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MolNFT v1 · #65427 · protein

Crystal structure of carbon-sulfur lyase involved in aluminum resistance (YP_878183.1) from clostridium novyi nt at 2.90 a resolution

3GWP: “Crystal structure of carbon-sulfur lyase involved in aluminum resistance (YP_878183.1) from clostridium novyi…”. X-ray diffraction, 15 pockets (best druggability 0.86). MolNFT v1 #65427 on GenesisL1: 3D structure, binding sites and…

PDB
3GWP
Type
protein
Length
1,696 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Carbon-sulfur lyase involved in aluminum resistance
UniProt
A0Q0N1
Pockets
15 · best druggability 0.86

Structure

x-ray diffraction · 3 distinct chains · 44% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ACarbon-sulfur lyase involved in aluminum resistanceprotein42443% helix, 14% strandA0Q0N1
B, DCarbon-sulfur lyase involved in aluminum resistanceprotein42744% helix, 13% strandA0Q0N1
CCarbon-sulfur lyase involved in aluminum resistanceprotein41844% helix, 13% strandA0Q0N1

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16370.860.9166empty
210080.810.83143empty
35050.700.8038empty
45810.700.7971empty
55260.680.7838empty

Interfaces

6 interfaces between chains.

  • A–B · 2602 Ų buried · 25 hydrogen bonds · protein-protein
  • C–D · 2559 Ų buried · 23 hydrogen bonds · protein-protein
  • B–D · 2307 Ų buried · 29 hydrogen bonds · protein-protein
  • A–C · 2175 Ų buried · 30 hydrogen bonds · protein-protein
  • B–C · 241 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 47 modified (engineered, cofactor).

Compared structures

  • 3GWP · Crystal structure of carbon-sulfur lyase involved in aluminum resistance (YP_878183.1)… · the same entry in another collection · chain A against A, TM-score 1.00

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