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Crystal structure of magnetospirillum gryphiswaldense msr-1 holo-fur

Analyse Crystal structure of magnetospirillum gryphiswaldense msr-1 holo-fur in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4RAZ
Type
protein
Length
268 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
DNA-binding transcriptional dual regulator of siderophore biosynthesis and TRANSPORT(FUR…
UniProt
V6F4Q0
Ligands
MN
Pockets
2 · best druggability 0.42

Structure

x-ray diffraction · 1 distinct chain · 43% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BDNA-binding transcriptional dual regulator of siderophore biosynthesis and TRANSPORT(FUR family)protein13443% helix, 25% strandV6F4Q0

Ligands and binding sites

  • MN · Manganese (II) ion · metal · 4 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 3 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11190.420.7617empty
21020.400.7718empty

Interfaces

1 interface between chains.

  • A–B · 1500 Ų buried · 26 hydrogen bonds · protein-protein

Compared structures

  • 4RAZ · Crystal structure of Magnetospirillum gryphiswaldense MSR-1 holo-Fur · the same entry in another collection · chain A against A, TM-score 1.00

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