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Structure of human MTHFD2 in complex with TH7299

Analyse Structure of human MTHFD2 in complex with TH7299 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6S4E
Type
protein
Length
292 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bifunctional methylenetetrahydrofolate DEHYDROGENASE/CYCLOHYDROLASE, mitochondrial
EC
1.5.1.15, 3.5.4.9
UniProt
P13995
Ligands
9L9, NAD, PO4
Pockets
4 · best druggability 0.68

Structure

x-ray diffraction · 1 distinct chain · 40% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABifunctional methylenetetrahydrofolate DEHYDROGENASE/CYCLOHYDROLASE, mitochondrial (EC 1.5.1.15, 3.5.4.9)protein29240% helix, 16% strandP13995

Ligands and binding sites

  • 9L9 · (2S)-2-[[4-[[2,4-bis(azanyl)-6-oxidanylidene-1H-pyrimidin-5-yl]carbamoylamino]phenyl]carbonylamino]pentanedioic acid · ligand · chains A
  • NAD · Nicotinamide-adenine-dinucleotide · ligand · chains A
  • PO4 · Phosphate ion · ion · 4 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14960.680.79479L9, NAD
2900.360.7416PO4
3580.300.7519empty
4510.290.7614PO4

Compared structures

  • 6S4E · Structure of human MTHFD2 in complex with TH7299 · the same entry in another collection · chain A against A, TM-score 1.00
  • P13995 · AlphaFold monomer V2.0 prediction for bifunctional methylenetetrahydrofolate… · a predicted model of the same protein · chain A against A, TM-score 0.99

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