Research workbench
Rdc refined solution structure of the thap zinc finger of THAP1 in complex with its 16BP RRM1 DNA target
Analyse Rdc refined solution structure of the thap zinc finger of THAP1 in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2L1G
- Type
- protein + DNA
- Length
- 119 residues
- Chains
- 3
- Method
- solution nmr
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Thap domain-containing protein 1; DNA (5'-D(*GP*CP*TP*TP*GP*TP*GP*TP*GP*GP*GP*CP*AP*GP*CP*…
- UniProt
- Q9NVV9
- Ligands
- ZN
Structure
solution nmr · 3 distinct chains · 18% helix, 7% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Thap domain-containing protein 1 | protein | 87 | 18% helix, 7% strand | Q9NVV9 |
| B | DNA (5'-D(*GP*CP*TP*TP*GP*TP*GP*TP*GP*GP*GP*CP*AP*GP*CP*G)- 3') | dna | 16 | — | — |
| C | DNA (5'- D(P*CP*GP*CP*TP*GP*CP*CP*CP*AP*CP*AP*CP*AP*AP*GP*C)-3') | dna | 16 | — | — |
Ligands and binding sites
- ZN · Zinc ion · metal · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Interfaces
3 interfaces between chains.
- B–C · 787 Ų buried · 82 hydrogen bonds · nucleic-nucleic
- A–B · 611 Ų buried · 13 hydrogen bonds · protein-nucleic
- A–C · 579 Ų buried · 17 hydrogen bonds · protein-nucleic
Compared structures
- 2L1G · RDC refined solution structure of the THAP zinc finger of THAP1 in complex with its 16bp… · the same entry in another collection · chain A against A, TM-score 1.00
- Q9NVV9 · AlphaFold monomer V2.0 prediction for thap domain-containing protein 1 (Q9NVV9) · a predicted model of the same protein · chain A against A, TM-score 0.67
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 Q9NVV9
- Elsewhere: RCSB PDB 2L1G · PDBe 2L1G · UniProt Q9NVV9
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