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PDB: 312 件

4EWS
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Crystal structure of cholesteryl ester transfer protein in complex with inhibitors
分子名称: 1,2-DILINOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE, CETP, CHLORIDE ION, ...
著者Liu, S, Qiu, X.
登録日2012-04-27
公開日2012-09-05
最終更新日2023-09-13
実験手法X-RAY DIFFRACTION (2.59 Å)
主引用文献Crystal structures of cholesteryl ester transfer protein in complex with inhibitors.
J.Biol.Chem., 287, 2012
6KKU
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human KCC1 structure determined in NaCl and GDN
分子名称: 2-[2-[(1~{S},2~{S},4~{S},5'~{R},6~{R},7~{S},8~{R},9~{S},12~{S},13~{R},16~{S})-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icos-18-ene-6,2'-oxane]-16-yl]oxyethyl]propane-1,3-diol, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, CHLORIDE ION, ...
著者Liu, S, Chang, S, Ye, S, Bai, X, Guo, J.
登録日2019-07-27
公開日2019-10-23
最終更新日2020-07-29
実験手法ELECTRON MICROSCOPY (3.5 Å)
主引用文献Cryo-EM structures of the human cation-chloride cotransporter KCC1.
Science, 366, 2019
4F2A
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BU of 4f2a by Molmil
Crystal structure of cholestryl esters transfer protein in complex with inhibitors
分子名称: (2R)-3-{[4-(4-chloro-3-ethylphenoxy)pyrimidin-2-yl][3-(1,1,2,2-tetrafluoroethoxy)benzyl]amino}-1,1,1-trifluoropropan-2-ol, 1,2-DIOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE, CHLORIDE ION, ...
著者Liu, S, Qiu, X.
登録日2012-05-07
公開日2012-09-05
最終更新日2020-07-29
実験手法X-RAY DIFFRACTION (3.11 Å)
主引用文献Crystal structures of cholesteryl ester transfer protein in complex with inhibitors.
J.Biol.Chem., 287, 2012
3VEV
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Glucokinase in complex with an activator and glucose
分子名称: (2S)-3-cyclopentyl-N-(5-methylpyridin-2-yl)-2-[2-oxo-4-(trifluoromethyl)pyridin-1(2H)-yl]propanamide, Glucokinase, SODIUM ION, ...
著者Liu, S.
登録日2012-01-09
公開日2012-02-08
最終更新日2023-09-13
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Insights into Mechanism of Glucokinase Activation: OBSERVATION OF MULTIPLE DISTINCT PROTEIN CONFORMATIONS.
J.Biol.Chem., 287, 2012
3VF6
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Glucokinase in complex with glucose and activator
分子名称: 6-({(2S)-3-cyclopentyl-2-[4-(trifluoromethyl)-1H-imidazol-1-yl]propanoyl}amino)pyridine-3-carboxylic acid, Glucokinase, SODIUM ION, ...
著者Liu, S.
登録日2012-01-09
公開日2012-02-08
最終更新日2024-02-28
実験手法X-RAY DIFFRACTION (1.86 Å)
主引用文献Insights into Mechanism of Glucokinase Activation: OBSERVATION OF MULTIPLE DISTINCT PROTEIN CONFORMATIONS.
J.Biol.Chem., 287, 2012
3VEY
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glucokinase in complex with glucose and ATPgS
分子名称: 6-methoxy-N-(1-methyl-1H-pyrazol-3-yl)quinazolin-4-amine, Glucokinase, PHOSPHOTHIOPHOSPHORIC ACID-ADENYLATE ESTER, ...
著者Liu, S.
登録日2012-01-09
公開日2012-02-08
最終更新日2024-02-28
実験手法X-RAY DIFFRACTION (2.25 Å)
主引用文献Insights into Mechanism of Glucokinase Activation: OBSERVATION OF MULTIPLE DISTINCT PROTEIN CONFORMATIONS.
J.Biol.Chem., 287, 2012
4Q9O
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BU of 4q9o by Molmil
Crystal structure of Upps + inhibitor
分子名称: 3-(2-chlorophenyl)-5-methyl-N-[4-(propan-2-yl)phenyl]-1,2-oxazole-4-carboxamide, Isoprenyl transferase, SULFATE ION
著者Liu, S, Qiu, X.
登録日2014-05-01
公開日2014-10-15
最終更新日2024-02-28
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Discovery and structural characterization of an allosteric inhibitor of bacterial cis-prenyltransferase.
Protein Sci., 24, 2015
4QEB
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Dcps in complex with covalent inhibitor targeting Tyrosine
分子名称: 3-{[(2,4-diaminoquinazolin-5-yl)oxy]methyl}benzenesulfonic acid, PHOSPHATE ION, m7GpppX diphosphatase
著者Liu, S.
登録日2014-05-15
公開日2015-05-20
最終更新日2023-09-20
実験手法X-RAY DIFFRACTION (3.21 Å)
主引用文献Human Dcps in complex with covalent inhibitor
To be Published
4QDV
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Dcps in complex with covalent ligand
分子名称: 4-{[(2,4-diaminoquinazolin-5-yl)oxy]methyl}benzenesulfonic acid, GLYCEROL, PHOSPHATE ION, ...
著者Liu, S.
登録日2014-05-14
公開日2015-05-20
最終更新日2024-03-06
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Dcps in complex with covalent ligands targeting Tyrosines
To be Published
4QDE
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Dcps in complex with covalent inhibitor
分子名称: 2-{[(2,4-diaminoquinazolin-5-yl)oxy]methyl}benzenesulfonic acid, PHOSPHATE ION, m7GpppX diphosphatase
著者Liu, S.
登録日2014-05-13
公開日2015-05-13
最終更新日2023-09-20
実験手法X-RAY DIFFRACTION (2.9 Å)
主引用文献Dcps in complex with covalent inhibitors
To be Published
4Q9M
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Crystal structure of UPPs in complex with FPP and an allosteric inhibitor
分子名称: 3-(2-chlorophenyl)-5-methyl-N-[4-(propan-2-yl)phenyl]-1,2-oxazole-4-carboxamide, CADMIUM ION, FARNESYL DIPHOSPHATE, ...
著者Liu, S, Qiu, X.
登録日2014-05-01
公開日2014-10-15
最終更新日2024-02-28
実験手法X-RAY DIFFRACTION (2.06 Å)
主引用文献Discovery and structural characterization of an allosteric inhibitor of bacterial cis-prenyltransferase.
Protein Sci., 24, 2015
2MA1
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BU of 2ma1 by Molmil
Solution structure of HRDC1 domain of RecQ helicase from Deinococcus radiodurans
分子名称: DNA helicase RecQ
著者Liu, S, Zhang, W, Gao, Z, Ming, Q, Hou, H, Lan, W, Wu, H, Cao, C, Dong, Y.
登録日2013-06-24
公開日2013-07-10
最終更新日2024-05-15
実験手法SOLUTION NMR
主引用文献NMR structure of the N-terminal-most HRDC1 domain of RecQ helicase from Deinococcus radiodurans
To be Published
4TN6
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BU of 4tn6 by Molmil
CK1d in complex with inhibitor
分子名称: 4-{4-(4-fluorophenyl)-1-[1-(1,2-oxazol-3-ylmethyl)piperidin-4-yl]-1H-imidazol-5-yl}pyrimidin-2-amine, Casein kinase I isoform delta, SULFATE ION
著者Liu, S.
登録日2014-06-03
公開日2015-08-12
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (2.41 Å)
主引用文献CK1D IN COMPLEX WITH inhibitor
To Be Published
3SIU
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BU of 3siu by Molmil
Structure of a hPrp31-15.5K-U4atac 5' stem loop complex, monomeric form
分子名称: NHP2-like protein 1, SULFATE ION, U4/U6 small nuclear ribonucleoprotein Prp31, ...
著者Liu, S, Ghalei, H, Luhrmann, R, Wahl, M.C.
登録日2011-06-20
公開日2011-08-10
最終更新日2023-09-13
実験手法X-RAY DIFFRACTION (2.626 Å)
主引用文献Structural basis for the dual U4 and U4atac snRNA-binding specificity of spliceosomal protein hPrp31.
Rna, 17, 2011
2I80
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BU of 2i80 by Molmil
Allosteric inhibition of Staphylococcus aureus D-alanine:D-alanine ligase revealed by crystallographic studies
分子名称: 3-CHLORO-2,2-DIMETHYL-N-[4-(TRIFLUOROMETHYL)PHENYL]PROPANAMIDE, D-alanine-D-alanine ligase
著者Liu, S, Chang, J.S, Herberg, J.T, Horng, M.-M, Tomich, P.K, Lin, A.H, Marotti, K.R.
登録日2006-08-31
公開日2006-09-26
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.19 Å)
主引用文献Allosteric inhibition of Staphylococcus aureus D-alanine:D-alanine ligase revealed by crystallographic studies.
Proc.Natl.Acad.Sci.Usa, 103, 2006
2FYS
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BU of 2fys by Molmil
Crystal structure of Erk2 complex with KIM peptide derived from MKP3
分子名称: Dual specificity protein phosphatase 6, Mitogen-activated protein kinase 1
著者Liu, S, Sun, J.P, Zhou, B, Zhang, Z.Y.
登録日2006-02-08
公開日2006-04-11
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Structural basis of docking interactions between ERK2 and MAP kinase phosphatase 3
Proc.Natl.Acad.Sci.Usa, 103, 2006
3SIV
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BU of 3siv by Molmil
Structure of a hPrp31-15.5K-U4atac 5' stem loop complex, dimeric form
分子名称: NHP2-like protein 1, U4/U6 small nuclear ribonucleoprotein Prp31, U4atac snRNA
著者Liu, S, Ghalei, H, Luhrmann, R, Wahl, M.C.
登録日2011-06-20
公開日2011-08-10
最終更新日2023-09-13
実験手法X-RAY DIFFRACTION (3.304 Å)
主引用文献Structural basis for the dual U4 and U4atac snRNA-binding specificity of spliceosomal protein hPrp31.
Rna, 17, 2011
2I8C
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BU of 2i8c by Molmil
Allosteric inhibition of Staphylococcus aureus D-alanine:D-alanine ligase revealed by crystallographic studies
分子名称: ADENOSINE-5'-DIPHOSPHATE, D-alanine-D-alanine ligase, MAGNESIUM ION, ...
著者Liu, S, Chang, J.S, Herberg, J.T, Horng, M, Tomich, P.K, Lin, A.H, Marotti, K.R.
登録日2006-09-01
公開日2006-09-26
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.46 Å)
主引用文献Allosteric inhibition of Staphylococcus aureus D-alanine:D-alanine ligase revealed by crystallographic studies.
Proc.Natl.Acad.Sci.Usa, 103, 2006
2GV9
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Crystal structure of the Herpes Simplex virus type 1 DNA polymerase
分子名称: DNA polymerase, GUANIDINE, MERCURY (II) ION, ...
著者Liu, S.
登録日2006-05-02
公開日2006-05-16
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (2.68 Å)
主引用文献Crystal structure of the herpes simplex virus 1 DNA polymerase.
J.Biol.Chem., 281, 2006
5W4W
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BU of 5w4w by Molmil
Identification and Profiling of a Selective and Brain Penetrant Radioligand for In Vivo Target Occupancy Measurement of Casein Kinase 1 (CK1) Inhibitors
分子名称: 4-[3-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]-6-methyl-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-5-one, Casein kinase I isoform delta, SULFATE ION
著者Liu, S.
登録日2017-06-13
公開日2017-06-28
最終更新日2024-03-13
実験手法X-RAY DIFFRACTION (1.99 Å)
主引用文献Identification and Profiling of a Selective and Brain Penetrant Radioligand for in Vivo Target Occupancy Measurement of Casein Kinase 1 (CK1) Inhibitors.
ACS Chem Neurosci, 8, 2017
2I87
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BU of 2i87 by Molmil
Allosteric inhibition of Staphylococcus aureus D-alanine:D-alanine ligase revealed by crystallographic studies
分子名称: D-alanine-D-alanine ligase, SULFATE ION
著者Liu, S, Chang, J.S, Herberg, J.T, Horng, M, Tomich, P.K, Lin, A.H, Marotti, K.R.
登録日2006-09-01
公開日2006-10-03
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Allosteric inhibition of Staphylococcus aureus D-alanine:D-alanine ligase revealed by crystallographic studies.
Proc.Natl.Acad.Sci.Usa, 103, 2006
4KIK
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Human IkB kinase beta
分子名称: Inhibitor of nuclear factor kappa-B kinase subunit beta, K-252A
著者Liu, S, Mosyak, L.
登録日2013-05-02
公開日2013-06-26
最終更新日2013-08-28
実験手法X-RAY DIFFRACTION (2.83 Å)
主引用文献Crystal Structure of a Human I kappa B Kinase beta Asymmetric Dimer.
J.Biol.Chem., 288, 2013
4NV5
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C50A mutant of Synechococcus VKOR, C2 crystal form (dehydrated)
分子名称: UBIQUINONE-10, VKORC1/thioredoxin domain protein
著者Liu, S, Cheng, W, Fowle Grider, R, Shen, G, Li, W.
登録日2013-12-04
公開日2014-02-12
実験手法X-RAY DIFFRACTION (2.79 Å)
主引用文献Structures of an intramembrane vitamin K epoxide reductase homolog reveal control mechanisms for electron transfer.
Nat Commun, 5, 2014
4NV6
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C212A mutant of Synechococcus VKOR
分子名称: UBIQUINONE-10, VKORC1/thioredoxin domain protein
著者Liu, S, Cheng, W, Fowle Grider, R, Shen, G, Li, W.
登録日2013-12-04
公開日2014-02-12
実験手法X-RAY DIFFRACTION (4.19 Å)
主引用文献Structures of an intramembrane vitamin K epoxide reductase homolog reveal control mechanisms for electron transfer.
Nat Commun, 5, 2014
4NV2
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C50A mutant of Synechococcus VKOR, C2221 crystal form
分子名称: UBIQUINONE-10, VKORC1/thioredoxin domain protein
著者Liu, S, Cheng, W, Fowle Grider, R, Shen, G, Li, W.
登録日2013-12-04
公開日2014-02-12
実験手法X-RAY DIFFRACTION (3.61 Å)
主引用文献Structures of an intramembrane vitamin K epoxide reductase homolog reveal control mechanisms for electron transfer.
Nat Commun, 5, 2014

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件を2024-08-21に公開中

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