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Crystal structure of human TEAD2 transcription factor in complex with flufenamic acid derivative

Analyse Crystal structure of human TEAD2 transcription factor in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6VAH
Type
protein
Length
403 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transcriptional enhancer factor tef-4
UniProt
Q15562
Ligands
QZ1, UNX
Pockets
4 · best druggability 0.84

Structure

x-ray diffraction · 2 distinct chains · 19% helix, 50% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATranscriptional enhancer factor tef-4protein20819% helix, 49% strandQ15562
BTranscriptional enhancer factor tef-4protein19518% helix, 51% strandQ15562

Ligands and binding sites

  • QZ1 · 2-fluoro-6-[(3-hexylphenyl)amino]benzoic acid · ligand · 2 copies · chains A, B
  • UNX · Unknown atom or ion · ion · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15590.840.8956QZ1
24300.770.8663QZ1
3850.330.7417empty
4620.330.7616empty

Interfaces

1 interface between chains.

  • A–B · 589 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 6VAH · Crystal structure of human TEAD2 transcription factor in complex with Flufenamic acid… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q15562 · AlphaFold monomer V2.0 prediction for transcriptional enhancer factor tef-4 (Q15562) · a predicted model of the same protein · chain B against A, TM-score 0.98

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