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MolNFT v1 · #149904 · protein

Structure of cuta from synechococcus elongatus PCC7942 complexed with bis-tris molecule

6GDV · Periplasmic divalent cation tolerance protein: “Structure of cuta from synechococcus elongatus PCC7942 complexed with bis-tris molecule”. X-ray diffraction, 4 pockets (best druggability 0.86). MolNFT v1 #149904 on GenesisL1: 3D…

PDB
6GDV
Type
protein
Length
323 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Periplasmic divalent cation tolerance protein
UniProt
Q31KX8
Pockets
4 · best druggability 0.86

Structure

x-ray diffraction · 3 distinct chains · 33% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APeriplasmic divalent cation tolerance proteinprotein10834% helix, 42% strandQ31KX8
BPeriplasmic divalent cation tolerance proteinprotein10533% helix, 42% strandQ31KX8
CPeriplasmic divalent cation tolerance proteinprotein11033% helix, 41% strandQ31KX8

Ligands and binding sites

  • BTB · 2-[bis-(2-hydroxy-ethyl)-amino]-2-hydroxymethyl-propane-1,3-diol · additive · chains A, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13540.860.9537empty
21300.650.8720empty
31500.570.8221empty
41110.570.8418BTB

Interfaces

3 interfaces between chains.

  • B–C · 1165 Ų buried · 13 hydrogen bonds · protein-protein
  • A–B · 1163 Ų buried · 12 hydrogen bonds · protein-protein
  • A–C · 1106 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 6GDV · Structure of CutA from Synechococcus elongatus PCC7942 complexed with Bis-Tris molecule · the same entry in another collection · chain A against A, TM-score 1.00

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