GL1X · GenesisL1 explorer

Research workbench

Crystal structure of the STH1 bromodomain from S.CEREVISIAE

Analyse Crystal structure of the STH1 bromodomain from S.CEREVISIAE in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6MR4
Type
protein
Length
648 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Nuclear protein STH1/NPS1
EC
3.6.4.12
UniProt
P32597
Pockets
9 · best druggability 0.82

Structure

x-ray diffraction · 3 distinct chains · 61% helix, 2% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CNuclear protein STH1/NPS1 (EC 3.6.4.12)protein10961% helix, 2% strandP32597
BNuclear protein STH1/NPS1 (EC 3.6.4.12)protein10661% helix, 2% strandP32597
D, E, FNuclear protein STH1/NPS1 (EC 3.6.4.12)protein10861% helix, 2% strandP32597

Pockets

9 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14700.820.8866empty
27660.690.7654empty
36970.640.7364empty
4840.510.8315empty
5810.510.8316empty

Interfaces

8 interfaces between chains.

  • A–F · 1022 Ų buried · 14 hydrogen bonds · protein-protein
  • B–F · 330 Ų buried · 5 hydrogen bonds · protein-protein
  • C–F · 283 Ų buried · 6 hydrogen bonds · protein-protein
  • D–F · 216 Ų buried · 2 hydrogen bonds · protein-protein
  • E–F · 209 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 6MR4 · Crystal structure of the Sth1 bromodomain from S.cerevisiae · the same entry in another collection · chain F against F, TM-score 1.00
  • P32597 · AlphaFold monomer V2.0 prediction for nuclear protein STH1/NPS1 (P32597) · a predicted model of the same protein · chain D against A, TM-score 0.98

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.