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Crystal structure of gamma-chymotrypsin at pH 5.6, room temperature

Analyse Crystal structure of gamma-chymotrypsin at pH 5.6, room temperature in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5R48
Type
protein
Length
245 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Gamma-chymotrypsin; Peptide swpw; Peptide tpgvy
EC
3.4.21.1
UniProt
P00766
Ligands
IOD, SO4

Structure

x-ray diffraction · 5 distinct chains · 11% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGamma-chymotrypsin (EC 3.4.21.1)protein100% helix, 0% strandP00766
BGamma-chymotrypsin (EC 3.4.21.1)protein1312% helix, 40% strandP00766
CGamma-chymotrypsin (EC 3.4.21.1)protein9525% helix, 40% strandP00766
DPeptide swpwprotein40% helix, 50% strand—
EPeptide tpgvyprotein50% helix, 60% strand—

Ligands and binding sites

  • IOD · Iodide ion · ion · chains B
  • SO4 · Sulfate ion · ion · chains B, C

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

Interfaces

8 interfaces between chains.

  • B–C · 2927 Ų buried · 40 hydrogen bonds · protein-protein
  • A–B · 472 Ų buried · 1 hydrogen bond · protein-protein
  • C–E · 394 Ų buried · 10 hydrogen bonds · protein-protein
  • C–D · 375 Ų buried · 9 hydrogen bonds · protein-protein
  • D–E · 302 Ų buried · 23 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 disulfide (disulfide).

Compared structures

  • 5R48 · Crystal Structure of gamma-Chymotrypsin at pH 5.6, room temperature · the same entry in another collection · chain E against E, TM-score 1.00
  • P00766 · AlphaFold monomer V2.0 prediction for chymotrypsinogen a (P00766) · a predicted model of the same protein · chain C against A, TM-score 0.99

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