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Crystal structure of the NMB1088 protein from neisseria meningitidis. northeast structural genomics consortium target MR91

Analyse Crystal structure of the NMB1088 protein from neisseria meningitidis. northeast… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3BID
Type
protein
Length
466 residues
Chains
8
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
UPF0339 protein NMB1088
UniProt
Q7DDI1
Pockets
1 · best druggability 0.26

Structure

x-ray diffraction · 4 distinct chains · 20% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, FUPF0339 protein NMB1088protein5821% helix, 34% strandQ7DDI1
B, D, HUPF0339 protein NMB1088protein5721% helix, 35% strandQ7DDI1
EUPF0339 protein NMB1088protein6120% helix, 34% strandQ7DDI1
GUPF0339 protein NMB1088protein6020% helix, 33% strandQ7DDI1

Pockets

1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1640.260.7213empty

Interfaces

10 interfaces between chains.

  • A–B · 1564 Ų buried · 19 hydrogen bonds · protein-protein
  • C–D · 1556 Ų buried · 16 hydrogen bonds · protein-protein
  • G–H · 1485 Ų buried · 16 hydrogen bonds · protein-protein
  • E–F · 1441 Ų buried · 18 hydrogen bonds · protein-protein
  • B–H · 298 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 modified (engineered).

Compared structures

  • 3BID · Crystal structure of the NMB1088 protein from Neisseria meningitidis. Northeast… · the same entry in another collection · chain H against H, TM-score 1.00
  • Q7DDI1 · AlphaFold monomer V2.0 prediction for UPF0339 protein NMB1088 (Q7DDI1) · a predicted model of the same protein · chain B against A, TM-score 0.93

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