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MolNFT v1 · #124244 · protein

Crystal structure of GTP cyclohydrolase-ib with tris

5K9G · GTP cyclohydrolase FOLE2: “Crystal structure of GTP cyclohydrolase-ib with tris”. X-ray diffraction, 1 ligand (ZN), 7 pockets (best druggability 0.53). MolNFT v1 #124244 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
5K9G
Type
protein
Length
488 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
GTP cyclohydrolase FOLE2
EC
3.5.4.16
UniProt
Q5F9K6
Ligands
ZN
Pockets
7 · best druggability 0.53

Structure

x-ray diffraction · 2 distinct chains · 27% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGTP cyclohydrolase FOLE2 (EC 3.5.4.16)protein24527% helix, 45% strandQ5F9K6
BGTP cyclohydrolase FOLE2 (EC 3.5.4.16)protein24327% helix, 45% strandQ5F9K6

Ligands and binding sites

  • ZN · Zinc ion · metal · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 8 copies · chains A, B
  • TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · chains A, B
  • FMT · Formic acid · additive · chains B

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

Pockets

7 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1500.530.8817empty
2550.530.8817empty
31150.490.8026ZN, TRS, FMT
41220.490.7925ZN
5530.370.8013EDO

Interfaces

1 interface between chains.

  • A–B · 1660 Ų buried · 37 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (nonstandard).

Compared structures

  • 5K9G · Crystal Structure of GTP Cyclohydrolase-IB with Tris · the same entry in another collection · chain A against A, TM-score 1.00
  • Q5F9K6 · AlphaFold monomer V2.0 prediction for GTP cyclohydrolase FOLE2 (Q5F9K6) · a predicted model of the same protein · chain B against A, TM-score 0.99

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