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MolNFT v1 · #171520 · protein

Inhibitory human GTP cyclohydrolase I - gfrp complex

6Z85 · GTP cyclohydrolase 1: “Inhibitory human GTP cyclohydrolase I - gfrp complex”. Electron microscopy, 2 ligands (HBI, ZN), 20 pockets (best druggability 0.88). MolNFT v1 #171520 on GenesisL1: 3D structure, binding sites and pockets in…

PDB
6Z85
Type
protein
Length
2,360 residues
Chains
20
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
GTP cyclohydrolase 1; GTP cyclohydrolase 1 feedback regulatory protein
EC
3.5.4.16
UniProt
P30793, P30047
Ligands
HBI, ZN
Pockets
20 · best druggability 0.88

Structure

electron microscopy · 2 distinct chains · 33% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, D, B, E, G, H, I, J, FGTP cyclohydrolase 1 (EC 3.5.4.16)protein15541% helix, 28% strandP30793
K, L, M, N, O, P, Q, R, S, TGTP cyclohydrolase 1 feedback regulatory proteinprotein8120% helix, 36% strandP30047

Ligands and binding sites

  • HBI · 7,8-dihydrobiopterin · ligand · 10 copies · chains A, E, C, B, D, G, F, H, I, J
  • ZN · Zinc ion · metal · 10 copies · chains A, C, D, B, E, G, H, I, J, F

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

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19700.880.90106HBI
27010.870.9191HBI
3920.780.9822empty
4990.780.9722empty
5920.770.9722empty

Interfaces

55 interfaces between chains.

  • D–H · 1506 Ų buried · 7 hydrogen bonds · protein-protein
  • C–I · 1502 Ų buried · 8 hydrogen bonds · protein-protein
  • E–G · 1494 Ų buried · 6 hydrogen bonds · protein-protein
  • A–F · 1492 Ų buried · 6 hydrogen bonds · protein-protein
  • B–J · 1487 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 6Z85 · inhibitory human GTP cyclohydrolase I - GFRP complex · the same entry in another collection · chain T against T, TM-score 1.00

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