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Crystal structure of the titin M10-obscurin ig domain 1 complex

Analyse Crystal structure of the titin M10-obscurin ig domain 1 complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4UOW
Type
protein
Length
3,420 residues
Chains
36
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Titin; Obscurin
EC
2.7.11.1
UniProt
Q8WZ42, Q5VST9
Ligands
NA, CL
Pockets
20 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 3% helix, 63% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
0, 2, 4, 6, 8, A, C, E, G, I, K, M, O, Q, S, U, W, YTitin (EC 2.7.11.1)protein973% helix, 61% strandQ8WZ42
1, 3, 5, 7, 9, B, D, F, H, J, L, N, P, R, T, V, X, ZObscurin (EC 2.7.11.1)protein933% helix, 66% strandQ5VST9

Ligands and binding sites

  • NA · Sodium ion · metal · chains P
  • CL · Chloride ion · ion · 8 copies · chains 0, 1, A, B, E, F, M, N, Q, R, S, T, W, X, Y, Z

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
18900.740.78105empty
27790.730.7985empty
37980.730.7957empty
48130.730.7868empty
57510.730.7983empty

Interfaces

74 interfaces between chains.

  • 8–9 · 710 Ų buried · 15 hydrogen bonds · protein-protein
  • K–L · 709 Ų buried · 13 hydrogen bonds · protein-protein
  • A–B · 708 Ų buried · 16 hydrogen bonds · protein-protein
  • I–J · 707 Ų buried · 13 hydrogen bonds · protein-protein
  • 2–3 · 705 Ų buried · 15 hydrogen bonds · protein-protein

Compared structures

  • 4UOW · Crystal structure of the titin M10-Obscurin Ig domain 1 complex · the same entry in another collection · chain 0 against 0, TM-score 1.00

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