GL1X · GenesisL1 explorer

MolNFT v1 · #91229 · protein

Mutagenesis of zinc ligand residue CYS221 reveals plasticity in the imp-1 metallo-B-lactamase active site

4F6Z · Beta-lactamase: “Mutagenesis of zinc ligand residue CYS221 reveals plasticity in the imp-1 metallo-B-lactamase active site”. X-ray diffraction, 1 ligand (ZN), 1 pocket (best druggability 0.51). MolNFT v1 #91229 on GenesisL1: 3D…

PDB
4F6Z
Type
protein
Length
221 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-lactamase
UniProt
Q79MP6
Ligands
ZN
Pockets
1 · best druggability 0.51

Structure

x-ray diffraction · 1 distinct chain · 26% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-lactamaseprotein22126% helix, 32% strandQ79MP6

Ligands and binding sites

  • ZN · Zinc ion · metal · chains A
  • FLC · Citrate anion · 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11940.510.7730FLC

Compared structures

  • 4F6Z · Mutagenesis of zinc ligand residue Cys221 reveals plasticity in the IMP-1… · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.