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Crystal structure of ispd from mycobacterium smegmatis in complex with cmp

Analyse Crystal structure of ispd from mycobacterium smegmatis in complex with cmp in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2XWM
Type
protein
Length
442 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase
EC
2.7.7.60
UniProt
A0R560
Ligands
C5P
Pockets
2 · best druggability 0.82

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase (EC 2.7.7.60)protein22038% helix, 24% strandA0R560
B2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase (EC 2.7.7.60)protein22239% helix, 23% strandA0R560

Ligands and binding sites

  • C5P · Cytidine-5'-monophosphate · ligand · 2 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110960.820.8396C5P
2590.280.7412empty

Interfaces

1 interface between chains.

  • A–B · 1595 Ų buried · 28 hydrogen bonds · protein-protein

Compared structures

  • 2XWM · Crystal structure of IspD from Mycobacterium smegmatis in complex with CMP · the same entry in another collection · chain A against A, TM-score 1.00

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