MolNFT v1 · #104378 · protein
TRNA-guanine transglycosylase (tgt) mutant V262D in complex with 6- amino-2-{[2-(morpholin-4-YL)ETHYL]AMINO}-1H,7H,8H-IMIDAZO[4,5- G]QUINAZOLIN-8-one
4Q8P · Queuine tRNA-ribosyltransferase: “TRNA-guanine transglycosylase (tgt) mutant V262D in complex with 6…”. X-ray diffraction, 2 ligands (CKR, ZN), 2 pockets (best druggability 0.64). MolNFT v1 #104378 on GenesisL1: 3D structure…
- PDB
- 4Q8P
- Type
- protein
- Length
- 368 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Queuine tRNA-ribosyltransferase
- EC
- 2.4.2.29
- UniProt
- P28720
- Ligands
- CKR, ZN
- Pockets
- 2 · best druggability 0.64
Structure
x-ray diffraction · 1 distinct chain · 44% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Queuine tRNA-ribosyltransferase (EC 2.4.2.29) | protein | 368 | 44% helix, 19% strand | P28720 |
Ligands and binding sites
- CKR · 6-amino-2-[(2-morpholin-4-ylethyl)amino]-3,7-dihydro-8H-imidazo[4,5-g]quinazolin-8-one · ligand · chains A
- ZN · Zinc ion · metal · chains A
- GOL · Glycerol · additive · 3 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 283 | 0.64 | 0.81 | 34 | CKR |
| 2 | 77 | 0.35 | 0.76 | 17 | empty |
Compared structures
- 4Q8P · tRNA-Guanine Transglycosylase (TGT) Mutant V262D in Complex with… · the same entry in another collection · 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 P28720
- Elsewhere: RCSB PDB 4Q8P · PDBe 4Q8P · UniProt P28720
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