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Crystal structure of E. COLI hype, a hydrogenase maturation protein

Analyse Crystal structure of E. COLI hype, a hydrogenase maturation protein in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2I6R
Type
protein
Length
1,274 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hype protein
UniProt
Q7ABB2
Pockets
11 · best druggability 0.81

Structure

x-ray diffraction · 4 distinct chains · 35% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHype proteinprotein31634% helix, 26% strandQ7ABB2
BHype proteinprotein31536% helix, 26% strandQ7ABB2
CHype proteinprotein32134% helix, 26% strandQ7ABB2
DHype proteinprotein32235% helix, 26% strandQ7ABB2

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17300.810.8474empty
211110.800.81103empty
37430.790.8377empty
47830.770.8175empty
57160.760.8176empty

Interfaces

3 interfaces between chains.

  • C–D · 2748 Ų buried · 44 hydrogen bonds · protein-protein
  • A–B · 2668 Ų buried · 46 hydrogen bonds · protein-protein
  • B–D · 607 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 2I6R · Crystal structure of E. coli HypE, a hydrogenase maturation protein · the same entry in another collection · chain A against A, TM-score 1.00

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