POLYKETIDE/NON- ribosomal peptide… · the same entry in another collection · chain A against A, TM-score 1.00

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