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Oxacilloyl-acylated MECR1 extracellular antibiotic-sensor domain.

Analyse Oxacilloyl-acylated MECR1 extracellular antibiotic-sensor domain. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2IWD
Type
protein
Length
246 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Methicillin resistance MECR1 protein
UniProt
P0A0B0
Ligands
1S6
Pockets
1 · best druggability 0.38

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMethicillin resistance MECR1 proteinprotein24637% helix, 26% strandP0A0B0

Ligands and binding sites

  • 1S6 · (2R,4S)-5,5-dimethyl-2-[(1R)-1-{[(5-methyl-3-phenyl-1,2-oxazol-4-yl)carbonyl]amino}-2-oxoethyl]-1,3-thiazolidine-4-carb oxylic acid · ligand · 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
11320.380.73291S6

Modifications

Observed in the structure: 1 covalent (covalent ligand).

Compared structures

  • 2IWD · Oxacilloyl-acylated MecR1 extracellular antibiotic-sensor domain. · the same entry in another collection · chain A against A, TM-score 1.00
  • P0A0B0 · AlphaFold monomer V2.0 prediction for methicillin resistance MECR1 protein (P0A0B0) · a predicted model of the same protein · chain A against A, TM-score 0.99

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