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Structure of agra lyttr domain in complex with promoters

Analyse Structure of agra lyttr domain in complex with promoters in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4XYQ
Type
protein + DNA
Length
135 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
DNA (5'-D(*TP*TP*TP*AP*AP*CP*AP*GP*TP*TP*AP*AP*GP*TP*AP*T)- 3'); DNA…
UniProt
Q5HEG2
Pockets
3 · best druggability 0.45

Structure

x-ray diffraction · 3 distinct chains · 16% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BDNA (5'-D(*TP*TP*TP*AP*AP*CP*AP*GP*TP*TP*AP*AP*GP*TP*AP*T)- 3')dna16——
CDNA (5'-D(*AP*AP*TP*AP*CP*TP*TP*AP*AP*CP*TP*GP*TP*TP*AP*A)- 3')dna16——
AAccessory gene regulator aprotein10316% helix, 49% strandQ5HEG2

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · chains B, A

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11640.450.7622empty
21100.380.7616empty
3530.250.7311empty

Interfaces

3 interfaces between chains.

  • B–C · 666 Ų buried · 48 hydrogen bonds · nucleic-nucleic
  • C–A · 502 Ų buried · 8 hydrogen bonds · protein-nucleic
  • B–A · 360 Ų buried · 8 hydrogen bonds · protein-nucleic

Compared structures

  • 4XYQ · Structure of AgrA LytTR domain in complex with promoters · the same entry in another collection · chain B against B, TM-score 1.00
  • Q5HEG2 · AlphaFold monomer V2.0 prediction for accessory gene regulator a (Q5HEG2) · a predicted model of the same protein · chain A against A, TM-score 0.95

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