Research workbench
NMR solution structure of the extended pbx homeodomain bound to DNA
Analyse NMR solution structure of the extended pbx homeodomain bound to DNA in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1LFU
- Type
- protein + DNA
- Length
- 110 residues
- Chains
- 3
- Method
- solution nmr
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- 5'-D(*GP*CP*GP*CP*AP*TP*GP*AP*TP*TP*GP*CP*CP*C)-3'…
- UniProt
- P41778
- Pockets
- 2 · best druggability 0.45
Structure
solution nmr · 3 distinct chains · 63% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | 5'-D(*GP*CP*GP*CP*AP*TP*GP*AP*TP*TP*GP*CP*CP*C)-3' | dna | 14 | — | — |
| B | 5'-D(*GP*GP*GP*CP*AP*AP*TP*CP*AP*TP*GP*CP*GP*C)-3' | dna | 14 | — | — |
| P | Homeobox protein PBX1 | protein | 82 | 63% helix, 0% strand | P41778 |
Pockets
2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 81 | 0.45 | 0.81 | 16 | empty |
| 2 | 66 | 0.29 | 0.74 | 15 | empty |
Interfaces
3 interfaces between chains.
- A–B · 636 Ų buried · 51 hydrogen bonds · nucleic-nucleic
- B–P · 572 Ų buried · 9 hydrogen bonds · protein-nucleic
- A–P · 501 Ų buried · 10 hydrogen bonds · protein-nucleic
Compared structures
- 1LFU · NMR Solution Structure of the Extended PBX Homeodomain Bound to DNA · the same entry in another collection · chain A against A, TM-score 1.00
- P41778 · AlphaFold monomer V2.0 prediction for pre-B-cell leukemia transcription factor 1 (P41778) · a predicted model of the same protein · chain P against A, TM-score 0.70
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 P41778
- Elsewhere: RCSB PDB 1LFU · PDBe 1LFU · UniProt P41778
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