|
13FL
Structure of FabS1CE2_P2a in complex with the N-terminal domain of PD-L1
Deposited 2026-05-04
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain C
19–132(114 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
mmCIF provides none of the parsed conditions
|
Resolution 2.22 Å
R-free 0.239
|
|
3BIK
Crystal Structure of the PD-1/PD-L1 Complex
Deposited 2007-11-30
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–239(222 aa)
Fragment:EXTRACELLULAR REGION
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 6;298 K;20% PEG 3350, 200MM NH4H2PO4, pH 6.00, VAPOR DIFFUSION, SITTING DROP, temperature 298K
|
Resolution 2.65 Å
R-free 0.268
|
|
3BIS
Crystal Structure of the PD-L1
Deposited 2007-11-30
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
18–239(222 aa)
Fragment:EXTRACELLULAR REGION
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 6.5;298 K;20% PEG 3350, 0.1 M NaCacodylate, 0.2 M ammonium formate or ammonium fluoride, pH 6.50, VAPOR DIFFUSION, SITTING DROP, temperature 298K
|
Resolution 2.64 Å
R-free 0.292
|
|
3BIS
Crystal Structure of the PD-L1
Deposited 2007-11-30
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain B
18–239(222 aa)
Fragment:EXTRACELLULAR REGION
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 6.5;298 K;20% PEG 3350, 0.1 M NaCacodylate, 0.2 M ammonium formate or ammonium fluoride, pH 6.50, VAPOR DIFFUSION, SITTING DROP, temperature 298K
|
Resolution 2.64 Å
R-free 0.292
|
|
3FN3
Dimeric Structure of PD-L1
Deposited 2008-12-23
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
19–238(220 aa)
Fragment:extracellular domain
Chain B
19–238(220 aa)
Fragment:extracellular domain
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 5.5;291 K;15% PEG 3350 (w/v), 0.2M ammonium acetate (NH4Ac), 0.1M BIS-Tris pH 5.5, VAPOR DIFFUSION, HANGING DROP, temperature 291K
|
Resolution 2.70 Å
R-free 0.296
|
|
4Z18
CRYSTAL STRUCTURE OF HUMAN PD-L1
Deposited 2015-03-27
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
19–239(221 aa)
Fragment:UNP RESIDUES 19-339
Chain B
19–239(221 aa)
Fragment:UNP RESIDUES 19-339
|
Not recorded
|
CL CHLORIDE ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;PEG 3350, sodium chloride, hepes
|
Resolution 1.95 Å
R-free 0.246
|
|
4ZQK
Structure of the complex of human programmed death-1 (PD-1) and its ligand PD-L1.
Deposited 2015-05-10
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–132(115 aa)
|
Not recorded
|
NA SODIUM ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 5.5;295 K;0.1 M BIS-Tris pH 5.5, 1.84 M ammonium sulfate
|
Resolution 2.45 Å
R-free 0.253
|
|
5C3T
PD-1 binding domain from human PD-L1
Deposited 2015-06-17
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
18–134(117 aa)
Fragment:UNP residues 18-134
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;295.15 K;1.84 Na Formate
|
Resolution 1.80 Å
R-free 0.178
|
|
5GGT
PD-L1 in complex with BMS-936559 Fab
Deposited 2016-06-16
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain A
18–134(117 aa)
Fragment:UNP residues 18-134
|
Mutation:Q57E
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;0.1M imidazole, pH 9.0, 1.2M sodium citrate
|
Resolution 2.80 Å
R-free 0.269
|
|
5GRJ
Crystal structure of human PD-L1 with monoclonal antibody avelumab
Deposited 2016-08-11
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain A
18–238(221 aa)
Fragment:UNP residues 18-238
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
EVAPORATION;pH 7.5;291 K;0.2 M magnesium chloride hexahydrate, 0.1 M HEPES-Na, 30%(v/v) iso-Propanol
|
Resolution 3.21 Å
R-free 0.238
|
|
5IUS
Crystal structure of human PD-L1 in complex with high affinity PD-1 mutant
Deposited 2016-03-18
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain C
18–239(222 aa)
|
Not recorded
|
CL CHLORIDE ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 6.4;293 K;0.1 M bis-TRIS pH 6.4, 17% PEG MME 5000, 2 mM LiCl
|
Resolution 2.89 Å
R-free 0.260
|
|
5IUS
Crystal structure of human PD-L1 in complex with high affinity PD-1 mutant
Deposited 2016-03-18
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain D
18–239(222 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 6.4;293 K;0.1 M bis-TRIS pH 6.4, 17% PEG MME 5000, 2 mM LiCl
|
Resolution 2.89 Å
R-free 0.260
|
|
5J89
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
Deposited 2016-04-07
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain C
2–134(133 aa)
Chain D
2–134(133 aa)
|
Not recorded
|
6GX N-{2-[({2-methoxy-6-[(2-methyl[1,1'-biphenyl]-3-yl)methoxy]pyridin-3-yl}methyl)amino]ethyl}acetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 8;293 K;0.01M Tris pH=8.5, 0.3M sodium chloride, 27% (w/v) PEG 4000
|
Resolution 2.20 Å
R-free 0.256
|
|
5J89
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
Deposited 2016-04-07
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
2–134(133 aa)
Chain B
2–134(133 aa)
|
Not recorded
|
6GX N-{2-[({2-methoxy-6-[(2-methyl[1,1'-biphenyl]-3-yl)methoxy]pyridin-3-yl}methyl)amino]ethyl}acetamide × 1
EDO 1,2-ETHANEDIOL × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 8;293 K;0.01M Tris pH=8.5, 0.3M sodium chloride, 27% (w/v) PEG 4000
|
Resolution 2.20 Å
R-free 0.256
|
|
5J8O
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
Deposited 2016-04-08
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
6GZ (2R)-1-({3-bromo-4-[(2-methyl[1,1'-biphenyl]-3-yl)methoxy]phenyl}methyl)piperidine-2-carboxylic acid × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 8;293 K;0.2 M ammonium formate and 20% (w/v) PEG 3350
|
Resolution 2.30 Å
R-free 0.305
|
|
5JDR
Structure of PD-L1
Deposited 2016-04-17
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–239(222 aa)
Fragment:UNP RESIDUES 18-239
Chain B
18–239(222 aa)
Fragment:UNP RESIDUES 18-239
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
LIQUID DIFFUSION;295 K;0.2 M Ammonium Acetate, 20% PEG 3350
|
Resolution 2.70 Å
R-free 0.276
|
|
5JDS
Crystal structure of PD-L1 complexed with a nanobody at 1.7 Angstron resolution
Deposited 2016-04-17
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–132(115 aa)
Fragment:UNP RESIDUES 18-132
|
Not recorded
|
NA SODIUM ION × 2
CL CHLORIDE ION × 3
SO4 SULFATE ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
LIQUID DIFFUSION;295 K;2M NaCl, 1.4M (NH4)2SO4
|
Resolution 1.70 Å
R-free 0.204
|
|
5N2D
Structure of PD-L1/small-molecule inhibitor complex
Deposited 2017-02-07
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 4
PDB declaration: tetrameric
|
Chain A
2–134(133 aa)
Chain B
2–134(133 aa)
Chain C
2–134(133 aa)
Chain D
2–134(133 aa)
|
Not recorded
|
8J8 ~{N}-[2-[[2,6-dimethoxy-4-[(2-methyl-3-phenyl-phenyl)methoxy]phenyl]methylamino]ethyl]ethanamide × 2
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M Tris pH 8.5, 0.2 M magnesium chloride, 30% (w/v) PEG 4000
|
Resolution 2.35 Å
R-free 0.267
|
|
5N2F
Structure of PD-L1/small-molecule inhibitor complex
Deposited 2017-02-07
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
8HW 4-[[4-[[3-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-methyl-phenyl]methoxy]-2,5-bis(fluoranyl)phenyl]methylamino]-3-oxidanylidene-butanoic acid × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;0.01 M Tris pH 8.4 , 0.28 M sodium chloride, 27% (w/v) PEG 4000
|
Resolution 1.70 Å
R-free 0.230
|
|
5NIU
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
Deposited 2017-03-27
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
8YZ (2~{R})-2-[[2-[(3-cyanophenyl)methoxy]-4-[[3-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-methyl-phenyl]methoxy]-5-methyl-phenyl]methylamino]-3-oxidanyl-propanoic acid × 1
EDO 1,2-ETHANEDIOL × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;298 K;0.1 M Tris pH 8.5 containing 0.2 M magnesium chloride and 30% (w/v) PEG 4000
|
Resolution 2.01 Å
R-free 0.262
|
|
5NIU
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
Deposited 2017-03-27
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain C
18–134(117 aa)
Chain D
18–134(117 aa)
|
Not recorded
|
8YZ (2~{R})-2-[[2-[(3-cyanophenyl)methoxy]-4-[[3-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-methyl-phenyl]methoxy]-5-methyl-phenyl]methylamino]-3-oxidanyl-propanoic acid × 1
EDO 1,2-ETHANEDIOL × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;298 K;0.1 M Tris pH 8.5 containing 0.2 M magnesium chloride and 30% (w/v) PEG 4000
|
Resolution 2.01 Å
R-free 0.262
|
|
5O45
Structure of human PD-L1 in complex with inhibitor
Deposited 2017-05-26
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
17–134(118 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;0.2 M imidazole malate (pH 8.5) 27% PEG 10000
|
Resolution 0.99 Å
R-free 0.137
|
|
5O4Y
Structure of human PD-L1 in complex with inhibitor
Deposited 2017-05-31
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain B
18–132(115 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;0.2 M ammonium acetate (pH 5.5), 0.1 M Bis-Tris, 25% PEG 3350
|
Resolution 2.30 Å
R-free 0.262
|
|
5O4Y
Structure of human PD-L1 in complex with inhibitor
Deposited 2017-05-31
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain C
18–132(115 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;0.2 M ammonium acetate (pH 5.5), 0.1 M Bis-Tris, 25% PEG 3350
|
Resolution 2.30 Å
R-free 0.262
|
|
5O4Y
Structure of human PD-L1 in complex with inhibitor
Deposited 2017-05-31
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain E
18–132(115 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;0.2 M ammonium acetate (pH 5.5), 0.1 M Bis-Tris, 25% PEG 3350
|
Resolution 2.30 Å
R-free 0.262
|
|
5X8L
PD-L1 in complex with atezolizumab
Deposited 2017-03-03
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain A
18–134(117 aa)
Fragment:UNP residues 18-134
|
Mutation:Q47E
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;0.1M Sodium HEPES pH 7.5, 20% w/v PEG8000
|
Resolution 3.10 Å
R-free 0.256
|
|
5X8L
PD-L1 in complex with atezolizumab
Deposited 2017-03-03
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain B
18–134(117 aa)
Fragment:UNP residues 18-134
|
Mutation:Q47E
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;0.1M Sodium HEPES pH 7.5, 20% w/v PEG8000
|
Resolution 3.10 Å
R-free 0.256
|
|
5X8L
PD-L1 in complex with atezolizumab
Deposited 2017-03-03
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain C
18–134(117 aa)
Fragment:UNP residues 18-134
|
Mutation:Q47E
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;0.1M Sodium HEPES pH 7.5, 20% w/v PEG8000
|
Resolution 3.10 Å
R-free 0.256
|
|
5X8L
PD-L1 in complex with atezolizumab
Deposited 2017-03-03
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 4
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain D
18–134(117 aa)
Fragment:UNP residues 18-134
|
Mutation:Q47E
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;0.1M Sodium HEPES pH 7.5, 20% w/v PEG8000
|
Resolution 3.10 Å
R-free 0.256
|
|
5X8L
PD-L1 in complex with atezolizumab
Deposited 2017-03-03
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 5
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain E
18–134(117 aa)
Fragment:UNP residues 18-134
|
Mutation:Q47E
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;0.1M Sodium HEPES pH 7.5, 20% w/v PEG8000
|
Resolution 3.10 Å
R-free 0.256
|
|
5X8M
PD-L1 in complex with durvalumab
Deposited 2017-03-03
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain A
18–134(117 aa)
Fragment:UNP residues 18-134
|
Mutation:Q47E
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;0.2M Ammonium sulfate, 0.1M Bis-Tris pH 5.5, 25% w/v PEG 3350
|
Resolution 2.66 Å
R-free 0.219
|
|
5XJ4
Complex structure of durvalumab-scFv/PD-L1
Deposited 2017-04-29
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
19–238(220 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
EVAPORATION;pH 7;291 K;3.5 M sodium formate, pH 7.0
|
Resolution 2.30 Å
R-free 0.240
|
|
5XXY
Crystal structure of PD-L1 complexed with atezolizumab fab at 2.9A
Deposited 2017-07-05
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain A
18–133(116 aa)
Fragment:IgV domain,UNP residues 18-133
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 7;298 K;2M ammonium sulfate, 0.1M Tris PH 7.0
|
Resolution 2.90 Å
R-free 0.295
|
|
6L8R
membrane-bound PD-L1-CD
Deposited 2019-11-07
|
Different construct
Different oligomeric state
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
260–290(31 aa)
|
Not recorded
|
No recorded non-water small molecule
|
SOLUTION NMR
NMR measurement conditions
pH 6;300 K;Ionic strength (raw mmCIF value) 20;Pressure 1
NMR sample composition
0.5 mM 15N_13C_2H PD-L1-CD, 60 mM DMPG, 85 mM DHPC, 90% H2O/10% D2O | 90% H2O/10% D2O
NMR sample composition
0.5 mM 15N_13C PD-L1-CD, 60 mM 2H DMPG, 85 mM 2H DHPC, 90% H2O/10% D2O | 90% H2O/10% D2O
NMR sample composition
0.5 mM 15N_2H PD-L1-CD, 60 mM POPG, 85 mM 2H DHPC, 90% H2O/10% D2O | 90% H2O/10% D2O
|
Resolution not provided
|
|
6NM7
PD-L1 IgV domain bound to fragment
Deposited 2019-01-10
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
19–134(116 aa)
Chain B
19–134(116 aa)
|
Mutation:V76T
Mutation:V76T
|
22L 5-phenylthieno[2,3-d]pyrimidin-4(3H)-one × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291 K;0.056 M NaH2PO4, 1.344 M K2HPO4
|
Resolution 2.43 Å
R-free 0.269
|
|
6NM8
IgV-V76T BMS compound 105
Deposited 2019-01-10
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
19–134(116 aa)
Chain B
19–134(116 aa)
|
Mutation:V76T
Mutation:V76T
|
KSD N-({2,6-dimethoxy-4-[(2-methyl[1,1'-biphenyl]-3-yl)methoxy]phenyl}methyl)-D-alanine × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 8.5;291 K;29% PEG 4000, 0.28 M NaCl, 0.01 M Tris
|
Resolution 2.79 Å
R-free 0.304
|
|
6NNV
PD-L1 IgV domain complex with macro-cyclic peptide
Deposited 2019-01-15
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Fragment:UNP residues 18-134
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
EVAPORATION;291 K;0.056 M sodium phosphate monobasic, 1.344 M potassium phosphate dibasic
|
Resolution 1.92 Å
R-free 0.253
|
|
6NNV
PD-L1 IgV domain complex with macro-cyclic peptide
Deposited 2019-01-15
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain B
18–134(117 aa)
Fragment:UNP residues 18-134
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
EVAPORATION;291 K;0.056 M sodium phosphate monobasic, 1.344 M potassium phosphate dibasic
|
Resolution 1.92 Å
R-free 0.253
|
|
6NNV
PD-L1 IgV domain complex with macro-cyclic peptide
Deposited 2019-01-15
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain C
18–134(117 aa)
Fragment:UNP residues 18-134
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
EVAPORATION;291 K;0.056 M sodium phosphate monobasic, 1.344 M potassium phosphate dibasic
|
Resolution 1.92 Å
R-free 0.253
|
|
6NNV
PD-L1 IgV domain complex with macro-cyclic peptide
Deposited 2019-01-15
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 4
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain D
18–134(117 aa)
Fragment:UNP residues 18-134
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
EVAPORATION;291 K;0.056 M sodium phosphate monobasic, 1.344 M potassium phosphate dibasic
|
Resolution 1.92 Å
R-free 0.253
|
|
6NOJ
PD-L1 IgV domain V76T with fragment
Deposited 2019-01-16
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Fragment:UNP residues 18-134
Chain B
18–134(117 aa)
Fragment:UNP residues 18-134
|
Not recorded
|
KW7 methyl 3-amino-4-(2-fluorophenyl)-1H-pyrrole-2-carboxylate × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
EVAPORATION;291 K;0.056 M sodium phosphate monobasic, 1.344 M potassium phosphate dibasic
|
Resolution 2.33 Å
R-free 0.245
|
|
6NOS
PD-L1 IgV domain V76T with fragment
Deposited 2019-01-16
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Fragment:UNP residues 18-134
Chain B
18–134(117 aa)
Fragment:UNP residues 18-134
|
Not recorded
|
KWA 1-[5-(3,5-dichlorophenyl)furan-2-yl]-N-methylmethanamine × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
EVAPORATION;291 K;0.056 M sodium phosphate monobasic, 1.344 M potassium phosphate dibasic
|
Resolution 2.70 Å
R-free 0.275
|
|
6NP9
PD-L1 IgV domain V76T with fragment
Deposited 2019-01-17
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
|
Mutation:V76T
|
SO4 SULFATE ION × 4
|
X-RAY DIFFRACTION
X-ray crystallization conditions
EVAPORATION;291 K;Ammonium Sulfate
|
Resolution 1.27 Å
R-free 0.218
|
|
6PV9
Human PD-L1 bound to a macrocyclic peptide which blocks the PD-1/PD-L1 interaction
Deposited 2019-07-19
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
19–239(221 aa)
Fragment:extracellular domain (UNP residues 19-239)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 5.5;293 K;20% PEG3000, 0.1 M sodium citrate, pH 5.5
|
Resolution 2.00 Å
R-free 0.226
|
|
6R3K
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
Deposited 2019-03-20
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
EDO 1,2-ETHANEDIOL × 1
JQT (2~{S},4~{R})-1-[[5-chloranyl-2-[(3-cyanophenyl)methoxy]-4-[[3-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-methyl-phenyl]methoxy]phenyl]methyl]-4-oxidanyl-pyrrolidine-2-carboxylic acid × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;298 K;0.01 M Tris pH 8.4 containing 0.28 M sodium chloride and 27% (w/v) PEG 4000
|
Resolution 2.20 Å
R-free 0.259
|
|
6R3K
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
Deposited 2019-03-20
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain C
18–134(117 aa)
Chain D
18–134(117 aa)
|
Not recorded
|
EDO 1,2-ETHANEDIOL × 1
JQT (2~{S},4~{R})-1-[[5-chloranyl-2-[(3-cyanophenyl)methoxy]-4-[[3-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-methyl-phenyl]methoxy]phenyl]methyl]-4-oxidanyl-pyrrolidine-2-carboxylic acid × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;298 K;0.01 M Tris pH 8.4 containing 0.28 M sodium chloride and 27% (w/v) PEG 4000
|
Resolution 2.20 Å
R-free 0.259
|
|
6RPG
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with inhibitor
Deposited 2019-05-14
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
KDW ~{N}-[2-[[4-[[3-[3-[[4-[(2-acetamidoethylamino)methyl]-5-[(5-cyanopyridin-3-yl)methoxy]-2-methyl-phenoxy]methyl]-2-methyl-phenyl]-2-methyl-phenyl]methoxy]-2-[(5-cyanopyridin-3-yl)methoxy]-5-methyl-phenyl]methylamino]ethyl]ethanamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M BIS-Tris pH 5.4, 0.2 M ammonium sulfate and 23 % (w/v) PEG 3350
|
Resolution 2.70 Å
R-free 0.281
|
|
6VQN
Co-crystal structure of human PD-L1 complexed with Compound A
Deposited 2020-02-05
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
R81 N,N'-(2,2'-dimethyl[1,1'-biphenyl]-3,3'-diyl)bis(5-{[(2-hydroxyethyl)amino]methyl}pyridine-2-carboxamide) × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;100 mM NaCitrate, pH 6.5 and 22% (w/v) PEG 3000
|
Resolution 2.49 Å
R-free 0.228
|
|
6VQN
Co-crystal structure of human PD-L1 complexed with Compound A
Deposited 2020-02-05
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain C
18–134(117 aa)
|
Not recorded
|
R81 N,N'-(2,2'-dimethyl[1,1'-biphenyl]-3,3'-diyl)bis(5-{[(2-hydroxyethyl)amino]methyl}pyridine-2-carboxamide) × 2
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;100 mM NaCitrate, pH 6.5 and 22% (w/v) PEG 3000
|
Resolution 2.49 Å
R-free 0.228
|
|
6YCR
Structure of human PD-L1 in complex with inhibitor
Deposited 2020-03-18
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;1.0M succinic acid, 0.1M HEPES pH 7.0, 1% w/v PEG 2000 MME
|
Resolution 1.54 Å
R-free 0.180
|
|
7BEA
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with inhibitor
Deposited 2020-12-22
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
TK2 2-(aminomethyl)-6-[(2-methyl-3-phenyl-phenyl)methoxy]-~{N}-(2-phenylethyl)imidazo[1,2-a]pyridin-3-amine × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 8.5;298 K;1.2 M Sodium citrate tribasic dihydrate
0.01 M Sodium borate, pH 8.5
|
Resolution 2.45 Å
|
|
7C88
Complex structure of JS003 and PD-L1
Deposited 2020-05-29
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain M
1–136(136 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291 K;0.1M Na HEPES 7.0, 15% w/v PEG 20000
|
Resolution 2.00 Å
R-free 0.258
|
|
7C88
Complex structure of JS003 and PD-L1
Deposited 2020-05-29
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain C
1–136(136 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291 K;0.1M Na HEPES 7.0, 15% w/v PEG 20000
|
Resolution 2.00 Å
R-free 0.258
|
|
7CZD
Crystal structure of PD-L1 in complex with a VHH
Deposited 2020-09-08
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain B
19–134(116 aa)
|
Not recorded
|
EDO 1,2-ETHANEDIOL × 3
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291 K;0.2 M ammonium sulfate, 0.1 M Bis-Tris pH 5.5, 25% w/v PEG 3350
|
Resolution 1.64 Å
R-free 0.184
|
|
7CZD
Crystal structure of PD-L1 in complex with a VHH
Deposited 2020-09-08
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain D
19–134(116 aa)
|
Not recorded
|
EDO 1,2-ETHANEDIOL × 3
PEG DI(HYDROXYETHYL)ETHER × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291 K;0.2 M ammonium sulfate, 0.1 M Bis-Tris pH 5.5, 25% w/v PEG 3350
|
Resolution 1.64 Å
R-free 0.184
|
|
7DCV
Structure of the transmembrane domain of human PD-L1
Deposited 2020-10-27
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental method
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
232–290(59 aa)
|
Mutation:C250A, M266L, M267L, C272S
|
No recorded non-water small molecule
|
SOLUTION NMR
NMR measurement conditions
pH 6;310 K;Ionic strength (raw mmCIF value) 20;Pressure 1
NMR sample composition
20 mM MES, 30 mM DMPC, 60 mM DHPC, 90% H2O/10% D2O | 90% H2O/10% D2O
NMR sample composition
20 mM MES, 30 mM [U-2H] DMPC, 60 mM [U-2H] DHPC, 90% H2O/10% D2O | 90% H2O/10% D2O
|
Resolution not provided
|
|
7DY7
Discovery of Novel Small-molecule Inhibitors of PD-1/PD-L1 Axis that Promotes PD-L1 Internalization and Degradation
Deposited 2021-01-20
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
HOU 2-[[3-[[5-(2-methyl-3-phenyl-phenyl)-1,3,4-oxadiazol-2-yl]amino]phenyl]methylamino]ethanol × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;289.15 K;PEG 3350,ammonium acetate
|
Resolution 2.42 Å
R-free 0.240
|
|
7NLD
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
Deposited 2021-02-22
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain C
18–134(117 aa)
Chain D
18–134(117 aa)
|
Not recorded
|
UGZ N-(2-((2'-chloro-3'-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-3-methoxy-[1,1'-biphenyl]-4-yl)(methyl)amino)ethyl)methanesulfonamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION;293 K;0.1M sodium cocdylate pH 6.5; 25% PEG4000
|
Resolution 2.30 Å
R-free 0.294
|
|
7NLD
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
Deposited 2021-02-22
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
UGZ N-(2-((2'-chloro-3'-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-3-methoxy-[1,1'-biphenyl]-4-yl)(methyl)amino)ethyl)methanesulfonamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION;293 K;0.1M sodium cocdylate pH 6.5; 25% PEG4000
|
Resolution 2.30 Å
R-free 0.294
|
|
7NLD
Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
Deposited 2021-02-22
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain E
18–134(117 aa)
Chain F
18–134(117 aa)
|
Not recorded
|
UGZ N-(2-((2'-chloro-3'-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-3-methoxy-[1,1'-biphenyl]-4-yl)(methyl)amino)ethyl)methanesulfonamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION;293 K;0.1M sodium cocdylate pH 6.5; 25% PEG4000
|
Resolution 2.30 Å
R-free 0.294
|
|
7OUN
Structure of human PD-L1 in complex with macrocyclic inhibitor
Deposited 2021-06-12
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
17–134(118 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 6.24;298 K;0.1M sodium citrate 1.95M ammonium sulphate
|
Resolution 1.90 Å
R-free 0.246
|
|
7SJQ
Ex silico engineering of cystine-dense peptides yielding a potent bispecific T-cell engager
Deposited 2021-10-18
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
|
Not recorded
|
GOL GLYCEROL × 1
NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1
SO4 SULFATE ION × 1
NA SODIUM ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;300 K;Sodium Citrate pH 7, ammonium sulfate
|
Resolution 2.00 Å
R-free 0.232
|
|
7TPS
Crystal structure of ALPN-202 (engineered CD80 vIgD) in complex with PD-L1
Deposited 2022-01-26
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Other combination
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain B
19–227(209 aa)
|
Non-standard monomer:Yes (specific site not provided by mmCIF)
|
NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 3
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION;293 K;0.03 M sodium nitrate, 0.03 M sodium
phosphate dibasic, 0.03 M ammonium sulfate, 0.1 M sodium HEPES/MOPS (acid), pH 7.5, 20% v/v glycerol, 10% w/v
PEG 4000
|
Resolution 3.15 Å
R-free 0.291
|
|
7TPS
Crystal structure of ALPN-202 (engineered CD80 vIgD) in complex with PD-L1
Deposited 2022-01-26
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Other combination
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain D
19–227(209 aa)
|
Not recorded
|
NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 3
GOL GLYCEROL × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION;293 K;0.03 M sodium nitrate, 0.03 M sodium
phosphate dibasic, 0.03 M ammonium sulfate, 0.1 M sodium HEPES/MOPS (acid), pH 7.5, 20% v/v glycerol, 10% w/v
PEG 4000
|
Resolution 3.15 Å
R-free 0.291
|
|
7UX5
Structure of PDL1 in complex with FP28136, a Helicon Polypeptide
Deposited 2022-05-05
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
|
Not recorded
|
WHL N,N'-(1,4-phenylene)diacetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291.15 K;0.1 M TRIS pH 8, 25% v/v PEG 350 MME.
|
Resolution 3.35 Å
R-free 0.301
|
|
7UX5
Structure of PDL1 in complex with FP28136, a Helicon Polypeptide
Deposited 2022-05-05
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain C
18–134(117 aa)
|
Not recorded
|
WHL N,N'-(1,4-phenylene)diacetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291.15 K;0.1 M TRIS pH 8, 25% v/v PEG 350 MME.
|
Resolution 3.35 Å
R-free 0.301
|
|
7UX5
Structure of PDL1 in complex with FP28136, a Helicon Polypeptide
Deposited 2022-05-05
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain E
18–134(117 aa)
|
Not recorded
|
WHL N,N'-(1,4-phenylene)diacetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291.15 K;0.1 M TRIS pH 8, 25% v/v PEG 350 MME.
|
Resolution 3.35 Å
R-free 0.301
|
|
7UX5
Structure of PDL1 in complex with FP28136, a Helicon Polypeptide
Deposited 2022-05-05
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 4
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain G
18–134(117 aa)
|
Not recorded
|
WHL N,N'-(1,4-phenylene)diacetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291.15 K;0.1 M TRIS pH 8, 25% v/v PEG 350 MME.
|
Resolution 3.35 Å
R-free 0.301
|
|
7UX5
Structure of PDL1 in complex with FP28136, a Helicon Polypeptide
Deposited 2022-05-05
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 5
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain I
18–134(117 aa)
|
Not recorded
|
WHL N,N'-(1,4-phenylene)diacetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291.15 K;0.1 M TRIS pH 8, 25% v/v PEG 350 MME.
|
Resolution 3.35 Å
R-free 0.301
|
|
7UX5
Structure of PDL1 in complex with FP28136, a Helicon Polypeptide
Deposited 2022-05-05
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 6
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain K
18–134(117 aa)
|
Not recorded
|
WHL N,N'-(1,4-phenylene)diacetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291.15 K;0.1 M TRIS pH 8, 25% v/v PEG 350 MME.
|
Resolution 3.35 Å
R-free 0.301
|
|
7UXO
Structure of PDL1 in complex with FP30790, a Helicon Polypeptide
Deposited 2022-05-05
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
|
Not recorded
|
NH2 AMINO GROUP × 1
WHL N,N'-(1,4-phenylene)diacetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291.15 K;0.1 M Sodium acetate pH 4.6, 2.0 M Sodium formate.
|
Resolution 2.25 Å
R-free 0.250
|
|
7UXP
Structure of PDL1 in complex with FP28132, a Helicon Polypeptide
Deposited 2022-05-05
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
|
Not recorded
|
NH2 AMINO GROUP × 1
WHL N,N'-(1,4-phenylene)diacetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291.15 K;0.1 M MES pH 6.5, 1.6 M Magnesium sulfate.
|
Resolution 2.62 Å
R-free 0.286
|
|
7UXP
Structure of PDL1 in complex with FP28132, a Helicon Polypeptide
Deposited 2022-05-05
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain B
18–134(117 aa)
|
Not recorded
|
NH2 AMINO GROUP × 1
WHL N,N'-(1,4-phenylene)diacetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291.15 K;0.1 M MES pH 6.5, 1.6 M Magnesium sulfate.
|
Resolution 2.62 Å
R-free 0.286
|
|
7UXQ
Structure of PDL1 in complex with FP28135, a Helicon Polypeptide
Deposited 2022-05-05
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
|
Not recorded
|
EDO 1,2-ETHANEDIOL × 4
WHL N,N'-(1,4-phenylene)diacetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291.15 K;1.1 M Sodium Malonate pH 7.0, 0.1 M HEPES pH 7.0, 0.5% v/v Jeffamine ED-2001 Reagent pH 7.0.
|
Resolution 2.89 Å
R-free 0.228
|
|
7UXQ
Structure of PDL1 in complex with FP28135, a Helicon Polypeptide
Deposited 2022-05-05
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain B
18–134(117 aa)
|
Not recorded
|
EDO 1,2-ETHANEDIOL × 6
WHL N,N'-(1,4-phenylene)diacetamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291.15 K;1.1 M Sodium Malonate pH 7.0, 0.1 M HEPES pH 7.0, 0.5% v/v Jeffamine ED-2001 Reagent pH 7.0.
|
Resolution 2.89 Å
R-free 0.228
|
|
7VUN
Design, modification, evaluation and cocrystal studies of novel phthalimides regulating PD-1/PD-L1 interaction
Deposited 2021-11-03
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 8
PDB declaration: octameric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
Chain C
18–134(117 aa)
Chain D
18–134(117 aa)
Chain E
18–134(117 aa)
Chain F
18–134(117 aa)
Chain G
18–134(117 aa)
Chain H
18–134(117 aa)
|
Not recorded
|
8H7 (2~{S},3~{S})-2-[[6-[(3-cyanophenyl)methoxy]-2-(2-methyl-3-phenyl-phenyl)-1,3-bis(oxidanylidene)isoindol-5-yl]methylamino]-3-oxidanyl-butanoic acid × 4
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;289.15 K;PEG 3350, 1,4 - Dioxane, Tris
|
Resolution 2.70 Å
R-free 0.289
|
|
7XAD
Crystal strucutre of PD-L1 and DBL2_02 designed protein binder
Deposited 2022-03-17
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
1–238(238 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291 K;0.2 M potassium/sodium tartrate, 0.1 M Bis Tris propane, pH 6.5 ,20 % w/v PEG 3350
|
Resolution 3.00 Å
R-free 0.294
|
|
7XAD
Crystal strucutre of PD-L1 and DBL2_02 designed protein binder
Deposited 2022-03-17
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain D
1–238(238 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291 K;0.2 M potassium/sodium tartrate, 0.1 M Bis Tris propane, pH 6.5 ,20 % w/v PEG 3350
|
Resolution 3.00 Å
R-free 0.294
|
|
7XAD
Crystal strucutre of PD-L1 and DBL2_02 designed protein binder
Deposited 2022-03-17
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain F
1–238(238 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291 K;0.2 M potassium/sodium tartrate, 0.1 M Bis Tris propane, pH 6.5 ,20 % w/v PEG 3350
|
Resolution 3.00 Å
R-free 0.294
|
|
7XAD
Crystal strucutre of PD-L1 and DBL2_02 designed protein binder
Deposited 2022-03-17
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 4
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain H
1–238(238 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;291 K;0.2 M potassium/sodium tartrate, 0.1 M Bis Tris propane, pH 6.5 ,20 % w/v PEG 3350
|
Resolution 3.00 Å
R-free 0.294
|
|
7XAE
Crystal strucutre of PD-L1 and 3ONJA protein
Deposited 2022-03-17
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
1–238(238 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M Sodium citrate tribasic dihydrate pH 5.5, 16% w/v Polyethylene glycol 8,000
|
Resolution 3.44 Å
R-free 0.262
|
|
7XAE
Crystal strucutre of PD-L1 and 3ONJA protein
Deposited 2022-03-17
|
Different construct
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain B
1–238(238 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M Sodium citrate tribasic dihydrate pH 5.5, 16% w/v Polyethylene glycol 8,000
|
Resolution 3.44 Å
R-free 0.262
|
|
7YDS
The structure of the bispecific antibody targeted PD-L1 and 4-1BB
Deposited 2022-07-04
|
Different construct
Different mutation/modification
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain A
1–136(136 aa)
|
Mutation:N35Q
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;289.15 K;18% PEG4000, 0.1M Bis-tris pH 6.2
|
Resolution 2.30 Å
R-free 0.246
|
|
8ALX
Structure of human PD-L1 in complex with inhibitor
Deposited 2022-08-01
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
|
Not recorded
|
ACT ACETATE ION × 3
GOL GLYCEROL × 2
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;1.4 M sodium acetate trihydrate; 0.1 M sodium cacodylate pH 6.5
|
Resolution 1.10 Å
R-free 0.136
|
|
8AOK
Complex of PD-L1 with VHH6
Deposited 2022-08-08
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
|
Not recorded
|
PEG DI(HYDROXYETHYL)ETHER × 3
ACY ACETIC ACID × 1
OXM OXAMIC ACID × 1
EDO 1,2-ETHANEDIOL × 2
FMT FORMIC ACID × 1
PG4 TETRAETHYLENE GLYCOL × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 7.5;291 K;0.1 M HEPES:MOPS, pH 7.5, 0.02 M Ammonium acetate, 0.02 M Potassium sodium tartrate tetrahydrate, 0.02 M Sodium citrate tribasic dihydrate, 0.02 M Sodium formate, 0.02M Sodium oxamate,
10% (w/v) PEG 20000 and 20% (v/v) PEG 500-MME.
|
Resolution 1.60 Å
R-free 0.185
|
|
8AOM
Complex of PD-L1 with VHH1
Deposited 2022-08-08
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
19–239(221 aa)
|
Not recorded
|
MG MAGNESIUM ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 7.5;291 K;0.1 M MOPS, pH 7.5, and 12% (w/v) PEG 8000
|
Resolution 2.20 Å
R-free 0.245
|
|
8JBA
Discovery and Crystallography Study of Novel Oxadiazole Analogs as Small Molecule PD-1/PD-L1 inhibitors
Deposited 2023-05-08
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
AU9 (2~{S})-2-[[3-[[5-[(2-methyl-3-phenyl-phenoxy)methyl]-1,3,4-oxadiazol-2-yl]sulfanylmethyl]phenyl]methylamino]-3-oxidanyl-propanoic acid × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;289.15 K;Tris, Potassium sodium tartrate tetrahydrate
|
Resolution 2.60 Å
R-free 0.257
|
|
8K5N
Discovery of Novel PD-L1 Inhibitors That Induce Dimerization and Degradation of PD-L1 Based on Fragment Coupling Strategy
Deposited 2023-07-22
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
I7M 3-[(1~{S})-1-[6-methoxy-3-methyl-5-[[[(2~{S})-5-oxidanylidenepyrrolidin-2-yl]methylamino]methyl]pyridin-2-yl]oxy-2,3-dihydro-1~{H}-inden-4-yl]-2-methyl-~{N}-[5-[[[(2~{S})-5-oxidanylidenepyrrolidin-2-yl]methylamino]methyl]pyridin-2-yl]benzamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;289.15 K;Ammonium acetate, PEG 3350
|
Resolution 2.20 Å
R-free 0.234
|
|
8OR1
Co-crystal strucutre of PD-L1 with low molecular weight inhibitor
Deposited 2023-04-12
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–133(116 aa)
Chain B
18–133(116 aa)
|
Not recorded
|
VYC 5-[[5-[[2-chloranyl-3-(2-fluorophenyl)phenyl]methoxy]-2-[(~{E})-2-hydroxyethyliminomethyl]phenoxy]methyl]pyridine-3-carbonitrile × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;2.0 M Ammonium sulfate, 0.1 M Sodium acetate pH 5.0
|
Resolution 3.50 Å
R-free 0.296
|
|
8P1O
Solubilizer tag effect on PD-L1/inhibitor binding properties for m-terphenyl derivatives
Deposited 2023-05-12
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
2–134(133 aa)
Chain B
2–134(133 aa)
|
Not recorded
|
WEW (3~{R})-1-[[4-[2-chloranyl-3-(2,3-dihydro-1,4-benzodioxin-6-yl)phenyl]-2-methoxy-phenyl]methyl]-~{N}-(2-hydroxyethyl)pyrrolidine-3-carboxamide × 1
CL CHLORIDE ION × 2
SO4 SULFATE ION × 2
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;27 % w/v PEG 3350, 0.1 M Bis-Tris propane, pH 7.0 and 0.2 M Lithium sulfate
|
Resolution 2.17 Å
R-free 0.289
|
|
8P64
Co-crystal structure of PD-L1 with low molecular weight inhibitor
Deposited 2023-05-25
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
X1Q ~{N}-[[1-[(~{E})-2-(2-methyl-3-phenyl-phenyl)ethenyl]-1,2,3,4-tetrazol-5-yl]methyl]ethanamine × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;1.2 M S38 sodium citrate tribasic dihydrate 0.01 M sodium borate, pH 8.5
|
Resolution 3.31 Å
R-free 0.297
|
|
8RPB
Structure of S79 Fab in complex with IgV domain of human PD-L1
Deposited 2024-01-15
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 3
PDB declaration: trimeric
|
Chain P
18–133(116 aa)
|
Not recorded
|
CL CHLORIDE ION × 1
GOL GLYCEROL × 3
SO4 SULFATE ION × 6
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293.15 K;0.1M Tris pH 8.0, 1.6M Li2SO4
|
Resolution 2.79 Å
R-free 0.251
|
|
8XR5
Crystal structure of PD-L1 complexed with small molecule inhibitor X18
Deposited 2024-01-06
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
19–134(116 aa)
Chain B
19–134(116 aa)
|
Not recorded
|
A1LV3 (2~{R})-2-[[2-(2,1,3-benzoxadiazol-5-ylmethoxy)-5-chloranyl-4-[[2-fluoranyl-3-[3-[3-(4-oxidanylpiperidin-1-yl)propoxy]phenyl]phenyl]methoxy]phenyl]methylamino]-3-oxidanyl-propanoic acid × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;289 K;19% PEG3350 and 0.2 M Ammonium tartrate dibasic
|
Resolution 1.95 Å
R-free 0.257
|
|
8ZNL
PD-L1 de novo designed binder with picomolar binding affinity
Deposited 2024-05-27
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain B
19–132(114 aa)
|
Not recorded
|
BR BROMIDE ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION;293 K;buffer containing 0.03M Sodium fluoride; 0.03M Sodium bromide; 0.03M Sodium iodide; 0.1 M (Imidazole/MES) pH6.5, 12.5% v/v MPD; 12.5% PEG1000; 12.5% w/v PEG 3350.
|
Resolution 1.77 Å
R-free 0.275
|
|
8ZNL
PD-L1 de novo designed binder with picomolar binding affinity
Deposited 2024-05-27
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain D
19–132(114 aa)
|
Not recorded
|
BR BROMIDE ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION;293 K;buffer containing 0.03M Sodium fluoride; 0.03M Sodium bromide; 0.03M Sodium iodide; 0.1 M (Imidazole/MES) pH6.5, 12.5% v/v MPD; 12.5% PEG1000; 12.5% w/v PEG 3350.
|
Resolution 1.77 Å
R-free 0.275
|
|
8ZNL
PD-L1 de novo designed binder with picomolar binding affinity
Deposited 2024-05-27
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain F
19–132(114 aa)
|
Not recorded
|
BR BROMIDE ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION;293 K;buffer containing 0.03M Sodium fluoride; 0.03M Sodium bromide; 0.03M Sodium iodide; 0.1 M (Imidazole/MES) pH6.5, 12.5% v/v MPD; 12.5% PEG1000; 12.5% w/v PEG 3350.
|
Resolution 1.77 Å
R-free 0.275
|
|
8ZNL
PD-L1 de novo designed binder with picomolar binding affinity
Deposited 2024-05-27
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 4
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain H
19–132(114 aa)
|
Not recorded
|
BR BROMIDE ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION;293 K;buffer containing 0.03M Sodium fluoride; 0.03M Sodium bromide; 0.03M Sodium iodide; 0.1 M (Imidazole/MES) pH6.5, 12.5% v/v MPD; 12.5% PEG1000; 12.5% w/v PEG 3350.
|
Resolution 1.77 Å
R-free 0.275
|
|
9EO0
Small-Molecule Inhibitors of Programmed Cell Death-1/Programmed Death-Ligand 1
Deposited 2024-03-14
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
A1H56 ~{N}-[3-[3-[[5-[(2-hydroxyethylamino)methyl]pyridin-2-yl]carbonylamino]-2-methyl-phenyl]-2-methyl-phenyl]-5-[[3-(methylsulfonylamino)propylamino]methyl]pyridine-2-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293.15 K;0.1 M Sodium HEPES 7.5 25 % w/v PEG 3350
|
Resolution 2.50 Å
R-free 0.302
|
|
9EO0
Small-Molecule Inhibitors of Programmed Cell Death-1/Programmed Death-Ligand 1
Deposited 2024-03-14
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain C
18–134(117 aa)
Chain F
18–134(117 aa)
|
Not recorded
|
A1H56 ~{N}-[3-[3-[[5-[(2-hydroxyethylamino)methyl]pyridin-2-yl]carbonylamino]-2-methyl-phenyl]-2-methyl-phenyl]-5-[[3-(methylsulfonylamino)propylamino]methyl]pyridine-2-carboxamide × 1
SO4 SULFATE ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293.15 K;0.1 M Sodium HEPES 7.5 25 % w/v PEG 3350
|
Resolution 2.50 Å
R-free 0.302
|
|
9EO0
Small-Molecule Inhibitors of Programmed Cell Death-1/Programmed Death-Ligand 1
Deposited 2024-03-14
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain D
18–134(117 aa)
Chain E
18–134(117 aa)
|
Not recorded
|
A1H56 ~{N}-[3-[3-[[5-[(2-hydroxyethylamino)methyl]pyridin-2-yl]carbonylamino]-2-methyl-phenyl]-2-methyl-phenyl]-5-[[3-(methylsulfonylamino)propylamino]methyl]pyridine-2-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293.15 K;0.1 M Sodium HEPES 7.5 25 % w/v PEG 3350
|
Resolution 2.50 Å
R-free 0.302
|
|
9ERY
Co-crystal strucutre of PD-L1 with low molecular weight inhibitor
Deposited 2024-03-25
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
VVH 5-[[5-[[2-[bis(fluoranyl)methyl]-3-(2,3-dihydro-1,4-benzodioxin-6-yl)phenyl]methoxy]-2-[(2-hydroxyethylamino)methyl]phenoxy]methyl]pyridine-3-carbonitrile × 1
SO4 SULFATE ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;2.0 M Ammonium sulfate and 0.1 M Sodium cacodylate pH 6.5
|
Resolution 2.70 Å
R-free 0.276
|
|
9HRT
Structure of human PD-L1 in complex with clinically evaluated inhibitor
Deposited 2024-12-18
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
A1IXH (2~{R})-2-[[3-[(~{E})-2-[3-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-methyl-phenyl]ethenyl]-4-(trifluoromethyl)phenyl]methylamino]-2-methyl-3-oxidanyl-propanoic acid × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;0.2M Ammonium sulfate; 0.1 soudium cacodylate; 6.53% w/v PEG 8000
|
Resolution 2.30 Å
R-free 0.263
|
|
9I0U
Structure of human PD-L1 in complex with clinically evaluated inhibitor
Deposited 2025-01-15
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
GOL GLYCEROL × 2
A1IZJ (5~{S})-5-[[[5-[2-chloranyl-3-[2-chloranyl-3-[6-methoxy-5-[[[(2~{S})-5-oxidanylidenepyrrolidin-2-yl]methylamino]methyl]pyrazin-2-yl]phenyl]phenyl]-3-methoxy-pyrazin-2-yl]methylamino]methyl]pyrrolidin-2-one × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;2.0M ammonium sulfate; 0.1M sodium acetate pH 4.6
|
Resolution 1.46 Å
R-free 0.202
|
|
9I0W
Structure of human PD-L1 in complex with clinically evaluated inhibitor
Deposited 2025-01-15
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
A1IZP (3~{R})-1-[[7-(iminomethyl)-2-[2-methyl-3-[2-methyl-3-[[3-[[(3~{R})-3-oxidanylpyrrolidin-1-yl]methyl]-1,7-naphthyridin-8-yl]amino]phenyl]phenyl]-1,3-benzoxazol-5-yl]methyl]pyrrolidine-3-carboxylic acid × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;293 K;0.2 M ammonium sulfate, 0.1 M Bis-Tris pH 5.5, 25% w/v PEG 3350
|
Resolution 2.10 Å
R-free 0.299
|
|
9IJT
Crystal Structure of human Programmed cell death 1 ligand 1 (PD-L1) bound to Small molecule inhibitor Compound-10
Deposited 2024-06-25
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 4
PDB declaration: tetrameric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
Chain C
18–134(117 aa)
Chain D
18–134(117 aa)
|
Not recorded
|
A1L2P (2~{S})-1-[[4-methoxy-2-[(2-methyl-3-phenyl-phenyl)methoxy]pyrimidin-5-yl]methyl]piperidine-2-carboxylic acid × 2
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;pH 8.5;299 K;0.1M Tris pH 8.5, 0.1M Magnesium chloride, 25% PEG 4000
|
Resolution 2.05 Å
R-free 0.260
|
|
9INU
Novel PD-L1/VISTA dual inhibitor as potential immunotherapy agents
Deposited 2024-07-08
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain B
18–134(117 aa)
|
Not recorded
|
A1D9R (2~{S})-2-[[6-methoxy-2-[(2-methyl-3-phenyl-phenyl)amino]pyrimidin-4-yl]methylamino]-3-oxidanyl-propanoic acid × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, HANGING DROP;289.15 K;Tris, potassium sodium tartrate tetrahydrate
|
Resolution 2.70 Å
R-free 0.287
|
|
9KSB
Crystal structure of X163
Deposited 2024-11-29
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
18–134(117 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
mmCIF provides none of the parsed conditions
|
Resolution 3.00 Å
R-free 0.279
|
|
9KSB
Crystal structure of X163
Deposited 2024-11-29
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain B
18–134(117 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
mmCIF provides none of the parsed conditions
|
Resolution 3.00 Å
R-free 0.279
|
|
9KSB
Crystal structure of X163
Deposited 2024-11-29
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain C
18–134(117 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
mmCIF provides none of the parsed conditions
|
Resolution 3.00 Å
R-free 0.279
|
|
9KSB
Crystal structure of X163
Deposited 2024-11-29
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 4
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain D
18–134(117 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
mmCIF provides none of the parsed conditions
|
Resolution 3.00 Å
R-free 0.279
|
|
9KSB
Crystal structure of X163
Deposited 2024-11-29
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 5
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain E
18–134(117 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
mmCIF provides none of the parsed conditions
|
Resolution 3.00 Å
R-free 0.279
|
|
9KSB
Crystal structure of X163
Deposited 2024-11-29
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 6
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain F
18–134(117 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
mmCIF provides none of the parsed conditions
|
Resolution 3.00 Å
R-free 0.279
|
|
9LJ3
Crystal structure of P25
Deposited 2025-01-14
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain B
18–134(117 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;289.15 K;0.2 M Sodium phosphate dibasic dihydrate,pH 9.1
20% w/v Polyethylene glycol 3,350
|
Resolution 3.15 Å
R-free 0.285
|
|
9LJ3
Crystal structure of P25
Deposited 2025-01-14
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain A
18–134(117 aa)
|
Not recorded
|
A1EJ6 3-[[4-chloranyl-2-[(2-hydroxyethylamino)methyl]-5-[[2-methyl-3-[3-[2-[2-[(3~{R})-3-oxidanylpyrrolidin-1-yl]ethoxy]ethoxy]phenyl]phenyl]methoxy]phenoxy]methyl]benzenecarbonitrile × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;289.15 K;0.2 M Sodium phosphate dibasic dihydrate,pH 9.1
20% w/v Polyethylene glycol 3,350
|
Resolution 3.15 Å
R-free 0.285
|
|
9LJ3
Crystal structure of P25
Deposited 2025-01-14
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain C
18–134(117 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;289.15 K;0.2 M Sodium phosphate dibasic dihydrate,pH 9.1
20% w/v Polyethylene glycol 3,350
|
Resolution 3.15 Å
R-free 0.285
|
|
9LJ3
Crystal structure of P25
Deposited 2025-01-14
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 4
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain D
18–134(117 aa)
|
Not recorded
|
A1EJ6 3-[[4-chloranyl-2-[(2-hydroxyethylamino)methyl]-5-[[2-methyl-3-[3-[2-[2-[(3~{R})-3-oxidanylpyrrolidin-1-yl]ethoxy]ethoxy]phenyl]phenyl]methoxy]phenoxy]methyl]benzenecarbonitrile × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;289.15 K;0.2 M Sodium phosphate dibasic dihydrate,pH 9.1
20% w/v Polyethylene glycol 3,350
|
Resolution 3.15 Å
R-free 0.285
|
|
9LJ3
Crystal structure of P25
Deposited 2025-01-14
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 5
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain E
18–134(117 aa)
|
Not recorded
|
A1EJ6 3-[[4-chloranyl-2-[(2-hydroxyethylamino)methyl]-5-[[2-methyl-3-[3-[2-[2-[(3~{R})-3-oxidanylpyrrolidin-1-yl]ethoxy]ethoxy]phenyl]phenyl]methoxy]phenoxy]methyl]benzenecarbonitrile × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;289.15 K;0.2 M Sodium phosphate dibasic dihydrate,pH 9.1
20% w/v Polyethylene glycol 3,350
|
Resolution 3.15 Å
R-free 0.285
|
|
9LJ3
Crystal structure of P25
Deposited 2025-01-14
|
Different construct
Different oligomeric state
Different experimental conditions
Different structure-quality metrics
|
Assembly 6
Protein monomer
Monomer;Protein × 1
PDB declaration: monomeric
|
Chain F
18–134(117 aa)
|
Not recorded
|
No recorded non-water small molecule
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;289.15 K;0.2 M Sodium phosphate dibasic dihydrate,pH 9.1
20% w/v Polyethylene glycol 3,350
|
Resolution 3.15 Å
R-free 0.285
|
|
9MAP
Crystal structure of GAGWLP and PD-L1
Deposited 2025-03-14
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein heterocomplex
Heteromer;Protein × 12
PDB declaration: dodecameric
|
Chain A
18–133(116 aa)
|
Not recorded
|
PO4 PHOSPHATE ION × 6
CA CALCIUM ION × 6
CL CHLORIDE ION × 6
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;289.15 K;pH 6.0,2.04M NaH2PO4 and K2HPO4
|
Resolution 3.00 Å
R-free 0.284
|
|
9MAP
Crystal structure of GAGWLP and PD-L1
Deposited 2025-03-14
|
Different construct
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein heterocomplex
Heteromer;Protein × 8
PDB declaration: octameric
|
Chain A
18–133(116 aa)
|
Not recorded
|
PO4 PHOSPHATE ION × 4
CA CALCIUM ION × 4
CL CHLORIDE ION × 4
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;289.15 K;pH 6.0,2.04M NaH2PO4 and K2HPO4
|
Resolution 3.00 Å
R-free 0.284
|
|
9MAP
Crystal structure of GAGWLP and PD-L1
Deposited 2025-03-14
|
Different construct
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein heterocomplex
Heteromer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–133(116 aa)
|
Not recorded
|
PO4 PHOSPHATE ION × 1
CA CALCIUM ION × 1
CL CHLORIDE ION × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;289.15 K;pH 6.0,2.04M NaH2PO4 and K2HPO4
|
Resolution 3.00 Å
R-free 0.284
|
|
9QSM
small molecule inhibitor in complex with PD-L1
Deposited 2025-04-05
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 1
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain A
18–134(117 aa)
Chain D
18–134(117 aa)
|
Not recorded
|
A1JAE ~{N}-[2-chloranyl-3-[2-chloranyl-3-[4-[[[2-(hydroxymethyl)-1,3-bis(oxidanyl)propan-2-yl]amino]methyl]-3-methoxy-phenyl]phenyl]phenyl]-5-[[[2-(hydroxymethyl)-1,3-bis(oxidanyl)propan-2-yl]amino]methyl]pyridine-2-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;0.1MBis-Tris 6.520% w/v PEG 5000 MME
|
Resolution 1.75 Å
R-free 0.270
|
|
9QSM
small molecule inhibitor in complex with PD-L1
Deposited 2025-04-05
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 2
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain B
18–134(117 aa)
Chain C
18–134(117 aa)
|
Not recorded
|
A1JAE ~{N}-[2-chloranyl-3-[2-chloranyl-3-[4-[[[2-(hydroxymethyl)-1,3-bis(oxidanyl)propan-2-yl]amino]methyl]-3-methoxy-phenyl]phenyl]phenyl]-5-[[[2-(hydroxymethyl)-1,3-bis(oxidanyl)propan-2-yl]amino]methyl]pyridine-2-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;0.1MBis-Tris 6.520% w/v PEG 5000 MME
|
Resolution 1.75 Å
R-free 0.270
|
|
9QSM
small molecule inhibitor in complex with PD-L1
Deposited 2025-04-05
|
Different construct
Different mutation/modification
Different oligomeric state
Different ligand/ion
Different experimental conditions
Different structure-quality metrics
|
Assembly 3
Protein homooligomer
Homooligomer;Protein × 2
PDB declaration: dimeric
|
Chain E
18–134(117 aa)
Chain F
18–134(117 aa)
|
Not recorded
|
A1JAE ~{N}-[2-chloranyl-3-[2-chloranyl-3-[4-[[[2-(hydroxymethyl)-1,3-bis(oxidanyl)propan-2-yl]amino]methyl]-3-methoxy-phenyl]phenyl]phenyl]-5-[[[2-(hydroxymethyl)-1,3-bis(oxidanyl)propan-2-yl]amino]methyl]pyridine-2-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray crystallization conditions
VAPOR DIFFUSION, SITTING DROP;293 K;0.1MBis-Tris 6.520% w/v PEG 5000 MME
|
Resolution 1.75 Å
R-free 0.270
|