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Crystal structure of complex of BBKI and Bovine Trypsin

Analyse Crystal structure of complex of BBKI and Bovine Trypsin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6DWH
Type
protein
Length
2,316 residues
Chains
12
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2
Source
Bauhinia bauhinioides; Bos taurus
Molecule
Cationic trypsin; Kunitz-type inihibitor
EC
3.4.21.4
UniProt
P00760, Q6VEQ7
Ligands
NA, CL
Pockets
20 · best druggability 0.79

Structure

x-ray diffraction · resolution 2 · 2 distinct chains · 6% helix, 40% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FCationic trypsin (EC 3.4.21.4)protein22311% helix, 37% strandP00760
G, H, I, J, K, LKunitz-type inihibitorprotein1630% helix, 45% strandQ6VEQ7

Ligands and binding sites

  • NA · Sodium ion · metal · 8 copies · chains C, E, I, J, L, F
  • CL · Chloride ion · ion · 2 copies · chains D, J, F, L

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

Pockets

20 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15080.790.8654empty
24770.770.8550empty
31860.690.8830empty
41770.670.8731empty
51840.670.8731empty

Interfaces

13 interfaces between chains.

  • E–K · 994 Ų buried · 23 hydrogen bonds · protein-protein
  • D–J · 990 Ų buried · 23 hydrogen bonds · protein-protein
  • B–H · 985 Ų buried · 20 hydrogen bonds · protein-protein
  • F–L · 977 Ų buried · 22 hydrogen bonds · protein-protein
  • A–G · 967 Ų buried · 23 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 36 disulfide (disulfide).

Compared structures

  • 6DWH · Crystal structure of complex of bbki and bovine trypsin · the same entry in another collection · chain J against J, TM-score 1.00

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