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Crystal structure of the mycobacterium tuberculosis tat-secreted protein RV2525C, monoclinic crystal form I

Analyse Crystal structure of the mycobacterium tuberculosis tat-secreted protein… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4PMO
Type
protein
Length
422 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tat-secreted protein RV2525C
UniProt
P95028
Ligands
NA
Pockets
3 · best druggability 0.62

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BTat-secreted protein RV2525Cprotein21134% helix, 23% strandP95028

Ligands and binding sites

  • NA · Sodium ion · metal · 6 copies · chains A, B
  • FMT · Formic acid · additive · 10 copies · chains A, B
  • GOL · Glycerol · additive · 6 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12310.620.8228GOL, FMT
21730.490.7730GOL, FMT
31520.480.7727GOL, FMT

Interfaces

1 interface between chains.

  • A–B · 278 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 4PMO · Crystal structure of the Mycobacterium tuberculosis Tat-secreted protein Rv2525c… · the same entry in another collection · chain A against A, TM-score 1.00

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