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Human P97 double hexamer conformer II with atpgammas bound

Analyse Human P97 double hexamer conformer II with atpgammas bound in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7VCS
Type
protein
Length
9,192 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
AGS, MG
Pockets
20 · best druggability 0.84

Structure

electron microscopy · 1 distinct chain · 40% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, J, K, LTransitional endoplasmic reticulum ATPase (EC 3.6.4.6)protein76640% helix, 15% strandP55072

Ligands and binding sites

  • AGS · Phosphothiophosphoric acid-adenylate ester · ligand · 24 copies · chains A, F, B, C, D, E, G, L, H, I, J, K
  • MG · Magnesium ion · metal · 12 copies · chains A, B, C, D, E, F, G, H, I, J, K, L

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
110270.840.85138AGS, MG
210340.840.85124AGS, MG
39170.830.85124AGS, MG
48730.820.84110empty
58030.810.8493AGS

Interfaces

24 interfaces between chains.

  • H–I · 4220 Ų buried · 31 hydrogen bonds · protein-protein
  • B–C · 4186 Ų buried · 26 hydrogen bonds · protein-protein
  • C–D · 4021 Ų buried · 34 hydrogen bonds · protein-protein
  • G–L · 3968 Ų buried · 22 hydrogen bonds · protein-protein
  • A–B · 3928 Ų buried · 20 hydrogen bonds · protein-protein

Compared structures

  • 7VCS · Human p97 double hexamer conformer II with ATPgammaS bound · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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