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Activation of ribokinase by monovalent cations

Analyse Activation of ribokinase by monovalent cations in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1GQT
Type
protein
Length
1,223 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ribokinase
EC
2.7.1.15
UniProt
P05054
Ligands
RIB, ACP, CS
Pockets
11 · best druggability 0.75

Structure

x-ray diffraction · 3 distinct chains · 39% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DRibokinase (EC 2.7.1.15)protein30539% helix, 25% strandP05054
BRibokinase (EC 2.7.1.15)protein30739% helix, 24% strandP05054
CRibokinase (EC 2.7.1.15)protein30639% helix, 25% strandP05054

Ligands and binding sites

  • RIB · alpha-D-ribofuranose · ligand · 4 copies · chains A, B, C, D
  • ACP · Phosphomethylphosphonic acid adenylate ester · ligand · 3 copies · chains A, B, C, D
  • CS · Cesium ion · metal · 4 copies · chains A, B, C, D

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

Pockets

11 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19400.750.7853empty
25170.740.8253ACP, RIB
35820.730.8156ACP, RIB
45250.720.8153ACP, RIB
55060.690.8049RIB

Interfaces

3 interfaces between chains.

  • C–D · 1129 Ų buried · 11 hydrogen bonds · protein-protein
  • A–B · 1118 Ų buried · 10 hydrogen bonds · protein-protein
  • B–D · 461 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 1GQT · Activation of Ribokinase by Monovalent Cations · the same entry in another collection · chain A against A, TM-score 1.00

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