+Open data
-Basic information
Entry | Database: PDB / ID: 8q54 | ||||||
---|---|---|---|---|---|---|---|
Title | N5-methyl-H4MPT:CoM methyltransferase -coenzyme M complex + CoM | ||||||
Components | (Tetrahydromethanopterin S-methyltransferase subunit ...) x 7 | ||||||
Keywords | TRANSFERASE / methanogenesis / tetrahydromethanopterin / coenzyme M / vitamin B12 / Na+ transport | ||||||
Function / homology | Function and homology information tetrahydromethanopterin S-methyltransferase / tetrahydromethanopterin S-methyltransferase activity / methyltransferase complex / methanogenesis, from carbon dioxide / vesicle membrane / cobalt ion binding / sodium ion transport / one-carbon metabolic process / methylation / plasma membrane / cytoplasm Similarity search - Function | ||||||
Biological species | Methanothermobacter marburgensis (archaea) | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.39 Å | ||||||
Authors | Aziz, I. / Vonck, J. / Ermler, U. | ||||||
Funding support | Germany, 1items
| ||||||
Citation | Journal: To Be Published Title: Cryo-EM structure of the methanogenic Na+ translocating N5-methyl-H4MPT:CoM methyltransferase complex Authors: Aziz, I. / Kayastha, K. / Kaltwasser, S. / Vonck, J. / Welsch, S. / Murohy, B.J. / Kahnt, J. / Wu, D. / Wagner, T. / Shima, S. / Ermler, U. | ||||||
History |
|
-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
---|
-Downloads & links
-Download
PDBx/mmCIF format | 8q54.cif.gz | 1.1 MB | Display | PDBx/mmCIF format |
---|---|---|---|---|
PDB format | pdb8q54.ent.gz | Display | PDB format | |
PDBx/mmJSON format | 8q54.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 8q54_validation.pdf.gz | 2 MB | Display | wwPDB validaton report |
---|---|---|---|---|
Full document | 8q54_full_validation.pdf.gz | 2.1 MB | Display | |
Data in XML | 8q54_validation.xml.gz | 106.2 KB | Display | |
Data in CIF | 8q54_validation.cif.gz | 154.7 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/q5/8q54 ftp://data.pdbj.org/pub/pdb/validation_reports/q5/8q54 | HTTPS FTP |
-Related structure data
Related structure data | 18162MC M: map data used to model this data C: citing same article (ref.) |
---|---|
Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
-Assembly
Deposited unit |
|
---|---|
1 |
|
-Components
-Tetrahydromethanopterin S-methyltransferase subunit ... , 7 types, 21 molecules AaQBbRCcSDdTEeUFfVGgW
#1: Protein | Mass: 25640.320 Da / Num. of mol.: 3 / Source method: isolated from a natural source Source: (natural) Methanothermobacter marburgensis (archaea) References: UniProt: P80184 #2: Protein | Mass: 10725.471 Da / Num. of mol.: 3 / Source method: isolated from a natural source Source: (natural) Methanothermobacter marburgensis (archaea) References: UniProt: Q59584 #3: Protein | Mass: 27132.244 Da / Num. of mol.: 3 / Source method: isolated from a natural source Source: (natural) Methanothermobacter marburgensis (archaea) References: UniProt: P80185 #4: Protein | Mass: 22783.881 Da / Num. of mol.: 3 / Source method: isolated from a natural source Source: (natural) Methanothermobacter marburgensis (archaea) References: UniProt: P80183 #5: Protein | Mass: 31253.289 Da / Num. of mol.: 3 / Source method: isolated from a natural source Source: (natural) Methanothermobacter marburgensis (archaea) References: UniProt: P80186 #6: Protein | Mass: 7325.928 Da / Num. of mol.: 3 / Source method: isolated from a natural source Source: (natural) Methanothermobacter marburgensis (archaea) References: UniProt: Q50773 #7: Protein | Mass: 9519.042 Da / Num. of mol.: 3 / Source method: isolated from a natural source Source: (natural) Methanothermobacter marburgensis (archaea) References: UniProt: Q50774 |
---|
-Non-polymers , 5 types, 112 molecules
#8: Chemical | #9: Chemical | ChemComp-JCV / [( Mass: 1706.543 Da / Num. of mol.: 12 / Source method: obtained synthetically / Formula: C98H193O19P #10: Chemical | ChemComp-NA / #11: Chemical | #12: Water | ChemComp-HOH / | |
---|
-Details
Has ligand of interest | Y |
---|
-Experimental details
-Experiment
Experiment | Method: ELECTRON MICROSCOPY |
---|---|
EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
-Sample preparation
Component | Name: Methyl-H4MPT:CoM methyltransferase / Type: COMPLEX / Entity ID: #1-#7 / Source: NATURAL |
---|---|
Molecular weight | Value: 430 kDa/nm / Experimental value: YES |
Source (natural) | Organism: Methanothermobacter marburgensis (archaea) |
Buffer solution | pH: 7 |
Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
Vitrification | Cryogen name: ETHANE |
-Electron microscopy imaging
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
---|---|
Microscopy | Model: FEI TITAN KRIOS |
Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2100 nm / Nominal defocus min: 1200 nm |
Image recording | Electron dose: 73.9 e/Å2 / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) |
-Processing
EM software | Name: PHENIX / Version: 1.20.1_4487: / Category: model refinement | ||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
Particle selection | Num. of particles selected: 910067 | ||||||||||||||||||||||||
3D reconstruction | Resolution: 2.39 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 87173 / Symmetry type: POINT | ||||||||||||||||||||||||
Refine LS restraints |
|