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Crystal structure of monomeric reversibly photoswitchable red fluorescent protein rstagrfp in the on state

Analyse Crystal structure of monomeric reversibly photoswitchable red fluorescent… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3U8C
Type
protein
Length
892 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fluorescent protein rstagrfp
Ligands
NRQ
Pockets
14 · best druggability 0.86

Structure

x-ray diffraction · 1 distinct chain · 4% helix, 57% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DFluorescent protein rstagrfpprotein2234% helix, 57% strand—

Ligands and binding sites

  • NRQ · {(4Z)-4-(4-hydroxybenzylidene)-2-[3-(methylthio) propanimidoyl]-5-oxo-4,5-dihydro-1H-imidazol-1-yl}acetic acid · ligand · 4 copies · chains A, B, C, D
  • GOL · Glycerol · additive · chains A, C, D

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

Pockets

14 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15190.860.9252empty
21140.770.9732NRQ
31210.770.9635NRQ
41030.760.9632NRQ
51050.750.9633NRQ

Interfaces

6 interfaces between chains.

  • A–D · 1531 Ų buried · 30 hydrogen bonds · protein-protein
  • B–C · 1511 Ų buried · 28 hydrogen bonds · protein-protein
  • C–D · 911 Ų buried · 13 hydrogen bonds · protein-protein
  • A–B · 900 Ų buried · 15 hydrogen bonds · protein-protein
  • A–C · 110 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 cofactor (chromophore).

Compared structures

  • 3U8C · Crystal structure of monomeric reversibly photoswitchable red fluorescent protein… · the same entry in another collection · chain A against A, TM-score 1.00

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