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0.9A resolution crystal structure of alpha-lytic protease complexed with a transition state analogue, meosuc-ala-ala-pro-val boronic acid

Analyse 0.9A resolution crystal structure of alpha-lytic protease complexed with a… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2H5D
Type
protein
Length
201 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alpha-lytic protease; Meosuc-ala-ala-pro-ala boronic acid inhibitor
EC
3.4.21.12
UniProt
P00778
Ligands
MSU, B2V, SO4

Structure

x-ray diffraction · 2 distinct chains · 7% helix, 55% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAlpha-lytic protease (EC 3.4.21.12)protein1987% helix, 55% strandP00778
BMeosuc-ala-ala-pro-ala boronic acid inhibitorprotein30% helix, 33% strand—

Ligands and binding sites

  • MSU · Succinic acid monomethyl ester · ligand · chains A, B
  • B2V · Valine boronic acid · ligand · chains A, B
  • SO4 · Sulfate ion · ion · 8 copies · chains A, B
  • GOL · Glycerol · additive · chains A, B

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

Interfaces

1 interface between chains.

  • A–B · 229 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 covalent, 3 disulfide (covalent ligand, disulfide).

Compared structures

  • 2H5D · 0.9A resolution crystal structure of alpha-lytic protease complexed with a transition… · the same entry in another collection · chain A against A, TM-score 1.00
  • P00778 · AlphaFold monomer V2.0 prediction for alpha-lytic protease (P00778) · a predicted model of the same protein · chain A against A, TM-score 1.00

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