GL1X · GenesisL1 explorer

Research workbench

Crystal structure of bifidobacterium longum multiple inositol polyphosphate phosphatase apo form

Analyse Crystal structure of bifidobacterium longum multiple inositol polyphosphate… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6RXD
Type
protein
Length
1,018 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Histidine acid phosphatase
UniProt
B7GTV0
Ligands
ZN
Pockets
8 · best druggability 0.75

Structure

x-ray diffraction · 1 distinct chain · 46% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BHistidine acid phosphataseprotein50946% helix, 13% strandB7GTV0

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 copies · chains A, B

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

Pockets

8 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19260.750.7887empty
29690.740.7791empty
34790.620.7647empty
44030.590.7649empty
51040.360.7423empty

Interfaces

1 interface between chains.

  • A–B · 941 Ų buried · 17 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 6RXD · Crystal Structure of Bifidobacterium longum Multiple Inositol Polyphosphate Phosphatase… · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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