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- PDB-9jiv: Macrophage migration inhibitory factor Y100H mutant (MIF(Y100H)) -

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Basic information

Entry
Database: PDB / ID: 9jiv
TitleMacrophage migration inhibitory factor Y100H mutant (MIF(Y100H))
ComponentsMacrophage migration inhibitory factor
KeywordsCYTOKINE / Macrophage migration inhibitory factor
Function / homology
Function and homology information


positive regulation of prostaglandin secretion involved in immune response / positive regulation of myeloid leukocyte cytokine production involved in immune response / dopachrome isomerase activity / phenylpyruvate tautomerase / L-dopachrome isomerase / phenylpyruvate tautomerase activity / positive regulation of arachidonate secretion / cytokine receptor binding / negative regulation of myeloid cell apoptotic process / negative regulation of macrophage chemotaxis ...positive regulation of prostaglandin secretion involved in immune response / positive regulation of myeloid leukocyte cytokine production involved in immune response / dopachrome isomerase activity / phenylpyruvate tautomerase / L-dopachrome isomerase / phenylpyruvate tautomerase activity / positive regulation of arachidonate secretion / cytokine receptor binding / negative regulation of myeloid cell apoptotic process / negative regulation of macrophage chemotaxis / negative regulation of mature B cell apoptotic process / carboxylic acid metabolic process / positive regulation of lipopolysaccharide-mediated signaling pathway / positive regulation of chemokine (C-X-C motif) ligand 2 production / prostaglandin biosynthetic process / negative regulation of protein metabolic process / negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator / regulation of macrophage activation / chemoattractant activity / protein homotrimerization / negative regulation of DNA damage response, signal transduction by p53 class mediator / positive regulation of cAMP/PKA signal transduction / negative regulation of cellular senescence / positive regulation of phosphorylation / positive regulation of B cell proliferation / Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation / negative regulation of cell migration / positive regulation of cytokine production / cytokine activity / Cell surface interactions at the vascular wall / DNA damage response, signal transduction by p53 class mediator / positive regulation of fibroblast proliferation / positive regulation of tumor necrosis factor production / cellular senescence / protease binding / secretory granule lumen / vesicle / ficolin-1-rich granule lumen / cell surface receptor signaling pathway / positive regulation of ERK1 and ERK2 cascade / inflammatory response / negative regulation of gene expression / innate immune response / positive regulation of cell population proliferation / Neutrophil degranulation / negative regulation of apoptotic process / cell surface / extracellular space / extracellular exosome / extracellular region / nucleoplasm / identical protein binding / plasma membrane / cytoplasm / cytosol
Similarity search - Function
Macrophage migration inhibitory factor, conserved site / Macrophage migration inhibitory factor family signature. / Macrophage migration inhibitory factor / Macrophage migration inhibitory factor (MIF) / Tautomerase/MIF superfamily
Similarity search - Domain/homology
ISOPROPYL ALCOHOL / Macrophage migration inhibitory factor
Similarity search - Component
Biological speciesHomo sapiens (human)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.25 Å
AuthorsHimiyama, T. / Okamoto, Y.
Funding support Japan, 5items
OrganizationGrant numberCountry
Japan Science and TechnologyJPMJAX1913 Japan
Japan Science and TechnologyJPMJPR22A4 Japan
Japan Science and TechnologyJPMJFR212H Japan
Japan Society for the Promotion of Science (JSPS)21H05118 Japan
Japan Society for the Promotion of Science (JSPS)24K08609 Japan
CitationJournal: Nat Commun / Year: 2025
Title: A cytokine-based designer enzyme with an abiological multinuclear metal center exhibits intrinsic and extrinsic catalysis.
Authors: Ueno, A. / Takida, F. / Kita, T. / Ishii, T. / Himiyama, T. / Mabuchi, T. / Okamoto, Y.
History
DepositionSep 12, 2024Deposition site: PDBJ / Processing site: PDBJ
Revision 1.0Aug 6, 2025Provider: repository / Type: Initial release
Revision 1.1Aug 13, 2025Group: Database references / Category: citation
Item: _citation.journal_volume / _citation.page_first ..._citation.journal_volume / _citation.page_first / _citation.page_last / _citation.pdbx_database_id_PubMed / _citation.title

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Macrophage migration inhibitory factor
B: Macrophage migration inhibitory factor
C: Macrophage migration inhibitory factor
hetero molecules


Theoretical massNumber of molelcules
Total (without water)38,22413
Polymers37,3843
Non-polymers84110
Water10,178565
1


  • Idetical with deposited unit
  • defined by author&software
  • Evidence: light scattering
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area8800 Å2
ΔGint-88 kcal/mol
Surface area13140 Å2
MethodPISA
Unit cell
Length a, b, c (Å)67.917, 68.172, 87.315
Angle α, β, γ (deg.)90.000, 90.000, 90.000
Int Tables number19
Space group name H-MP212121

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Components

#1: Protein Macrophage migration inhibitory factor / MIF / Glycosylation-inhibiting factor / GIF / L-dopachrome isomerase / L-dopachrome tautomerase / ...MIF / Glycosylation-inhibiting factor / GIF / L-dopachrome isomerase / L-dopachrome tautomerase / Phenylpyruvate tautomerase


Mass: 12461.225 Da / Num. of mol.: 3 / Mutation: Y100H
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: MIF, GLIF, MMIF / Production host: Escherichia coli (E. coli)
References: UniProt: P14174, phenylpyruvate tautomerase, L-dopachrome isomerase
#2: Chemical
ChemComp-SO4 / SULFATE ION


Mass: 96.063 Da / Num. of mol.: 4 / Source method: obtained synthetically / Formula: SO4
#3: Chemical ChemComp-GOL / GLYCEROL / GLYCERIN / PROPANE-1,2,3-TRIOL


Mass: 92.094 Da / Num. of mol.: 3 / Source method: obtained synthetically / Formula: C3H8O3
#4: Chemical ChemComp-IPA / ISOPROPYL ALCOHOL / 2-PROPANOL


Mass: 60.095 Da / Num. of mol.: 3 / Source method: obtained synthetically / Formula: C3H8O
#5: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 565 / Source method: isolated from a natural source / Formula: H2O
Has ligand of interestN
Has protein modificationN

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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: 2.7 Å3/Da / Density % sol: 54.5 %
Crystal growTemperature: 293 K / Method: vapor diffusion, hanging drop / pH: 7.5
Details: 2.0M ammonium sulfate, 20mM Tris-HCl buffer (pH 7.5), 3% isopropanol

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Data collection

DiffractionMean temperature: 100 K / Serial crystal experiment: N
Diffraction sourceSource: SYNCHROTRON / Site: SPring-8 / Beamline: BL45XU / Wavelength: 1 Å
DetectorType: DECTRIS EIGER X 16M / Detector: PIXEL / Date: Nov 22, 2021
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1 Å / Relative weight: 1
ReflectionResolution: 1.25→48.161 Å / Num. obs: 112191 / % possible obs: 99.7 % / Redundancy: 8.4 % / CC1/2: 0.999 / Rmerge(I) obs: 0.046 / Net I/σ(I): 19.7
Reflection shellResolution: 1.25→1.27 Å / Rmerge(I) obs: 0.681 / Mean I/σ(I) obs: 3 / Num. unique obs: 5484 / CC1/2: 0.845

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Processing

Software
NameVersionClassification
REFMAC5.8.0419refinement
XDSdata reduction
Aimlessdata scaling
MOLREPphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.25→48.161 Å / Cor.coef. Fo:Fc: 0.982 / Cor.coef. Fo:Fc free: 0.976 / SU B: 1.152 / SU ML: 0.022 / Cross valid method: THROUGHOUT / ESU R: 0.033 / ESU R Free: 0.034
Details: Hydrogens have been added in their riding positions
RfactorNum. reflection% reflection
Rfree0.1517 5670 5.058 %
Rwork0.1254 106438 -
all0.127 --
obs-112108 99.676 %
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: BABINET MODEL PLUS MASK
Displacement parametersBiso mean: 16.159 Å2
Baniso -1Baniso -2Baniso -3
1-0.008 Å20 Å2-0 Å2
2--0.023 Å20 Å2
3----0.031 Å2
Refinement stepCycle: LAST / Resolution: 1.25→48.161 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms2595 0 50 565 3210
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.0130.0122796
X-RAY DIFFRACTIONr_bond_other_d0.0010.0162620
X-RAY DIFFRACTIONr_angle_refined_deg1.8581.7913819
X-RAY DIFFRACTIONr_angle_other_deg0.7011.7196026
X-RAY DIFFRACTIONr_dihedral_angle_1_deg5.7645363
X-RAY DIFFRACTIONr_dihedral_angle_2_deg6.605515
X-RAY DIFFRACTIONr_dihedral_angle_3_deg10.88710427
X-RAY DIFFRACTIONr_dihedral_angle_6_deg17.27610116
X-RAY DIFFRACTIONr_chiral_restr0.1130.2430
X-RAY DIFFRACTIONr_chiral_restr_other0.0210.23
X-RAY DIFFRACTIONr_gen_planes_refined0.010.023370
X-RAY DIFFRACTIONr_gen_planes_other0.0010.02644
X-RAY DIFFRACTIONr_nbd_refined0.2320.2483
X-RAY DIFFRACTIONr_symmetry_nbd_other0.1940.22439
X-RAY DIFFRACTIONr_nbtor_refined0.1760.21349
X-RAY DIFFRACTIONr_symmetry_nbtor_other0.0810.21463
X-RAY DIFFRACTIONr_xyhbond_nbd_refined0.2340.2330
X-RAY DIFFRACTIONr_symmetry_xyhbond_nbd_other0.1510.21
X-RAY DIFFRACTIONr_symmetry_nbd_refined0.1510.26
X-RAY DIFFRACTIONr_nbd_other0.2010.233
X-RAY DIFFRACTIONr_symmetry_xyhbond_nbd_refined0.2260.232
X-RAY DIFFRACTIONr_mcbond_it3.6731.5211428
X-RAY DIFFRACTIONr_mcbond_other3.6681.5211428
X-RAY DIFFRACTIONr_mcangle_it4.7052.7421799
X-RAY DIFFRACTIONr_mcangle_other4.7042.7421800
X-RAY DIFFRACTIONr_scbond_it7.6881.8741368
X-RAY DIFFRACTIONr_scbond_other7.6851.8741369
X-RAY DIFFRACTIONr_scangle_it10.2863.292020
X-RAY DIFFRACTIONr_scangle_other10.2833.292021
X-RAY DIFFRACTIONr_lrange_it15.9721.553172
X-RAY DIFFRACTIONr_lrange_other13.12316.9292961
X-RAY DIFFRACTIONr_rigid_bond_restr4.6735416
LS refinement shell

Refine-ID: X-RAY DIFFRACTION / Total num. of bins used: 20

Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRfactor allNum. reflection allFsc freeFsc work% reflection obs (%)WRfactor Rwork
1.25-1.2820.2153800.1978140.19182250.9660.97499.62310.16
1.282-1.3180.2084030.18175760.18380180.9710.97799.51360.151
1.318-1.3560.193880.15973760.16178010.9760.98299.52570.13
1.356-1.3970.1684210.14171240.14275770.980.98699.57770.115
1.397-1.4430.1543630.12169750.12373510.9830.9999.82320.098
1.443-1.4940.1633680.11367500.11671250.9830.99199.90180.095
1.494-1.550.1443640.10665190.10868960.9860.99399.81150.091
1.55-1.6130.1553060.10262950.10566140.9850.99399.80350.09
1.613-1.6850.133620.09659850.09863710.9890.99499.62330.086
1.685-1.7670.1382520.158030.10260800.9880.99399.58880.093
1.767-1.8630.1322720.09655270.09758010.9890.99499.96550.091
1.863-1.9750.1282790.10152280.10255310.990.99499.56610.1
1.975-2.1120.1342740.10248810.10451620.9890.99399.86440.105
2.112-2.280.1462570.11345830.11548560.9860.99299.67050.119
2.28-2.4970.1422410.12142000.12344650.9870.99199.46250.131
2.497-2.7910.1652080.13138040.13240450.9840.9999.18420.143
2.791-3.2210.1621860.13534270.13636210.9820.98899.77910.152
3.221-3.9410.1451410.13129250.13230730.9870.98999.77220.153
3.941-5.5550.1411400.13322830.13324230.990.991000.162
5.555-48.1610.212650.20213630.20214350.9670.97199.51220.241

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