1BN5
| HUMAN METHIONINE AMINOPEPTIDASE 2 | 分子名称: | COBALT (II) ION, METHIONINE AMINOPEPTIDASE, TERTIARY-BUTYL ALCOHOL | 著者 | Liu, S, Widom, J, Kemp, C.W, Crews, C.M, Clardy, J.C. | 登録日 | 1998-07-31 | 公開日 | 1999-07-31 | 最終更新日 | 2023-08-09 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Structure of human methionine aminopeptidase-2 complexed with fumagillin. Science, 282, 1998
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1BOA
| HUMAN METHIONINE AMINOPEPTIDASE 2 COMPLEXED WITH ANGIOGENESIS INHIBITOR FUMAGILLIN | 分子名称: | COBALT (II) ION, FUMAGILLIN, METHIONINE AMINOPEPTIDASE | 著者 | Liu, S, Widom, J, Kemp, C.W, Crews, C.M, Clardy, J.C. | 登録日 | 1998-08-01 | 公開日 | 1999-08-01 | 最終更新日 | 2023-08-09 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Structure of human methionine aminopeptidase-2 complexed with fumagillin. Science, 282, 1998
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1B6A
| HUMAN METHIONINE AMINOPEPTIDASE 2 COMPLEXED WITH TNP-470 | 分子名称: | (1R,2S,3S,4R)-4-hydroxy-2-methoxy-4-methyl-3-[(2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]cyclohexyl (chloroacetyl)carbamate, COBALT (II) ION, METHIONINE AMINOPEPTIDASE | 著者 | Liu, S, Clardy, J.C. | 登録日 | 1999-01-13 | 公開日 | 2000-01-13 | 最終更新日 | 2023-08-02 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Structure of human methionine aminopeptidase-2 complexed with fumagillin. Science, 282, 1998
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1B59
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6WV5
| Human VKOR C43S mutant with vitamin K1 epoxide | 分子名称: | (2R,3R)-2-hydroxy-3-methyl-2-[(2E,7S)-3,7,11,15-tetramethylhexadec-2-en-1-yl]-2,3-dihydronaphthalene-1,4-dione, Vitamin K epoxide reductase Cys43Ser mutant, termini restrained by green fluorescent protein | 著者 | Liu, S, Sukumar, N, Li, W. | 登録日 | 2020-05-05 | 公開日 | 2020-11-11 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Structural basis of antagonizing the vitamin K catalytic cycle for anticoagulation. Science, 371, 2021
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6WV6
| Human VKOR with phenindione | 分子名称: | (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate, Phenindione, Vitamin K epoxide reductase, ... | 著者 | Liu, S, Sukumar, N, Li, W. | 登録日 | 2020-05-05 | 公開日 | 2020-11-11 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | Structural basis of antagonizing the vitamin K catalytic cycle for anticoagulation. Science, 371, 2021
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6WV3
| Human VKOR with warfarin | 分子名称: | (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate, S-WARFARIN, Vitamin K epoxide reductase, ... | 著者 | Liu, S, Sukumar, N, Li, W. | 登録日 | 2020-05-05 | 公開日 | 2020-11-11 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.197 Å) | 主引用文献 | Structural basis of antagonizing the vitamin K catalytic cycle for anticoagulation. Science, 371, 2021
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6WVH
| Human VKOR with Brodifacoum | 分子名称: | (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate, Brodifacoum, Vitamin K epoxide reductase, ... | 著者 | Liu, S, Sukumar, N, Li, W. | 登録日 | 2020-05-06 | 公開日 | 2020-11-11 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (1.99 Å) | 主引用文献 | Structural basis of antagonizing the vitamin K catalytic cycle for anticoagulation. Science, 371, 2021
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6WVB
| Takifugu rubripes VKOR-like with warfarin | 分子名称: | S-WARFARIN, Vitamin K epoxide reductase-like protein, termini restrained by green fluorescent protein | 著者 | Liu, S, Sukumar, N, Li, W. | 登録日 | 2020-05-05 | 公開日 | 2020-11-11 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.872 Å) | 主引用文献 | Structural basis of antagonizing the vitamin K catalytic cycle for anticoagulation. Science, 371, 2021
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6WV4
| Human VKOR C43S with warfarin | 分子名称: | S-WARFARIN, Vitamin K epoxide reductase Cys43Ser mutant, termini restrained by green fluorescent protein | 著者 | Liu, S, Sukumar, N, Li, W. | 登録日 | 2020-05-05 | 公開日 | 2020-11-11 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (3.012 Å) | 主引用文献 | Structural basis of antagonizing the vitamin K catalytic cycle for anticoagulation. Science, 371, 2021
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6WV8
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4YHU
| Yeast Prp3 C-terminal fragment 296-469 | 分子名称: | U4/U6 small nuclear ribonucleoprotein PRP3, YTTRIUM (III) ION | 著者 | Liu, S, Wahl, M.C. | 登録日 | 2015-02-27 | 公開日 | 2015-07-22 | 最終更新日 | 2015-09-30 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | A composite double-/single-stranded RNA-binding region in protein Prp3 supports tri-snRNP stability and splicing. Elife, 4, 2015
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1D3G
| HUMAN DIHYDROOROTATE DEHYDROGENASE COMPLEXED WITH BREQUINAR ANALOG | 分子名称: | 2-BIPHENYL-4-YL-6-FLUORO-3-METHYL-QUINOLINE-4-CARBOXYLIC ACID, ACETATE ION, DECYLAMINE-N,N-DIMETHYL-N-OXIDE, ... | 著者 | Liu, S, Neidhardt, E.A, Grossman, T.H, Ocain, T, Clardy, J. | 登録日 | 1999-09-29 | 公開日 | 2000-09-13 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | Structures of human dihydroorotate dehydrogenase in complex with antiproliferative agents. Structure Fold.Des., 8, 2000
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1D3H
| HUMAN DIHYDROOROTATE DEHYDROGENASE COMPLEXED WITH ANTIPROLIFERATIVE AGENT A771726 | 分子名称: | (2Z)-2-cyano-3-hydroxy-N-[4-(trifluoromethyl)phenyl]but-2-enamide, ACETATE ION, DIHYDROOROTATE DEHYDROGENASE, ... | 著者 | Liu, S, Neidhardt, E.A, Grossman, T.H, Ocain, T, Clardy, J. | 登録日 | 1999-09-29 | 公開日 | 2000-08-13 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | 主引用文献 | Structures of human dihydroorotate dehydrogenase in complex with antiproliferative agents. Structure Fold.Des., 8, 2000
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6WVE
| Chicken SPCS1 | 分子名称: | Green fluorescent protein,Chicken Signal Peptidase Complex Subunit 1,Green fluorescent protein | 著者 | Liu, S, Li, W. | 登録日 | 2020-05-05 | 公開日 | 2021-01-13 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.429 Å) | 主引用文献 | Termini restraining of small membrane proteins enables structure determination at near-atomic resolution. Sci Adv, 6, 2020
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6WVF
| E.coli DsbB C104S with ubiquinone | 分子名称: | Green fluorescent protein,Disulfide bond formation protein B,Green fluorescent protein, UBIQUINONE-1 | 著者 | Liu, S, Li, W. | 登録日 | 2020-05-05 | 公開日 | 2021-01-13 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.9 Å) | 主引用文献 | Termini restraining of small membrane proteins enables structure determination at near-atomic resolution. Sci Adv, 6, 2020
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6WVI
| VKOR-like from Takifugu rubripes | 分子名称: | (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate, Vitamin K epoxide reductase-like protein, termini restrained by green fluorescent protein | 著者 | Liu, S, Sukumar, N, Li, W. | 登録日 | 2020-05-06 | 公開日 | 2020-11-11 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Structural basis of antagonizing the vitamin K catalytic cycle for anticoagulation. Science, 371, 2021
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6WV7
| Human VKOR with Chlorophacinone | 分子名称: | Chlorophacinone, Vitamin K epoxide reductase, termini restrained by green fluorescent protein | 著者 | Liu, S, Sukumar, N, Li, W. | 登録日 | 2020-05-05 | 公開日 | 2020-11-11 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.483 Å) | 主引用文献 | Structural basis of antagonizing the vitamin K catalytic cycle for anticoagulation. Science, 371, 2021
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6WV9
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6WVA
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4ZA1
| Crystal Structure of NosA Involved in Nosiheptide Biosynthesis | 分子名称: | 2,3-DIHYDROXY-1,4-DITHIOBUTANE, NosA | 著者 | Liu, S, Guo, H, Zhang, T, Han, L, Yao, P, Zhang, Y, Rong, N, Yu, Y, Lan, W, Wang, C, Ding, J, Wang, R, Liu, W, Cao, C. | 登録日 | 2015-04-13 | 公開日 | 2015-08-19 | 最終更新日 | 2024-03-20 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Structure-based Mechanistic Insights into Terminal Amide Synthase in Nosiheptide-Represented Thiopeptides Biosynthesis Sci Rep, 5, 2015
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8EGU
| Branched chain ketoacid dehydrogenase kinase complexes | 分子名称: | (2~{S})-3-methyl-2-[pentanoyl-[[4-[2-(2~{H}-1,2,3,4-tetrazol-5-yl)phenyl]phenyl]methyl]amino]butanoic acid, ADENOSINE-5'-DIPHOSPHATE, SULFATE ION, ... | 著者 | Liu, S. | 登録日 | 2022-09-13 | 公開日 | 2023-03-08 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (1.923 Å) | 主引用文献 | Structural studies identify angiotensin II receptor blocker-like compounds as branched-chain ketoacid dehydrogenase kinase inhibitors. J.Biol.Chem., 299, 2023
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8EGF
| Branched chain ketoacid dehydrogenase kinase in complex with inhibitor | 分子名称: | (5P)-5-(4'-methyl[1,1'-biphenyl]-2-yl)-1H-tetrazole, ADENOSINE-5'-DIPHOSPHATE, POTASSIUM ION, ... | 著者 | Liu, S. | 登録日 | 2022-09-12 | 公開日 | 2023-03-08 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (1.85 Å) | 主引用文献 | Structural studies identify angiotensin II receptor blocker-like compounds as branched-chain ketoacid dehydrogenase kinase inhibitors. J.Biol.Chem., 299, 2023
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8EGD
| Branched chain ketoacid dehydrogenase kinase in complex with inhibitor | 分子名称: | 5-(4-methoxyphenyl)-1H-tetrazole, ADENOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, ... | 著者 | Liu, S. | 登録日 | 2022-09-12 | 公開日 | 2023-03-08 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (2.047 Å) | 主引用文献 | Structural studies identify angiotensin II receptor blocker-like compounds as branched-chain ketoacid dehydrogenase kinase inhibitors. J.Biol.Chem., 299, 2023
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8EGQ
| Branched chain ketoacid dehydrogenase kinase complexes | 分子名称: | (2S)-2-ethyl-4-{[(2'M)-2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl}-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine, ADENOSINE-5'-DIPHOSPHATE, SULFATE ION, ... | 著者 | Liu, S. | 登録日 | 2022-09-13 | 公開日 | 2023-03-08 | 最終更新日 | 2023-10-25 | 実験手法 | X-RAY DIFFRACTION (1.955 Å) | 主引用文献 | Structural studies identify angiotensin II receptor blocker-like compounds as branched-chain ketoacid dehydrogenase kinase inhibitors. J.Biol.Chem., 299, 2023
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