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- PDB-1ysx: Solution structure of domain 3 from human serum albumin complexed... -

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Basic information

Entry
Database: PDB / ID: 1ysx
TitleSolution structure of domain 3 from human serum albumin complexed to an anti-apoptotic ligand directed against Bcl-xL and Bcl-2
ComponentsSerum albumin
KeywordsAPOPTOSIS / COMPLEX
Function / homology
Function and homology information


exogenous protein binding / Ciprofloxacin ADME / enterobactin binding / cellular response to calcium ion starvation / Heme biosynthesis / HDL remodeling / negative regulation of mitochondrial depolarization / Prednisone ADME / Heme degradation / Aspirin ADME ...exogenous protein binding / Ciprofloxacin ADME / enterobactin binding / cellular response to calcium ion starvation / Heme biosynthesis / HDL remodeling / negative regulation of mitochondrial depolarization / Prednisone ADME / Heme degradation / Aspirin ADME / antioxidant activity / toxic substance binding / Scavenging of heme from plasma / Recycling of bile acids and salts / cellular response to starvation / platelet alpha granule lumen / fatty acid binding / Post-translational protein phosphorylation / Cytoprotection by HMOX1 / Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) / pyridoxal phosphate binding / Platelet degranulation / protein-folding chaperone binding / blood microparticle / copper ion binding / endoplasmic reticulum lumen / Golgi apparatus / endoplasmic reticulum / protein-containing complex / DNA binding / extracellular space / extracellular exosome / extracellular region / identical protein binding / nucleus / cytoplasm
Similarity search - Function
Serum albumin/Alpha-fetoprotein/Afamin / ALB/AFP/VDB / Serum albumin, N-terminal / Serum albumin, conserved site / Serum albumin-like / Serum albumin family / Albumin domain signature. / Albumin domain profile. / serum albumin
Similarity search - Domain/homology
Biological speciesHomo sapiens (human)
MethodSOLUTION NMR / simulated annealing
AuthorsOltersdorf, T. / Elmore, S.W. / Shoemaker, A.R. / Armstrong, R.C. / Augeri, D.J. / Belli, B.A. / Bruncko, M. / Deckwerth, T.L. / Dinges, J. / Hajduk, P.J. ...Oltersdorf, T. / Elmore, S.W. / Shoemaker, A.R. / Armstrong, R.C. / Augeri, D.J. / Belli, B.A. / Bruncko, M. / Deckwerth, T.L. / Dinges, J. / Hajduk, P.J. / Joseph, M.K. / Kitada, S. / Korsmeyer, S.J. / Kunzer, A.R. / Letai, A. / Li, C. / Mitten, M.J. / Nettesheim, D.G. / Ng, S. / Nimmer, P.M. / O'Connor, J.M. / Oleksijew, A. / Petros, A.M. / Reed, J.C. / Shen, W. / Tahir, S.K. / Thompson, C.B. / Tomaselli, K.J. / Wang, B. / Wendt, M.D. / Zhang, H. / Fesik, S.W. / Rosenberg, S.H.
CitationJournal: Nature / Year: 2005
Title: An inhibitor of Bcl-2 family proteins induces regression of solid tumours
Authors: Oltersdorf, T. / Elmore, S.W. / Shoemaker, A.R. / Armstrong, R.C. / Augeri, D.J. / Belli, B.A. / Bruncko, M. / Deckwerth, T.L. / Dinges, J. / Hajduk, P.J. / Joseph, M.K. / Kitada, S. / ...Authors: Oltersdorf, T. / Elmore, S.W. / Shoemaker, A.R. / Armstrong, R.C. / Augeri, D.J. / Belli, B.A. / Bruncko, M. / Deckwerth, T.L. / Dinges, J. / Hajduk, P.J. / Joseph, M.K. / Kitada, S. / Korsmeyer, S.J. / Kunzer, A.R. / Letai, A. / Li, C. / Mitten, M.J. / Nettesheim, D.G. / Ng, S. / Nimmer, P.M. / O'Connor, J.M. / Oleksijew, A. / Petros, A.M. / Reed, J.C. / Shen, W. / Tahir, S.K. / Thompson, C.B. / Tomaselli, K.J. / Wang, B. / Wendt, M.D. / Zhang, H. / Fesik, S.W. / Rosenberg, S.H.
History
DepositionFeb 9, 2005Deposition site: RCSB / Processing site: RCSB
Revision 1.0Jun 7, 2005Provider: repository / Type: Initial release
Revision 1.1Apr 30, 2008Group: Version format compliance
Revision 1.2Jul 13, 2011Group: Version format compliance
Revision 1.3Mar 2, 2022Group: Database references / Derived calculations
Category: database_2 / pdbx_struct_assembly ...database_2 / pdbx_struct_assembly / pdbx_struct_oper_list / struct_site
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _struct_site.pdbx_auth_asym_id / _struct_site.pdbx_auth_comp_id / _struct_site.pdbx_auth_seq_id
Revision 1.4May 22, 2024Group: Data collection / Category: chem_comp_atom / chem_comp_bond

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: Serum albumin
hetero molecules


Theoretical massNumber of molelcules
Total (without water)23,2662
Polymers22,6861
Non-polymers5801
Water00
1


  • Idetical with deposited unit
  • defined by author
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
NMR ensembles
DataCriteria
Number of conformers (submitted / calculated)1 / -
Representative

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Components

#1: Protein Serum albumin


Mass: 22686.324 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: ALB / Plasmid: pET15b / Species (production host): Escherichia coli / Production host: Escherichia coli BL21(DE3) (bacteria) / Strain (production host): BL21(DE3) / References: UniProt: P02768
#2: Chemical ChemComp-4EB / 4-({2-[(2,4-DIMETHYLPHENYL)SULFANYL]ETHYL}AMINO)-N-[(4'-FLUORO-1,1'-BIPHENYL-4-YL)CARBONYL]-3-NITROBENZENESULFONAMIDE


Mass: 579.662 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C29H26FN3O5S2

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Experimental details

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Experiment

ExperimentMethod: SOLUTION NMR
NMR experiment
Conditions-IDExperiment-IDSolution-IDType
1113D 13C-separated NOESY
1213D 13C-edited 12C-filtered NOESY

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Sample preparation

DetailsContents: 0.5 mM Human serum albumin domain 3 U-15N,13C, 50 mM sodium phosphate, 150 mM sodium chloride, 0.1 mM EDTA, 100% D2O
Solvent system: 100% D2O
Sample conditionsIonic strength: 200 mM / pH: 6.5 / Pressure: ambient / Temperature: 303 K

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NMR measurement

RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M
Radiation wavelengthRelative weight: 1
NMR spectrometerType: Bruker DRX / Manufacturer: Bruker / Model: DRX / Field strength: 800 MHz

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Processing

NMR softwareName: X-PLOR / Version: 3.1 / Developer: Brunger / Classification: refinement
RefinementMethod: simulated annealing / Software ordinal: 1
NMR ensembleConformers submitted total number: 1

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