GL1X · GenesisL1 explorer

MolNFT v1 · #118598 · protein

Sandercyanin fluorescent protein purified from sander vitreus

5F6Z: “Sandercyanin fluorescent protein purified from sander vitreus”. X-ray diffraction, 2 ligands (BLA, NAG), 9 pockets (best druggability 0.79). MolNFT v1 #118598 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
5F6Z
Type
protein
Length
664 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Sandercyanin fluorescent protein
Ligands
BLA, NAG
Pockets
9 · best druggability 0.79

Structure

x-ray diffraction · 1 distinct chain · 14% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DSandercyanin fluorescent proteinprotein16614% helix, 45% strand—

Ligands and binding sites

  • BLA · Biliverdine IX alpha · ligand · 4 copies · chains A, D, B, C
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13430.790.8943BLA
23350.780.8843BLA
33250.780.8943BLA
43710.780.8742BLA
59530.720.7695empty

Interfaces

6 interfaces between chains.

  • B–C · 678 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 673 Ų buried · 2 hydrogen bonds · protein-protein
  • A–D · 671 Ų buried · 4 hydrogen bonds · protein-protein
  • B–D · 665 Ų buried · 4 hydrogen bonds · protein-protein
  • C–D · 250 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide, 4 glycan (disulfide, N-glycosylation).

Compared structures

  • 5F6Z · Sandercyanin Fluorescent Protein purified from Sander vitreus · the same entry in another collection · chain B against B, TM-score 1.00

Analyse

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