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MolNFT v1 · #185850 · protein

In situ structure of nebulin bound to actin filament in skeletal sarcomere

7QIM · Acts protein: “In situ structure of nebulin bound to actin filament in skeletal sarcomere”. Electron microscopy, 2 ligands (ADP, MG), 19 pockets (best druggability 0.85). MolNFT v1 #185850 on GenesisL1: 3D structure, binding sites…

PDB
7QIM
Type
protein
Length
2,030 residues
Chains
7
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Acts protein; Nebulin (mouse)
UniProt
A0A7K7PM04
Ligands
ADP, MG
Pockets
19 · best druggability 0.85

Structure

electron microscopy · 3 distinct chains · 53% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
C, B, A, D, EActs proteinprotein37143% helix, 18% strandA0A7K7PM04
FNebulin (mouse)protein10573% helix, 0% strand—
GNebulin (mouse)protein7073% helix, 0% strand—

Ligands and binding sites

  • ADP · Adenosine-5'-diphosphate · ligand · 5 copies · chains C, B, A, D, E
  • MG · Magnesium ion · metal · 5 copies · chains C, B, A, D, E

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

Pockets

19 pockets found on a 1 Å grid, 18 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15590.850.9082ADP, MG
25010.850.9178ADP, MG
35770.840.8976empty
43600.820.9165ADP, MG
55960.820.8784empty

Interfaces

17 interfaces between chains.

  • C–A · 1209 Ų buried · 7 hydrogen bonds · protein-protein
  • B–D · 1207 Ų buried · 7 hydrogen bonds · protein-protein
  • C–E · 1201 Ų buried · 8 hydrogen bonds · protein-protein
  • E–F · 685 Ų buried · 3 hydrogen bonds · protein-protein
  • C–F · 667 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 modified (methylation).

Compared structures

  • 7QIM · In situ structure of nebulin bound to actin filament in skeletal sarcomere · the same entry in another collection · chain C against C, TM-score 1.00

Analyse

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