MolNFT v1 · #2315 · protein + DNA
Ecorv-T93A/DNA/CA2+
1BSS · 5'-D(*AP*AP*AP*GP*AP*TP*AP*TP*CP*TP*T)-3': “Ecorv-T93A/DNA/CA2+”. X-ray diffraction, 1 ligand (CA), 5 pockets (best druggability 0.85). MolNFT v1 #2315 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 1BSS
- Type
- protein + DNA
- Length
- 480 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- 5'-D(*AP*AP*AP*GP*AP*TP*AP*TP*CP*TP*T)-3'; Ecorv endonuclease
- EC
- 3.1.21.4
- UniProt
- P04390
- Ligands
- CA
- Pockets
- 5 · best druggability 0.85
Structure
x-ray diffraction · 3 distinct chains · 32% helix, 30% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| C, D | 5'-D(*AP*AP*AP*GP*AP*TP*AP*TP*CP*TP*T)-3' | dna | 11 | — | — |
| A | Ecorv endonuclease (EC 3.1.21.4) | protein | 230 | 33% helix, 31% strand | P04390 |
| B | Ecorv endonuclease (EC 3.1.21.4) | protein | 228 | 31% helix, 29% strand | P04390 |
Ligands and binding sites
- CA · Calcium ion · metal · 2 copies · chains A, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 945 | 0.85 | 0.87 | 87 | CA |
| 2 | 183 | 0.63 | 0.84 | 29 | empty |
| 3 | 209 | 0.53 | 0.78 | 27 | empty |
| 4 | 183 | 0.49 | 0.77 | 27 | empty |
| 5 | 68 | 0.33 | 0.76 | 10 | empty |
Interfaces
6 interfaces between chains.
- A–B · 1384 Ų buried · 8 hydrogen bonds · protein-protein
- D–B · 736 Ų buried · 11 hydrogen bonds · protein-nucleic
- C–A · 724 Ų buried · 16 hydrogen bonds · protein-nucleic
- C–D · 498 Ų buried · 43 hydrogen bonds · nucleic-nucleic
- D–A · 471 Ų buried · 13 hydrogen bonds · protein-nucleic
Compared structures
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 P04390
- Elsewhere: RCSB PDB 1BSS · PDBe 1BSS · UniProt P04390
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