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Directed evolution of transaminases by ancestral reconstruction. using old proteins for new chemistries

Analyse Directed evolution of transaminases by ancestral reconstruction. using old… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5KR5
Type
protein
Length
909 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
4-aminobutyrate transaminase
EC
2.6.1.18
Ligands
PLP, CA
Pockets
6 · best druggability 0.70

Structure

x-ray diffraction · 2 distinct chains · 44% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A4-aminobutyrate transaminase (EC 2.6.1.18)protein45544% helix, 18% strand—
B4-aminobutyrate transaminase (EC 2.6.1.18)protein45444% helix, 18% strand—

Ligands and binding sites

  • PLP · Pyridoxal-5'-phosphate · ligand · 2 copies · chains A, B
  • CA · Calcium ion · metal · 3 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · additive · 3 copies · chains A, B

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

Pockets

6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1570.700.9727PLP
25130.690.7949empty
35160.680.7853empty
41300.440.7620empty
5500.310.7713empty

Interfaces

1 interface between chains.

  • A–B · 5559 Ų buried · 79 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 5KR5 · Directed Evolution of Transaminases By Ancestral Reconstruction. Using Old Proteins for… · the same entry in another collection · chain A against A, TM-score 1.00

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