-
1
-
-
0035399464
-
Combinatorial control of protein phosphatase-1
-
Bollen M. Combinatorial control of protein phosphatase-1. Trends Biochem. Sci. 26 (2001) 426-431
-
(2001)
Trends Biochem. Sci.
, vol.26
, pp. 426-431
-
-
Bollen, M.1
-
3
-
-
0037081563
-
Protein phosphatase 1 - targeted in many directions
-
Cohen P.T. Protein phosphatase 1 - targeted in many directions. J. Cell Sci. 115 (2002) 241-256
-
(2002)
J. Cell Sci.
, vol.115
, pp. 241-256
-
-
Cohen, P.T.1
-
4
-
-
0036034909
-
Molecular enzymology underlying regulation of protein phosphatase-1 by natural toxins
-
Holmes C.F., Maynes J.T., Perreault K.R., Dawson J.F., and James M.N. Molecular enzymology underlying regulation of protein phosphatase-1 by natural toxins. Curr. Med. Chem. 9 (2002) 1981-1989
-
(2002)
Curr. Med. Chem.
, vol.9
, pp. 1981-1989
-
-
Holmes, C.F.1
Maynes, J.T.2
Perreault, K.R.3
Dawson, J.F.4
James, M.N.5
-
5
-
-
1642603545
-
Modified norcantharidins; synthesis, protein phosphatases 1 and 2A inhibition, and anticancer activity
-
Hart M.E., Chamberlin A.R., Walkom C., Sakoff J.A., and Mccluskey A. Modified norcantharidins; synthesis, protein phosphatases 1 and 2A inhibition, and anticancer activity. Bioorg. Med. Chem. Lett. 14 (2004) 1969-1973
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 1969-1973
-
-
Hart, M.E.1
Chamberlin, A.R.2
Walkom, C.3
Sakoff, J.A.4
Mccluskey, A.5
-
6
-
-
43049183607
-
Natural products as a robust source of new drugs and drug leads: past successes and present day issues
-
Rishton G.M. Natural products as a robust source of new drugs and drug leads: past successes and present day issues. Am. J. Cardiol. 101 (2008) 43D-49D
-
(2008)
Am. J. Cardiol.
, vol.101
-
-
Rishton, G.M.1
-
7
-
-
0033018801
-
The design, synthesis, and biological evaluation of analogues of the serine-threonine protein phosphatase 1 and 2A selective inhibitor microcystin LA: rational modifications imparting PP1 selectivity
-
Aggen J.B., Humphrey J.M., Gauss C.M., Huang H.B., Nairn A.C., and Chamberlin A.R. The design, synthesis, and biological evaluation of analogues of the serine-threonine protein phosphatase 1 and 2A selective inhibitor microcystin LA: rational modifications imparting PP1 selectivity. Bioorg. Med. Chem. 7 (1999) 543-564
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 543-564
-
-
Aggen, J.B.1
Humphrey, J.M.2
Gauss, C.M.3
Huang, H.B.4
Nairn, A.C.5
Chamberlin, A.R.6
-
8
-
-
0036035538
-
The microcystins and nodularins: cyclic polypeptide inhibitors of PP1 and PP2A
-
Gulledgea B.M., Aggena J.B., Huangb H.B., Nairnc A.C., and Chamberlin A.R. The microcystins and nodularins: cyclic polypeptide inhibitors of PP1 and PP2A. Curr. Med. Chem. 9 (2002) 1991-2003
-
(2002)
Curr. Med. Chem.
, vol.9
, pp. 1991-2003
-
-
Gulledgea, B.M.1
Aggena, J.B.2
Huangb, H.B.3
Nairnc, A.C.4
Chamberlin, A.R.5
-
9
-
-
0036032442
-
Okadaic acid: the archetypal serine/threonine protein phosphatase inhibitor
-
Dounay A.B., and Forsyth C.J. Okadaic acid: the archetypal serine/threonine protein phosphatase inhibitor. Curr. Med. Chem. 9 (2002) 1939-1980
-
(2002)
Curr. Med. Chem.
, vol.9
, pp. 1939-1980
-
-
Dounay, A.B.1
Forsyth, C.J.2
-
10
-
-
0022551475
-
Calyculin A, a novel antitumor metabolite from the mairne sponge Discodermia calyx
-
Kato Y., Fusetani N., Matsunaga S., Hashimoto K., Fujita S., and Furua T.J. Calyculin A, a novel antitumor metabolite from the mairne sponge Discodermia calyx. J. Am. Chem. Soc. 108 (1986) 2780-2781
-
(1986)
J. Am. Chem. Soc.
, vol.108
, pp. 2780-2781
-
-
Kato, Y.1
Fusetani, N.2
Matsunaga, S.3
Hashimoto, K.4
Fujita, S.5
Furua, T.J.6
-
11
-
-
0026015352
-
Cyanobacterial nodularin is a potent inhibitor of type 1 and type 2A protein phosphatases
-
Honkanen R.E., Dukelow M., Zwiller J., Moore R.E., Khatra B.S., and Boynton A.L. Cyanobacterial nodularin is a potent inhibitor of type 1 and type 2A protein phosphatases. Mol. Pharmacol. 40 (1991) 577-583
-
(1991)
Mol. Pharmacol.
, vol.40
, pp. 577-583
-
-
Honkanen, R.E.1
Dukelow, M.2
Zwiller, J.3
Moore, R.E.4
Khatra, B.S.5
Boynton, A.L.6
-
12
-
-
0023196773
-
A new antibiotic, tautomycin
-
Cheng X.C., Kihara T., Kusakabe H., Magae J., Kobayashi Y., Fang R.P., et al. A new antibiotic, tautomycin. J. Antibiot. (Tokyo) 40 (1987) 907-909
-
(1987)
J. Antibiot. (Tokyo)
, vol.40
, pp. 907-909
-
-
Cheng, X.C.1
Kihara, T.2
Kusakabe, H.3
Magae, J.4
Kobayashi, Y.5
Fang, R.P.6
-
13
-
-
0021017333
-
Novel antitumor agents CI-920, PD 113,270 and PD 113,271. II. Isolation and characterization
-
Stampwala S.S., Bunge R.H., Hurley T.R., Willmer N.E., Brankiewicz A.J., Steinman C.E., et al. Novel antitumor agents CI-920, PD 113,270 and PD 113,271. II. Isolation and characterization. J. Antibiot. (Tokyo) 36 (1983) 1601-1605
-
(1983)
J. Antibiot. (Tokyo)
, vol.36
, pp. 1601-1605
-
-
Stampwala, S.S.1
Bunge, R.H.2
Hurley, T.R.3
Willmer, N.E.4
Brankiewicz, A.J.5
Steinman, C.E.6
-
14
-
-
0024428817
-
Medical uses of mylabris in ancient China and recent studies
-
Wang G.S. Medical uses of mylabris in ancient China and recent studies. J. Ethnopharmacol. 26 (1989) 147-162
-
(1989)
J. Ethnopharmacol.
, vol.26
, pp. 147-162
-
-
Wang, G.S.1
-
15
-
-
53849124027
-
Belizeanic Acid: a potent protein phosphatase 1 inhibitor belonging to the okadaic Acid class, with an unusual skeleton
-
Cruz P.G., Fernandez J.J., Norte M., and Daranas A.H. Belizeanic Acid: a potent protein phosphatase 1 inhibitor belonging to the okadaic Acid class, with an unusual skeleton. Chemistry 14 (2008) 6948-6956
-
(2008)
Chemistry
, vol.14
, pp. 6948-6956
-
-
Cruz, P.G.1
Fernandez, J.J.2
Norte, M.3
Daranas, A.H.4
-
16
-
-
0035941284
-
Crystal structure of the tumor-promoter okadaic acid bound to protein phosphatase-1
-
Maynes J.T., Bateman K.S., Cherney M.M., Das A.K., Luu H.A., Holmes C.F., et al. Crystal structure of the tumor-promoter okadaic acid bound to protein phosphatase-1. J. Biol. Chem. 276 (2001) 44078-44082
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 44078-44082
-
-
Maynes, J.T.1
Bateman, K.S.2
Cherney, M.M.3
Das, A.K.4
Luu, H.A.5
Holmes, C.F.6
-
17
-
-
0036111253
-
Crystal structure of the complex between calyculin A and the catalytic subunit of protein phosphatase 1
-
Kita A., Matsunaga S., Takai A., Kataiwa H., Wakimoto T., Fusetani N., et al. Crystal structure of the complex between calyculin A and the catalytic subunit of protein phosphatase 1. Structure 10 (2002) 715-724
-
(2002)
Structure
, vol.10
, pp. 715-724
-
-
Kita, A.1
Matsunaga, S.2
Takai, A.3
Kataiwa, H.4
Wakimoto, T.5
Fusetani, N.6
-
18
-
-
0029094754
-
Three-dimensional structure of the catalytic subunit of protein serine/threonine phosphatase-1
-
Goldberg J., Huang H.B., Kwon Y.G., Greengard P., Nairn A.C., and Kuriyan J. Three-dimensional structure of the catalytic subunit of protein serine/threonine phosphatase-1. Nature 376 (1995) 745-753
-
(1995)
Nature
, vol.376
, pp. 745-753
-
-
Goldberg, J.1
Huang, H.B.2
Kwon, Y.G.3
Greengard, P.4
Nairn, A.C.5
Kuriyan, J.6
-
19
-
-
30344447686
-
Crystal structures of protein phosphatase-1 bound to motuporin and dihydromicrocystin-LA: elucidation of the mechanism of enzyme inhibition by cyanobacterial toxins
-
Maynes J.T., Luu H.A., Cherney M.M., Andersen R.J., Williams D., Holmes C.F., et al. Crystal structures of protein phosphatase-1 bound to motuporin and dihydromicrocystin-LA: elucidation of the mechanism of enzyme inhibition by cyanobacterial toxins. J. Mol. Biol. 356 (2006) 111-120
-
(2006)
J. Mol. Biol.
, vol.356
, pp. 111-120
-
-
Maynes, J.T.1
Luu, H.A.2
Cherney, M.M.3
Andersen, R.J.4
Williams, D.5
Holmes, C.F.6
-
20
-
-
33846118688
-
Crystal structure of a protein phosphatase 2A heterotrimeric holoenzyme
-
Cho U.S., and Xu W. Crystal structure of a protein phosphatase 2A heterotrimeric holoenzyme. Nature 445 (2007) 53-57
-
(2007)
Nature
, vol.445
, pp. 53-57
-
-
Cho, U.S.1
Xu, W.2
-
21
-
-
33750006297
-
Structure of protein phosphatase 2A core enzyme bound to tumor-inducing toxins
-
Xing Y., Xu Y., Chen Y., Jeffrey P.D., Chao Y., Lin Z., et al. Structure of protein phosphatase 2A core enzyme bound to tumor-inducing toxins. Cell 127 (2006) 341-353
-
(2006)
Cell
, vol.127
, pp. 341-353
-
-
Xing, Y.1
Xu, Y.2
Chen, Y.3
Jeffrey, P.D.4
Chao, Y.5
Lin, Z.6
-
22
-
-
5644290640
-
Crystal structure and mutagenesis of a protein phosphatase-1:calcineurin hybrid elucidate the role of the beta12-beta13 loop in inhibitor binding
-
Maynes J.T., Perreault K.R., Cherney M.M., Luu H.A., James M.N., and Holmes C.F. Crystal structure and mutagenesis of a protein phosphatase-1:calcineurin hybrid elucidate the role of the beta12-beta13 loop in inhibitor binding. J. Biol. Chem. 279 (2004) 43198-43206
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 43198-43206
-
-
Maynes, J.T.1
Perreault, K.R.2
Cherney, M.M.3
Luu, H.A.4
James, M.N.5
Holmes, C.F.6
-
23
-
-
0030806027
-
A model for binding of structurally diverse natural product inhibitors of protein phosphatases PP1 and PP2A
-
Gupta V., Ogawa A.K., Du X., Houk K.N., and Armstrong R.W. A model for binding of structurally diverse natural product inhibitors of protein phosphatases PP1 and PP2A. J. Med. Chem. 40 (1997) 3199-3206
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3199-3206
-
-
Gupta, V.1
Ogawa, A.K.2
Du, X.3
Houk, K.N.4
Armstrong, R.W.5
-
24
-
-
0037200054
-
The specificity of extracellular signal-regulated kinase 2 dephosphorylation by protein phosphatases
-
Zhou B., Wang Z.X., Zhao Y., Brautigan D.L., and Zhang Z.Y. The specificity of extracellular signal-regulated kinase 2 dephosphorylation by protein phosphatases. J. Biol. Chem. 277 (2002) 31818-31825
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 31818-31825
-
-
Zhou, B.1
Wang, Z.X.2
Zhao, Y.3
Brautigan, D.L.4
Zhang, Z.Y.5
-
25
-
-
0037420824
-
The selective inhibition of phosphatases by natural toxins: the anhydride domain of tautomycin is not a primary factor in controlling PP1/PP2A selectivity
-
Liu W., Sheppeck II J.E., Colby D.A., Huang H.B., Nairn A.C., and Chamberlin A.R. The selective inhibition of phosphatases by natural toxins: the anhydride domain of tautomycin is not a primary factor in controlling PP1/PP2A selectivity. Bioorg. Med. Chem. Lett. 13 (2003) 1597-1600
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1597-1600
-
-
Liu, W.1
Sheppeck II, J.E.2
Colby, D.A.3
Huang, H.B.4
Nairn, A.C.5
Chamberlin, A.R.6
-
26
-
-
0030035016
-
Molecular shape analysis and activity of tautomycin, a protein phosphatase inhibitor
-
Sugiyama Y., Ohtani I.I., Isobe M., Takai A., Ubukata M., and Isono K. Molecular shape analysis and activity of tautomycin, a protein phosphatase inhibitor. Bioorg. Med. Chem. Lett. 6 (1996) 3-8
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 3-8
-
-
Sugiyama, Y.1
Ohtani, I.I.2
Isobe, M.3
Takai, A.4
Ubukata, M.5
Isono, K.6
-
27
-
-
0029785147
-
Mapping the protein universe
-
Holm L., and Sander C. Mapping the protein universe. Science 273 (1996) 595-603
-
(1996)
Science
, vol.273
, pp. 595-603
-
-
Holm, L.1
Sander, C.2
-
28
-
-
0030065764
-
Tyrosine-272 is involved in the inhibition of protein phosphatase-1 by multiple toxins
-
Zhang L., Zhang Z., Long F., and Lee E.Y. Tyrosine-272 is involved in the inhibition of protein phosphatase-1 by multiple toxins. Biochemistry 35 (1996) 1606-1611
-
(1996)
Biochemistry
, vol.35
, pp. 1606-1611
-
-
Zhang, L.1
Zhang, Z.2
Long, F.3
Lee, E.Y.4
-
29
-
-
0028132006
-
Purification of type 1 protein (serine/threonine) phosphatases by microcystin-Sepharose affinity chromatography
-
Moorhead G., Mackintosh R.W., Morrice N., Gallagher T., and Mackintosh C. Purification of type 1 protein (serine/threonine) phosphatases by microcystin-Sepharose affinity chromatography. FEBS Lett. 356 (1994) 46-50
-
(1994)
FEBS Lett.
, vol.356
, pp. 46-50
-
-
Moorhead, G.1
Mackintosh, R.W.2
Morrice, N.3
Gallagher, T.4
Mackintosh, C.5
-
30
-
-
0037420802
-
A new model of the tautomycin-PP1 complex that is not analogous to the corresponding okadaic acid structure
-
Colby D.A., Liu W., Sheppeck J.E., Huang H.B., Nairn A.C., and Chamberlin A.R. A new model of the tautomycin-PP1 complex that is not analogous to the corresponding okadaic acid structure. Bioorg. Med. Chem. Lett. 13 (2003) 1601-1605
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 1601-1605
-
-
Colby, D.A.1
Liu, W.2
Sheppeck, J.E.3
Huang, H.B.4
Nairn, A.C.5
Chamberlin, A.R.6
-
31
-
-
0035929178
-
Tautomycetin is a novel and specific inhibitor of serine/threonine protein phosphatase type 1, PP1
-
Mitsuhashi S., Matsuura N., Ubukata M., Oikawa H., Shima H., and Kikuchi K. Tautomycetin is a novel and specific inhibitor of serine/threonine protein phosphatase type 1, PP1. Biochem. Biophys. Res. Commun. 287 (2001) 328-331
-
(2001)
Biochem. Biophys. Res. Commun.
, vol.287
, pp. 328-331
-
-
Mitsuhashi, S.1
Matsuura, N.2
Ubukata, M.3
Oikawa, H.4
Shima, H.5
Kikuchi, K.6
-
32
-
-
0035848412
-
Importance of the C28-C38 hydrophobic domain of okadaic acid for potent inhibition of protein serine-threonine phosphatases 1 and 2A
-
Frydrychowski V.A., Urbanek R.A., Dounay A.B., and Forsyth C.J. Importance of the C28-C38 hydrophobic domain of okadaic acid for potent inhibition of protein serine-threonine phosphatases 1 and 2A. Bioorg. Med. Chem. Lett. 11 (2001) 647-649
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 647-649
-
-
Frydrychowski, V.A.1
Urbanek, R.A.2
Dounay, A.B.3
Forsyth, C.J.4
-
33
-
-
0032055256
-
Different moieties of tautomycin involved in protein phosphatase inhibition and induction of apoptosis
-
Kawamura T., Matsuzawa S., Mizuno Y., Kikuchi K., Oikawa H., Oikawa M., et al. Different moieties of tautomycin involved in protein phosphatase inhibition and induction of apoptosis. Biochem. Pharmacol. 55 (1998) 995-1003
-
(1998)
Biochem. Pharmacol.
, vol.55
, pp. 995-1003
-
-
Kawamura, T.1
Matsuzawa, S.2
Mizuno, Y.3
Kikuchi, K.4
Oikawa, H.5
Oikawa, M.6
-
34
-
-
33845404441
-
Structure of the protein phosphatase 2A holoenzyme
-
Xu Y., Xing Y., Chen Y., Chao Y., Lin Z., Fan E., et al. Structure of the protein phosphatase 2A holoenzyme. Cell 127 (2006) 1239-1251
-
(2006)
Cell
, vol.127
, pp. 1239-1251
-
-
Xu, Y.1
Xing, Y.2
Chen, Y.3
Chao, Y.4
Lin, Z.5
Fan, E.6
-
35
-
-
34547807709
-
Molecular biology of cantharidin in cancer cells
-
Rauh R., Kahl S., Boechzelt H., Bauer R., Kaina B., and Efferth T. Molecular biology of cantharidin in cancer cells. Chin. Med. 2 (2007) 8
-
(2007)
Chin. Med.
, vol.2
, pp. 8
-
-
Rauh, R.1
Kahl, S.2
Boechzelt, H.3
Bauer, R.4
Kaina, B.5
Efferth, T.6
-
36
-
-
0037075845
-
Serine-threonine protein phosphatase inhibitors: development of potential therapeutic strategies
-
Mccluskey A., Sim A.T., and Sakoff J.A. Serine-threonine protein phosphatase inhibitors: development of potential therapeutic strategies. J. Med. Chem. 45 (2002) 1151-1175
-
(2002)
J. Med. Chem.
, vol.45
, pp. 1151-1175
-
-
Mccluskey, A.1
Sim, A.T.2
Sakoff, J.A.3
-
37
-
-
1842431395
-
Protein phosphatase inhibition: structure based design. Towards new therapeutic agents
-
Sakoff J.A., and Mccluskey A. Protein phosphatase inhibition: structure based design. Towards new therapeutic agents. Curr. Pharm. Des. 10 (2004) 1139-1159
-
(2004)
Curr. Pharm. Des.
, vol.10
, pp. 1139-1159
-
-
Sakoff, J.A.1
Mccluskey, A.2
-
38
-
-
0030934346
-
Structure-based design of novel calcineurin (PP2B) inhibitors
-
Tatlock J.H., Linton M.A., Hou X.J., Kissinger C.R., Pelletier L.A., Showalter R.E., et al. Structure-based design of novel calcineurin (PP2B) inhibitors. Bioorg. Med. Chem. Lett. 7 (1997) 1007-1012
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 1007-1012
-
-
Tatlock, J.H.1
Linton, M.A.2
Hou, X.J.3
Kissinger, C.R.4
Pelletier, L.A.5
Showalter, R.E.6
-
39
-
-
33751419975
-
Strategies to maximize heterologous protein expression in Escherichia coli with minimal cost
-
Peti W., and Page R. Strategies to maximize heterologous protein expression in Escherichia coli with minimal cost. Protein Expr. Purif. 51 (2007) 1-10
-
(2007)
Protein Expr. Purif.
, vol.51
, pp. 1-10
-
-
Peti, W.1
Page, R.2
-
41
-
-
0028103275
-
The CCP4 suite: programs for protein crystallography
-
The CCP4 suite: programs for protein crystallography. Acta Crystallogr. D 50 (1994) 760-763
-
(1994)
Acta Crystallogr. D
, vol.50
, pp. 760-763
-
-
-
42
-
-
0031059866
-
Processing of X-ray diffraction data collected in oscillation mode
-
Otwinowski Z., and Minor W. Processing of X-ray diffraction data collected in oscillation mode. Methods Enzymol. 276 (1997) 307-326
-
(1997)
Methods Enzymol.
, vol.276
, pp. 307-326
-
-
Otwinowski, Z.1
Minor, W.2
-
43
-
-
0030924992
-
Refinement of macromolecular structures by the maximum-likelihood method
-
Murshudov G.N., Vagin A.A., and Dodson E.J. Refinement of macromolecular structures by the maximum-likelihood method. Acta Crystallogr. D 53 (1997) 240-255
-
(1997)
Acta Crystallogr. D
, vol.53
, pp. 240-255
-
-
Murshudov, G.N.1
Vagin, A.A.2
Dodson, E.J.3
-
44
-
-
13244281317
-
Coot: model-building tools for molecular graphics
-
Emsley P., and Cowtan K. Coot: model-building tools for molecular graphics. Acta Crystallogr. D 60 (2004) 2126-2132
-
(2004)
Acta Crystallogr. D
, vol.60
, pp. 2126-2132
-
-
Emsley, P.1
Cowtan, K.2
-
45
-
-
0035182073
-
Use of TLS parameters to model anisotropic displacements in macromolecular refinement
-
Winn M.D., Isupov M.N., and Murshudov G.N. Use of TLS parameters to model anisotropic displacements in macromolecular refinement. Acta Crystallogr. D 57 (2001) 122-133
-
(2001)
Acta Crystallogr. D
, vol.57
, pp. 122-133
-
-
Winn, M.D.1
Isupov, M.N.2
Murshudov, G.N.3
-
46
-
-
0000127585
-
Automated refinement of protein models
-
Lamzin V.S., and Wilson K.S. Automated refinement of protein models. Acta Crystallogr. D 49 (1993) 129-147
-
(1993)
Acta Crystallogr. D
, vol.49
, pp. 129-147
-
-
Lamzin, V.S.1
Wilson, K.S.2
-
47
-
-
34547592557
-
MolProbity: all-atom contacts and structure validation for proteins and nucleic acids
-
Davis I.W., Leaver-Fay A., Chen V.B., Block J.N., Kapral G.J., Wang X., et al. MolProbity: all-atom contacts and structure validation for proteins and nucleic acids. Nucleic Acids Res. 35 (2007) W375-W383
-
(2007)
Nucleic Acids Res.
, vol.35
-
-
Davis, I.W.1
Leaver-Fay, A.2
Chen, V.B.3
Block, J.N.4
Kapral, G.J.5
Wang, X.6
-
48
-
-
0025398721
-
WHAT IF: a molecular modeling and drug design program
-
29
-
Vriend G. WHAT IF: a molecular modeling and drug design program. J. Mol. Graph. 8 (1990) 52-56 29
-
(1990)
J. Mol. Graph.
, vol.8
, pp. 52-56
-
-
Vriend, G.1
-
50
-
-
7544226311
-
PRODRG: a tool for high-throughput crystallography of protein-ligand complexes
-
Schuttelkopf A.W., and Van Aalten D.M. PRODRG: a tool for high-throughput crystallography of protein-ligand complexes. Acta Crystallogr. D 60 (2004) 1355-1363
-
(2004)
Acta Crystallogr. D
, vol.60
, pp. 1355-1363
-
-
Schuttelkopf, A.W.1
Van Aalten, D.M.2
-
51
-
-
43249097539
-
Iterative-build OMIT maps: map improvement by iterative model building and refinement without model bias
-
Terwilliger T.C., Grosse-Kunstleve R.W., Afonine P.V., Moriarty N.W., Adams P.D., Read R.J., et al. Iterative-build OMIT maps: map improvement by iterative model building and refinement without model bias. Acta Crystallogr. D 64 (2008) 515-524
-
(2008)
Acta Crystallogr. D
, vol.64
, pp. 515-524
-
-
Terwilliger, T.C.1
Grosse-Kunstleve, R.W.2
Afonine, P.V.3
Moriarty, N.W.4
Adams, P.D.5
Read, R.J.6
|