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Basis for a switch in substrate specificity: crystal structure of selected variant of cre site-specific recombinase, alshg bound to the engineered recognition site LOXM7

Analyse Basis for a switch in substrate specificity: crystal structure of selected… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1PVP
Type
protein + DNA
Length
707 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
34-mer; Recombinase cre
UniProt
P06956
Pockets
11 · best druggability 0.80

Structure

x-ray diffraction · 4 distinct chains · 56% helix, 6% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
C34-merdna32——
D34-merdna34——
ARecombinase creprotein32356% helix, 4% strandP06956
BRecombinase creprotein31857% helix, 9% strandP06956

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16780.800.8569empty
23340.640.8039empty
32460.590.8028empty
43090.580.7730empty
5720.470.8322empty

Interfaces

6 interfaces between chains.

  • A–B · 1539 Ų buried · 25 hydrogen bonds · protein-protein
  • C–B · 1500 Ų buried · 39 hydrogen bonds · protein-nucleic
  • D–B · 1375 Ų buried · 27 hydrogen bonds · protein-nucleic
  • D–A · 1290 Ų buried · 26 hydrogen bonds · protein-nucleic
  • C–D · 712 Ų buried · 73 hydrogen bonds · nucleic-nucleic

Compared structures

  • 1PVP · Basis for a switch in substrate specificity: crystal structure of selected variant of cre… · the same entry in another collection · chain C against C, TM-score 1.00

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