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MolNFT v1 · #115338 · protein

Fic protein from neisseria meningitidis (nmfic) mutant E102R in dimeric form

5CGL · Adenosine monophosphate-protein transferase nmfic: “Fic protein from neisseria meningitidis (nmfic) mutant E102R in dimeric form”. X-ray diffraction, 3 pockets (best druggability 0.67). MolNFT v1 #115338 on GenesisL1: 3D structure…

PDB
5CGL
Type
protein
Length
324 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Adenosine monophosphate-protein transferase nmfic
EC
2.7.7.-
UniProt
Q7DDR9
Pockets
3 · best druggability 0.67

Structure

x-ray diffraction · 2 distinct chains · 65% helix, 3% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAdenosine monophosphate-protein transferase nmfic (EC 2.7.7.-)protein16165% helix, 3% strandQ7DDR9
BAdenosine monophosphate-protein transferase nmfic (EC 2.7.7.-)protein16365% helix, 3% strandQ7DDR9

Ligands and binding sites

  • PEG · Di(hydroxyethyl)ether · additive · 2 copies · chains A, B

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

Pockets

3 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1940.670.9126empty
2930.670.9126empty
32490.500.7544PEG

Interfaces

1 interface between chains.

  • A–B · 471 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • Q7DDR9 · AlphaFold monomer V2.0 prediction for protein adenylyltransferase nmfic (Q7DDR9) · a predicted model of the same protein · chain B against A, TM-score 1.00

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