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Structure of the trypsin induced serpin-type proteinase inhibitor, miropin.

Analyse Structure of the trypsin induced serpin-type proteinase inhibitor, miropin. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5NCT
Type
protein
Length
363 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Serpin-type proteinase inhibitor, miropin
UniProt
G8UQY8
Pockets
2 · best druggability 0.65

Structure

x-ray diffraction · 2 distinct chains · 28% helix, 37% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASerpin-type proteinase inhibitor, miropinprotein32731% helix, 36% strandG8UQY8
CSerpin-type proteinase inhibitor, miropinprotein360% helix, 53% strandG8UQY8

Ligands and binding sites

  • GOL · Glycerol · additive · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11840.650.8423empty
2580.300.7518empty

Interfaces

1 interface between chains.

  • A–C · 2577 Ų buried · 46 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 5NCT · Structure of the trypsin induced serpin-type proteinase inhibitor, miropin. · the same entry in another collection · chain A against A, TM-score 1.00

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