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Conserved hypothetical protein from clostridium thermocellum cth-2968

Analyse Conserved hypothetical protein from clostridium thermocellum cth-2968 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1XRG
Type
protein
Length
400 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative translation initiation inhibitor, yjgf family
Ligands
UNX
Pockets
6 · best druggability 0.81

Structure

x-ray diffraction · 3 distinct chains · 27% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APutative translation initiation inhibitor, yjgf familyprotein12529% helix, 30% strand—
BPutative translation initiation inhibitor, yjgf familyprotein13825% helix, 32% strand—
CPutative translation initiation inhibitor, yjgf familyprotein13728% helix, 33% strand—

Ligands and binding sites

  • UNX · Unknown atom or ion · ion · 17 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11300.810.9926UNX
21780.600.8224empty
31740.580.8223empty
41940.580.8022UNX
5840.420.7924UNX

Interfaces

3 interfaces between chains.

  • B–C · 1252 Ų buried · 20 hydrogen bonds · protein-protein
  • A–B · 1226 Ų buried · 20 hydrogen bonds · protein-protein
  • A–C · 1012 Ų buried · 12 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 5 modified (engineered).

Compared structures

  • 1XRG · Conserved hypothetical protein from Clostridium thermocellum Cth-2968 · the same entry in another collection · chain A against A, TM-score 1.00

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