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Cryo-EM structure of the multiple peptide resistance factor (mprf) loaded with two lysyl-phosphatidylglycerol molecules
Analyse Cryo-EM structure of the multiple peptide resistance factor (mprf) loaded with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7DUW
- Type
- protein
- Length
- 1,640 residues
- Chains
- 2
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Bifunctional lysylphosphatidylglycerol FLIPPASE/SYNTHETASE mprf
- UniProt
- A0A6P1C618
- Ligands
- EV9, LHG, PGT, J4U
- Pockets
- 15 · best druggability 0.86
Structure
electron microscopy · 1 distinct chain · 64% helix, 11% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Bifunctional lysylphosphatidylglycerol FLIPPASE/SYNTHETASE mprf | protein | 820 | 64% helix, 11% strand | A0A6P1C618 |
Ligands and binding sites
- EV9 · [(2~{R})-3-[[(2~{S})-3-[(2~{S})-2,6-bis(azanyl) hexanoyl]oxy-2-oxidanyl-propoxy]-oxidanyl-phosphoryl]oxy-2-hexadecanoyloxy-propyl] hexadecanoate · ligand · 4 copies · chains A, B
- LHG · 1,2-dipalmitoyl-phosphatidyl-glycerole · ligand · 2 copies · chains A, B
- PGT · (1S)-2-{[{[(2R)-2,3-dihydroxypropyl]oxy}(hydroxy) phosphoryl]oxy}-1-[(palmitoyloxy)methyl]ethyl stearate · ligand · 2 copies · chains A, B
- J4U · (2~{R},3~{S},4~{S},5~{S},6~{S})-2-(hydroxymethyl)-6-[(2~{R},3~{S},4~{R},5~{R},6~{R})-2-(hydroxymethyl)-6-[2-[[(2~{R},3~{S},4~{R},5~{R},6~{S})-6-(hydroxymethyl)-5-[(2~{S},3~{R},4~{S},5~{S},6~{R})-6-(hydroxymethyl)-3,4,5-tris(oxidanyl)oxan-2-yl]oxy-3,4-bis(oxidanyl)oxan-2-yl]oxymethyl]-4-[(1~{R},2~{R}, 4~{S},5'~{R},6~{R},7~{R},8~{R},9~{S},12~{S},13~{R}, 16~{S})-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icos-18-ene-6,2'-oxane]-16-yl]oxy-butoxy]-4,5-bis(oxidanyl)oxa · ligand · 2 copies · chains A, B
- LMT · Dodecyl-beta-D-maltoside · additive · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
15 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1010 | 0.86 | 0.86 | 97 | PGT |
| 2 | 1105 | 0.84 | 0.85 | 121 | EV9 |
| 3 | 1144 | 0.84 | 0.85 | 116 | EV9 |
| 4 | 790 | 0.82 | 0.84 | 57 | LMT, EV9 |
| 5 | 804 | 0.82 | 0.84 | 61 | LMT, EV9 |
Interfaces
1 interface between chains.
- A–B · 649 Ų buried · 11 hydrogen bonds · protein-protein
Compared structures
- 7DUW · Cryo-EM structure of the multiple peptide resistance factor (MprF) loaded with two… · the same entry in another collection · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt A0A6P1C618
- Elsewhere: RCSB PDB 7DUW · PDBe 7DUW · UniProt A0A6P1C618
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