GL1X · GenesisL1 explorer

MolNFT v1 · #77429 · protein

Methylmalonyl-CoA mutase, substrate-free state (poor quality structure)

3REQ: “Methylmalonyl-CoA mutase, substrate-free state (poor quality structure)”. X-ray diffraction, 2 ligands (B12, ADN), 15 pockets (best druggability 0.86). MolNFT v1 #77429 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
3REQ
Type
protein
Length
1,345 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Methylmalonyl-CoA mutase
EC
5.4.99.2
UniProt
P11653, P11652
Ligands
B12, ADN
Pockets
15 · best druggability 0.86

Structure

x-ray diffraction · 2 distinct chains · 46% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMethylmalonyl-CoA mutase (EC 5.4.99.2)protein72547% helix, 9% strandP11653
BMethylmalonyl-CoA mutase (EC 5.4.99.2)protein62045% helix, 12% strandP11652

Ligands and binding sites

  • B12 · Cobalamin · ligand · chains A
  • ADN · Adenosine · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17370.860.9089B12
24990.710.8153empty
3950.680.9224empty
4510.670.9622empty
52990.650.8139empty

Interfaces

1 interface between chains.

  • A–B · 5328 Ų buried · 75 hydrogen bonds · protein-protein

Compared structures

  • 3REQ · Methylmalonyl-CoA mutase, substrate-free state (poor quality structure) · the same entry in another collection · chain A against A, TM-score 1.00
  • P11652 · AlphaFold monomer V2.0 prediction for methylmalonyl-CoA mutase small subunit (P11652) · a predicted model of the same protein · chain B against A, TM-score 0.99
  • P11653 · AlphaFold monomer V2.0 prediction for methylmalonyl-CoA mutase large subunit (P11653) · a predicted model of the same protein · chain A against A, TM-score 0.93

Analyse

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