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Crystal structure of TEM1 beta-lactamase mutant I263A

Analyse Crystal structure of TEM1 beta-lactamase mutant I263A in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6APA
Type
protein
Length
1,052 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-lactamase tem
EC
3.5.2.6
UniProt
P62593
Pockets
10 · best druggability 0.75

Structure

x-ray diffraction · 1 distinct chain · 43% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DBeta-lactamase tem (EC 3.5.2.6)protein26343% helix, 18% strandP62593

Pockets

10 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19120.750.7975empty
210830.740.7784empty
33320.560.7535empty
42070.540.7926empty
52060.450.7329empty

Interfaces

5 interfaces between chains.

  • A–B · 677 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 494 Ų buried · 10 hydrogen bonds · protein-protein
  • A–C · 201 Ų buried · 1 hydrogen bond · protein-protein
  • B–D · 189 Ų buried · 1 hydrogen bond · protein-protein
  • A–D · 82 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 6APA · Crystal structure of TEM1 beta-lactamase mutant I263A · the same entry in another collection · chain B against B, TM-score 1.00
  • P62593 · AlphaFold monomer V2.0 prediction for beta-lactamase tem (P62593) · a predicted model of the same protein · chain B against A, TM-score 1.00

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