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MolNFT v1 · #15862 · protein

Crystallographic analyses of NADH peroxidase CYS42ALA and CYS42SER mutants: active site structure, mechanistic implications, and an unusual environment of ARG303

1NHP: “Crystallographic analyses of NADH peroxidase CYS42ALA and CYS42SER mutants: active site structure…”. X-ray diffraction, 2 ligands (FAD, SO4), 3 pockets (best druggability 0.78). MolNFT v1 #15862 on GenesisL1: 3D structure, binding…

PDB
1NHP
Type
protein
Length
447 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NADH peroxidase
EC
1.11.1.1
UniProt
P37062
Ligands
FAD, SO4
Pockets
3 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 27% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANADH peroxidase (EC 1.11.1.1)protein44727% helix, 30% strandP37062

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · chains A
  • SO4 · Sulfate ion · ion · 2 copies · 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
110510.780.8095SO4, FAD
2730.470.8219empty
3510.270.7413empty

Compared structures

  • 1NHP · Crystallographic analyses of NADH peroxidase CYS42ALA and CYS42SER mutants: active site… · the same entry in another collection · chain A against A, TM-score 1.00
  • P37062 · AlphaFold monomer V2.0 prediction for NADH peroxidase (P37062) · a predicted model of the same protein · chain A against A, TM-score 1.00

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