Research workbench
Human factor xiii with calcium bound in the ion site
Analyse Human factor xiii with calcium bound in the ion site in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1EVU
- Type
- protein
- Length
- 1,416 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Coagulation factor xiii
- EC
- 2.3.2.13
- UniProt
- P00488
- Ligands
- CA
- Pockets
- 17 · best druggability 0.86
Structure
x-ray diffraction · 2 distinct chains · 15% helix, 41% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Coagulation factor xiii (EC 2.3.2.13) | protein | 708 | 15% helix, 41% strand | P00488 |
| B | Coagulation factor xiii (EC 2.3.2.13) | protein | 708 | 15% helix, 42% strand | P00488 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
17 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 977 | 0.86 | 0.87 | 124 | PGO |
| 2 | 822 | 0.85 | 0.88 | 104 | empty |
| 3 | 453 | 0.68 | 0.80 | 39 | empty |
| 4 | 130 | 0.65 | 0.88 | 28 | empty |
| 5 | 128 | 0.61 | 0.86 | 35 | empty |
Interfaces
1 interface between chains.
- A–B · 2894 Ų buried · 48 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 1 modified (acetylation).
Compared structures
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 P00488
- Elsewhere: RCSB PDB 1EVU · PDBe 1EVU · UniProt P00488
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