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6-Deoxyerythronolide B synthase (DEBS) module 1 in complex with antibody fragment 1B2: "turnstile closed" state (TE-free)

Analyse 6-Deoxyerythronolide B synthase (DEBS) module 1 in complex with antibody… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7M7J
Type
protein
Length
3,124 residues
Chains
6
Method
electron microscopy
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
4.3
Source
Homo sapiens; Saccharopolyspora erythraea
Molecule
EryAI; 1B2 (heavy chain); 1B2 (light chain)
UniProt
Q5UNP6
Pockets
20 · best druggability 0.78

Structure

electron microscopy · resolution 4.3 · 5 distinct chains · 28% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BEryAIprotein91235% helix, 13% strandQ5UNP6
AEryAIprotein139035% helix, 14% strandQ5UNP6
C, E1B2 (heavy chain)protein2053% helix, 46% strand—
D1B2 (light chain)protein2063% helix, 34% strand—
F1B2 (light chain)protein2064% helix, 33% strand—

Pockets

20 pockets found on a 1 Å grid, 19 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19550.780.80116empty
21230.770.9637empty
33620.750.8664empty
45990.740.8174empty
54530.710.8142empty

Interfaces

11 interfaces between chains.

  • B–A · 4804 Ų buried · 83 hydrogen bonds · protein-protein
  • E–F · 1592 Ų buried · 7 hydrogen bonds · protein-protein
  • C–D · 1573 Ų buried · 4 hydrogen bonds · protein-protein
  • B–E · 922 Ų buried · 10 hydrogen bonds · protein-protein
  • A–C · 863 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 7M7J · 6-deoxyerythronolide B synthase (debs) module 1 in complex with antibody fragment 1B2… · the same entry in another collection · chain A against A, TM-score 1.00

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