[English] 日本語

- EMDB-38391: Cryo-EM complex structure between hydroxylase and regulatory comp... -
+
Open data
-
Basic information
Entry | ![]() | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Title | Cryo-EM complex structure between hydroxylase and regulatory component from soluble methane monooxygenase | |||||||||
![]() | ||||||||||
![]() |
| |||||||||
![]() | soluble methane monooxygenase / hydroxylase / regulatory component / oxidoreductase | |||||||||
Function / homology | ![]() methane metabolic process / methane monooxygenase [NAD(P)H] activity / oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen / monooxygenase activity / metal ion binding Similarity search - Function | |||||||||
Biological species | ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.85 Å | |||||||||
![]() | Hwang Y / Ryu B / Pozharski E / Lee SJ | |||||||||
Funding support | ![]()
| |||||||||
![]() | ![]() Title: Heartbeat-like dynamics drives oxygen activation in methane monooxygenase Authors: Hwang Y / Ryu B / Lee DH / Hong HJ / Na JG / Song CG / Kang HG / Pozharski E / Lee SJ | |||||||||
History |
|
-
Structure visualization
Supplemental images |
---|
-
Downloads & links
-EMDB archive
Map data | ![]() | 110.8 MB | ![]() | |
---|---|---|---|---|
Header (meta data) | ![]() ![]() | 22.9 KB 22.9 KB | Display Display | ![]() |
FSC (resolution estimation) | ![]() | 12.7 KB | Display | ![]() |
Images | ![]() | 171.7 KB | ||
Masks | ![]() | 216 MB | ![]() | |
Filedesc metadata | ![]() | 7.3 KB | ||
Others | ![]() ![]() | 3.5 MB 3.5 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 8xiwMC ![]() 8yrdC M: atomic model generated by this map C: citing same article ( |
---|---|
Similar structure data | Similarity search - Function & homology ![]() |
-
Links
EMDB pages | ![]() ![]() |
---|---|
Related items in Molecule of the Month |
-
Map
File | ![]() | ||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.849 Å | ||||||||||||||||||||||||||||||||||||
Density |
| ||||||||||||||||||||||||||||||||||||
Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
|
-Supplemental data
-Mask #1
File | ![]() | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Projections & Slices |
| ||||||||||||
Density Histograms |
-Half map: #1
File | emd_38391_half_map_1.map | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Projections & Slices |
| ||||||||||||
Density Histograms |
-Half map: #2
File | emd_38391_half_map_2.map | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Projections & Slices |
| ||||||||||||
Density Histograms |
-
Sample components
-Entire : Cryo-EM structure of soluble methane monooxygenase hydroxylase in...
Entire | Name: Cryo-EM structure of soluble methane monooxygenase hydroxylase in complex with regulatory subunit |
---|---|
Components |
|
-Supramolecule #1: Cryo-EM structure of soluble methane monooxygenase hydroxylase in...
Supramolecule | Name: Cryo-EM structure of soluble methane monooxygenase hydroxylase in complex with regulatory subunit type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#4 |
---|---|
Source (natural) | Organism: ![]() |
-Macromolecule #1: Methane monooxygenase
Macromolecule | Name: Methane monooxygenase / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 59.97923 KDa |
Sequence | String: MAISLATKAA TDALKVNRAP VGVEPQEVHK WLQSFNWDFK ENRTKYATKY HMANQTKEQF KVIAKEYARM EAAKDERQFG TLLDGLTRL GAGNKVHPRW GETMKVISNF LEVGEYNAIA ASAMLWDSAT AAEQKNGYLA QVLDEIRHTH QCAFINHYYS K HYHDPAGH ...String: MAISLATKAA TDALKVNRAP VGVEPQEVHK WLQSFNWDFK ENRTKYATKY HMANQTKEQF KVIAKEYARM EAAKDERQFG TLLDGLTRL GAGNKVHPRW GETMKVISNF LEVGEYNAIA ASAMLWDSAT AAEQKNGYLA QVLDEIRHTH QCAFINHYYS K HYHDPAGH NDARRTRAIG PLWKGMKRVF ADGFISGDAV ECSVNLQLVG EACFTNPLIV AVTEWASANG DEITPTVFLS VE TDELRHM ANGYQTVVSI ANDPAAAKYL NTDLNNAFWT QQKYFTPALG YLFEYGSKFK VEPWVKTWNR WVYEDWGGIW IGR LGKYGV ESPRSLRDAK TDAYWAHHDL ALAAYALWPL GFARLALPDE EDQEWFEANY PGWADHYGKI YNEWKKLGYE DPKS GFIPY AWLLANGHDV YIDRVSQVPF IPSLAKGSGS LRVHEFNGKK HSLTDDWGER MWLSEPERYE CHNLFEQYEG RELSE VIAE GHGVRSDGKT LIAQPHVRGD NLWTLEDIKR AGCVFPNPLA KF UniProtKB: Methane monooxygenase |
-Macromolecule #2: Methane monooxygenase
Macromolecule | Name: Methane monooxygenase / type: protein_or_peptide / ID: 2 / Number of copies: 2 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 45.239246 KDa |
Sequence | String: MSQPQSSQVT KRGLTDPERA AIIAAAVPDH ALDTQRKYHY FIQPRWKRLS EYEQLSCYAQ PNPDWIAGGL DWGDWTQKFH GGRPSWGNE STELRTTDWY RHRDPARRWH APYVKDKSEE ARYTQRFLAA YSSEGSIRTI DAYWRDEILN KYYGALLYNE Y GLFNAHSS ...String: MSQPQSSQVT KRGLTDPERA AIIAAAVPDH ALDTQRKYHY FIQPRWKRLS EYEQLSCYAQ PNPDWIAGGL DWGDWTQKFH GGRPSWGNE STELRTTDWY RHRDPARRWH APYVKDKSEE ARYTQRFLAA YSSEGSIRTI DAYWRDEILN KYYGALLYNE Y GLFNAHSS VGRDCLSDTI RQSATFAGLD KVDNAQMIQM ERLFIAKLVP GFDASTDVPK KIWTTDPIYA GARGAVEEIW QG IQDWNEI LWAGHAVYDA TFGQFARREF FQRLATVYGD TLTPFFTAQS QTYFQTTRGA IEDLFVYCLA NDPEFGAHNR TFL NAWTEH YLARSVTALK DFVGIYAKVE KVAGATDRAG VSEALQRVFG DWKVDYADKI GFNIDVDQKV DAVLAGFKN UniProtKB: Methane monooxygenase |
-Macromolecule #3: Methane monooxygenase
Macromolecule | Name: Methane monooxygenase / type: protein_or_peptide / ID: 3 / Number of copies: 2 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 19.379207 KDa |
Sequence | String: MAKREPIHEN STRTEWEGKI AKLNSVDQAT KFIQDFRVAY SSPFRKSYDL DVDYQYIERK IEERLSVLKT EKLSVADLVT KATTGEDAA AVEAAWIAKM KAAESKYAAE RIHIEFRQLY KPPVLPVNVF LRTDAALGTI LMELRNTDYY ATPLEGLRKE R GVKVLHLQ A UniProtKB: Methane monooxygenase |
-Macromolecule #4: Methane monooxygenase
Macromolecule | Name: Methane monooxygenase / type: protein_or_peptide / ID: 4 / Number of copies: 1 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 14.916896 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MSSAHNAYNA GIMQKTGKAF ADEFFAEENQ VVHESNAVVL VLMKSDEIDA IIEDMVLKGG KAKNPSIVVE DKAGFWWIKA DGAIEIDAA EASDLLGKPF SVYDLLVNVS STVGRAYTLG TKFTITSELM GLDRALTDI UniProtKB: Methane monooxygenase |
-Macromolecule #5: FE (III) ION
Macromolecule | Name: FE (III) ION / type: ligand / ID: 5 / Number of copies: 4 / Formula: FE |
---|---|
Molecular weight | Theoretical: 55.845 Da |
-Macromolecule #6: water
Macromolecule | Name: water / type: ligand / ID: 6 / Number of copies: 94 / Formula: HOH |
---|---|
Molecular weight | Theoretical: 18.015 Da |
Chemical component information | ![]() ChemComp-HOH: |
-Experimental details
-Structure determination
Method | cryo EM |
---|---|
![]() | single particle reconstruction |
Aggregation state | particle |
-
Sample preparation
Concentration | 2.0 mg/mL |
---|---|
Buffer | pH: 6.5 |
Grid | Model: Quantifoil R1.2/1.3 / Material: COPPER / Mesh: 200 / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 60 sec. / Pretreatment - Atmosphere: AIR / Pretreatment - Pressure: 101.325 kPa |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277.15 K / Instrument: FEI VITROBOT MARK IV |
-
Electron microscopy
Microscope | TFS KRIOS |
---|---|
Temperature | Min: 70.0 K / Max: 70.0 K |
Specialist optics | Energy filter - Name: GIF Bioquantum / Energy filter - Slit width: 20 eV |
Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Digitization - Dimensions - Width: 5760 pixel / Digitization - Dimensions - Height: 4092 pixel / Number grids imaged: 1 / Number real images: 9471 / Average exposure time: 5.24 sec. / Average electron dose: 58.2 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | C2 aperture diameter: 70.0 µm / Calibrated defocus max: 3.8000000000000003 µm / Calibrated defocus min: 0.445 µm / Calibrated magnification: 58893 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.3000000000000003 µm / Nominal defocus min: 0.9 µm / Nominal magnification: 105000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |