MolNFT v1 · #82724 · protein
Crystal structure of G52A-P55G mutant of L-serine-O-acetyltransferase found in D-cycloserine biosynthetic pathway
3VVM · Homoserine O-acetyltransferase: “Crystal structure of G52A-P55G mutant of L-serine-O-acetyltransferase found in D-cycloserine biosynthetic…”. X-ray diffraction, 8 pockets (best druggability 0.72). MolNFT v1 #82724 on GenesisL1: 3D…
- PDB
- 3VVM
- Type
- protein
- Length
- 737 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Homoserine O-acetyltransferase
- EC
- 2.3.1.31
- UniProt
- D2Z028
- Pockets
- 8 · best druggability 0.72
Structure
x-ray diffraction · 2 distinct chains · 39% helix, 18% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Homoserine O-acetyltransferase (EC 2.3.1.31) | protein | 368 | 40% helix, 18% strand | D2Z028 |
| B | Homoserine O-acetyltransferase (EC 2.3.1.31) | protein | 369 | 39% helix, 18% strand | D2Z028 |
Pockets
8 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 440 | 0.72 | 0.82 | 44 | empty |
| 2 | 452 | 0.70 | 0.80 | 47 | empty |
| 3 | 91 | 0.66 | 0.91 | 24 | empty |
| 4 | 246 | 0.59 | 0.79 | 32 | empty |
| 5 | 103 | 0.49 | 0.81 | 19 | empty |
Interfaces
1 interface between chains.
- A–B · 2169 Ų buried · 33 hydrogen bonds · protein-protein
Compared structures
- 3VVM · Crystal structure of G52A-P55G mutant of L-serine-O-acetyltransferase found in… · the same entry in another collection · chain B against B, TM-score 1.00
- D2Z028 · AlphaFold monomer V2.0 prediction for L-SERINE/HOMOSERINE O-acetyltransferase (D2Z028) · a predicted model of the same protein · 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 D2Z028
- Elsewhere: RCSB PDB 3VVM · PDBe 3VVM · UniProt D2Z028
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