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MolNFT v1 · #114212 · protein

Crystal structure of the catalytic domain of mmp-13 complexed with 4- oxo-N-(3-(2-(1H-1,2,4-triazol-3-YLSULFANYL)ETHOXY)BENZYL)-3,4- dihydroquinazoline-2-carboxamide

5B5P · Collagenase 3: “Crystal structure of the catalytic domain of mmp-13 complexed with 4…”. X-ray diffraction, 3 ligands (WNN, CA, ZN), 1 pocket (best druggability 0.74). MolNFT v1 #114212 on GenesisL1: 3D structure, binding sites and…

PDB
5B5P
Type
protein
Length
332 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
WNN, CA, ZN
Pockets
1 · best druggability 0.74

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
ACollagenase 3 (EC 3.4.24.-)protein16723% helix, 19% strandP45452
BCollagenase 3 (EC 3.4.24.-)protein16524% helix, 18% strandP45452

Ligands and binding sites

  • WNN · 4-oxo-N-{3-[2-(1H-1,2,4-triazol-3-ylsulfanyl)ethoxy]benzyl}-3,4-dihydroquinazoline-2-carboxamide · ligand · 2 copies · chains A, B
  • CA · Calcium ion · metal · 6 copies · chains A, B
  • ZN · Zinc ion · metal · 4 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
111130.740.77109WNN

Interfaces

1 interface between chains.

  • A–B · 1252 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 5B5P · 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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