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SERINE/THREONINE phosphatase Z1 (candida albicans) binds to inhibitor microcystin-lr

Analyse SERINE/THREONINE phosphatase Z1 (candida albicans) binds to inhibitor… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5JPF
Type
protein
Length
294 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
SERINE/THREONINE-protein phosphatase; Microcystin-lr
EC
3.1.3.16
UniProt
C4YM68
Ligands
1ZN, FGA, DAM, MN
Pockets
2 · best druggability 0.53

Structure

x-ray diffraction · 2 distinct chains · 35% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASERINE/THREONINE-protein phosphatase (EC 3.1.3.16)protein29036% helix, 20% strandC4YM68
MMicrocystin-lrprotein40% helix, 0% strand—

Ligands and binding sites

  • 1ZN · (2S,3S,4E,6E,8S,9S)-3-amino-9-methoxy-2,6,8-trimethyl-10-phenyldeca-4,6-dienoic acid · ligand · chains A, M
  • FGA · Gamma-D-glutamic acid · ligand · chains A, M
  • DAM · N-methyl-alpha-beta-dehydroalanine · ligand · chains A, M
  • MN · Manganese (II) ion · metal · 2 copies · chains A
  • MLI · Malonate ion · additive · 3 copies · chains A

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
11970.530.78341ZN, FGA, MN, MLI
2730.310.7422empty

Interfaces

1 interface between chains.

  • A–M · 237 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 covalent, 1 d-amino, 1 modified (covalent ligand, D-amino acid, nonstandard).

Compared structures

  • 5JPF · Serine/Threonine phosphatase Z1 (Candida albicans) binds to inhibitor microcystin-LR · the same entry in another collection · chain M against M, TM-score 1.00

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