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MolNFT v1 · #116926 · protein

Crystal structure of human PRMT8 in complex with sah

5DST · Protein arginine N-methyltransferase 8: “Crystal structure of human PRMT8 in complex with sah”. X-ray diffraction, 1 ligand (SAH), 20 pockets (best druggability 0.72). MolNFT v1 #116926 on GenesisL1: 3D structure, binding sites and…

PDB
5DST
Type
protein
Length
4,744 residues
Chains
15
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein arginine N-methyltransferase 8
EC
2.1.1.-
UniProt
Q9NR22
Ligands
SAH
Pockets
20 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 26% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, D, E, G, J, K, L, M, N, OProtein arginine N-methyltransferase 8 (EC 2.1.1.-)protein31626% helix, 39% strandQ9NR22
C, F, H, IProtein arginine N-methyltransferase 8 (EC 2.1.1.-)protein31726% helix, 38% strandQ9NR22

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · 15 copies · chains A, B, C, D, E, F, G, H, I, J, K, L, M, N, O

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
12190.720.8832SAH
22230.710.8731SAH
32320.700.8633SAH
42790.700.8539SAH
52820.700.8539SAH

Interfaces

32 interfaces between chains.

  • A–B · 1739 Ų buried · 12 hydrogen bonds · protein-protein
  • E–F · 1734 Ų buried · 12 hydrogen bonds · protein-protein
  • G–H · 1726 Ų buried · 12 hydrogen bonds · protein-protein
  • K–L · 1723 Ų buried · 11 hydrogen bonds · protein-protein
  • C–D · 1719 Ų buried · 11 hydrogen bonds · protein-protein

Compared structures

  • 5DST · Crystal structure of human PRMT8 in complex with SAH · the same entry in another collection · chain J against J, TM-score 1.00

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