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8KCK
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BU of 8kck by Molmil
De novo design protein -N9
分子名称: De novo design protein -N9
著者Wang, S, Liu, Y.
登録日2023-08-07
公開日2024-08-14
実験手法X-RAY DIFFRACTION (1.35 Å)
主引用文献De novo design protein -N9
To Be Published
8KCV
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BU of 8kcv by Molmil
Crystal structure of UDA01-CAAMDDFQL
分子名称: Beta2-microglobulin, MHC class I antigen, peptide of AIV
著者Tang, Z, Zhang, N.
登録日2023-08-08
公開日2024-08-14
実験手法X-RAY DIFFRACTION (2.39 Å)
主引用文献Structure of duck MHC UDA01
To Be Published
8KD8
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BU of 8kd8 by Molmil
N(5)-hydroxyornithine:cis-anhydromevalonyl coenzyme A-N(5)-transacylase sidF N-terminal domain
分子名称: N(5)-hydroxyornithine:cis-anhydromevalonyl coenzyme A-N(5)-transacylase sidF
著者Poonsiri, T, Demitri, N, Benini, S.
登録日2023-08-09
公開日2024-08-14
実験手法X-RAY DIFFRACTION (2.581 Å)
主引用文献N(5)-hydroxyornithine:cis-anhydromevalonyl coenzyme A-N(5)-transacylase sidF N-terminal domain
To Be Published
8KDK
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BU of 8kdk by Molmil
Crystal structure of CcbF in complex with PLP
分子名称: CcbF
著者Mori, T, Lyu, S, Kadlcik, S, Abe, I.
登録日2023-08-09
公開日2024-08-14
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Crystal structure of CcbF in complex with PLP
To Be Published
8KDL
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BU of 8kdl by Molmil
Crystal structure of LmbF in complex with PLP
分子名称: Aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme, GLYCEROL
著者Mori, T, Lyu, S, Kadlcik, S, Abe, I.
登録日2023-08-09
公開日2024-08-14
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Structure of LmbF in complex with PLP
To Be Published
8KDQ
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BU of 8kdq by Molmil
De novo design protein -T03
分子名称: De novo design protein -T03
著者Wang, S, Liu, Y.
登録日2023-08-09
公開日2024-08-14
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献De novo design protein -T03
To Be Published
8KDU
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BU of 8kdu by Molmil
Crystal structure of trypsin with its substrate
分子名称: (2~{R})-2-benzamido-5-carbamimidamido-pentanoic acid, ARGININE, CALCIUM ION, ...
著者Akbar, Z, Ahmad, M.S.
登録日2023-08-10
公開日2024-08-14
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Crystal structure of trypsin with its substrate
To Be Published
8PWD
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BU of 8pwd by Molmil
Crystal structure of VDR in complex Des-C-Ring and Aromatic-D-Ring analog 3c
分子名称: (1R,3S,5Z)-4-methylidene-5-[(E)-3-[3-[7,7,7-tris(fluoranyl)-6-oxidanyl-6-(trifluoromethyl)hept-3-ynyl]phenyl]pent-2-enylidene]cyclohexane-1,3-diol, Nuclear receptor coactivator 2, Vitamin D3 receptor A
著者Rochel, N.
登録日2023-07-20
公開日2024-08-14
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Novel Des-C-Ring and Aromatic-D-Ring analogs Acting as Potent Agonists of the Vitamin D Receptor (VDR)
To Be Published
8PWF
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BU of 8pwf by Molmil
crystal structure of VDR in complex with Des-C-Ring and Aromatic-D-Ring analog 2
分子名称: (1R,3S,5Z)-4-methylidene-5-[(E)-3-[3-[7,7,7-tris(fluoranyl)-6-oxidanyl-6-(trifluoromethyl)heptyl]phenyl]pent-2-enylidene]cyclohexane-1,3-diol, Nuclear receptor coactivator 2, Vitamin D3 receptor A
著者rochel, N.
登録日2023-07-20
公開日2024-08-14
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Novel Des-C-Ring and Aromatic-D-Ring analogs Acting as Potent Agonists of the Vitamin D Receptor (VDR)
To Be Published
8Q23
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BU of 8q23 by Molmil
HsNMT1 in complex with both MyrCoA and Ac-D-ORN-SFSKPR inhibitor peptide
分子名称: ACE-ORD-SER-PHE-SER-LYS-PRO-ARG, CHLORIDE ION, GLYCEROL, ...
著者Dian, C, Giglione, C, Meinnel, T.
登録日2023-08-01
公開日2024-08-14
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献HsNMT1 in complex with both MyrCoA and Ac-D-ORN-SFSKPR inhibitor peptide
to be published
8Q24
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BU of 8q24 by Molmil
HsNMT1 in complex with both MyrCoA and (DAB)SFSKPR inhibitor peptide
分子名称: CHLORIDE ION, DAB-SER-PHE-SER-LYS-PRO-ARG, GLYCEROL, ...
著者Dian, C, Giglione, C, Meinnel, T.
登録日2023-08-01
公開日2024-08-14
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献HsNMT1 in complex with both MyrCoA and Dab-SFSKPR inhibitor peptide
to be published
8Q26
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BU of 8q26 by Molmil
HsNMT1 in complex with both MyrCoA and GNCFSKPR inhibitor peptide
分子名称: CHLORIDE ION, COENZYME A, Glycylpeptide N-tetradecanoyltransferase 1, ...
著者Dian, C, Giglione, C, Meinnel, T.
登録日2023-08-01
公開日2024-08-14
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献HsNMT1 in complex with both MyrCoA and GNCFSKPR inhibitor peptide
to be published
8Q2Z
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BU of 8q2z by Molmil
HsNMT1 in complex with both MyrCoA and GNLLSKFR peptide
分子名称: CHLORIDE ION, COENZYME A, GLYCEROL, ...
著者Dian, C, Giglione, C, Meinnel, T.
登録日2023-08-03
公開日2024-08-14
実験手法X-RAY DIFFRACTION (1.88 Å)
主引用文献HsNMT1 in complex with both MyrCoA and GNLLSKFR inhibitor peptide
to be published
8Q3D
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BU of 8q3d by Molmil
HsNMT1 in complex with both MyrCoA and GNCFSKPR(NH2) inhibitor peptide
分子名称: CHLORIDE ION, COENZYME A, GLYCEROL, ...
著者Dian, C, Giglione, C, Meinnel, T.
登録日2023-08-04
公開日2024-08-14
実験手法X-RAY DIFFRACTION (2.15 Å)
主引用文献HsNMT1 in complex with both MyrCoA and GNCFSKPR(NH2) inhibitor peptide
to be published
8Q3S
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BU of 8q3s by Molmil
HsNMT1 in complex with both MyrCoA and GNCFSKAR inhibitor peptide
分子名称: CHLORIDE ION, COENZYME A, GLY-ASN-CYS-PHE-SER-LYS-ALA-ARG, ...
著者Dian, C, Giglione, C, Meinnel, T.
登録日2023-08-04
公開日2024-08-14
実験手法X-RAY DIFFRACTION (1.78 Å)
主引用文献HsNMT1 in complex with both MyrCoA and GNCFSKAR inhibitor peptide
to be published
8Q3T
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BU of 8q3t by Molmil
HsNMT1 in complex with both MyrCoA and GNCFSKPRVPTK inhibitor peptide
分子名称: CHLORIDE ION, COENZYME A, GLYCEROL, ...
著者Dian, C, Giglione, C, Meinnel, T.
登録日2023-08-04
公開日2024-08-14
実験手法X-RAY DIFFRACTION (1.96 Å)
主引用文献HsNMT1 in complex with both MyrCoA and GNCFSKPR inhibitor peptide
to be published
8QFT
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BU of 8qft by Molmil
X-ray structure of non-toxic non-hemagglutinin (NTNH) protein from botulinum neurotoxin serotype X
分子名称: non-toxic non-hemagglutinin protein X
著者Skerlova, J, Masuyer, G, Stenmark, P.
登録日2023-09-04
公開日2024-08-14
実験手法X-RAY DIFFRACTION (3.3 Å)
主引用文献X-ray structure of non-toxic non-hemagglutinin (NTNH) protein from botulinum neurotoxin serotype X
To Be Published
8QQH
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BU of 8qqh by Molmil
Structure of beta-galactosidase from Desulfurococcus amyloliticus
分子名称: Beta-galactosidase
著者Samygina, V.R, Kil, Y, Sergeev, R.S, Rychkov, G.N.
登録日2023-10-04
公開日2024-08-14
実験手法X-RAY DIFFRACTION (2.15 Å)
主引用文献The archaeal highly thermostable GH35 family beta-galactosidase Da beta Gal has a unique seven domain protein fold.
Febs J., 2024
7ZYN
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BU of 7zyn by Molmil
Crystal Structure of EGFR-T790M/C797S in Complex with WZ4002
分子名称: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, Epidermal growth factor receptor, N-{3-[(5-chloro-2-{[2-methoxy-4-(4-methylpiperazin-1-yl)phenyl]amino}pyrimidin-4-yl)oxy]phenyl}prop-2-enamide
著者Niggenaber, J, Kleinboelting, S, Mueller, M.P, Rauh, D.
登録日2022-05-25
公開日2023-05-03
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Addressing the Osimertinib Resistance Mutation EGFR-L858R/C797S with Reversible Aminopyrimidines.
Acs Med.Chem.Lett., 14, 2023
7ZYM
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BU of 7zym by Molmil
Crystal Structure of EGFR-T790M/C797S in Complex with Brigatinib
分子名称: 5-chloro-N~4~-[2-(dimethylphosphoryl)phenyl]-N~2~-{2-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl}pyrimidine-2,4-diamine, Epidermal growth factor receptor
著者Niggenaber, J, Kleinboelting, S, Mueller, M.P, Rauh, D.
登録日2022-05-25
公開日2023-05-03
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Addressing the Osimertinib Resistance Mutation EGFR-L858R/C797S with Reversible Aminopyrimidines.
Acs Med.Chem.Lett., 14, 2023
7ZYP
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BU of 7zyp by Molmil
Crystal Structure of EGFR-T790M/C797S in Complex with Reversible Aminopyrimidine 9
分子名称: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, Epidermal growth factor receptor, propan-2-yl 2-[[4-(4-azanylpiperidin-1-yl)-2-methoxy-phenyl]amino]-4-(1-methylindol-3-yl)pyrimidine-5-carboxylate
著者Niggenaber, J, Kleinboelting, S, Mueller, M.P, Rauh, D.
登録日2022-05-25
公開日2023-05-03
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Addressing the Osimertinib Resistance Mutation EGFR-L858R/C797S with Reversible Aminopyrimidines.
Acs Med.Chem.Lett., 14, 2023
7ZYQ
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BU of 7zyq by Molmil
Crystal Structure of EGFR-T790M/V948R in Complex with Reversible Aminopyrimidine 13
分子名称: CHLORIDE ION, Epidermal growth factor receptor, SODIUM ION, ...
著者Niggenaber, J, Mueller, M.P, Rauh, D.
登録日2022-05-25
公開日2023-05-03
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Addressing the Osimertinib Resistance Mutation EGFR-L858R/C797S with Reversible Aminopyrimidines.
Acs Med.Chem.Lett., 14, 2023
4I43
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BU of 4i43 by Molmil
Crystal structure of Prp8:Aar2 complex
分子名称: A1 cistron-splicing factor AAR2, Pre-mRNA-splicing factor 8
著者Galej, W.P, Oubridge, C, Newman, A.J, Nagai, K.
登録日2012-11-27
公開日2013-01-23
最終更新日2023-09-20
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Crystal structure of Prp8 reveals active site cavity of the spliceosome.
Nature, 493, 2013
7QB1
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BU of 7qb1 by Molmil
PPARg in complex with inhibitor
分子名称: 3-[(3,4-dichlorophenyl)methyl]-4-oxidanylidene-6-phenoxy-phthalazine-1-carboxylic acid, Peroxisome proliferator-activated receptor gamma, SULFATE ION
著者Petersen, J.
登録日2021-11-17
公開日2022-05-04
最終更新日2024-05-01
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Discovery by Virtual Screening of an Inhibitor of CDK5-Mediated PPAR gamma Phosphorylation.
Acs Med.Chem.Lett., 13, 2022
4HAS
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BU of 4has by Molmil
Crystal structure of PX domain of human sorting nexin SNX27
分子名称: 1,2-ETHANEDIOL, CITRIC ACID, Sorting nexin-27
著者Froese, D.S, Krojer, T, Strain-Damerell, C, Allerston, C, Kiyani, W, Burgess-Brown, N, von Delft, F, Arrowsmith, C, Bountra, C, Edwards, A, Yue, W.W, Structural Genomics Consortium (SGC)
登録日2012-09-27
公開日2013-04-24
最終更新日2024-02-28
実験手法X-RAY DIFFRACTION (1.74 Å)
主引用文献Crystal structure of PX domain of human sorting nexin SNX27
To be Published

223790

件を2024-08-14に公開中

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