Research workbench
The structure of a nonadecapeptide of the fifth EGF domain of thrombomodulin complexed with thrombin
Analyse The structure of a nonadecapeptide of the fifth EGF domain of thrombomodulin… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1HLT
- Type
- protein
- Length
- 573 residues
- Chains
- 5
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Alpha-thrombin (small subunit); Alpha-thrombin (large subunit); Thrombomodulin
- UniProt
- P00734, P07204
- Ligands
- 0G6
- Pockets
- 6 · best druggability 0.56
Structure
x-ray diffraction · 3 distinct chains · 14% helix, 30% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| L, J | Alpha-thrombin (small subunit) | protein | 27 | 44% helix, 0% strand | P00734 |
| H, K | Alpha-thrombin (large subunit) | protein | 251 | 11% helix, 33% strand | P00734 |
| R | Thrombomodulin | protein | 17 | 0% helix, 24% strand | P07204 |
Ligands and binding sites
- 0G6 · D-phenylalanyl-N-[(2S,3S)-6-{[amino(iminio)methyl]amino}-1-chloro-2-hydroxyhexan-3-yl]-L-prolinamide · ligand · 2 copies · chains H, K
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
6 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 225 | 0.56 | 0.78 | 40 | 0G6 |
| 2 | 183 | 0.52 | 0.78 | 32 | 0G6 |
| 3 | 82 | 0.40 | 0.78 | 15 | empty |
| 4 | 75 | 0.38 | 0.77 | 21 | empty |
| 5 | 63 | 0.37 | 0.78 | 17 | empty |
Interfaces
5 interfaces between chains.
- J–K · 1102 Ų buried · 22 hydrogen bonds · protein-protein
- L–H · 1091 Ų buried · 19 hydrogen bonds · protein-protein
- H–R · 463 Ų buried · 5 hydrogen bonds · protein-protein
- K–R · 463 Ų buried · 6 hydrogen bonds · protein-protein
- H–K · 135 Ų buried · 0 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 8 disulfide, 4 covalent (disulfide, covalent ligand).
Compared structures
- 1HLT · The structure of a nonadecapeptide of the fifth EGF domain of thrombomodulin complexed… · the same entry in another collection · chain R against R, TM-score 1.00
- P00734 · AlphaFold monomer V2.0 prediction for prothrombin (P00734) · a predicted model of the same protein · chain K against A, TM-score 0.92
- P07204 · AlphaFold monomer V2.0 prediction for thrombomodulin (P07204) · a predicted model of the same protein · chain R against A, TM-score 0.38
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P00734
- Every structure of UniProt P07204
- Elsewhere: RCSB PDB 1HLT · PDBe 1HLT · UniProt P00734 · UniProt P07204
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