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Crystal structure of trypsin inhibitor 1 from Senna obtusifolia

Analyse Crystal structure of trypsin inhibitor 1 from Senna obtusifolia in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6KV2
Type
protein
Length
710 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.003
Source
Senna obtusifolia
Molecule
Trypsin inhibitor 1
EC
1.2.3.4
Pockets
7 · best druggability 0.81

Structure

x-ray diffraction · resolution 2.003 · 4 distinct chains · 2% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATrypsin inhibitor 1 (EC 1.2.3.4)protein1833% helix, 46% strand—
BTrypsin inhibitor 1 (EC 1.2.3.4)protein1914% helix, 43% strand—
DTrypsin inhibitor 1 (EC 1.2.3.4)protein1660% helix, 48% strand—
CTrypsin inhibitor 1 (EC 1.2.3.4)protein1702% helix, 49% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19850.810.82129empty
21430.500.7927empty
3900.430.7919empty
4890.400.7724empty
51200.370.7426empty

Interfaces

5 interfaces between chains.

  • B–C · 869 Ų buried · 8 hydrogen bonds · protein-protein
  • B–D · 718 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 670 Ų buried · 6 hydrogen bonds · protein-protein
  • A–D · 665 Ų buried · 3 hydrogen bonds · protein-protein
  • A–B · 553 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 14 modified, 8 disulfide (engineered, disulfide).

Compared structures

  • 6KV2 · Crystal structure of trypsin inhibitor 1 from senna obtusifolia · the same entry in another collection · chain A against A, TM-score 1.00

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