8H78: Human MMP-2 catalytic domain

Crystal structure of human MMP-2 catalytic domain in complex with inhibitor. Determined by X-ray diffraction at 2.4 Å resolution. Released 18 Jan 2023.

Method
X-ray diffraction
Resolution
2.4 Å
Organism
Homo sapiens
Chains
2
Atoms
2,804
Mol. weight
40.05 kDa
Ligands
L2U, 2HP, CA, ZN
Released
18 Jan 2023

Explore 8H78 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

8H78 contains 6 α-helices and 20 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chains A and B: 3 helices, 10 β-strands

ElementResiduesLengthSheet
β-strand411
β-strand15-2062
β-strand2213
α-helix29-4416
β-strand50-5342
β-strand61-6662
β-strand84-8632
β-strand97-10042
β-strand105-10624
β-strand113-11424
α-helix115-12612
β-strand12911
α-helix153-16311

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Matrix metalloproteinase-2A, Bprotein168Homo sapiensP08253 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>8H78_1 Matrix metalloproteinase-2 (chains A, B)
MYNFFPRKPKWDKNQITYRIIGYTPDLAPETVDDAFARAFQVWSDVTPLRFSRIYDGEAD
IMINFGRWEHGDGYPFDGKDGLLAHAFAPGTGVGGDSHFDDDELWTLGKGVGYSLFLVAA
HAFGHAMGLEHSQDPGALMAPIYTYTKNFRLSQDDIKGIQELYGASPD

Ligands and cofactors

IDNameFormulaCopies
L2U(2~{R})-2-[[4-[(4-aminocarbonylphenyl)carbonylamino]phenyl]sulfonylamino]-5-[(2…C41 H57 N9 O13 S2
2HPDihydrogenphosphate ionH2 O4 P1
CACalcium ionCa6
ZNZinc ionZn4

Primary citation

Discovery of TP0597850: A Selective, Chemically Stable, and Slow Tight-Binding Matrix Metalloproteinase-2 Inhibitor with a Phenylbenzamide-Pentapeptide Hybrid Scaffold. Takeuchi, T., Nomura, Y., Tamita, T. et al. J Med Chem (2023) 66:822-836. DOI 10.1021/acs.jmedchem.2c01698 · PubMed

Other PDB entries of the same protein (UniProt P08253 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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