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MolNFT v1 · #111700 · protein

Crystal structure of TAF1 BD2 bromodomain bound to a butyryllysine peptide

4YYM · Transcription initiation factor tfiid subunit 1: “Crystal structure of TAF1 BD2 bromodomain bound to a butyryllysine peptide”. X-ray diffraction, 1 ligand (CA), 1 pocket (best druggability 0.78). MolNFT v1 #111700 on GenesisL1: 3D…

PDB
4YYM
Type
protein
Length
272 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Transcription initiation factor tfiid subunit 1; Histone H4
UniProt
P21675, P62805
Ligands
CA
Pockets
1 · best druggability 0.78

Structure

x-ray diffraction · 3 distinct chains · 71% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATranscription initiation factor tfiid subunit 1protein13273% helix, 0% strandP21675
BTranscription initiation factor tfiid subunit 1protein13372% helix, 0% strandP21675
ZHistone H4protein70% helix, 0% strandP62805

Ligands and binding sites

  • CA · Calcium ion · metal · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11810.780.9323empty

Interfaces

3 interfaces between chains.

  • A–B · 652 Ų buried · 2 hydrogen bonds · protein-protein
  • B–Z · 349 Ų buried · 4 hydrogen bonds · protein-protein
  • A–Z · 275 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (nonstandard).

Compared structures

  • 4YYM · Crystal structure of TAF1 BD2 Bromodomain bound to a butyryllysine peptide · the same entry in another collection · chain A against A, TM-score 1.00
  • P21675 · AlphaFold monomer V2.0 prediction for transcription initiation factor tfiid subunit 1… · a predicted model of the same protein · chain B against A, TM-score 0.96

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