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Crystal structure of hexameric cbs-CP12 protein from bloom-forming cyanobacteria, yb-derivative at 2.8 a resolution

Analyse Crystal structure of hexameric cbs-CP12 protein from bloom-forming… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5NPL
Type
protein
Length
537 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Similar to TR|Q8YYT1|Q8YYT1
UniProt
A8YJ50
Ligands
DO3, YB
Pockets
10 · best druggability 0.79

Structure

x-ray diffraction · 3 distinct chains · 46% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASimilar to TR|Q8YYT1|Q8YYT1protein18146% helix, 17% strandA8YJ50
BSimilar to TR|Q8YYT1|Q8YYT1protein17746% helix, 17% strandA8YJ50
CSimilar to TR|Q8YYT1|Q8YYT1protein17945% helix, 17% strandA8YJ50

Ligands and binding sites

  • DO3 · 10-((2R)-2-hydroxypropyl)-1,4,7,10-tetraazacyclododecane 1,4,7-triacetic acid · ligand · 2 copies · chains A, B
  • YB · Ytterbium (III) ion · metal · 17 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13910.790.8841empty
22660.580.7825empty
3630.540.8823empty
41880.530.7830empty
51950.500.7623empty

Interfaces

2 interfaces between chains.

  • B–C · 1877 Ų buried · 24 hydrogen bonds · protein-protein
  • A–B · 1566 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 disulfide (disulfide).

Compared structures

  • 5NPL · Crystal structure of hexameric CBS-CP12 protein from bloom-forming cyanobacteria… · the same entry in another collection · chain A against A, TM-score 1.00

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