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Crystal structure of zebrafish TRAP1 with amppnp and mitoq

Analyse Crystal structure of zebrafish TRAP1 with amppnp and mitoq in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7EXP
Type
protein
Length
1,173 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
TNF receptor-associated protein 1
UniProt
A8WFV1
Ligands
ANP, 05M, CO, MG
Pockets
20 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 41% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATNF receptor-associated protein 1protein57440% helix, 22% strandA8WFV1
BTNF receptor-associated protein 1protein59941% helix, 21% strandA8WFV1

Ligands and binding sites

  • ANP · Phosphoaminophosphonic acid-adenylate ester · ligand · 2 copies · chains A, B
  • 05M · 2,3-dimethoxy-5-methyl-6-[10-(triphenyl-$l^{5}-phosphanyl)decyl]cyclohexa-2,5-diene-1,4-dione · ligand · chains A, B
  • CO · Cobalt (II) ion · metal · 4 copies · chains A, B
  • MG · Magnesium ion · metal · 2 copies · chains A, B

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

Pockets

20 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12970.790.9045ANP, MG
23230.770.8944ANP, MG
3940.680.9328empty
44620.650.7840empty
52320.560.7831empty

Interfaces

1 interface between chains.

  • A–B · 5247 Ų buried · 65 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent (covalent ligand).

Compared structures

  • 7EXP · Crystal structure of zebrafish TRAP1 with AMPPNP and MitoQ · the same entry in another collection · chain A against A, TM-score 1.00

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