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MolNFT v1 · #147285 · protein

Cryo-EM structure of C. elegans GDP-microtubule

6E88 · Tubulin alpha-2 chain: “Cryo-EM structure of C. elegans GDP-microtubule”. Electron microscopy, 2 ligands (GTP, GDP), 20 pockets (best druggability 0.87). MolNFT v1 #147285 on GenesisL1: 3D structure, binding sites and pockets in…

PDB
6E88
Type
protein
Length
5,160 residues
Chains
12
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tubulin alpha-2 chain; Tubulin beta-2 chain
UniProt
P34690, P52275
Ligands
GTP, GDP
Pockets
20 · best druggability 0.87

Structure

electron microscopy · 2 distinct chains · 43% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, H, L, I, MTubulin alpha-2 chainprotein43441% helix, 14% strandP34690
B, D, J, N, K, OTubulin beta-2 chainprotein42645% helix, 17% strandP52275

Ligands and binding sites

  • GTP · Guanosine-5'-triphosphate · ligand · 6 copies · chains A, B, C, D, H, J, L, N, I, K, M, O
  • GDP · Guanosine-5'-diphosphate · ligand · 6 copies · chains B, C, D, J, L, N, K, M, O

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
14980.870.9469GTP
25000.870.9364GTP
35190.870.9372GTP
47470.860.8999GDP
54980.860.9264GTP

Interfaces

17 interfaces between chains.

  • C–D · 2043 Ų buried · 23 hydrogen bonds · protein-protein
  • A–B · 2033 Ų buried · 24 hydrogen bonds · protein-protein
  • I–K · 2027 Ų buried · 25 hydrogen bonds · protein-protein
  • H–J · 2025 Ų buried · 21 hydrogen bonds · protein-protein
  • M–O · 2021 Ų buried · 22 hydrogen bonds · protein-protein

Compared structures

  • 6E88 · Cryo-EM structure of C. elegans GDP-microtubule · the same entry in another collection · chain O against O, TM-score 1.00

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