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Crystal structure of the zebrafish cap-specific adenosine methyltransferase bound to SAH and m7G-capped RNA

Analyse Crystal structure of the zebrafish cap-specific adenosine methyltransferase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6IS0
Type
protein + RNA
Length
470 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.8
Source
Danio rerio; SYNTHETIC CONSTRUCT
Molecule
PDX1 C-terminal-inhibiting factor 1; m7G-capped RNA
UniProt
A0A0R4IKJ1
Ligands
SAH, M7G
Pockets
3 · best druggability 0.77

Structure

x-ray diffraction · resolution 1.8 · 2 distinct chains · 50% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APDX1 C-terminal-inhibiting factor 1protein46750% helix, 13% strandA0A0R4IKJ1
Cm7G-capped RNArna3——

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · chains A
  • M7G · 7N-methyl-8-hydroguanosine-5'-diphosphate · ligand · chains A
  • EDO · 1,2-ethanediol · additive · 4 copies · chains A
  • B3P · 2-[3-(2-hydroxy-1,1-dihydroxymethyl-ethylamino)-propylamino]-2-hydroxymethyl-propane-1,3-diol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111710.770.79114SAH, EDO
2790.310.7315M7G
3560.270.7312empty

Interfaces

1 interface between chains.

  • A–C · 244 Ų buried · 11 hydrogen bonds · protein-nucleic

Modifications

Observed in the structure: 2 modified (nucleotide modification).

Compared structures

  • 6IS0 · Crystal structure of the zebrafish cap-specific adenosine methyltransferase bound to sah… · the same entry in another collection · chain A against A, TM-score 1.00

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