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MolNFT v1 · #186661 · protein

Cryo-EM structure of human P97-E470D mutant bound to atpgs.

7RLF · Transitional endoplasmic reticulum ATPase: “Cryo-EM structure of human P97-E470D mutant bound to atpgs.”. Electron microscopy, 2 ligands (AGS, MG), 20 pockets (best druggability 0.79). MolNFT v1 #186661 on GenesisL1: 3D structure…

PDB
7RLF
Type
protein
Length
4,368 residues
Chains
6
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transitional endoplasmic reticulum ATPase
EC
3.6.4.6
UniProt
P55072
Ligands
AGS, MG
Pockets
20 · best druggability 0.79

Structure

electron microscopy · 1 distinct chain · 40% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FTransitional endoplasmic reticulum ATPase (EC 3.6.4.6)protein72840% helix, 16% strandP55072

Ligands and binding sites

  • AGS · Phosphothiophosphoric acid-adenylate ester · ligand · 12 copies · chains A, F, B, C, D, E
  • MG · Magnesium ion · metal · 12 copies · chains A, B, C, D, E, F

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
16150.790.8480AGS, MG
26270.790.8480AGS, MG
34790.780.8678AGS, MG
46190.780.8480AGS, MG
53990.780.8764AGS, MG

Interfaces

12 interfaces between chains.

  • B–C · 3741 Ų buried · 37 hydrogen bonds · protein-protein
  • C–D · 3734 Ų buried · 39 hydrogen bonds · protein-protein
  • A–B · 3711 Ų buried · 34 hydrogen bonds · protein-protein
  • A–F · 3706 Ų buried · 36 hydrogen bonds · protein-protein
  • E–F · 3704 Ų buried · 34 hydrogen bonds · protein-protein

Compared structures

  • 7RLF · Cryo-EM structure of human p97-E470D mutant bound to ATPgS. · the same entry in another collection · chain A against A, TM-score 1.00

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