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Undecorated gtpgammas microtubule

Analyse Undecorated gtpgammas microtubule in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6DPW
Type
protein
Length
5,154 residues
Chains
12
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tubulin alpha-1B chain; Tubulin beta chain
UniProt
Q2XVP4, P02554
Ligands
GTP, GSP, MG
Pockets
20 · best druggability 0.86

Structure

electron microscopy · 2 distinct chains · 49% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, E, J, K, LTubulin alpha-1B chainprotein43047% helix, 17% strandQ2XVP4
B, D, F, G, H, ITubulin beta chainprotein42950% helix, 20% strandP02554

Ligands and binding sites

  • GTP · Guanosine-5'-triphosphate · ligand · 6 copies · chains A, H, C, I, E, G, F, J, B, K, D, L
  • GSP · 5'-guanosine-diphosphate-monothiophosphate · ligand · 6 copies · chains A, B, C, D, E, F, G, H, I
  • MG · Magnesium ion · metal · 6 copies · chains A, C, E, J, K, L

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

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13880.860.9456GSP
23950.850.9362GSP
32710.840.9644GTP, MG
42550.830.9542GTP, MG
52680.830.9545GTP, MG

Interfaces

17 interfaces between chains.

  • A–H · 1972 Ų buried · 21 hydrogen bonds · protein-protein
  • B–K · 1971 Ų buried · 21 hydrogen bonds · protein-protein
  • D–L · 1964 Ų buried · 21 hydrogen bonds · protein-protein
  • C–I · 1962 Ų buried · 21 hydrogen bonds · protein-protein
  • E–G · 1962 Ų buried · 21 hydrogen bonds · protein-protein

Compared structures

  • 6DPW · Undecorated GTPgammaS microtubule · the same entry in another collection · chain A against A, TM-score 1.00

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