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Crystal structure of the catalytic domain of mmp-13 complexed with 4- (2-((6-fluoro-2-((3-METHOXYBENZYL)CARBAMOYL)-4-oxo-3,4- dihydroquinazolin-5-YL)OXY)ETHYL)BENZOIC acid

Analyse Crystal structure of the catalytic domain of mmp-13 complexed with 4… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3WV1
Type
protein
Length
334 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Collagenase 3
EC
3.4.24.-
UniProt
P45452
Ligands
WHH, ZN, CA, NA
Pockets
1 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 24% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACollagenase 3 (EC 3.4.24.-)protein17024% helix, 18% strandP45452
BCollagenase 3 (EC 3.4.24.-)protein16424% helix, 18% strandP45452

Ligands and binding sites

  • WHH · 4-[2-({6-fluoro-2-[(3-methoxybenzyl)carbamoyl]-4-oxo-3,4-dihydroquinazolin-5-yl}oxy)ethyl]benzoic acid · ligand · 2 copies · chains A, B
  • ZN · Zinc ion · metal · 4 copies · chains A, B
  • CA · Calcium ion · metal · 4 copies · chains A, B
  • NA · Sodium ion · metal · 2 copies · chains A, B
  • FMT · Formic acid · additive · 2 copies · chains A, B

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
111840.750.77118FMT, WHH, ZN

Interfaces

1 interface between chains.

  • A–B · 1123 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 3WV1 · Crystal structure of the catalytic domain of MMP-13 complexed with… · the same entry in another collection · chain A against A, TM-score 1.00

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