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Crystal structure of mycolic acid cyclopropane synthase CMAA1 complexed with sah and dddmab

Analyse Crystal structure of mycolic acid cyclopropane synthase CMAA1 complexed with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1KPH
Type
protein
Length
1,138 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cyclopropane-fatty-acyl-phospholipid synthase 1
EC
2.1.1.79
UniProt
Q11195
Ligands
SAH, 10A, CO3
Pockets
11 · best druggability 0.84

Structure

x-ray diffraction · 2 distinct chains · 50% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACyclopropane-fatty-acyl-phospholipid synthase 1 (EC 2.1.1.79)protein28351% helix, 16% strandQ11195
B, C, DCyclopropane-fatty-acyl-phospholipid synthase 1 (EC 2.1.1.79)protein28549% helix, 16% strandQ11195

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · 4 copies · chains A, B, C, D
  • 10A · Didecyl-dimethyl-ammonium · ligand · 4 copies · chains A, B, C, D
  • CO3 · Carbonate ion · ion · 4 copies · chains A, B, C, D

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

Pockets

11 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14510.840.9168CO3, SAH, 10A
24420.840.9163CO3, SAH, 10A
34450.840.9166CO3, SAH, 10A
44430.810.8948empty
51590.790.9536SAH

Interfaces

3 interfaces between chains.

  • A–D · 651 Ų buried · 7 hydrogen bonds · protein-protein
  • B–C · 429 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 184 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 1KPH · Crystal Structure of mycolic acid cyclopropane synthase CmaA1 complexed with SAH and… · the same entry in another collection · chain A against A, TM-score 1.00

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