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MolNFT v1 · #151902 · protein

Crystal structure of tp domain from chlamydia trachomatis penicillin- binding protein 3 in complex with meropenem

6I1H · Penicillin-binding PROTEIN,PENICILLIN-binding protein: “Crystal structure of tp domain from chlamydia trachomatis penicillin- binding protein 3 in complex with…”. X-ray diffraction, 1 ligand (MER), 4 pockets (best druggability…

PDB
6I1H
Type
protein
Length
676 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Penicillin-binding PROTEIN,PENICILLIN-binding protein
EC
2.4.1.129
UniProt
A0A0E9FXJ8
Ligands
MER
Pockets
4 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 34% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APenicillin-binding PROTEIN,PENICILLIN-binding protein (EC 2.4.1.129)protein34033% helix, 21% strandA0A0E9FXJ8
BPenicillin-binding PROTEIN,PENICILLIN-binding protein (EC 2.4.1.129)protein33635% helix, 21% strandA0A0E9FXJ8

Ligands and binding sites

  • MER · (4R,5S)-3-{[(3S,5S)-5-(dimethylcarbamoyl)pyrrolidin-3-yl]sulfanyl}-5-[(2S,3R)-3-hydroxy-1-oxobutan-2-yl]-4-methyl-4,5-dihydro-1H-pyrrole-2-carboxylic acid · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1760.720.9621empty
27980.720.7888MER
32430.530.7633MER
41510.440.7621empty

Interfaces

1 interface between chains.

  • A–B · 865 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 6I1H · Crystal structure of TP domain from Chlamydia trachomatis Penicillin-Binding Protein 3 in… · the same entry in another collection · chain A against A, TM-score 1.00

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