MolNFT v1 · #136893 · protein
Crystal structure of N102A mutant of human macrophage migration inhibitory factor
5V70: “Crystal structure of N102A mutant of human macrophage migration inhibitory factor”. X-ray diffraction, 1 ligand (SO4), 5 pockets (best druggability 0.83). MolNFT v1 #136893 on GenesisL1: 3D structure, binding sites and pockets in…
- PDB
- 5V70
- Type
- protein
- Length
- 342 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Macrophage migration inhibitory factor
- EC
- 5.3.2.1, 5.3.3.12
- UniProt
- P14174
- Ligands
- SO4
- Pockets
- 5 · best druggability 0.83
Structure
x-ray diffraction · 1 distinct chain · 39% helix, 31% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C | Macrophage migration inhibitory factor (EC 5.3.2.1, 5.3.3.12) | protein | 114 | 39% helix, 31% strand | P14174 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · 5 copies · chains A, B, C
- GOL · Glycerol · additive · 3 copies · chains A, C, B
- IPA · Isopropyl alcohol · additive · 3 copies · chains B, C, A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 391 | 0.83 | 0.92 | 44 | empty |
| 2 | 52 | 0.52 | 0.87 | 13 | GOL |
| 3 | 54 | 0.51 | 0.87 | 13 | GOL |
| 4 | 62 | 0.50 | 0.85 | 13 | GOL |
| 5 | 100 | 0.34 | 0.73 | 18 | empty |
Interfaces
3 interfaces between chains.
- A–C · 1140 Ų buried · 18 hydrogen bonds · protein-protein
- A–B · 1134 Ų buried · 18 hydrogen bonds · protein-protein
- B–C · 1125 Ų buried · 17 hydrogen bonds · protein-protein
Compared structures
- 5V70 · Crystal structure of N102A mutant of human macrophage migration inhibitory factor · the same entry in another collection · chain A against A, TM-score 1.00
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 P14174
- Elsewhere: RCSB PDB 5V70 · PDBe 5V70 · UniProt P14174
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