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NMR solution structure of the PHI0 pki nes peptide in complex with CRM1-rangtp

Analyse NMR solution structure of the PHI0 pki nes peptide in complex with CRM1-rangtp in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2L1L
Type
protein
Length
154 residues
Chains
2
Method
solution nmr
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Camp-dependent protein kinase inhibitor alpha; Exportin-1
UniProt
P61925, O14980
Pockets
2 · best druggability 0.32

Structure

solution nmr · 2 distinct chains · 62% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACamp-dependent protein kinase inhibitor alphaprotein2730% helix, 0% strandP61925
BExportin-1protein12769% helix, 0% strandO14980

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1630.320.7517empty
2600.280.7316empty

Interfaces

1 interface between chains.

  • A–B · 862 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 2L1L · NMR Solution Structure of the Phi0 PKI NES Peptide in Complex with CRM1-RanGTP · the same entry in another collection · chain A against A, TM-score 1.00
  • O14980 · AlphaFold monomer V2.0 prediction for exportin-1 (O14980) · a predicted model of the same protein · chain B against A, TM-score 0.99
  • P61925 · AlphaFold monomer V2.0 prediction for camp-dependent protein kinase inhibitor alpha… · a predicted model of the same protein · chain A against A, TM-score 0.32

Analyse

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