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Three-dimensional structure of ribonulcease T1 complexed with an isosteric phosphonate analogue of gpu: alternate substrate binding modes and catalysis.

Analyse Three-dimensional structure of ribonulcease T1 complexed with an isosteric… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1B2M
Type
protein + RNA
Length
214 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
5'-R(*GP*(U34))-3'; Ribonuclease T1
EC
3.1.27.3
UniProt
P00651
Pockets
2 · best druggability 0.35

Structure

x-ray diffraction · 2 distinct chains · 15% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
C, D, E5'-R(*GP*(U34))-3'rna2——
A, BRibonuclease T1 (EC 3.1.27.3)protein10415% helix, 31% strandP00651

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1710.350.7713empty
2580.340.7816empty

Interfaces

8 interfaces between chains.

  • C–A · 314 Ų buried · 12 hydrogen bonds · protein-nucleic
  • D–B · 305 Ų buried · 13 hydrogen bonds · protein-nucleic
  • A–B · 278 Ų buried · 7 hydrogen bonds · protein-protein
  • D–A · 199 Ų buried · 0 hydrogen bonds · protein-nucleic
  • E–B · 101 Ų buried · 1 hydrogen bond · protein-nucleic

Modifications

Observed in the structure: 4 disulfide, 3 modified (disulfide, nucleotide modification).

Compared structures

  • 1B2M · Three-dimensional structure of ribonulcease T1 complexed with an isosteric phosphonate… · the same entry in another collection · chain A against A, TM-score 1.00
  • P00651 · AlphaFold monomer V2.0 prediction for guanyl-specific ribonuclease T1 (P00651) · a predicted model of the same protein · chain A against A, TM-score 0.99

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