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Cryo-EM structure of human P97 bound to cb-5083 and ADP.

Analyse Cryo-EM structure of human P97 bound to cb-5083 and ADP. in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7RLI
Type
protein
Length
8,820 residues
Chains
12
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transitional endoplasmic reticulum ATPase
EC
3.6.4.6
UniProt
P55072
Ligands
JDP, ADP
Pockets
20 · best druggability 0.84

Structure

electron microscopy · 1 distinct chain · 38% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, J, K, LTransitional endoplasmic reticulum ATPase (EC 3.6.4.6)protein73538% helix, 12% strandP55072

Ligands and binding sites

  • JDP · 1-[4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl]-2-methyl-1H-indole-4-carboxamide · ligand · 12 copies · chains A, B, C, D, E, F, G, H, I, J, K, L
  • ADP · Adenosine-5'-diphosphate · ligand · 12 copies · chains A, F, B, C, D, E, G, L, H, I, J, K

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
111050.840.85136ADP
29510.840.85109empty
311430.840.85130ADP
411420.840.85142ADP
58640.830.85101empty

Interfaces

31 interfaces between chains.

  • J–K · 3790 Ų buried · 40 hydrogen bonds · protein-protein
  • E–F · 3766 Ų buried · 42 hydrogen bonds · protein-protein
  • B–C · 3736 Ų buried · 39 hydrogen bonds · protein-protein
  • K–L · 3718 Ų buried · 37 hydrogen bonds · protein-protein
  • A–F · 3717 Ų buried · 38 hydrogen bonds · protein-protein

Compared structures

  • 7RLI · Cryo-EM structure of human p97 bound to CB-5083 and ADP. · the same entry in another collection · chain A against A, TM-score 1.00

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