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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
469 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
PDX1 C-terminal-inhibiting factor 1; M7G-capped RNA
UniProt
A0A0R4IKJ1
Ligands
M7G, SAH
Pockets
3 · best druggability 0.78

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
APDX1 C-terminal-inhibiting factor 1protein46750% helix, 13% strandA0A0R4IKJ1
CM7G-capped RNArna2——

Ligands and binding sites

  • M7G · 7N-methyl-8-hydroguanosine-5'-diphosphate · ligand · 2 copies · chains A, C
  • SAH · S-adenosyl-L-homocysteine · 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
19950.780.79100SAH, EDO
2830.310.7316M7G
3520.250.7312empty

Interfaces

1 interface between chains.

  • A–C · 157 Ų buried · 9 hydrogen bonds · protein-nucleic

Modifications

Observed in the structure: 1 covalent, 1 modified (covalent ligand, nucleotide modification).

Compared structures

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

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