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Wild-type ampt from thermus thermophilus

Analyse Wild-type ampt from thermus thermophilus in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2AYI
Type
protein
Length
1,985 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aminopeptidase T
EC
3.4.11.-
UniProt
P42778
Ligands
ZN
Pockets
20 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 36% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, EAminopeptidase T (EC 3.4.11.-)protein39736% helix, 24% strandP42778

Ligands and binding sites

  • ZN · Zinc ion · metal · 10 copies · chains A, B, C, D, E

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

Pockets

20 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19630.830.8488empty
211500.790.8082ZN
36260.720.7943empty
46140.720.7940empty
511720.720.7587ZN

Interfaces

4 interfaces between chains.

  • D–E · 1644 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 1635 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 561 Ų buried · 11 hydrogen bonds · protein-protein
  • A–E · 526 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 2AYI · Wild-type AmpT from Thermus thermophilus · the same entry in another collection · chain B against B, TM-score 1.00
  • P42778 · AlphaFold monomer V2.0 prediction for aminopeptidase T (P42778) · a predicted model of the same protein · chain C against A, TM-score 0.99

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