MolNFT v1 · #64200 · protein
SAC3:SUS1:CDC31 complex
3FWC · Cell division control protein 31: “SAC3:SUS1:CDC31 complex”. X-ray diffraction, 1 ligand (SO4), 19 pockets (best druggability 0.57). MolNFT v1 #64200 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 3FWC
- Type
- protein
- Length
- 1,626 residues
- Chains
- 16
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Cell division control protein 31; Nuclear mRNA export protein SAC3; Protein SUS1
- UniProt
- P06704, P46674, Q6WNK7
- Ligands
- SO4
- Pockets
- 19 · best druggability 0.57
Structure
x-ray diffraction · 14 distinct chains · 75% helix, 2% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Cell division control protein 31 | protein | 145 | 58% helix, 6% strand | P06704 |
| B | Nuclear mRNA export protein SAC3 | protein | 83 | 94% helix, 0% strand | P46674 |
| C | Protein SUS1 | protein | 87 | 77% helix, 0% strand | Q6WNK7 |
| D | Protein SUS1 | protein | 86 | 81% helix, 0% strand | Q6WNK7 |
| E | Cell division control protein 31 | protein | 150 | 59% helix, 5% strand | P06704 |
| F, N | Nuclear mRNA export protein SAC3 | protein | 84 | 96% helix, 0% strand | P46674 |
| G, K | Protein SUS1 | protein | 88 | 78% helix, 0% strand | Q6WNK7 |
| H | Protein SUS1 | protein | 92 | 82% helix, 0% strand | Q6WNK7 |
| I | Cell division control protein 31 | protein | 147 | 61% helix, 4% strand | P06704 |
| J | Nuclear mRNA export protein SAC3 | protein | 78 | 97% helix, 0% strand | P46674 |
| L | Protein SUS1 | protein | 84 | 81% helix, 0% strand | Q6WNK7 |
| M | Cell division control protein 31 | protein | 148 | 60% helix, 5% strand | P06704 |
| O | Protein SUS1 | protein | 89 | 82% helix, 0% strand | Q6WNK7 |
| P | Protein SUS1 | protein | 93 | 83% helix, 0% strand | Q6WNK7 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · 4 copies · chains A, B, C, E, F, G, I, J, K, M, N, O
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
19 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 210 | 0.57 | 0.79 | 25 | SO4 |
| 2 | 203 | 0.54 | 0.78 | 28 | SO4 |
| 3 | 197 | 0.53 | 0.78 | 26 | SO4 |
| 4 | 266 | 0.52 | 0.75 | 37 | empty |
| 5 | 174 | 0.51 | 0.78 | 23 | SO4 |
Interfaces
23 interfaces between chains.
- J–K · 1658 Ų buried · 8 hydrogen bonds · protein-protein
- F–G · 1645 Ų buried · 9 hydrogen bonds · protein-protein
- N–O · 1644 Ų buried · 10 hydrogen bonds · protein-protein
- B–C · 1615 Ų buried · 7 hydrogen bonds · protein-protein
- M–N · 1518 Ų buried · 13 hydrogen bonds · protein-protein
Compared structures
- 3FWC · Sac3:Sus1:Cdc31 complex · the same entry in another collection · chain G against G, 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 P06704
- Every structure of UniProt P46674
- Every structure of UniProt Q6WNK7
- Elsewhere: RCSB PDB 3FWC · PDBe 3FWC · UniProt P06704 · UniProt P46674 · UniProt Q6WNK7
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