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MolNFT v1 · #111839 · protein

Crystal structure of human SPT16 mid-AID/H3-H4 tetramer fact histone complex

4Z2M · Fact complex subunit SPT16: “Crystal structure of human SPT16 mid-AID/H3-H4 tetramer fact histone complex”. X-ray diffraction, 5 pockets (best druggability 0.67). MolNFT v1 #111839 on GenesisL1: 3D structure, binding sites and…

PDB
4Z2M
Type
protein
Length
565 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fact complex subunit SPT16; Histone H3.1; Histone H4
UniProt
Q9Y5B9, P68431, P62805
Pockets
5 · best druggability 0.67

Structure

x-ray diffraction · 5 distinct chains · 45% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BFact complex subunit SPT16protein27124% helix, 38% strandQ9Y5B9
GHistone H3.1protein7764% helix, 5% strandP68431
HHistone H4protein7166% helix, 7% strandP62805
IHistone H3.1protein7667% helix, 5% strandP68431
JHistone H4protein7060% helix, 6% strandP62805

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16070.670.7753empty
22060.510.7720empty
32230.480.7431empty
41220.360.7325empty
5820.320.7417empty

Interfaces

7 interfaces between chains.

  • G–H · 2147 Ų buried · 13 hydrogen bonds · protein-protein
  • I–J · 1992 Ų buried · 9 hydrogen bonds · protein-protein
  • G–I · 591 Ų buried · 5 hydrogen bonds · protein-protein
  • B–H · 515 Ų buried · 7 hydrogen bonds · protein-protein
  • B–I · 459 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 4Z2M · Crystal structure of human SPT16 Mid-AID/H3-H4 tetramer FACT Histone complex · the same entry in another collection · chain B against B, TM-score 1.00
  • Q9Y5B9 · AlphaFold monomer V2.0 prediction for fact complex subunit SPT16 (Q9Y5B9) · a predicted model of the same protein · chain B against A, TM-score 0.98

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