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Scytonema hofmannii tnsc bound to amppnp and DNA

Analyse Scytonema hofmannii tnsc bound to amppnp and DNA in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7PLH
Type
protein + DNA
Length
1,864 residues
Chains
9
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Shtnsc; DNA (5'- D(P*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*T)…
Ligands
ANP, MG
Pockets
20 · best druggability 0.81

Structure

electron microscopy · 2 distinct chains · 54% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, GShtnscprotein26054% helix, 8% strand—
H, IDNA (5'- D(P*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*TP*AP*T) -3')dna22——

Ligands and binding sites

  • ANP · Phosphoaminophosphonic acid-adenylate ester · ligand · 7 copies · chains A, B, C, D, E, F, G
  • MG · Magnesium ion · metal · 7 copies · chains A, B, C, D, E, F, G

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
14460.810.8955empty
24920.790.8750ANP, MG
35340.780.8558ANP, MG
44680.780.8650ANP, MG
53290.780.8956empty

Interfaces

24 interfaces between chains.

  • C–D · 1191 Ų buried · 16 hydrogen bonds · protein-protein
  • F–G · 1169 Ų buried · 13 hydrogen bonds · protein-protein
  • E–F · 1164 Ų buried · 18 hydrogen bonds · protein-protein
  • A–B · 1128 Ų buried · 12 hydrogen bonds · protein-protein
  • B–C · 1117 Ų buried · 13 hydrogen bonds · protein-protein

Compared structures

  • 7PLH · Scytonema hofmannii TnsC bound to AMPPNP and DNA · the same entry in another collection · chain A against A, TM-score 1.00

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