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Structure of thiamine-monophosphate kinase from acinetobacter baumannii in complex with adenosine diphosphate (ADP) and thiamine diphosphate (tpp), orthorhombic crystal form

Analyse Structure of thiamine-monophosphate kinase from acinetobacter baumannii in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6MFM
Type
protein
Length
608 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Thiamine-monophosphate kinase
EC
2.7.4.16
UniProt
A0A0D5YC82
Ligands
TPP, ADP, MG, NA
Pockets
2 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 33% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AThiamine-monophosphate kinase (EC 2.7.4.16)protein30433% helix, 28% strandA0A0D5YC82
BThiamine-monophosphate kinase (EC 2.7.4.16)protein30433% helix, 27% strandA0A0D5YC82

Ligands and binding sites

  • TPP · Thiamine diphosphate · ligand · 2 copies · chains A, B
  • ADP · Adenosine-5'-diphosphate · ligand · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 8 copies · chains A, B
  • NA · Sodium ion · metal · 4 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14980.790.8665TPP, MG, NA, ADP
24560.780.8659ADP, NA, MG, TPP

Interfaces

1 interface between chains.

  • A–B · 2613 Ų buried · 43 hydrogen bonds · protein-protein

Compared structures

  • 6MFM · Structure of thiamine-monophosphate kinase from Acinetobacter baumannii in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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