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- PDB-6d48: Cell Surface Receptor -

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Basic information

Entry
Database: PDB / ID: 6d48
TitleCell Surface Receptor
ComponentsMyeloid cell surface antigen CD33
KeywordsIMMUNE SYSTEM / Sialic Acid Binding / Transmembrane / Receptor / Siglec
Function / homology
Function and homology information


immune response-inhibiting signal transduction / positive regulation of protein tyrosine phosphatase activity / negative regulation of monocyte activation / sialic acid binding / negative regulation of interleukin-8 production / negative regulation of interleukin-1 beta production / tertiary granule membrane / negative regulation of calcium ion transport / negative regulation of tumor necrosis factor production / specific granule membrane ...immune response-inhibiting signal transduction / positive regulation of protein tyrosine phosphatase activity / negative regulation of monocyte activation / sialic acid binding / negative regulation of interleukin-8 production / negative regulation of interleukin-1 beta production / tertiary granule membrane / negative regulation of calcium ion transport / negative regulation of tumor necrosis factor production / specific granule membrane / positive regulation of protein secretion / cell-cell adhesion / peroxisome / Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell / cell-cell signaling / signaling receptor activity / carbohydrate binding / protein phosphatase binding / cell adhesion / negative regulation of cell population proliferation / external side of plasma membrane / Neutrophil degranulation / Golgi apparatus / cell surface / signal transduction / nucleoplasm / plasma membrane
Similarity search - Function
Immunoglobulin / Immunoglobulin domain / Immunoglobulin V-set domain / Immunoglobulin V-set domain / Immunoglobulin subtype / Immunoglobulin / Ig-like domain profile. / Immunoglobulin-like domain / Immunoglobulin-like domain superfamily / Immunoglobulins ...Immunoglobulin / Immunoglobulin domain / Immunoglobulin V-set domain / Immunoglobulin V-set domain / Immunoglobulin subtype / Immunoglobulin / Ig-like domain profile. / Immunoglobulin-like domain / Immunoglobulin-like domain superfamily / Immunoglobulins / Immunoglobulin-like fold / Immunoglobulin-like / Sandwich / Mainly Beta
Similarity search - Domain/homology
Myeloid cell surface antigen CD33
Similarity search - Component
Biological speciesHomo sapiens (human)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.776 Å
AuthorsHermans, S.J. / Miles, L.A. / Parker, M.W.
CitationJournal: Iscience / Year: 2019
Title: Small Molecule Binding to Alzheimer Risk Factor CD33 Promotes A beta Phagocytosis.
Authors: Miles, L.A. / Hermans, S.J. / Crespi, G.A.N. / Gooi, J.H. / Doughty, L. / Nero, T.L. / Markulic, J. / Ebneth, A. / Wroblowski, B. / Oehlrich, D. / Trabanco, A.A. / Rives, M.L. / Royaux, I. / ...Authors: Miles, L.A. / Hermans, S.J. / Crespi, G.A.N. / Gooi, J.H. / Doughty, L. / Nero, T.L. / Markulic, J. / Ebneth, A. / Wroblowski, B. / Oehlrich, D. / Trabanco, A.A. / Rives, M.L. / Royaux, I. / Hancock, N.C. / Parker, M.W.
History
DepositionApr 17, 2018Deposition site: RCSB / Processing site: RCSB
Revision 1.0Apr 17, 2019Provider: repository / Type: Initial release
Revision 1.1Oct 30, 2019Group: Data collection / Database references / Category: citation / citation_author
Item: _citation.country / _citation.journal_abbrev ..._citation.country / _citation.journal_abbrev / _citation.journal_id_CSD / _citation.journal_id_ISSN / _citation.journal_volume / _citation.page_first / _citation.page_last / _citation.pdbx_database_id_DOI / _citation.pdbx_database_id_PubMed / _citation.title / _citation.year
Revision 1.2Oct 4, 2023Group: Data collection / Database references ...Data collection / Database references / Derived calculations / Refinement description
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_initial_refinement_model / struct_conn
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _struct_conn.pdbx_dist_value / _struct_conn.ptnr1_auth_asym_id / _struct_conn.ptnr1_auth_seq_id / _struct_conn.ptnr1_label_asym_id / _struct_conn.ptnr1_label_seq_id / _struct_conn.ptnr2_auth_asym_id / _struct_conn.ptnr2_auth_seq_id / _struct_conn.ptnr2_label_asym_id / _struct_conn.ptnr2_label_seq_id / _struct_conn.ptnr2_symmetry

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
E: Myeloid cell surface antigen CD33
F: Myeloid cell surface antigen CD33
G: Myeloid cell surface antigen CD33
H: Myeloid cell surface antigen CD33


Theoretical massNumber of molelcules
Total (without water)58,5934
Polymers58,5934
Non-polymers00
Water8,827490
1
E: Myeloid cell surface antigen CD33


Theoretical massNumber of molelcules
Total (without water)14,6481
Polymers14,6481
Non-polymers00
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
2
F: Myeloid cell surface antigen CD33


Theoretical massNumber of molelcules
Total (without water)14,6481
Polymers14,6481
Non-polymers00
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
3
G: Myeloid cell surface antigen CD33


Theoretical massNumber of molelcules
Total (without water)14,6481
Polymers14,6481
Non-polymers00
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
4
H: Myeloid cell surface antigen CD33


Theoretical massNumber of molelcules
Total (without water)14,6481
Polymers14,6481
Non-polymers00
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
Unit cell
Length a, b, c (Å)60.801, 41.543, 107.498
Angle α, β, γ (deg.)90.00, 96.55, 90.00
Int Tables number4
Space group name H-MP1211

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Components

#1: Protein
Myeloid cell surface antigen CD33 / Sialic acid-binding Ig-like lectin 3 / Siglec-3 / gp67


Mass: 14648.298 Da / Num. of mol.: 4
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: CD33, SIGLEC3 / Production host: Escherichia coli (E. coli) / References: UniProt: P20138
#2: Water ChemComp-HOH / water / Water


Mass: 18.015 Da / Num. of mol.: 490 / 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: 2.38 Å3/Da / Density % sol: 48.31 % / Description: Cubic
Crystal growTemperature: 293 K / Method: vapor diffusion, hanging drop / pH: 8.5 / Details: 25% PEG 4000 100 mM Tris-HCl pH 8.5 10% Glycerol

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: Australian Synchrotron / Beamline: MX2 / Wavelength: 0.9537 Å
DetectorType: ADSC QUANTUM 315r / Detector: CCD / Date: Nov 17, 2013
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.9537 Å / Relative weight: 1
ReflectionResolution: 1.776→42.48 Å / Num. obs: 51251 / % possible obs: 98.5 % / Redundancy: 3.4 % / CC1/2: 0.999 / Rmerge(I) obs: 0.044 / Rpim(I) all: 0.028 / Rrim(I) all: 0.052 / Net I/σ(I): 14.7
Reflection shellResolution: 1.776→1.81 Å / Redundancy: 3.2 % / Rmerge(I) obs: 0.391 / Mean I/σ(I) obs: 3.1 / Num. unique obs: 2673 / Rpim(I) all: 0.246 / Rrim(I) all: 0.464 / % possible all: 90.3

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Processing

Software
NameVersionClassification
PHENIX(1.11.1-2575_1496: ???)refinement
XDSdata reduction
Aimlessdata scaling
PHASERphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 1NKO
Resolution: 1.776→35.599 Å / SU ML: 0.18 / Cross valid method: FREE R-VALUE / σ(F): 1.34 / Phase error: 21.54 / Stereochemistry target values: ML
RfactorNum. reflection% reflection
Rfree0.2122 2485 4.85 %
Rwork0.1756 --
obs0.1774 51235 98.46 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL
Refinement stepCycle: LAST / Resolution: 1.776→35.599 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms4040 0 0 490 4530
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.014170
X-RAY DIFFRACTIONf_angle_d0.9795669
X-RAY DIFFRACTIONf_dihedral_angle_d12.7422503
X-RAY DIFFRACTIONf_chiral_restr0.062594
X-RAY DIFFRACTIONf_plane_restr0.008751
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
1.7761-1.81030.29061310.23052467X-RAY DIFFRACTION90
1.8103-1.84730.27681290.22072717X-RAY DIFFRACTION100
1.8473-1.88740.28641490.2062780X-RAY DIFFRACTION100
1.8874-1.93130.25261410.21772635X-RAY DIFFRACTION100
1.9313-1.97960.26181430.19612780X-RAY DIFFRACTION100
1.9796-2.03310.22481360.18612703X-RAY DIFFRACTION100
2.0331-2.0930.22071590.1682738X-RAY DIFFRACTION100
2.093-2.16050.22111180.1662723X-RAY DIFFRACTION100
2.1605-2.23770.19411330.17112735X-RAY DIFFRACTION100
2.2377-2.32730.20691380.17172726X-RAY DIFFRACTION100
2.3273-2.43320.21751340.17112773X-RAY DIFFRACTION100
2.4332-2.56140.22791560.1842694X-RAY DIFFRACTION99
2.5614-2.72190.2321360.18632736X-RAY DIFFRACTION100
2.7219-2.93190.20051280.17752745X-RAY DIFFRACTION99
2.9319-3.22680.22231620.18072722X-RAY DIFFRACTION99
3.2268-3.69330.20681400.16292687X-RAY DIFFRACTION98
3.6933-4.65160.16251310.14312728X-RAY DIFFRACTION97
4.6516-35.60610.2071210.18912661X-RAY DIFFRACTION92

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