GL1X · GenesisL1 explorer

MolNFT v1 · #121098 · protein

1.93 ångström resolution crystal structure of a pullulanase-specific type II secretion system integral cytoplasmic membrane protein gspl (C-terminal fragment; residues 309-397) from klebsiella pneumoniae subsp. pneumoniae ntuh-K2044

5HL8 · Type II secretion system protein L: “1.93 ångström resolution crystal structure of a pullulanase-specific type II secretion system integral…”. X-ray diffraction, 3 pockets (best druggability 0.50). MolNFT v1 #121098 on GenesisL1: 3D…

PDB
5HL8
Type
protein
Length
309 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Type II secretion system protein L
UniProt
A0A060VDE2
Pockets
3 · best druggability 0.50

Structure

x-ray diffraction · 3 distinct chains · 30% helix, 42% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BType II secretion system protein Lprotein8128% helix, 46% strandA0A060VDE2
CType II secretion system protein Lprotein7928% helix, 42% strandA0A060VDE2
DType II secretion system protein Lprotein6834% helix, 37% strandA0A060VDE2

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11750.500.7726empty
21050.430.7818empty
3700.330.7517empty

Interfaces

4 interfaces between chains.

  • B–C · 731 Ų buried · 15 hydrogen bonds · protein-protein
  • A–D · 551 Ų buried · 8 hydrogen bonds · protein-protein
  • A–B · 429 Ų buried · 9 hydrogen bonds · protein-protein
  • B–D · 125 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 modified (engineered).

Compared structures

  • 5HL8 · 1.93 Angstrom resolution crystal structure of a pullulanase-specific type II secretion… · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.