Research workbench
Bamabcde bound to substrate espp class 2
Analyse Bamabcde bound to substrate espp class 2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7TT0
- Type
- protein
- Length
- 962 residues
- Chains
- 5
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Outer membrane protein assembly factor bama; Outer membrane protein assembly factor bame…
- EC
- 3.4.21.-
- UniProt
- C3TPJ2, A0A3L5AP29, A0A1X3I1M6, W8SZY2, Q7BSW5
- Pockets
- 12 · best druggability 0.78
Structure
electron microscopy · 5 distinct chains · 28% helix, 32% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Outer membrane protein assembly factor bama | protein | 588 | 14% helix, 45% strand | C3TPJ2 |
| E | Outer membrane protein assembly factor bame | protein | 89 | 17% helix, 36% strand | A0A3L5AP29 |
| D | Outer membrane protein assembly factor bamd | protein | 213 | 78% helix, 0% strand | A0A1X3I1M6 |
| C | Outer membrane protein assembly factor bamc | protein | 48 | 15% helix, 0% strand | W8SZY2 |
| P | MALTOSE/MALTODEXTRIN-binding periplasmic PROTEIN,SERINE protease espp chimera (EC 3.4.21.-) | protein | 24 | 0% helix, 67% strand | Q7BSW5 |
Pockets
12 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 827 | 0.78 | 0.82 | 88 | empty |
| 2 | 290 | 0.59 | 0.78 | 39 | empty |
| 3 | 255 | 0.57 | 0.78 | 34 | empty |
| 4 | 179 | 0.55 | 0.80 | 38 | empty |
| 5 | 126 | 0.53 | 0.82 | 20 | empty |
Interfaces
7 interfaces between chains.
- D–C · 1798 Ų buried · 20 hydrogen bonds · protein-protein
- A–D · 982 Ų buried · 11 hydrogen bonds · protein-protein
- A–E · 779 Ų buried · 8 hydrogen bonds · protein-protein
- E–D · 777 Ų buried · 7 hydrogen bonds · protein-protein
- A–P · 700 Ų buried · 19 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 2 disulfide (disulfide).
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 C3TPJ2
- Every structure of UniProt A0A3L5AP29
- Every structure of UniProt A0A1X3I1M6
- Every structure of UniProt W8SZY2
- Every structure of UniProt Q7BSW5
- Elsewhere: RCSB PDB 7TT0 · PDBe 7TT0 · UniProt C3TPJ2 · UniProt A0A3L5AP29 · UniProt A0A1X3I1M6 · UniProt W8SZY2 · UniProt Q7BSW5
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.