Research workbench
AP2 bound to heparin and TGN38 tyrosine cargo peptide
Analyse AP2 bound to heparin and TGN38 tyrosine cargo peptide in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7RWA
- Type
- protein
- Length
- 3,244 residues
- Chains
- 10
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Ap-2 complex subunit alpha-2; Ap-2 complex subunit beta; Ap-2 complex subunit mu; Ap-2…
- UniProt
- P17427, Q9DBG3, P84091, P62743
- Pockets
- 20 · best druggability 0.81
Structure
electron microscopy · 5 distinct chains · 54% helix, 13% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, a | Ap-2 complex subunit alpha-2 | protein | 600 | 71% helix, 1% strand | P17427 |
| B, b | Ap-2 complex subunit beta | protein | 496 | 67% helix, 0% strand | Q9DBG3 |
| M, m | Ap-2 complex subunit mu | protein | 379 | 13% helix, 46% strand | P84091 |
| S, s | Ap-2 complex subunit sigma | protein | 142 | 46% helix, 25% strand | P62743 |
| Y, y | Trans-golgi network integral membrane protein TGN38 peptide | protein | 5 | 0% helix, 60% strand | — |
Pockets
20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1037 | 0.81 | 0.83 | 125 | empty |
| 2 | 1060 | 0.81 | 0.82 | 131 | empty |
| 3 | 779 | 0.79 | 0.83 | 125 | empty |
| 4 | 1105 | 0.78 | 0.80 | 98 | empty |
| 5 | 939 | 0.78 | 0.80 | 127 | empty |
Interfaces
12 interfaces between chains.
- A–S · 493 Ų buried · 2 hydrogen bonds · protein-protein
- a–s · 491 Ų buried · 2 hydrogen bonds · protein-protein
- B–M · 369 Ų buried · 1 hydrogen bond · protein-protein
- b–m · 367 Ų buried · 1 hydrogen bond · protein-protein
- m–y · 350 Ų buried · 5 hydrogen bonds · protein-protein
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 P17427
- Every structure of UniProt Q9DBG3
- Every structure of UniProt P84091
- Every structure of UniProt P62743
- Elsewhere: RCSB PDB 7RWA · PDBe 7RWA · UniProt P17427 · UniProt Q9DBG3 · UniProt P84091 · UniProt P62743
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