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MolNFT v1 · #136080 · protein

Crystal structure of dhdps from chlamydomonas reinhardtii

5UI3 · Dihydrodipicolinate synthase: “Crystal structure of dhdps from chlamydomonas reinhardtii”. X-ray diffraction, 1 ligand (AKG), 10 pockets (best druggability 0.76). MolNFT v1 #136080 on GenesisL1: 3D structure, binding sites and…

PDB
5UI3
Type
protein
Length
1,221 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dihydrodipicolinate synthase
UniProt
A8I3W3
Ligands
AKG
Pockets
10 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 47% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
D, A, BDihydrodipicolinate synthaseprotein30547% helix, 14% strandA8I3W3
CDihydrodipicolinate synthaseprotein30647% helix, 14% strandA8I3W3

Ligands and binding sites

  • AKG · 2-oxoglutaric acid · ligand · 4 copies · chains D, 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14230.760.8553empty
23640.760.8647empty
31190.480.8019empty
4970.460.8019AKG
51110.460.7923AKG

Interfaces

5 interfaces between chains.

  • B–C · 1708 Ų buried · 27 hydrogen bonds · protein-protein
  • D–A · 1622 Ų buried · 23 hydrogen bonds · protein-protein
  • A–B · 675 Ų buried · 7 hydrogen bonds · protein-protein
  • D–C · 669 Ų buried · 8 hydrogen bonds · protein-protein
  • A–C · 42 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 covalent (covalent ligand).

Compared structures

  • 5UI3 · Crystal structure of DHDPS from chlamydomonas reinhardtii · the same entry in another collection · chain D against D, TM-score 1.00

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