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- PDB-6j0p: Crystal structure of HypX from Aquifex aeolicus (Crystal Form I) -

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Basic information

Entry
Database: PDB / ID: 6j0p
TitleCrystal structure of HypX from Aquifex aeolicus (Crystal Form I)
ComponentsHydrogenase regulation HoxX
KeywordsBIOSYNTHETIC PROTEIN / Hydrogenase / maturation / carbon monoxide
Function / homology
Function and homology information


biosynthetic process / catalytic activity
Similarity search - Function
[NiFe]-hydrogenase maturation factor, HypX/HoxX type / : / Formyl transferase, C-terminal / Formyl transferase, C-terminal domain / Formyl transferase-like, C-terminal domain superfamily / Formyl transferase, N-terminal / Formyl transferase / Formyl transferase, N-terminal domain superfamily / Enoyl-CoA hydratase/isomerase, conserved site / Enoyl-CoA hydratase/isomerase signature. ...[NiFe]-hydrogenase maturation factor, HypX/HoxX type / : / Formyl transferase, C-terminal / Formyl transferase, C-terminal domain / Formyl transferase-like, C-terminal domain superfamily / Formyl transferase, N-terminal / Formyl transferase / Formyl transferase, N-terminal domain superfamily / Enoyl-CoA hydratase/isomerase, conserved site / Enoyl-CoA hydratase/isomerase signature. / Enoyl-CoA hydratase/isomerase / Enoyl-CoA hydratase/isomerase / ClpP/crotonase-like domain superfamily
Similarity search - Domain/homology
COENZYME A / Hydrogenase regulation HoxX
Similarity search - Component
Biological speciesAquifex aeolicus (bacteria)
MethodX-RAY DIFFRACTION / SYNCHROTRON / SAD / Resolution: 1.79 Å
AuthorsMuraki, N. / Aono, S.
Funding support Japan, 1items
OrganizationGrant numberCountry
Japan Society for the Promotion of Science17H03093 Japan
CitationJournal: Commun Biol / Year: 2019
Title: Structural characterization of HypX responsible for CO biosynthesis in the maturation of NiFe-hydrogenase.
Authors: Muraki, N. / Ishii, K. / Uchiyama, S. / Itoh, S.G. / Okumura, H. / Aono, S.
History
DepositionDec 25, 2018Deposition site: PDBJ / Processing site: PDBJ
Revision 1.0Nov 6, 2019Provider: repository / Type: Initial release
Revision 1.1Mar 27, 2024Group: Data collection / Database references / Category: chem_comp_atom / chem_comp_bond / database_2
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: Hydrogenase regulation HoxX
B: Hydrogenase regulation HoxX
hetero molecules


Theoretical massNumber of molelcules
Total (without water)137,2526
Polymers135,5332
Non-polymers1,7194
Water7,062392
1
A: Hydrogenase regulation HoxX
hetero molecules


Theoretical massNumber of molelcules
Total (without water)68,6263
Polymers67,7661
Non-polymers8602
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area100 Å2
ΔGint-10 kcal/mol
Surface area24300 Å2
MethodPISA
2
B: Hydrogenase regulation HoxX
hetero molecules


Theoretical massNumber of molelcules
Total (without water)68,6263
Polymers67,7661
Non-polymers8602
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area0 Å2
ΔGint0 kcal/mol
Surface area24140 Å2
MethodPISA
Unit cell
Length a, b, c (Å)79.840, 124.300, 290.850
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number20
Space group name H-MC2221

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Components

#1: Protein Hydrogenase regulation HoxX / HypX


Mass: 67766.445 Da / Num. of mol.: 2
Source method: isolated from a genetically manipulated source
Details: SF file contains Friedel pairs.
Source: (gene. exp.) Aquifex aeolicus (strain VF5) (bacteria)
Strain: VF5 / Gene: hoxX, aq_1156 / Plasmid: pET15b / Production host: Escherichia coli BL21(DE3) (bacteria) / References: UniProt: O67224
#2: Chemical ChemComp-COA / COENZYME A


Mass: 767.534 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C21H36N7O16P3S
#3: Chemical ChemComp-GOL / GLYCEROL / GLYCERIN / PROPANE-1,2,3-TRIOL


Mass: 92.094 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C3H8O3
#4: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 392 / Source method: isolated from a natural source / Formula: H2O

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Experimental details

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Experiment

ExperimentMethod: X-RAY DIFFRACTION / Number of used crystals: 1

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Sample preparation

CrystalDensity Matthews: 2.74 Å3/Da / Density % sol: 55.16 %
Crystal growTemperature: 293 K / Method: vapor diffusion, sitting drop / Details: 20% PEG3350, HEPES-NaOH / PH range: 7.0 - 7.5

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Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: SPring-8 / Beamline: BL44XU / Wavelength: 0.9 Å
DetectorType: RAYONIX MX300HE / Detector: CCD / Date: Oct 12, 2017
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.9 Å / Relative weight: 1
ReflectionResolution: 1.79→42.47 Å / Num. obs: 134916 / % possible obs: 98.8 % / Redundancy: 7.5 % / Biso Wilson estimate: 28.65 Å2 / CC1/2: 0.999 / Rmerge(I) obs: 0.073 / Rpim(I) all: 0.029 / Rrim(I) all: 0.078 / Net I/σ(I): 16.77
Reflection shellResolution: 1.79→1.86 Å / Redundancy: 7.5 % / Rmerge(I) obs: 1.094 / Mean I/σ(I) obs: 1.6 / Num. unique obs: 11960 / CC1/2: 0.677 / Rpim(I) all: 0.4255 / Rrim(I) all: 1.175 / % possible all: 89.1

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Processing

Software
NameVersionClassification
PHENIX(1.13_2998: ???)refinement
XDSdata reduction
XSCALEdata scaling
PHENIXphasing
Cootmodel building
RefinementMethod to determine structure: SAD / Resolution: 1.79→42.47 Å / SU ML: 0.22 / Cross valid method: FREE R-VALUE / σ(F): 1.23 / Phase error: 19.48
RfactorNum. reflection% reflectionSelection details
Rfree0.196 6685 5 %Random selection
Rwork0.173 ---
obs0.1739 133690 98.74 %-
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å
Refinement stepCycle: LAST / Resolution: 1.79→42.47 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms9174 0 108 392 9674
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0079666
X-RAY DIFFRACTIONf_angle_d0.81313085
X-RAY DIFFRACTIONf_dihedral_angle_d15.7765790
X-RAY DIFFRACTIONf_chiral_restr0.0561360
X-RAY DIFFRACTIONf_plane_restr0.0051675
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
1.7932-1.81350.51592880.4725452X-RAY DIFFRACTION65
1.8135-1.83490.33484310.34078238X-RAY DIFFRACTION100
1.8349-1.85730.33484380.30988355X-RAY DIFFRACTION100
1.8573-1.88080.29534360.27128279X-RAY DIFFRACTION100
1.8808-1.90550.30164340.24438309X-RAY DIFFRACTION100
1.9055-1.93160.26924360.21978277X-RAY DIFFRACTION100
1.9316-1.95920.2194440.19998295X-RAY DIFFRACTION100
1.9592-1.98850.24384400.19138360X-RAY DIFFRACTION100
1.9885-2.01950.22524330.19278202X-RAY DIFFRACTION100
2.0195-2.05260.20854480.19568421X-RAY DIFFRACTION100
2.0526-2.0880.20444210.1988197X-RAY DIFFRACTION100
2.088-2.1260.21224340.19658329X-RAY DIFFRACTION100
2.126-2.16690.20874410.17758367X-RAY DIFFRACTION100
2.1669-2.21110.20584350.17648244X-RAY DIFFRACTION100
2.2111-2.25920.22114410.17798301X-RAY DIFFRACTION100
2.2592-2.31180.19364280.17618308X-RAY DIFFRACTION100
2.3118-2.36960.2224380.17038298X-RAY DIFFRACTION100
2.3696-2.43360.19574330.1768302X-RAY DIFFRACTION100
2.4336-2.50520.20544340.17448323X-RAY DIFFRACTION100
2.5052-2.58610.18624380.17388306X-RAY DIFFRACTION100
2.5861-2.67850.1994310.17188299X-RAY DIFFRACTION100
2.6785-2.78580.21534360.17258249X-RAY DIFFRACTION100
2.7858-2.91250.21284410.1798296X-RAY DIFFRACTION100
2.9125-3.06610.19624430.17118389X-RAY DIFFRACTION100
3.0661-3.25810.18554370.1728264X-RAY DIFFRACTION100
3.2581-3.50960.19074460.1588314X-RAY DIFFRACTION100
3.5096-3.86270.16434380.1528290X-RAY DIFFRACTION100
3.8627-4.42130.15844340.14118283X-RAY DIFFRACTION100
4.4213-5.5690.15114310.1438275X-RAY DIFFRACTION100
5.569-42.470.19784310.17288105X-RAY DIFFRACTION97
Refinement TLS params.

Method: refined / Refine-ID: X-RAY DIFFRACTION

IDL112)L122)L132)L222)L232)L332)S11 (Å °)S12 (Å °)S13 (Å °)S21 (Å °)S22 (Å °)S23 (Å °)S31 (Å °)S32 (Å °)S33 (Å °)T112)T122)T132)T222)T232)T332)Origin x (Å)Origin y (Å)Origin z (Å)
10.70260.0953-0.11080.73650.060.6421-0.04490.04450.0479-0.07270.03730.007-0.049-0.00580.02820.1521-0.0019-0.01360.15-0.0130.1779-15.0171-18.628120.6595
21.14430.00810.00261.02820.10980.71510.0075-0.2192-0.04770.2554-0.06140.0057-0.0122-0.01770.02540.2323-0.0151-0.00570.24770.0130.195420.8516-11.018456.9513
Refinement TLS group
IDRefine-IDRefine TLS-IDSelection details
1X-RAY DIFFRACTION1(chain 'A' and resid -1 through 562)
2X-RAY DIFFRACTION2(chain 'B' and resid -1 through 561)

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