1G2E
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1G2F
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![BU of 1g2f by Molmil](/molmil-images/mine/1g2f) | STRUCTURE OF A CYS2HIS2 ZINC FINGER/TATA BOX COMPLEX (TATAZF;CLONE #6) | 分子名称: | 5'-D(*GP*AP*CP*GP*CP*TP*AP*TP*AP*AP*AP*AP*GP*GP*AP*G)-3', 5'-D(*TP*CP*CP*TP*TP*TP*TP*AP*TP*AP*GP*CP*GP*TP*CP*C)-3', TATA BOX ZINC FINGER PROTEIN, ... | 著者 | Wolfe, S.A, Grant, R.A, Elrod-Erickson, M, Pabo, C.O. | 登録日 | 2000-10-18 | 公開日 | 2001-09-07 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Beyond the "recognition code": structures of two Cys2His2 zinc finger/TATA box complexes. Structure, 9, 2001
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1G2G
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![BU of 1g2g by Molmil](/molmil-images/mine/1g2g) | MINIMAL CONFORMATION OF THE ALPHA-CONOTOXIN IMI FOR THE ALPHA7 NEURONAL NICOTINIC ACETYLCHOLINE RECEPTOR RECOGNITION | 分子名称: | ALPHA-CONOTOXIN IMI | 著者 | Lamthanh, H, Jegou-Matheron, C, Servent, D, Menez, A, Lancelin, J.M. | 登録日 | 2000-10-19 | 公開日 | 2000-11-08 | 最終更新日 | 2022-02-23 | 実験手法 | SOLUTION NMR | 主引用文献 | Minimal conformation of the alpha-conotoxin ImI for the alpha7 neuronal nicotinic acetylcholine receptor recognition: correlated CD, NMR and binding studies. FEBS Lett., 454, 1999
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1G2H
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1G2I
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![BU of 1g2i by Molmil](/molmil-images/mine/1g2i) | CRYSTAL STRUCTURE OF A NOVEL INTRACELLULAR PROTEASE FROM PYROCOCCUS HORIKOSHII AT 2 A RESOLUTION | 分子名称: | PROTEASE I, SULFATE ION | 著者 | Du, X, Choi, I.-G, Kim, R, Jancarik, J, Kim, S.-H, Berkeley Structural Genomics Center (BSGC) | 登録日 | 2000-10-19 | 公開日 | 2000-11-08 | 最終更新日 | 2018-01-24 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Crystal structure of an intracellular protease from Pyrococcus horikoshii at 2-A resolution. Proc.Natl.Acad.Sci.USA, 97, 2000
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1G2J
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![BU of 1g2j by Molmil](/molmil-images/mine/1g2j) | RNA OCTAMER R(CCCP*GGGG) CONTAINING PHENYL RIBONUCLEOTIDE | 分子名称: | 5'-R(*CP*CP*CP*(PYY)P*GP*GP*GP*G)-3', CALCIUM ION | 著者 | Minasov, G, Matulic-Adamic, J, Wilds, C.J, Haeberli, P, Usman, N, Beigelman, L, Egli, M. | 登録日 | 2000-10-20 | 公開日 | 2000-12-06 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (1.97 Å) | 主引用文献 | Crystal structure of an RNA duplex containing phenyl-ribonucleotides, hydrophobic isosteres of the natural pyrimidines. RNA, 6, 2000
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1G2K
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![BU of 1g2k by Molmil](/molmil-images/mine/1g2k) | HIV-1 PROTEASE WITH CYCLIC SULFAMIDE INHIBITOR, AHA047 | 分子名称: | 3-(7-BENZYL-4,5-DIHYDROXY-1,1-DIOXO-3,6-BIS-PHENOXYMETHYL-1L6-[1,2,7]THIADIAZEPAN-2-YLMETHYL)-N-METHYL-BENZAMIDE, PROTEASE RETROPEPSIN | 著者 | Lindberg, J, Unge, T. | 登録日 | 2000-10-20 | 公開日 | 2001-06-01 | 最終更新日 | 2023-08-09 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Synthesis and comparative molecular field analysis (CoMFA) of symmetric and nonsymmetric cyclic sulfamide HIV-1 protease inhibitors. J.Med.Chem., 44, 2001
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1G2L
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![BU of 1g2l by Molmil](/molmil-images/mine/1g2l) | FACTOR XA INHIBITOR COMPLEX | 分子名称: | CALCIUM ION, COAGULATION FACTOR X, [(1-{2[(4-CARBAMIMIDOYL-PHENYLAMINO)-METHYL]-1-METHYL-1H-BENZOIMIDAZOL-5-YL}-CYCLOPROPYL)-PYRIDIN-2-YL-METHYLENEAMINOOXY]-ACETIC ACID ETHYL ESTER | 著者 | Nar, H. | 登録日 | 2000-10-20 | 公開日 | 2001-10-20 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Structural basis for inhibition promiscuity of dual specific thrombin and factor Xa blood coagulation inhibitors. Structure, 9, 2001
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1G2M
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![BU of 1g2m by Molmil](/molmil-images/mine/1g2m) | FACTOR XA INHIBITOR COMPLEX | 分子名称: | 4-{[1-METHYL-5-(2-METHYL-BENZOIMIDAZOL-1-YLMETHYL)-1H-BENZOIMIDAZOL-2-YLMETHYL]-AMINO}-BENZAMIDINE, CALCIUM ION, COAGULATION FACTOR X | 著者 | Nar, H. | 登録日 | 2000-10-20 | 公開日 | 2001-10-20 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (3.02 Å) | 主引用文献 | Structural basis for inhibition promiscuity of dual specific thrombin and factor Xa blood coagulation inhibitors. Structure, 9, 2001
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1G2N
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![BU of 1g2n by Molmil](/molmil-images/mine/1g2n) | CRYSTAL STRUCTURE OF THE LIGAND BINDING DOMAIN OF THE ULTRASPIRACLE PROTEIN USP, THE ORTHOLOG OF RXRS IN INSECTS | 分子名称: | L-ALPHA-PHOSPHATIDYL-BETA-OLEOYL-GAMMA-PALMITOYL-PHOSPHATIDYLETHANOLAMINE, ULTRASPIRACLE PROTEIN | 著者 | Billas, I.M.L, Moulinier, L, Rochel, N, Moras, D, Structural Proteomics in Europe (SPINE) | 登録日 | 2000-10-20 | 公開日 | 2001-04-21 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (1.65 Å) | 主引用文献 | Crystal structure of the ligand-binding domain of the ultraspiracle protein USP, the ortholog of retinoid X receptors in insects. J.Biol.Chem., 276, 2001
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1G2O
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![BU of 1g2o by Molmil](/molmil-images/mine/1g2o) | CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH A TRANSITION-STATE INHIBITOR | 分子名称: | 1,4-DIDEOXY-4-AZA-1-(S)-(9-DEAZAHYPOXANTHIN-9-YL)-D-RIBITOL, PHOSPHATE ION, PURINE NUCLEOSIDE PHOSPHORYLASE | 著者 | Shi, W, Basso, L.A, Tyler, P.C, Furneaux, R.H, Blanchard, J.S, Almo, S.C, Schramm, V.L. | 登録日 | 2000-10-20 | 公開日 | 2001-08-01 | 最終更新日 | 2023-09-20 | 実験手法 | X-RAY DIFFRACTION (1.75 Å) | 主引用文献 | Structures of purine nucleoside phosphorylase from Mycobacterium tuberculosis in complexes with immucillin-H and its pieces. Biochemistry, 40, 2001
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1G2P
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![BU of 1g2p by Molmil](/molmil-images/mine/1g2p) | CRYSTAL STRUCTURE OF ADENINE PHOSPHORIBOSYLTRANSFERASE | 分子名称: | ADENINE PHOSPHORIBOSYLTRANSFERASE 1, SULFATE ION | 著者 | Shi, W, Tanaka, K.S.E, Almo, S.C, Schramm, V.L. | 登録日 | 2000-10-20 | 公開日 | 2001-12-05 | 最終更新日 | 2023-08-09 | 実験手法 | X-RAY DIFFRACTION (1.75 Å) | 主引用文献 | Structural analysis of adenine phosphoribosyltransferase from Saccharomyces cerevisiae. Biochemistry, 40, 2001
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1G2Q
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1G2R
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![BU of 1g2r by Molmil](/molmil-images/mine/1g2r) | Structure of Cytosolic Protein of Unknown Function Coded by Gene from NUSA/INFB Region, a YlxR Homologue | 分子名称: | HYPOTHETICAL CYTOSOLIC PROTEIN, SULFATE ION | 著者 | Osipiuk, J, Gornicki, P, Maj, L, Joachimiak, A, Midwest Center for Structural Genomics (MCSG) | 登録日 | 2000-10-20 | 公開日 | 2001-08-29 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (1.35 Å) | 主引用文献 | Streptococcus pneumonia YlxR at 1.35 A shows a putative new fold. Acta Crystallogr.,Sect.D, 57, 2001
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1G2S
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1G2T
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1G2U
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![BU of 1g2u by Molmil](/molmil-images/mine/1g2u) | THE STRUCTURE OF THE MUTANT, A172V, OF 3-ISOPROPYLMALATE DEHYDROGENASE FROM THERMUS THERMOPHILUS HB8 : ITS THERMOSTABILITY AND STRUCTURE. | 分子名称: | 3-ISOPROPYLMALATE DEHYDROGENASE | 著者 | Qu, C, Akanuma, S, Tanaka, N, Moriyama, H, Oshima, T. | 登録日 | 2000-10-21 | 公開日 | 2000-11-01 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.1 Å) | 主引用文献 | Design, X-ray crystallography, molecular modelling and thermal stability studies of mutant enzymes at site 172 of 3-isopropylmalate dehydrogenase from Thermus thermophilus. Acta Crystallogr.,Sect.D, 57, 2001
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1G2V
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![BU of 1g2v by Molmil](/molmil-images/mine/1g2v) | THE STRUCTURAL BASIS OF THE CATALYTIC MECHANISM AND REGULATION OF GLUCOSE-1-PHOSPHATE THYMIDYLYLTRANSFERASE (RMLA). TTP COMPLEX. | 分子名称: | GLUCOSE-1-PHOSPHATE THYMIDYLYLTRANSFERASE, THYMIDINE-5'-TRIPHOSPHATE | 著者 | Blankenfeldt, W, Asuncion, M, Lam, J.S, Naismith, J.H. | 登録日 | 2000-10-21 | 公開日 | 2000-12-27 | 最終更新日 | 2023-08-09 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | The structural basis of the catalytic mechanism and regulation of glucose-1-phosphate thymidylyltransferase (RmlA). EMBO J., 19, 2000
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1G2W
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![BU of 1g2w by Molmil](/molmil-images/mine/1g2w) | E177S MUTANT OF THE PYRIDOXAL-5'-PHOSPHATE ENZYME D-AMINO ACID AMINOTRANSFERASE | 分子名称: | ACETATE ION, D-ALANINE AMINOTRANSFERASE, PYRIDOXAL-5'-PHOSPHATE | 著者 | Lepore, B.W, Ringe, D. | 登録日 | 2000-10-21 | 公開日 | 2000-11-15 | 最終更新日 | 2021-11-03 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Studies on an Active Site Residue, E177, That Affects Binding of the Coenzyme in D-Amino Acid Transaminase, and Mechanistic Studies on a Suicide Substrate Biochemistry and Molecular Biology of Vitamin B6 and PQQ-dependent Proteins, 10th Annual International Symposium on Vitamin B6, 2000
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1G2X
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![BU of 1g2x by Molmil](/molmil-images/mine/1g2x) | Sequence induced trimerization of krait PLA2: crystal structure of the trimeric form of krait PLA2 | 分子名称: | PHOSPHOLIPASE A2 | 著者 | Singh, G, Gourinath, S, Sharma, S, Bhanumathi, S, Paramsivam, M, Singh, T.P. | 登録日 | 2000-10-22 | 公開日 | 2003-06-17 | 最終更新日 | 2023-08-09 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Sequence-induced trimerization of phospholipase A2: structure of a trimeric isoform of PLA2 from common krait (Bungarus caeruleus) at 2.5 A resolution. Acta Crystallogr.,Sect.F, 61, 2005
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1G2Y
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![BU of 1g2y by Molmil](/molmil-images/mine/1g2y) | HNF-1ALPHA DIMERIZATION DOMAIN, WITH SELENOMETHIONINE SUBSTITUED AT LEU 12 | 分子名称: | HEPATOCYTE NUCLEAR FACTOR 1-ALPHA | 著者 | Rose, R.B, Endrizzi, J.A, Cronk, J.D, Holton, J, Alber, T. | 登録日 | 2000-10-23 | 公開日 | 2001-01-17 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (1 Å) | 主引用文献 | High-resolution structure of the HNF-1alpha dimerization domain. Biochemistry, 39, 2000
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1G2Z
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![BU of 1g2z by Molmil](/molmil-images/mine/1g2z) | DIMERIZATION DOMAIN OF HNF-1ALPHA WITH A LEU 13 SELENOMETHIONINE SUBSTITUTION | 分子名称: | HEPATOCYTE NUCLEAR FACTOR 1-ALPHA | 著者 | Rose, R.B, Endrizzi, J.A, Cronk, J.D, Holton, J, Alber, T. | 登録日 | 2000-10-23 | 公開日 | 2001-01-17 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (1.15 Å) | 主引用文献 | High-resolution structure of the HNF-1alpha dimerization domain. Biochemistry, 39, 2000
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1G30
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![BU of 1g30 by Molmil](/molmil-images/mine/1g30) | THROMBIN INHIBITOR COMPLEX | 分子名称: | HIRUDIN IIB, PROTHROMBIN, [(1-{2[(4-CARBAMIMIDOYL-PHENYLAMINO)-METHYL]-1-METHYL-1H-BENZOIMIDAZOL-5-YL}-CYCLOPROPYL)-PYRIDIN-2-YL-METHYLENEAMINOOXY]-ACETIC ACID ETHYL ESTER | 著者 | Nar, H. | 登録日 | 2000-10-23 | 公開日 | 2001-10-23 | 最終更新日 | 2018-10-03 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Structural basis for inhibition promiscuity of dual specific thrombin and factor Xa blood coagulation inhibitors. Structure, 9, 2001
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1G31
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![BU of 1g31 by Molmil](/molmil-images/mine/1g31) | GP31 CO-CHAPERONIN FROM BACTERIOPHAGE T4 | 分子名称: | GP31, PHOSPHATE ION, POTASSIUM ION | 著者 | Hunt, J.F, Van Der Vies, S.M, Henry, L, Deisenhofer, J. | 登録日 | 1998-03-27 | 公開日 | 1998-08-26 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Structural adaptations in the specialized bacteriophage T4 co-chaperonin Gp31 expand the size of the Anfinsen cage. Cell(Cambridge,Mass.), 90, 1997
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1G32
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![BU of 1g32 by Molmil](/molmil-images/mine/1g32) | THROMBIN INHIBITOR COMPLEX | 分子名称: | 4-{[1-METHYL-5-(2-METHYL-BENZOIMIDAZOL-1-YLMETHYL)-1H-BENZOIMIDAZOL-2-YLMETHYL]-AMINO}-BENZAMIDINE, HIRUDIN IIB, PROTHROMBIN | 著者 | Nar, H. | 登録日 | 2000-10-23 | 公開日 | 2001-10-23 | 最終更新日 | 2013-03-13 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Structural basis for inhibition promiscuity of dual specific thrombin and factor Xa blood coagulation inhibitors. Structure, 9, 2001
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