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MolNFT v1 · #188512 · protein

Hyperlytic variant of TAE1, type VI secretion amidase effector 1, from pseudomonas aeruginosa (CYS110SER)

7TVH · Peptidoglycan amidase TSE1: “Hyperlytic variant of TAE1, type VI secretion amidase effector 1, from pseudomonas aeruginosa (CYS110SER)”. X-ray diffraction, 4 pockets (best druggability 0.67). MolNFT v1 #188512 on GenesisL1: 3D…

PDB
7TVH
Type
protein
Length
584 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Peptidoglycan amidase TSE1
EC
3.4.19.11
UniProt
Q9I2Q1
Pockets
4 · best druggability 0.67

Structure

x-ray diffraction · 3 distinct chains · 38% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APeptidoglycan amidase TSE1 (EC 3.4.19.11)protein14538% helix, 21% strandQ9I2Q1
B, DPeptidoglycan amidase TSE1 (EC 3.4.19.11)protein14638% helix, 21% strandQ9I2Q1
CPeptidoglycan amidase TSE1 (EC 3.4.19.11)protein14738% helix, 20% strandQ9I2Q1

Pockets

4 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17460.670.7588empty
2790.530.8527empty
3790.510.8429empty
4780.280.7217empty

Interfaces

5 interfaces between chains.

  • A–B · 694 Ų buried · 6 hydrogen bonds · protein-protein
  • C–D · 689 Ų buried · 6 hydrogen bonds · protein-protein
  • A–D · 381 Ų buried · 5 hydrogen bonds · protein-protein
  • B–C · 370 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 50 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 7TVH · Hyperlytic variant of Tae1, Type VI secretion amidase effector 1, from Pseudomonas… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q9I2Q1 · AlphaFold monomer V2.0 prediction for peptidoglycan amidase TSE1 (Q9I2Q1) · a predicted model of the same protein · chain B against A, TM-score 0.99

Analyse

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