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MolNFT v1 · #71375 · protein

Crystal structure of the molybdopterin biosynthesis enzyme moab (TTHA0341) from thermus theromophilus HB8

3MCH · Molybdopterin biosynthesis enzyme, moab: “Crystal structure of the molybdopterin biosynthesis enzyme moab (TTHA0341) from thermus theromophilus HB8”. X-ray diffraction, 6 pockets (best druggability 0.71). MolNFT v1 #71375 on…

PDB
3MCH
Type
protein
Length
481 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Molybdopterin biosynthesis enzyme, moab
UniProt
Q5SLF2
Pockets
6 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CMolybdopterin biosynthesis enzyme, moabprotein15943% helix, 21% strandQ5SLF2
BMolybdopterin biosynthesis enzyme, moabprotein16342% helix, 21% strandQ5SLF2

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 2 copies · chains A, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14760.710.8243empty
22660.520.7540empty
32690.520.7538empty
42470.510.7635empty
51550.500.7823empty

Interfaces

3 interfaces between chains.

  • A–C · 822 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 800 Ų buried · 5 hydrogen bonds · protein-protein
  • B–C · 686 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 3MCH · Crystal structure of the molybdopterin biosynthesis enzyme MoaB (TTHA0341) from thermus… · the same entry in another collection · chain A against A, TM-score 1.00

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