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Crystal structure of mure from E.COLI
Analyse Crystal structure of mure from E.COLI in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7B53
- Type
- protein
- Length
- 964 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Udp-N-acetylmuramoyl-L-alanyl-D-glutamate--2,6- diaminopimelate ligase
- EC
- 6.3.2.13
- UniProt
- P22188
- Pockets
- 19 · best druggability 0.71
Structure
x-ray diffraction · 2 distinct chains · 35% helix, 24% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Udp-N-acetylmuramoyl-L-alanyl-D-glutamate--2,6- diaminopimelate ligase (EC 6.3.2.13) | protein | 487 | 35% helix, 24% strand | P22188 |
| B | Udp-N-acetylmuramoyl-L-alanyl-D-glutamate--2,6- diaminopimelate ligase (EC 6.3.2.13) | protein | 477 | 35% helix, 24% strand | P22188 |
Ligands and binding sites
- EDO · 1,2-ethanediol · additive · 4 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
19 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 784 | 0.71 | 0.77 | 77 | empty |
| 2 | 360 | 0.64 | 0.79 | 37 | empty |
| 3 | 231 | 0.62 | 0.82 | 26 | EDO |
| 4 | 130 | 0.48 | 0.79 | 18 | empty |
| 5 | 93 | 0.46 | 0.80 | 17 | empty |
Interfaces
1 interface between chains.
- A–B · 371 Ų buried · 4 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 P22188
- Elsewhere: RCSB PDB 7B53 · PDBe 7B53 · UniProt P22188
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