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MolNFT v1 · #51845 · protein

The structure of phycoerythrin from gloeobacter violaceus

2VJH · Phycoerythrin alpha chain: “The structure of phycoerythrin from gloeobacter violaceus”. X-ray diffraction, 2 ligands (PEB, PUB), 13 pockets (best druggability 0.70). MolNFT v1 #51845 on GenesisL1: 3D structure, binding sites and…

PDB
2VJH
Type
protein
Length
682 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Phycoerythrin alpha chain; Phycoerythrin beta subunit
UniProt
Q7NLD7, Q7NLD6
Ligands
PEB, PUB
Pockets
13 · best druggability 0.70

Structure

x-ray diffraction · 2 distinct chains · 76% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CPhycoerythrin alpha chainprotein16477% helix, 0% strandQ7NLD7
B, DPhycoerythrin beta subunitprotein17774% helix, 0% strandQ7NLD6

Ligands and binding sites

  • PEB · Phycoerythrobilin · ligand · 8 copies · chains A, B, C, D
  • PUB · Phycourobilin · ligand · 2 copies · chains B, D

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

Pockets

13 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14160.700.8257PEB
23130.680.8340empty
31270.680.8928PEB
41130.670.9028PEB
51300.560.8229PEB

Interfaces

5 interfaces between chains.

  • C–D · 1581 Ų buried · 19 hydrogen bonds · protein-protein
  • A–B · 1578 Ų buried · 19 hydrogen bonds · protein-protein
  • A–C · 928 Ų buried · 15 hydrogen bonds · protein-protein
  • A–D · 393 Ų buried · 7 hydrogen bonds · protein-protein
  • B–C · 388 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 cofactor, 4 covalent, 2 modified (phycoerythrobilin attachment, covalent ligand, nonstandard).

Compared structures

  • 2VJH · The structure of Phycoerythrin from Gloeobacter violaceus · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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