MolNFT v1 · #111128 · protein
Native bacteroidetes-affiliated GH5 cellulase linked with a polysaccharide utilization locus
4YHG: “Native bacteroidetes-affiliated GH5 cellulase linked with a polysaccharide utilization locus”. X-ray diffraction, 1 ligand (BGC), 3 pockets (best druggability 0.76). MolNFT v1 #111128 on GenesisL1: 3D structure, binding sites and…
- PDB
- 4YHG
- Type
- protein
- Length
- 750 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- GH5
- EC
- 3.2.1.4
- UniProt
- A0A076MPD7
- Ligands
- BGC
- Pockets
- 3 · best druggability 0.76
Structure
x-ray diffraction · 2 distinct chains · 43% helix, 13% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | GH5 (EC 3.2.1.4) | protein | 389 | 42% helix, 13% strand | A0A076MPD7 |
| B | GH5 (EC 3.2.1.4) | protein | 361 | 44% helix, 12% strand | A0A076MPD7 |
Ligands and binding sites
- BGC · beta-D-glucopyranose · sugar · 3 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 786 | 0.76 | 0.80 | 64 | empty |
| 2 | 385 | 0.64 | 0.78 | 32 | BGC |
| 3 | 197 | 0.48 | 0.75 | 25 | empty |
Interfaces
1 interface between chains.
- A–B · 656 Ų buried · 11 hydrogen bonds · protein-protein
Compared structures
- 4YHG · Native bacteroidetes-affiliated GH5 cellulase linked with a polysaccharide utilization… · the same entry in another collection · chain B against B, 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 A0A076MPD7
- Elsewhere: RCSB PDB 4YHG · PDBe 4YHG · UniProt A0A076MPD7
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