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MolNFT v1 · #188873 · protein

Structure of human SAMHD1 with non-hydrolysable dgtp analog

7UJN · Deoxynucleoside triphosphate triphosphohydrolase SAMHD1: “Structure of human SAMHD1 with non-hydrolysable dgtp analog”. Electron microscopy, 1 ligand (T8T), 20 pockets (best druggability 0.89). MolNFT v1 #188873 on GenesisL1: 3D…

PDB
7UJN
Type
protein
Length
1,948 residues
Chains
4
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Deoxynucleoside triphosphate triphosphohydrolase SAMHD1
EC
3.1.5.-
UniProt
Q9Y3Z3
Ligands
T8T
Pockets
20 · best druggability 0.89

Structure

electron microscopy · 1 distinct chain · 49% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DDeoxynucleoside triphosphate triphosphohydrolase SAMHD1 (EC 3.1.5.-)protein48749% helix, 11% strandQ9Y3Z3

Ligands and binding sites

  • T8T · 2'-deoxyguanosine-5'-O-(1-thiotriphosphate) · ligand · 12 copies · chains A, B, D, C

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

Pockets

20 pockets found on a 1 Å grid, 16 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19750.890.91142T8T
28010.880.91114T8T
32020.840.9827empty
42000.840.9729empty
510950.760.7976T8T

Interfaces

6 interfaces between chains.

  • A–D · 2167 Ų buried · 22 hydrogen bonds · protein-protein
  • B–C · 2158 Ų buried · 22 hydrogen bonds · protein-protein
  • A–B · 2030 Ų buried · 23 hydrogen bonds · protein-protein
  • C–D · 2029 Ų buried · 22 hydrogen bonds · protein-protein
  • B–D · 464 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 covalent (covalent ligand).

Compared structures

  • 7UJN · Structure of Human SAMHD1 with Non-Hydrolysable dGTP Analog · the same entry in another collection · chain A against A, TM-score 1.00

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