4MSV

Crystal structure of FASL and DcR3 complex

> Summary

Summary for 4MSV

Related4EN0 3MHD 4J6G 4KGG 4KGQ 3K51
DescriptorTumor necrosis factor receptor superfamily member 6B, Tumor necrosis factor ligand superfamily member 6, MAGNESIUM ION, ... (5 entities in total)
Functional Keywordsfasl, dcr3, tnf, tnfr, tnf6, structural genomics, psi-biology, new york structural genomics, research consortium, nysgrc, immunity, tnf supe cd95l, fas ligand, membrane, atoms-to-animals: the immune function network, ifn, jelly-roll fold, bind tnf receptor fas, protein structure initiative, new york structural genomics research consortium, cd95l, tnf superfamily, secreted protein, cytokine, immune system
Biological sourceHomo sapiens (human)
Cellular locationCell membrane; Single-pass type II membrane protein. Tumor necrosis factor ligand superfamily member 6, soluble form: Secreted . FasL intracellular domain: Nucleus P48023
Secreted O95407
Total number of polymer chains2
Total molecular weight36505.79
Authors
Primary citation
Liu, W.,Ramagopal, U.,Cheng, H.,Bonanno, J.B.,Toro, R.,Bhosle, R.,Zhan, C.,Almo, S.C.
Crystal Structure of the Complex of Human FasL and Its Decoy Receptor DcR3.
Structure, 24:2016-2023, 2016
PubMed: 27806260 (PDB entries with the same primary citation)
DOI: 10.1016/j.str.2016.09.009
MImport into Mendeley
Experimental method
X-RAY DIFFRACTION (2.5 Å)
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Structure validation

RfreeClashscoreRamachandran outliersSidechain outliersRSRZ outliers0.223305.0%4.3%MetricValuePercentile RanksWorseBetterPercentile relative to all X-ray structuresPercentile relative to X-ray structures of similar resolution

More Asymmetric unit images

Molmil generated image of 4msv
no rotation
Molmil generated image of 4msv
rotated about x axis by 90°
Molmil generated image of 4msv
rotated about y axis by 90°

More Biological unit images

Molmil generated image of 4msv
no rotation
Molmil generated image of 4msv
rotated about x axis by 90°
Molmil generated image of 4msv
rotated about y axis by 90°
(*)In the case of coarse surface representation, the asymmetric unit is shown as red ribbon representation.
Coordinate files for Biological unit (4msv.pdb1.gz [147.7 KB])

> Structural details

Entity

Chain IDDescriptionTypeChain lengthFormula weightNumber of moleculesDB Name (Accession)Biological sourceDescriptive keywords
BTumor necrosis factor receptor superfamily member 6Bpolymer17419044.31
UniProt (O95407)
Pfam (PF00020)
Homo sapiens (human)@PDBjDecoy receptor 3, DcR3, Decoy receptor for Fas ligand, M68
ATumor necrosis factor ligand superfamily member 6polymer15217345.11
UniProt (P48023)
Pfam (PF00229)
Homo sapiens (human)@PDBjApoptosis antigen ligand, APTL, CD95 ligand, CD95-L, Fas antigen ligand, Fas ligand, FasL, Tumor necrosis factor ligand superfamily member 6, membrane form, Tumor necrosis factor ligand superfamily member 6, soluble form, Receptor-binding FasL ectodomain, Soluble Fas ligand, sFasL, ADAM10-processed FasL form, APL, FasL intracellular domain, FasL ICD, SPPL2A-processed FasL form, SPA
MAGNESIUM IONnon-polymer24.31
GLYCEROLnon-polymer92.11
waterwater18.063

Sequence viewer

Contents of the asymmetric unit

PolymersNumber of chains2
Total molecular weight36389.4
Non-Polymers*Number of molecules2
Total molecular weight116.4
All*Total molecular weight36505.8
*Water molecules are not included.

> Experimental details

Refinement Statistics

Experimental method:X-RAY DIFFRACTION (2.5 Å)

Cell axes126.909126.909205.729
Cell angles90.0090.00120.00
SpacegroupH 3 2
Resolution limits48.52 - 2.50
the highest resolution shell value2.561 - 2.496
R-factor0.18914
R-work0.18744
the highest resolution shell value0.294
R-free0.22075
the highest resolution shell value0.390
RMSD bond length0.022
RMSD bond angle2.036

Data Collection Statistics

Resolution limits50.00 - 2.50
the highest resolution shell value -
Number of reflections22326
Rmerge_l_obs0.116
the highest resolution shell value0.826
Completeness100.0
Redundancy7.3
the highest resolution shell value7

Crystallization Conditions

crystal IDmethodpHpH rangetemperatureunit
1VAPOR DIFFUSION, SITTING DROP7290

Crystallization Reagents

IDcrystal IDsolution IDreagent nameconcentrationdetails
Crystallization Reagents in Literatures*
IDcrystal IDsolutionreagent nameconcentration (unit)details
Annotated Information is extracted from Literature Info*

> Functional details

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Functional Information from GO Data

ChainGOidnamespacecontents
B0005576cellular_componentextracellular region
B0005615cellular_componentextracellular space
B0005887cellular_componentintegral component of plasma membrane
B0004872molecular_functionreceptor activity
B0005031molecular_functiontumor necrosis factor-activated receptor activity
B0097190biological_processapoptotic signaling pathway
B0006955biological_processimmune response
B0006954biological_processinflammatory response
B0007275biological_processmulticellular organism development
B0043066biological_processnegative regulation of apoptotic process
B0042127biological_processregulation of cell proliferation
B0032496biological_processresponse to lipopolysaccharide
B0033209biological_processtumor necrosis factor-mediated signaling pathway
A0005901cellular_componentcaveola
A0060205cellular_componentcytoplasmic vesicle lumen
A0009897cellular_componentexternal side of plasma membrane
A0070062cellular_componentextracellular exosome
A0005576cellular_componentextracellular region
A0005615cellular_componentextracellular space
A0005887cellular_componentintegral component of plasma membrane
A0043202cellular_componentlysosomal lumen
A0005634cellular_componentnucleus
A0048471cellular_componentperinuclear region of cytoplasm
A0005886cellular_componentplasma membrane
A0005125molecular_functioncytokine activity
A0005123molecular_functiondeath receptor binding
A0005102molecular_functionreceptor binding
A0005164molecular_functiontumor necrosis factor receptor binding
A0006919biological_processactivation of cysteine-type endopeptidase activity involved in apoptotic process
A0097296biological_processactivation of cysteine-type endopeptidase activity involved in apoptotic signaling pathway
A0006915biological_processapoptotic process
A0097190biological_processapoptotic signaling pathway
A1903514biological_processrelease of sequestered calcium ion into cytosol by endoplasmic reticulum
A0007267biological_processcell-cell signaling
A0030644biological_processcellular chloride ion homeostasis
A0048388biological_processendosomal lumen acidification
A0097191biological_processextrinsic apoptotic signaling pathway
A0008625biological_processextrinsic apoptotic signaling pathway via death domain receptors
A0006955biological_processimmune response
A0006925biological_processinflammatory cell apoptotic process
A0070266biological_processnecroptotic process
A0097527biological_processnecroptotic signaling pathway
A0016525biological_processnegative regulation of angiogenesis
A1902042biological_processnegative regulation of extrinsic apoptotic signaling pathway via death domain receptors
A0000122biological_processnegative regulation of transcription from RNA polymerase II promoter
A0043065biological_processpositive regulation of apoptotic process
A0008284biological_processpositive regulation of cell proliferation
A2000353biological_processpositive regulation of endothelial cell apoptotic process
A0045742biological_processpositive regulation of epidermal growth factor receptor signaling pathway
A0043123biological_processpositive regulation of I-kappaB kinase/NF-kappaB signaling
A0043525biological_processpositive regulation of neuron apoptotic process
A1902041biological_processregulation of extrinsic apoptotic signaling pathway via death domain receptors
A0070848biological_processresponse to growth factor
A0032496biological_processresponse to lipopolysaccharide
A0046666biological_processretinal cell programmed cell death
A0007165biological_processsignal transduction
A0070231biological_processT cell apoptotic process
A0006351biological_processtranscription, DNA-templated
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Functional Information from PDB Data

site_idNumber of ResiduesDetails
AC16BINDING SITE FOR RESIDUE MG B 301
ChainResidue
BCYS132
BPRO133
BALA136
BSER159
BSER161
BHOH424

AC26BINDING SITE FOR RESIDUE GOL A 301
ChainResidue
AASN215
ATYR218
AGLN220
ALEU222
BLEU85
BARG89

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Functional Information from PDB atom coordinates for the "HETATM" binding sites

site_idNumber of ResiduesDetails
GOL_4msv_A_30110GLYCEROL binding site
ChainResidueligand
BLEU85GOL: GLYCEROL
BARG89GOL: GLYCEROL
AMET213-ASN215GOL: GLYCEROL
ATYR218-LEU222GOL: GLYCEROL

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Functional Information from PROSITE/UniProt

site_idNumber of ResiduesDetails
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Functional Information from SwissProt/UniProt

site_idNumber of ResiduesDetails
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Catalytic Information from CSA

site_idNumber of ResiduesDetails

> Sequence Neighbor

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