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MolNFT v1 · #191010 · protein

RNA binding induces an allosteric switch in CYP33 to repress MLL1 mediated transcription regulation

7ZEZ · Isoform 3 of peptidyl-prolyl cis-trans isomerase E: “RNA binding induces an allosteric switch in CYP33 to repress MLL1 mediated transcription regulation”. Solution nmr, 1 ligand (ZN), 1 pocket (best druggability 0.42). MolNFT v1…

PDB
7ZEZ
Type
protein
Length
170 residues
Chains
3
Method
solution nmr
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Isoform 3 of peptidyl-prolyl cis-trans isomerase E; Mll cleavage product N320; Histone H3
EC
5.2.1.8
UniProt
Q9UNP9, Q03164, B4E380
Ligands
ZN
Pockets
1 · best druggability 0.42

Structure

solution nmr · 3 distinct chains · 18% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AIsoform 3 of peptidyl-prolyl cis-trans isomerase E (EC 5.2.1.8)protein9324% helix, 30% strandQ9UNP9
BMll cleavage product N320protein6414% helix, 13% strandQ03164
DHistone H3protein130% helix, 8% strandB4E380

Ligands and binding sites

  • ZN · Zinc ion · metal · 2 copies · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11430.420.7523empty

Interfaces

3 interfaces between chains.

  • A–B · 909 Ų buried · 12 hydrogen bonds · protein-protein
  • B–D · 718 Ų buried · 8 hydrogen bonds · protein-protein
  • A–D · 43 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 modified (methylation).

Compared structures

  • 7ZEZ · Trimolecular complex Cyp33-RRMdelta alpha : MLL1-PHD3 : H3K4me3 · the same entry in another collection · chain A against A, TM-score 1.00
  • Q9UNP9 · AlphaFold monomer V2.0 prediction for peptidyl-prolyl cis-trans isomerase E (Q9UNP9) · a predicted model of the same protein · chain A against A, TM-score 0.79

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