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MMP-13 in complex with the peptide IMISF

Analyse MMP-13 in complex with the peptide IMISF in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6HV2
Type
protein
Length
171 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.709
Source
Homo sapiens
Molecule
Collagenase 3
EC
3.4.24.-
UniProt
P45452
Ligands
CA, ZN
Pockets
3 · best druggability 0.47

Structure

x-ray diffraction · resolution 1.709 · 2 distinct chains · 23% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACollagenase 3 (EC 3.4.24.-)protein16623% helix, 19% strandP45452
BCollagenase 3 (EC 3.4.24.-)protein50% helix, 40% strandP45452

Ligands and binding sites

  • CA · Calcium ion · metal · 3 copies · chains A
  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • GOL · Glycerol · additive · chains A, B

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

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1730.470.8318empty
2570.320.7617empty
3630.300.7413GOL

Interfaces

1 interface between chains.

  • A–B · 446 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 6HV2 · Mmp-13 in complex with the peptide imisf · the same entry in another collection · chain A against A, TM-score 1.00
  • P45452 · AlphaFold monomer V2.0 prediction for collagenase 3 (P45452) · a predicted model of the same protein · chain A against A, TM-score 0.97

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