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Crystal structure of the marr family transcriptional regulator SPO1453 from silicibacter pomeroyi dss-3

Analyse Crystal structure of the marr family transcriptional regulator SPO1453 from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3CDH
Type
protein
Length
270 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transcriptional regulator, marr family
UniProt
Q5LTG1
Ligands
SO4
Pockets
4 · best druggability 0.68

Structure

x-ray diffraction · 2 distinct chains · 73% helix, 6% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATranscriptional regulator, marr familyprotein13471% helix, 5% strandQ5LTG1
BTranscriptional regulator, marr familyprotein13674% helix, 7% strandQ5LTG1

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 6 copies · chains A, B
  • GOL · Glycerol · additive · 3 copies · chains A, B

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1520.680.9616GOL
23050.610.7832GOL
3600.460.8313empty
4690.320.7524empty

Interfaces

1 interface between chains.

  • A–B · 2509 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 modified (engineered).

Compared structures

  • 3CDH · Crystal structure of the MarR family transcriptional regulator SPO1453 from Silicibacter… · the same entry in another collection · chain A against A, TM-score 1.00

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