Research workbench
Crystal structure of the oxalate bound malyl-CoA lyase from roseiflexus castenholzii
Analyse Crystal structure of the oxalate bound malyl-CoA lyase from roseiflexus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6KKH
- Type
- protein
- Length
- 4,035 residues
- Chains
- 12
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HPCH/HPAI aldolase
- UniProt
- A7NHT0
- Ligands
- OXL, MG
- Pockets
- 20 · best druggability 0.87
Structure
x-ray diffraction · 11 distinct chains · 44% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | HPCH/HPAI aldolase | protein | 329 | 44% helix, 14% strand | A7NHT0 |
| B | HPCH/HPAI aldolase | protein | 345 | 43% helix, 15% strand | A7NHT0 |
| C | HPCH/HPAI aldolase | protein | 343 | 44% helix, 15% strand | A7NHT0 |
| D | HPCH/HPAI aldolase | protein | 328 | 45% helix, 15% strand | A7NHT0 |
| E | HPCH/HPAI aldolase | protein | 347 | 44% helix, 14% strand | A7NHT0 |
| F, L | HPCH/HPAI aldolase | protein | 342 | 46% helix, 14% strand | A7NHT0 |
| G | HPCH/HPAI aldolase | protein | 325 | 43% helix, 14% strand | A7NHT0 |
| H | HPCH/HPAI aldolase | protein | 316 | 43% helix, 14% strand | A7NHT0 |
| I | HPCH/HPAI aldolase | protein | 345 | 43% helix, 15% strand | A7NHT0 |
| J | HPCH/HPAI aldolase | protein | 346 | 45% helix, 15% strand | A7NHT0 |
| K | HPCH/HPAI aldolase | protein | 327 | 40% helix, 15% strand | A7NHT0 |
Ligands and binding sites
- OXL · Oxalate ion · ligand · 4 copies · chains B, C, A, F, H, I, G, L
- MG · Magnesium ion · metal · 2 copies · chains A, F, H, I
- TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · 4 copies · chains A, E, F, B, C, D, G, K, L, H, I, J
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
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 | 1093 | 0.87 | 0.88 | 103 | empty |
| 2 | 1095 | 0.86 | 0.87 | 112 | empty |
| 3 | 1123 | 0.86 | 0.87 | 91 | empty |
| 4 | 1199 | 0.85 | 0.86 | 102 | empty |
| 5 | 1141 | 0.85 | 0.86 | 85 | empty |
Interfaces
25 interfaces between chains.
- A–F · 2147 Ų buried · 24 hydrogen bonds · protein-protein
- H–I · 2120 Ų buried · 24 hydrogen bonds · protein-protein
- B–C · 1949 Ų buried · 20 hydrogen bonds · protein-protein
- G–L · 1880 Ų buried · 17 hydrogen bonds · protein-protein
- K–L · 1694 Ų buried · 20 hydrogen bonds · protein-protein
Compared structures
- 6KKH · Crystal structure of the oxalate bound malyl-CoA lyase from Roseiflexus castenholzii · the same entry in another collection · chain A against A, 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 A7NHT0
- Elsewhere: RCSB PDB 6KKH · PDBe 6KKH · UniProt A7NHT0
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