Research workbench
Bacillus subtilis lipase a with covalently bound rc-ipg- phosphonate-inhibitor
Analyse Bacillus subtilis lipase a with covalently bound rc-ipg- phosphonate-inhibitor in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1R4Z
- Type
- protein
- Length
- 358 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- P37957
Structure
x-ray diffraction · 1 distinct chain.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | — | protein | 179 | — | P37957 |
Compared structures
- 1R4Z · Bacillus subtilis lipase A with covalently bound Rc-IPG-phosphonate-inhibitor · the same entry in another collection · chain A against A, TM-score 1.00
- P37957 · AlphaFold monomer V2.0 prediction for lipase esta (P37957) · 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 P37957
- Elsewhere: RCSB PDB 1R4Z · PDBe 1R4Z · UniProt P37957
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