Loading
PDBj
メニューPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help
PDB: 8 件

7C2V
DownloadVisualize
BU of 7c2v by Molmil
Crystal Structure of IRAK4 kinase in complex with the inhibitor CA-4948
分子名称: 2-(2-methylpyridin-4-yl)-N-[2-morpholin-4-yl-5-[(3R)-3-oxidanylpyrrolidin-1-yl]-[1,3]oxazolo[4,5-b]pyridin-6-yl]-1,3-oxazole-4-carboxamide, Interleukin-1 receptor-associated kinase 4
著者Krishnamurthy, N.R, Robert, B.
登録日2020-05-09
公開日2020-11-25
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (2.44 Å)
主引用文献Discovery of CA-4948, an Orally Bioavailable IRAK4 Inhibitor for Treatment of Hematologic Malignancies.
Acs Med.Chem.Lett., 11, 2020
7C2W
DownloadVisualize
BU of 7c2w by Molmil
Crystal Structure of IRAK4 kinase in complex with a small molecule inhibitor
分子名称: Interleukin-1 receptor-associated kinase 4, N-(2-morpholin-4-yl-1,3-benzoxazol-6-yl)-6-pyridin-4-yl-pyridine-2-carboxamide
著者Krishnamurthy, N.R, Anirudha, L.
登録日2020-05-09
公開日2020-11-25
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (3.2 Å)
主引用文献Discovery of CA-4948, an Orally Bioavailable IRAK4 Inhibitor for Treatment of Hematologic Malignancies.
Acs Med.Chem.Lett., 11, 2020
1YBF
DownloadVisualize
BU of 1ybf by Molmil
Crystal structure of AMP nucleosidase from Bacteroides thetaiotaomicron VPI-5482
分子名称: AMP nucleosidase
著者Krishnamurthy, N.R, Swaminathan, S, Burley, S.K, New York SGX Research Center for Structural Genomics (NYSGXRC)
登録日2004-12-20
公開日2005-01-04
最終更新日2021-02-03
実験手法X-RAY DIFFRACTION (2.9 Å)
主引用文献Crystal structure of AMP nucleosidase from Bacteroides thetaiotaomicron
To be published
1XFJ
DownloadVisualize
BU of 1xfj by Molmil
Crystal structure of protein CC_0490 from Caulobacter crescentus, Pfam DUF152
分子名称: ACETATE ION, BETA-MERCAPTOETHANOL, GLYCEROL, ...
著者Krishnamurthy, N.R, Kumaran, D, Swaminathan, S, Burley, S.K, New York SGX Research Center for Structural Genomics (NYSGXRC)
登録日2004-09-14
公開日2004-09-21
最終更新日2021-02-03
実験手法X-RAY DIFFRACTION (1.75 Å)
主引用文献Crystal structure of a conserved hypothetical protein from Caulobacter crescentus
To be Published
1ZCC
DownloadVisualize
BU of 1zcc by Molmil
Crystal structure of glycerophosphodiester phosphodiesterase from Agrobacterium tumefaciens str.C58
分子名称: ACETATE ION, SULFATE ION, glycerophosphodiester phosphodiesterase
著者Krishnamurthy, N.R, Kumaran, D, Swaminathan, S, Burley, S.K, New York SGX Research Center for Structural Genomics (NYSGXRC)
登録日2005-04-11
公開日2005-05-03
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Crystal structure of glycerophosphodiester phosphodiesterase from Agrobacterium tumefaciens by SAD with a large asymmetric unit.
Proteins, 65, 2006
1U02
DownloadVisualize
BU of 1u02 by Molmil
Crystal structure of trehalose-6-phosphate phosphatase related protein
分子名称: GLYCEROL, MAGNESIUM ION, SODIUM ION, ...
著者Krishnamurthy, N.R, Kumaran, D, Swaminathan, S, Burley, S.K, New York SGX Research Center for Structural Genomics (NYSGXRC)
登録日2004-07-12
公開日2004-07-20
最終更新日2021-02-03
実験手法X-RAY DIFFRACTION (1.92 Å)
主引用文献Crystal structure of trehalose-6-phosphate phosphatase-related protein: biochemical and biological implications.
Protein Sci., 15, 2006
6INL
DownloadVisualize
BU of 6inl by Molmil
Crystal structure of CDK2 IN complex with Inhibitor CVT-313
分子名称: 2,2'-{[6-{[(4-methoxyphenyl)methyl]amino}-9-(propan-2-yl)-9H-purin-2-yl]azanediyl}di(ethan-1-ol), Cyclin-dependent kinase 2
著者Talapati, S.R, Krishnamurthy, N.R.
登録日2018-10-25
公開日2019-10-30
最終更新日2023-11-22
実験手法X-RAY DIFFRACTION (1.75 Å)
主引用文献Structure of cyclin-dependent kinase 2 (CDK2) in complex with the specific and potent inhibitor CVT-313.
Acta Crystallogr.,Sect.F, 76, 2020
4JOA
DownloadVisualize
BU of 4joa by Molmil
Crystal Structure of Human Anaplastic Lymphoma Kinase in complex with 7-azaindole based inhibitor
分子名称: 3-[1-(2,5-difluorobenzyl)-1H-pyrazol-4-yl]-5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine, ALK tyrosine kinase receptor
著者Hosahalli, S, Krishnamurthy, N.R, Lakshminarasimhan, A.
登録日2013-03-18
公開日2013-07-17
最終更新日2023-11-08
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献Discovery of 7-azaindole based anaplastic lymphoma kinase (ALK) inhibitors: wild type and mutant (L1196M) active compounds with unique binding mode
Bioorg.Med.Chem.Lett., 23, 2013

222926

件を2024-07-24に公開中

PDB statisticsPDBj update infoContact PDBjnumon