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MolNFT v1 · #21366 · protein

Ribosomal L7/L12 alpha-N-protein acetyltransferase in complex with coenzyme a (CoA free sulfhydryl)

1S7N · Acetyl transferase: “Ribosomal L7/L12 alpha-N-protein acetyltransferase in complex with coenzyme a (CoA free sulfhydryl)”. X-ray diffraction, 1 ligand (COA), 5 pockets (best druggability 0.78). MolNFT v1 #21366 on GenesisL1: 3D…

PDB
1S7N
Type
protein
Length
709 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Acetyl transferase
EC
2.3.1.-
UniProt
Q8ZPC0
Ligands
COA
Pockets
5 · best druggability 0.78

Structure

x-ray diffraction · 4 distinct chains · 38% helix, 37% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAcetyl transferase (EC 2.3.1.-)protein17738% helix, 37% strandQ8ZPC0
BAcetyl transferase (EC 2.3.1.-)protein17937% helix, 36% strandQ8ZPC0
CAcetyl transferase (EC 2.3.1.-)protein17639% helix, 37% strandQ8ZPC0
DAcetyl transferase (EC 2.3.1.-)protein17740% helix, 37% strandQ8ZPC0

Ligands and binding sites

  • COA · Coenzyme A · ligand · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18510.780.8176COA
28020.780.8162COA
38150.770.8068COA
47460.760.8061COA
51380.480.7825empty

Interfaces

3 interfaces between chains.

  • A–B · 959 Ų buried · 17 hydrogen bonds · protein-protein
  • C–D · 954 Ų buried · 13 hydrogen bonds · protein-protein
  • A–C · 313 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 1S7N · Ribosomal L7/L12 alpha-N-protein acetyltransferase in complex with Coenzyme A (CoA free… · the same entry in another collection · chain A against A, TM-score 1.00

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