3OXK
 
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5ZUH
 
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6DXS
 
 | Crystal structure of the LigJ hydratase E284Q mutant substrate complex with (3Z)-2-keto-4-carboxy-3-hexenedioate | 分子名称: | (2Z)-4-oxobut-2-ene-1,2,4-tricarboxylic acid, 4-oxalomesaconate hydratase, ZINC ION | 著者 | Mabanglo, M.F, Raushel, F.M, Hogancamp, T.N. | 登録日 | 2018-06-29 | 公開日 | 2018-09-26 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (1.65 Å) | 主引用文献 | Structure and Reaction Mechanism of the LigJ Hydratase: An Enzyme Critical for the Bacterial Degradation of Lignin in the Protocatechuate 4,5-Cleavage Pathway. Biochemistry, 57, 2018
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1OW5
 
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1MZT
 
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6EGC
 
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5WFN
 
 | Revised model of leiomodin 2-mediated actin regulation (alternate refinement of PDB 4RWT) | 分子名称: | Actin-5C, Leiomodin-2, MAGNESIUM ION, ... | 著者 | Yurtsever, Z, Eck, M.J, Dominguez, R. | 登録日 | 2017-07-12 | 公開日 | 2017-08-30 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (3 Å) | 主引用文献 | Crystal structure of leiomodin 2 in complex with actin: a structural and functional reexamination Biophys.J., 113, 2017
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1M3V
 
 | FLIN4: Fusion of the LIM binding domain of Ldb1 and the N-terminal LIM domain of LMO4 | 分子名称: | ZINC ION, fusion of the LIM interacting domain of ldb1 and the N-terminal LIM domain of LMO4 | 著者 | Deane, J.E, Mackay, J.P, Kwan, A.H.Y, Sum, E.Y, Visvader, J.E, Matthews, J.M. | 登録日 | 2002-06-30 | 公開日 | 2003-05-13 | 最終更新日 | 2024-05-15 | 実験手法 | SOLUTION NMR | 主引用文献 | Structural basis for the recognition of ldb1 by the N-terminal LIM domains of LMO2 and LMO4 EMBO J., 22, 2003
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1XQI
 
 | Crystal Structure Analysis of an NDP kinase from Pyrobaculum aerophilum | 分子名称: | 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, Nucleoside diphosphate kinase, TRIETHYLENE GLYCOL | 著者 | Pedelacq, J.D, Waldo, G.S, Cabantous, S, Liong, E.C, Berendzen, J, Terwilliger, T.C. | 登録日 | 2004-10-12 | 公開日 | 2005-09-20 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Structural and functional features of an NDP kinase from the hyperthermophile crenarchaeon Pyrobaculum aerophilum Protein Sci., 14, 2005
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1N2Y
 
 | SOLUTION STRUCTURE OF SS-CYCLIZED CATESTATIN FRAGMENT FROM CHROMOGRANIN A | 分子名称: | CATESTATIN | 著者 | Preece, N.E, Nguyen, M, Mahata, M, Mahata, S.K, Mahapatra, N.R, Tsigelny, I, O'Connor, D.T. | 登録日 | 2002-10-24 | 公開日 | 2002-11-13 | 最終更新日 | 2024-11-20 | 実験手法 | SOLUTION NMR | 主引用文献 | Conformational preferences and activities of peptides from the catecholamine
release-inhibitory (catestatin) region of chromogranin A Regul.Pept., 118, 2004
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1XFT
 
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1Y4O
 
 | Solution structure of a mouse cytoplasmic Roadblock/LC7 dynein light chain | 分子名称: | Dynein light chain 2A, cytoplasmic | 著者 | Song, J, Tyler, R.C, Lee, M.S, Tyler, E.M, Markley, J.L, Center for Eukaryotic Structural Genomics (CESG) | 登録日 | 2004-12-01 | 公開日 | 2005-01-18 | 最終更新日 | 2024-05-22 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structure of isoform 1 of Roadblock/LC7, a light chain in the dynein complex. J.Mol.Biol., 354, 2005
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1MM0
 
 | Solution structure of termicin, an antimicrobial peptide from the termite Pseudacanthotermes spiniger | 分子名称: | Termicin | 著者 | Da Silva, P, Jouvensal, L, Lamberty, M, Bulet, P, Caille, A, Vovelle, F. | 登録日 | 2002-09-02 | 公開日 | 2003-05-13 | 最終更新日 | 2024-10-23 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structure of termicin, an antimicrobial peptide from the termite Pseudacanthotermes spiniger PROTEIN SCI., 12, 2003
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1UPN
 
 | COMPLEX OF ECHOVIRUS TYPE 12 WITH DOMAINS 3 AND 4 OF ITS RECEPTOR DECAY ACCELERATING FACTOR (CD55) BY CRYO ELECTRON MICROSCOPY AT 16 A | 分子名称: | COMPLEMENT DECAY-ACCELERATING FACTOR, ECHOVIRUS 11 COAT PROTEIN VP1, ECHOVIRUS 11 COAT PROTEIN VP2, ... | 著者 | Bhella, D, Goodfellow, I.G, Roversi, P, Pettigrew, D, Chaudry, Y, Evans, D.J, Lea, S.M. | 登録日 | 2003-10-08 | 公開日 | 2004-01-07 | 最終更新日 | 2024-10-09 | 実験手法 | ELECTRON MICROSCOPY (16 Å) | 主引用文献 | The Structure of Echovirus Type 12 Bound to a Two-Domain Fragment of its Cellular Attachment Protein Decay-Accelerating Factor (Cd 55) J.Biol.Chem., 279, 2004
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2KN9
 
 | Solution structure of zinc-substituted rubredoxin B (Rv3250c) from Mycobacterium tuberculosis. Seattle Structural Genomics Center for Infectious Disease target MytuD.01635.a | 分子名称: | Rubredoxin, ZINC ION | 著者 | Buchko, G.W, Hewitt, S.N, Napuli, A.J, Van Voorhis, W.C, Seattle Structural Genomics Center for Infectious Disease (SSGCID) | 登録日 | 2009-08-20 | 公開日 | 2009-09-15 | 最終更新日 | 2024-05-01 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution-state NMR structure and biophysical characterization of zinc-substituted rubredoxin B (Rv3250c) from Mycobacterium tuberculosis. Acta Crystallogr.,Sect.F, 67, 2011
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2KOK
 
 | Solution structure of an arsenate reductase (ArsC) related protein from Brucella melitensis. Seattle Structural Genomics Center for Infectious Disease target BrabA.00007.a. | 分子名称: | arsenate reductase | 著者 | Buchko, G.W, Hewitt, S.N, Napuli, A.J, Van Voorhis, W.C, Seattle Structural Genomics Center for Infectious Disease (SSGCID) | 登録日 | 2009-09-23 | 公開日 | 2009-10-13 | 最終更新日 | 2024-05-08 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structure of an arsenate reductase-related protein, YffB, from Brucella melitensis, the etiological agent responsible for brucellosis. Acta Crystallogr.,Sect.F, 67, 2011
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2K5X
 
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5YIA
 
 | Crystal Structure of KNI-10343 bound Plasmepsin II (PMII) from Plasmodium falciparum | 分子名称: | (4R)-3-[(2S,3S)-3-[[(2R)-2-[2-(4-hydroxyphenyl)ethanoylamino]-3-methylsulfanyl-propanoyl]amino]-2-oxidanyl-4-phenyl-butanoyl]-5,5-dimethyl-N-[(1S,2R)-2-oxidanyl-2,3-dihydro-1H-inden-1-yl]-1,3-thiazolidine-4-carboxamide, 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE, GLYCEROL, ... | 著者 | Rathore, I, Mishra, V, Bhaumik, P. | 登録日 | 2017-10-03 | 公開日 | 2018-07-11 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Deciphering the mechanism of potent peptidomimetic inhibitors targeting plasmepsins - biochemical and structural insights. Febs J., 285, 2018
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5YIE
 
 | Crystal Structure of KNI-10742 bound Plasmepsin II (PMII) from Plasmodium falciparum | 分子名称: | (4R)-3-[(2S,3S)-3-[2-[4-[2-azanylethyl(ethyl)amino]-2,6-dimethyl-phenoxy]ethanoylamino]-2-oxidanyl-4-phenyl-butanoyl]-5,5-dimethyl-N-[(1S,2R)-2-oxidanyl-2,3-dihydro-1H-inden-1-yl]-1,3-thiazolidine-4-carboxamide, 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE, Plasmepsin II, ... | 著者 | Mishra, V, Rathore, I, Bhaumik, P. | 登録日 | 2017-10-04 | 公開日 | 2018-07-11 | 最終更新日 | 2024-11-13 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Deciphering the mechanism of potent peptidomimetic inhibitors targeting plasmepsins - biochemical and structural insights. Febs J., 285, 2018
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5YIC
 
 | Crystal Structure of KNI-10333 bound Plasmepsin II (PMII) from Plasmodium falciparum | 分子名称: | (4R)-3-[(2S,3S)-3-[[(2R)-2-[2-(4-aminophenyl)ethanoylamino]-3-methylsulfanyl-propanoyl]amino]-2-oxidanyl-4-phenyl-butanoyl]-5,5-dimethyl-N-[(1S,2R)-2-oxidanyl-2,3-dihydro-1H-inden-1-yl]-1,3-thiazolidine-4-carboxamide, 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE, GLYCEROL, ... | 著者 | Mishra, V, Rathore, I, Bhaumik, P. | 登録日 | 2017-10-03 | 公開日 | 2018-07-11 | 最終更新日 | 2024-11-06 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Deciphering the mechanism of potent peptidomimetic inhibitors targeting plasmepsins - biochemical and structural insights. Febs J., 285, 2018
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2LFM
 
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5YIB
 
 | Crystal Structure of KNI-10743 bound Plasmepsin II (PMII) from Plasmodium falciparum | 分子名称: | (4R)-3-[(2S,3S)-3-[2-[4-[2-(dimethylamino)ethyl-methyl-amino]-2,6-dimethyl-phenoxy]ethanoylamino]-2-oxidanyl-4-phenyl-butanoyl]-5,5-dimethyl-N-[(1S,2R)-2-oxidanyl-2,3-dihydro-1H-inden-1-yl]-1,3-thiazolidine-4-carboxamide, 1,2-ETHANEDIOL, 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE, ... | 著者 | Rathore, I, Mishra, V, Bhaumik, P. | 登録日 | 2017-10-03 | 公開日 | 2018-07-11 | 最終更新日 | 2024-11-20 | 実験手法 | X-RAY DIFFRACTION (2.15 Å) | 主引用文献 | Deciphering the mechanism of potent peptidomimetic inhibitors targeting plasmepsins - biochemical and structural insights. Febs J., 285, 2018
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5YID
 
 | Crystal Structure of KNI-10395 bound Plasmepsin II (PMII) from Plasmodium falciparum | 分子名称: | (4R)-N-[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]-3-[(2S,3S)-2-hydroxy-3-{[S-methyl-N-(phenylacetyl)-L-cysteinyl]ami no}-4-phenylbutanoyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxamide, 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE, Plasmepsin II, ... | 著者 | Mishra, V, Rathore, I, Bhaumik, P. | 登録日 | 2017-10-04 | 公開日 | 2018-07-11 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Deciphering the mechanism of potent peptidomimetic inhibitors targeting plasmepsins - biochemical and structural insights. Febs J., 285, 2018
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5YKD
 
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5YRX
 
 | Crystal structure of a hypothetical protein Rv3716c from Mycobacterium tuberculosis | 分子名称: | 1,2-ETHANEDIOL, CADMIUM ION, Nucleoid-associated protein Rv3716c | 著者 | Deka, G, Gopalan, A, Prabhavathi, M, Savithri, H.S, Raja, A, Murthy, M.R.N. | 登録日 | 2017-11-10 | 公開日 | 2018-05-16 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Structural and biophysical characterization of Rv3716c, a hypothetical protein from Mycobacterium tuberculosis Biochem. Biophys. Res. Commun., 495, 2018
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