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Crystal structure of mutant R43D/C273S of L-asparaginase I from yersinia pestis

Analyse Crystal structure of mutant R43D/C273S of L-asparaginase I from yersinia pestis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7R69
Type
protein
Length
1,242 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
L-asparaginase I
EC
3.5.1.1
UniProt
A0A3N4B0Q2
Pockets
8 · best druggability 0.82

Structure

x-ray diffraction · 4 distinct chains · 34% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AL-asparaginase I (EC 3.5.1.1)protein31934% helix, 21% strandA0A3N4B0Q2
BL-asparaginase I (EC 3.5.1.1)protein31234% helix, 20% strandA0A3N4B0Q2
CL-asparaginase I (EC 3.5.1.1)protein30834% helix, 20% strandA0A3N4B0Q2
DL-asparaginase I (EC 3.5.1.1)protein30334% helix, 21% strandA0A3N4B0Q2

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 13 copies · chains A, B, C, D

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

Pockets

8 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12200.820.9549EDO
22070.820.9637EDO
35230.730.8249empty
46200.730.8053empty
52090.490.7533empty

Interfaces

4 interfaces between chains.

  • C–D · 2050 Ų buried · 26 hydrogen bonds · protein-protein
  • A–B · 2022 Ų buried · 28 hydrogen bonds · protein-protein
  • B–D · 614 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 600 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 7R69 · Crystal structure of mutant R43D/C273S of L-Asparaginase I from Yersinia pestis · the same entry in another collection · chain A against A, TM-score 1.00

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