MolNFT v1 · #43488 · protein + DNA
LEF1 hmg domain (from mouse), complexed with DNA (15BP), NMR, 12 structures
2LEF · DNA (5'-D(*CP*AP*CP*CP*CP*TP*TP*TP*GP*AP*AP*GP*CP*TP*C)- 3'): “LEF1 hmg domain (from mouse), complexed with DNA (15BP), NMR, 12 structures”. Solution nmr, 2 pockets (best druggability 0.40). MolNFT v1 #43488 on GenesisL1: 3D…
- PDB
- 2LEF
- Type
- protein + DNA
- Length
- 116 residues
- Chains
- 3
- Method
- solution nmr
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- DNA (5'-D(*CP*AP*CP*CP*CP*TP*TP*TP*GP*AP*AP*GP*CP*TP*C)- 3'); DNA…
- UniProt
- P27782
- Pockets
- 2 · best druggability 0.40
Structure
solution nmr · 3 distinct chains · 57% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| B | DNA (5'-D(*CP*AP*CP*CP*CP*TP*TP*TP*GP*AP*AP*GP*CP*TP*C)- 3') | dna | 15 | — | — |
| C | DNA (5'-D(*GP*AP*GP*CP*TP*TP*CP*AP*AP*AP*GP*GP*GP*TP*G)- 3') | dna | 15 | — | — |
| A | Protein (lymphoid enhancer-binding factor) | protein | 86 | 57% helix, 0% strand | P27782 |
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 | 71 | 0.40 | 0.80 | 13 | empty |
| 2 | 91 | 0.38 | 0.76 | 16 | empty |
Interfaces
3 interfaces between chains.
- C–A · 1081 Ų buried · 27 hydrogen bonds · protein-nucleic
- B–A · 1051 Ų buried · 23 hydrogen bonds · protein-nucleic
- B–C · 659 Ų buried · 79 hydrogen bonds · nucleic-nucleic
Compared structures
- 2LEF · LEF1 hmg domain (from mouse), complexed with DNA (15BP), NMR, 12 structures · the same entry in another collection · chain B against B, TM-score 1.00
- P27782 · AlphaFold monomer V2.0 prediction for lymphoid enhancer-binding factor 1 (P27782) · a predicted model of the same protein · chain A against A, TM-score 0.81
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 P27782
- Elsewhere: RCSB PDB 2LEF · PDBe 2LEF · UniProt P27782
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