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Crystal structure of metallo-beta-lactamase smb-1 bound to hydrolyzed meropenem

Analyse Crystal structure of metallo-beta-lactamase smb-1 bound to hydrolyzed meropenem in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5AXO
Type
protein
Length
259 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Metallo-beta-lactamase
EC
3.5.2.6
UniProt
G5ELM3
Ligands
LMP, NA, ZN, SO4
Pockets
1 · best druggability 0.40

Structure

x-ray diffraction · 1 distinct chain · 36% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMetallo-beta-lactamase (EC 3.5.2.6)protein25936% helix, 23% strandG5ELM3

Ligands and binding sites

  • LMP · (2~{S},3~{R},4~{S})-2-[(2~{S},3~{R})-1,3-bis(oxidanyl)-1-oxidanylidene-butan-2-yl]-4-[(3~{S},5~{S})-5-(dimethylcarbamoyl)pyrrolidin-3-yl]sulfanyl-3-methyl-3,4-dihydro-2~{H}-pyrrole-5-carboxylic acid · ligand · chains A
  • NA · Sodium ion · metal · 10 copies · chains A
  • ZN · Zinc ion · metal · 2 copies · chains A
  • SO4 · Sulfate ion · ion · 3 copies · chains A
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · chains A

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

Pockets

1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1960.400.7728ZN, NA, LMP

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 5AXO · Crystal Structure of Metallo-beta-Lactamase SMB-1 Bound to Hydrolyzed Meropenem · the same entry in another collection · chain A against A, TM-score 1.00

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