GL1X · GenesisL1 explorer

MolNFT v1 · #111355 · protein

Doss gafa domain reduced nitric oxide bound crystal structure

4YOF · Redox sensor histidine kinase response regulator devs: “Doss gafa domain reduced nitric oxide bound crystal structure”. X-ray diffraction, 2 ligands (HEM, NO), 3 pockets (best druggability 0.80). MolNFT v1 #111355 on GenesisL1: 3D…

PDB
4YOF
Type
protein
Length
281 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Redox sensor histidine kinase response regulator devs
EC
2.7.13.3
UniProt
P9WGK2
Ligands
HEM, NO
Pockets
3 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARedox sensor histidine kinase response regulator devs (EC 2.7.13.3)protein14039% helix, 24% strandP9WGK2
BRedox sensor histidine kinase response regulator devs (EC 2.7.13.3)protein14137% helix, 26% strandP9WGK2

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
  • NO · Nitric oxide · ion · 2 copies · chains A, B

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

Pockets

3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13130.800.9032HEM, NO
23230.780.8833HEM, NO
31060.410.7620empty

Interfaces

1 interface between chains.

  • A–B · 672 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 4YOF · DosS GAFA Domain Reduced Nitric Oxide Bound Crystal Structure · the same entry in another collection · chain A against A, TM-score 1.00
  • P9WGK2 · AlphaFold monomer V2.0 prediction for oxygen sensor histidine kinase response regulator… · a predicted model of the same protein · chain B 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.