Research workbench
AlphaFold monomer V2.0 prediction for udp-N-acetylmuramate--L-alanine ligase (A3MR64)
Analyse AlphaFold monomer V2.0 prediction for udp-N-acetylmuramate--L-alanine ligase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- Accession
- A3MR64
- Type
- protein
- Length
- 465 residues
- Chains
- 1
- Collection
- MolNFT v1 / AlphaFold
- Contract
- 0xBf7491af3407816DFa88a5EA4c82e8A2B1D721eD
- Owner
- 0x5Be6db7bf0250FDCB4deFDb7f993cB6C300c26C2
- Molecule
- Udp-N-acetylmuramate--L-alanine ligase
- UniProt
- A3MR64
- Pockets
- 6 · best druggability 0.73
Structure
1 distinct chain · 38% helix, 25% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Udp-N-acetylmuramate--L-alanine ligase | protein | 465 | 38% helix, 25% strand | A3MR64 |
Pockets
6 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 572 | 0.73 | 0.81 | 72 | empty |
| 2 | 78 | 0.36 | 0.77 | 14 | empty |
| 3 | 55 | 0.33 | 0.77 | 14 | empty |
| 4 | 51 | 0.33 | 0.78 | 14 | empty |
| 5 | 51 | 0.31 | 0.77 | 14 | empty |
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 A3MR64
- Elsewhere: UniProt A3MR64 · AlphaFold DB A3MR64
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