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MolNFT v1 · #94949 · protein

Human P53 core domain with hot spot mutation R273H (form I)

4IBS · Cellular tumor antigen P53: “Human P53 core domain with hot spot mutation R273H (form I)”. X-ray diffraction, 1 ligand (ZN), 10 pockets (best druggability 0.64). MolNFT v1 #94949 on GenesisL1: 3D structure, binding sites and pockets…

PDB
4IBS
Type
protein
Length
775 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cellular tumor antigen P53
UniProt
P04637
Ligands
ZN
Pockets
10 · best druggability 0.64

Structure

x-ray diffraction · 2 distinct chains · 9% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACellular tumor antigen P53protein1939% helix, 34% strandP04637
B, C, DCellular tumor antigen P53protein1949% helix, 34% strandP04637

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 copies · chains A, B, C, D
  • EDO · 1,2-ethanediol · additive · chains D

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

Pockets

10 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15710.640.7678empty
24640.640.7768empty
33070.530.7537empty
41790.470.7637empty
51220.400.7519empty

Interfaces

4 interfaces between chains.

  • B–C · 549 Ų buried · 6 hydrogen bonds · protein-protein
  • A–D · 510 Ų buried · 11 hydrogen bonds · protein-protein
  • A–B · 480 Ų buried · 6 hydrogen bonds · protein-protein
  • C–D · 259 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 4IBS · Human p53 core domain with hot spot mutation R273H (form I) · the same entry in another collection · chain A against A, TM-score 1.00

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