GL1X · GenesisL1 explorer

MolNFT v1 · #88103 · protein

PIH1 N-terminal domain

4CKT · PIH1 domain-containing protein 1: “PIH1 N-terminal domain”. X-ray diffraction, 2 pockets (best druggability 0.57). MolNFT v1 #88103 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
4CKT
Type
protein
Length
275 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
PIH1 domain-containing protein 1; Telomere length regulation protein TEL2 homolog
UniProt
Q9CQJ2, Q9DC40
Pockets
2 · best druggability 0.57

Structure

x-ray diffraction · 4 distinct chains · 25% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APIH1 domain-containing protein 1protein12728% helix, 31% strandQ9CQJ2
BPIH1 domain-containing protein 1protein13226% helix, 27% strandQ9CQJ2
CTelomere length regulation protein TEL2 homologprotein80% helix, 0% strandQ9DC40
DTelomere length regulation protein TEL2 homologprotein80% helix, 0% strandQ9DC40

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11640.570.8132empty
21250.530.8122empty

Interfaces

3 interfaces between chains.

  • A–C · 450 Ų buried · 4 hydrogen bonds · protein-protein
  • A–B · 422 Ų buried · 2 hydrogen bonds · protein-protein
  • B–D · 365 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 modified (engineered, phosphorylation).

Compared structures

  • 4CKT · PIH1 N-terminal domain · the same entry in another collection · chain D against D, TM-score 1.00
  • Q9CQJ2 · AlphaFold monomer V2.0 prediction for PIH1 domain-containing protein 1 (Q9CQJ2) · a predicted model of the same protein · chain A against A, TM-score 0.96
  • Q9DC40 · AlphaFold monomer V2.0 prediction for telomere length regulation protein TEL2 homolog… · a predicted model of the same protein · chain C against A, TM-score 0.52

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