-
1
-
-
0036183496
-
Structural analyses reveal two distinct families of nucleoside phosphorylases
-
Pugmire M.J., Ealick S.E. Structural analyses reveal two distinct families of nucleoside phosphorylases. Biochem. J. 361:2002;1-25.
-
(2002)
Biochem. J.
, vol.361
, pp. 1-25
-
-
Pugmire, M.J.1
Ealick, S.E.2
-
2
-
-
0021689688
-
Phase I and pharmacokinetic studies of high-dose uridine intended for rescue from 5-fluorouracil toxicity
-
Leyva A., van Groeningen C.J., Kraal I., Gall H., Peters G.J., Lankelma J., Pinedo H.M. Phase I and pharmacokinetic studies of high-dose uridine intended for rescue from 5-fluorouracil toxicity. Cancer Res. 44:1984;5928-5933.
-
(1984)
Cancer Res.
, vol.44
, pp. 5928-5933
-
-
Leyva, A.1
Van Groeningen, C.J.2
Kraal, I.3
Gall, H.4
Peters, G.J.5
Lankelma, J.6
Pinedo, H.M.7
-
3
-
-
0022457607
-
Clinical and pharmacokinetic studies of prolonged administration of high-dose uridine intended for rescue from 5-fluorouracil toxicity
-
van Groeningen C.J., Leyva A., Kraal I., Peters G.J., Pinedo H.M. Clinical and pharmacokinetic studies of prolonged administration of high-dose uridine intended for rescue from 5-fluorouracil toxicity. Cancer Treat. Rep. 70:1986;745-750.
-
(1986)
Cancer Treat. Rep.
, vol.70
, pp. 745-750
-
-
Van Groeningen, C.J.1
Leyva, A.2
Kraal, I.3
Peters, G.J.4
Pinedo, H.M.5
-
4
-
-
0034257227
-
Modulation of 5-fluorouracil host toxicity by 5-(benzyloxybenzyl) barbituric acid acyclonucleoside, a uridine phosphorylase inhibitor, and 2′3′5′-tri-O-acetyluridine, a prodrug of uridine
-
Ashour O.M., Naguib F.N.M., Panzica R.P., Al Safarjalani O.N., el Kouni M.H. Modulation of 5-fluorouracil host toxicity by 5-(benzyloxybenzyl) barbituric acid acyclonucleoside, a uridine phosphorylase inhibitor, and 2′3′5′-tri-O-acetyluridine, a prodrug of uridine. Biochem. Pharmacol. 60:2000;427-431.
-
(2000)
Biochem. Pharmacol.
, vol.60
, pp. 427-431
-
-
Ashour, O.M.1
Naguib, F.N.M.2
Panzica, R.P.3
Al Safarjalani, O.N.4
El Kouni, M.H.5
-
5
-
-
15644382548
-
Phase I clinical and pharmacological studies of benzylacyclouridine, a uridine phosphorylase inhibitor
-
Pizzorno G., Yee L., Burtness B.A., Marsh J.C., Darnowski J.W., Chu M.Y.W., et al. Phase I clinical and pharmacological studies of benzylacyclouridine, a uridine phosphorylase inhibitor. Clin. Cancer Res. 4:1998;1165-1175.
-
(1998)
Clin. Cancer Res.
, vol.4
, pp. 1165-1175
-
-
Pizzorno, G.1
Yee, L.2
Burtness, B.A.3
Marsh, J.C.4
Darnowski, J.W.5
Chu, M.Y.W.6
-
6
-
-
0025021597
-
Three-dimensional structure of human erythrocytic purine nucleoside phosphorylase at 3.2 Å resolution
-
Ealick S.E., Rule S.A., Carter D.C., Greenhough T.J., Babu Y.S., Cook W.J., et al. Three-dimensional structure of human erythrocytic purine nucleoside phosphorylase at 3.2 Å resolution. J. Biol. Chem. 265:1990;1812-1820.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 1812-1820
-
-
Ealick, S.E.1
Rule, S.A.2
Carter, D.C.3
Greenhough, T.J.4
Babu, Y.S.5
Cook, W.J.6
-
7
-
-
0031575420
-
Crystal structure of calf spleen purine nucleoside phosphorylase in a complex with hypoxanthine at 2.15 Å resolution
-
Koellner G., Luić M., Shugar D., Saenger W., Bzowska A. Crystal structure of calf spleen purine nucleoside phosphorylase in a complex with hypoxanthine at 2.15 Å resolution. J. Mol. Biol. 265:1997;202-216.
-
(1997)
J. Mol. Biol.
, vol.265
, pp. 202-216
-
-
Koellner, G.1
Luić, M.2
Shugar, D.3
Saenger, W.4
Bzowska, A.5
-
8
-
-
0031572855
-
The crystal structure of Escherichia coli purine nucleoside phosphorylase: A comparison with the human enzyme reveals a conserved topology
-
Mao C., Cook W.J., Zhou M., Koszalka G.W., Krenitsky T.A., Ealick S.E. The crystal structure of Escherichia coli purine nucleoside phosphorylase: a comparison with the human enzyme reveals a conserved topology. Structure. 5:1997;1373-1383.
-
(1997)
Structure
, vol.5
, pp. 1373-1383
-
-
Mao, C.1
Cook, W.J.2
Zhou, M.3
Koszalka, G.W.4
Krenitsky, T.A.5
Ealick, S.E.6
-
9
-
-
0035902502
-
Structures of purine nucleoside phosphorylase from Mycobacterium tuberculosis in complexes with immucillin-H and its pieces
-
Shi W., Basso L.A., Santos D.S., Tyler P.C., Furneaux R.H., Blanchard J.S., Almo S.C., Schramm V.L. Structures of purine nucleoside phosphorylase from Mycobacterium tuberculosis in complexes with immucillin-H and its pieces. Biochemistry. 40:2001;8204-8215.
-
(2001)
Biochemistry
, vol.40
, pp. 8204-8215
-
-
Shi, W.1
Basso, L.A.2
Santos, D.S.3
Tyler, P.C.4
Furneaux, R.H.5
Blanchard, J.S.6
Almo, S.C.7
Schramm, V.L.8
-
10
-
-
0033579544
-
Crystal structure of the purine nucleoside phosphorylase (PNP) from Cellulomonas sp. and its implication for the mechanism for trimeric PNPs
-
Tebbe J., Bzowska A., Wielgus-Kutrowska B., Schröder W., Kazimierczuk Z., Shugar D., et al. Crystal structure of the purine nucleoside phosphorylase (PNP) from Cellulomonas sp. and its implication for the mechanism for trimeric PNPs. J. Mol. Biol. 294:1999;1239-1255.
-
(1999)
J. Mol. Biol.
, vol.294
, pp. 1239-1255
-
-
Tebbe, J.1
Bzowska, A.2
Wielgus-Kutrowska, B.3
Schröder, W.4
Kazimierczuk, Z.5
Shugar, D.6
-
11
-
-
0029027433
-
Atomic structure at 2.5 Å resolution of uridine phosphorylase from E. coli as refined in the monoclinic lattice
-
Morgunova E.Y., Mikhailov A.M., Popov A.N., Blagova E.V., Smirnova E.A., Vainshtein B.K., et al. Atomic structure at 2.5 Å resolution of uridine phosphorylase from E. coli as refined in the monoclinic lattice. FEBS Letters. 367:1995;183-187.
-
(1995)
FEBS Letters
, vol.367
, pp. 183-187
-
-
Morgunova, E.Y.1
Mikhailov, A.M.2
Popov, A.N.3
Blagova, E.V.4
Smirnova, E.A.5
Vainshtein, B.K.6
-
12
-
-
0037240345
-
Structure of Escherichia coli uridine phosphorylase at 2.0 Å resolution
-
Burling F.T., Kniewel R., Buglino J.A., Chadha T., Beckwith A., Lima C.D. Structure of Escherichia coli uridine phosphorylase at 2.0 Å resolution. Acta Crystallog. sect. D. 59:2003;73-76.
-
(2003)
Acta Crystallog. Sect. D
, vol.59
, pp. 73-76
-
-
Burling, F.T.1
Kniewel, R.2
Buglino, J.A.3
Chadha, T.4
Beckwith, A.5
Lima, C.D.6
-
13
-
-
0025160874
-
Three-dimensional structure of thymidine phosphorylase from Escherichia coli at 2.8 Å resolution
-
Walter M.R., Cook W.J., Cole L.B., Short S.A., Koszalka G.W., Krenitsky T.A., Ealick S.E. Three-dimensional structure of thymidine phosphorylase from Escherichia coli at 2.8 Å resolution. J. Biol. Chem. 265:1990;14016-14022.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 14016-14022
-
-
Walter, M.R.1
Cook, W.J.2
Cole, L.B.3
Short, S.A.4
Koszalka, G.W.5
Krenitsky, T.A.6
Ealick, S.E.7
-
14
-
-
0032516763
-
Structural and theoretical studies suggest domain movement produces an active conformation of thymidine phosphorylase
-
Pugmire M.J., Cook W.J., Jasanoff A., Walter M.R., Ealick S.E. Structural and theoretical studies suggest domain movement produces an active conformation of thymidine phosphorylase. J. Mol. Biol. 281:1998;285-299.
-
(1998)
J. Mol. Biol.
, vol.281
, pp. 285-299
-
-
Pugmire, M.J.1
Cook, W.J.2
Jasanoff, A.3
Walter, M.R.4
Ealick, S.E.5
-
15
-
-
0032533446
-
The crystal structure of pyrimidine nucleoside phosphorylase in a closed conformation
-
Pugmire M.J., Ealick S.E. The crystal structure of pyrimidine nucleoside phosphorylase in a closed conformation. Structure. 6:1998;1467-1479.
-
(1998)
Structure
, vol.6
, pp. 1467-1479
-
-
Pugmire, M.J.1
Ealick, S.E.2
-
16
-
-
0027135793
-
Structure-based design of inhibitors of purine nucleoside phosphorylase. 3. 9-Arylmethyl derivatives of 9-deazaguanine substituted on the methylene group
-
Erion M.D., Niwas S., Rose J.D., Ananthan S., Allen M., Secrist J.A. III, et al. Structure-based design of inhibitors of purine nucleoside phosphorylase. 3. 9-Arylmethyl derivatives of 9-deazaguanine substituted on the methylene group. J. Med. Chem. 36:1993;3771-3783.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3771-3783
-
-
Erion, M.D.1
Niwas, S.2
Rose, J.D.3
Ananthan, S.4
Allen, M.5
Secrist III, J.A.6
-
17
-
-
0026504301
-
Formycins a and B and some analogues: Selective inhibitors of bacterial (Escherichia coli) purine nucleoside phosphorylase
-
Bzowska A., Kulikowska E., Shugar D. Formycins A and B and some analogues: selective inhibitors of bacterial (Escherichia coli) purine nucleoside phosphorylase. Biochim. Biophys. Acta. 1120:1992;239-247.
-
(1992)
Biochim. Biophys. Acta
, vol.1120
, pp. 239-247
-
-
Bzowska, A.1
Kulikowska, E.2
Shugar, D.3
-
18
-
-
0032537481
-
One-third-the-sites transition-state inhibitors for purine nucleoside phosphorylase
-
Miles R.W., Tyler P.C., Furneaux R.H., Bagdassarian C.K., Schramm V.L. One-third-the-sites transition-state inhibitors for purine nucleoside phosphorylase. Biochemistry. 37:1998;8615-8621.
-
(1998)
Biochemistry
, vol.37
, pp. 8615-8621
-
-
Miles, R.W.1
Tyler, P.C.2
Furneaux, R.H.3
Bagdassarian, C.K.4
Schramm, V.L.5
-
19
-
-
0033519996
-
The 2.0 Å structure of malarial purine phosphoribosyltransferase in complex with a transition-state analogue inhibitor
-
Shi W., Li C.M., Tyler P.C., Furneaux R.H., Cahill S.M., Girvin M.E., et al. The 2.0 Å structure of malarial purine phosphoribosyltransferase in complex with a transition-state analogue inhibitor. Biochemistry. 38:1999;9872-9880.
-
(1999)
Biochemistry
, vol.38
, pp. 9872-9880
-
-
Shi, W.1
Li, C.M.2
Tyler, P.C.3
Furneaux, R.H.4
Cahill, S.M.5
Girvin, M.E.6
-
20
-
-
0034643828
-
Crystal structures of Giardia lamblia guanine phosphoribosyltransferase at 1.75 Å
-
Shi W., Munagala N.R., Wang C.C., Li C.M., Tyler P.C., Furneaux R.H., et al. Crystal structures of Giardia lamblia guanine phosphoribosyltransferase at 1.75 Å Biochemistry. 39:2000;6781-6790.
-
(2000)
Biochemistry
, vol.39
, pp. 6781-6790
-
-
Shi, W.1
Munagala, N.R.2
Wang, C.C.3
Li, C.M.4
Tyler, P.C.5
Furneaux, R.H.6
-
21
-
-
0028103275
-
The CCP4 suite: Programs for protein crystallography
-
Collaborative Computational Project, Number 4. The CCP4 suite: programs for protein crystallography. Acta Crystallog. sect. D. 50:1994;760-763.
-
(1994)
Acta Crystallog. Sect. D
, vol.50
, pp. 760-763
-
-
-
22
-
-
0035969964
-
Transition state structure of purine nucleoside phosphorylase and principles of atomic motion in enzymatic catalysis
-
Fedorov A., Shi W., Kicska G., Fedorov E., Tyler P.C., Furneaux R.H., et al. Transition state structure of purine nucleoside phosphorylase and principles of atomic motion in enzymatic catalysis. Biochemistry. 40:2001;853-860.
-
(2001)
Biochemistry
, vol.40
, pp. 853-860
-
-
Fedorov, A.1
Shi, W.2
Kicska, G.3
Fedorov, E.4
Tyler, P.C.5
Furneaux, R.H.6
-
23
-
-
0032479324
-
Crystal structure of the ternary complex of E. coli purine nucleoside phosphorylase with formycin B, a structural analogue of the substrate inosine, and phosphate (sulphate) at 2.1 Å resolution
-
Koellner G., Luić M., Shugar D., Saenger W., Bzowska A. Crystal structure of the ternary complex of E. coli purine nucleoside phosphorylase with formycin B, a structural analogue of the substrate inosine, and phosphate (sulphate) at 2.1 Å resolution. J. Mol. Biol. 280:1998;153-166.
-
(1998)
J. Mol. Biol.
, vol.280
, pp. 153-166
-
-
Koellner, G.1
Luić, M.2
Shugar, D.3
Saenger, W.4
Bzowska, A.5
-
24
-
-
0027729453
-
Purine nucleoside phosphorylase. Catalytic mechanism and transition-state analysis of the arsenolysis reaction
-
Kline P.C., Schramm V.L. Purine nucleoside phosphorylase. Catalytic mechanism and transition-state analysis of the arsenolysis reaction. Biochemistry. 32:1993;13212-13219.
-
(1993)
Biochemistry
, vol.32
, pp. 13212-13219
-
-
Kline, P.C.1
Schramm, V.L.2
-
25
-
-
0036303728
-
Open and closed conformation of the E. coli purine nucleoside phosphorylase active center and implications for the catalytic mechanism
-
Koellner G., Bzowska A., Wielgus-Kutrowska B., Luić M., Steiner T., Saenger W., Stepiński J. Open and closed conformation of the E. coli purine nucleoside phosphorylase active center and implications for the catalytic mechanism. J. Mol. Biol. 315:2002;351-371.
-
(2002)
J. Mol. Biol.
, vol.315
, pp. 351-371
-
-
Koellner, G.1
Bzowska, A.2
Wielgus-Kutrowska, B.3
Luić, M.4
Steiner, T.5
Saenger, W.6
Stepiński, J.7
-
26
-
-
0015217521
-
Cytoplasmic uridine phosphorylase of rat liver
-
Kraut A., Yamada E.W. Cytoplasmic uridine phosphorylase of rat liver. J. Biol. Chem. 246:1971;2021-2030.
-
(1971)
J. Biol. Chem.
, vol.246
, pp. 2021-2030
-
-
Kraut, A.1
Yamada, E.W.2
-
27
-
-
0032401829
-
Expression, characterization, and detection of human uridine phosphorylase and identification of variant uridine phosphorolytic activity in selected human tumors
-
Liu M., Cao D., Russel R., Handshumacher R.E., Pizzorno G. Expression, characterization, and detection of human uridine phosphorylase and identification of variant uridine phosphorolytic activity in selected human tumors. Cancer Res. 58:1998;5418-5424.
-
(1998)
Cancer Res.
, vol.58
, pp. 5418-5424
-
-
Liu, M.1
Cao, D.2
Russel, R.3
Handshumacher, R.E.4
Pizzorno, G.5
-
28
-
-
0021105251
-
Uridine phosphorylase from Escherichia coli B.: Kinetic studies on the mechanism of catalysis
-
Vita A., Huang C.Y., Magni G. Uridine phosphorylase from Escherichia coli B.: kinetic studies on the mechanism of catalysis. Arch. Biochem. Biophys. 226:1983;687-692.
-
(1983)
Arch. Biochem. Biophys.
, vol.226
, pp. 687-692
-
-
Vita, A.1
Huang, C.Y.2
Magni, G.3
-
29
-
-
0022586525
-
Uridine phosphorylase from Escherichia coli B. Enzymatic and molecular properties
-
Vita A., Amici A., Cacciamani T., Lancotti M., Magni G. Uridine phosphorylase from Escherichia coli B. Enzymatic and molecular properties. Int. J. Biochem. 18:1986;431-436.
-
(1986)
Int. J. Biochem.
, vol.18
, pp. 431-436
-
-
Vita, A.1
Amici, A.2
Cacciamani, T.3
Lancotti, M.4
Magni, G.5
-
30
-
-
0017227849
-
Uridine phosphorylase from Escherichia coli. Kinetic properties and mechanism
-
Krenitsky T.A. Uridine phosphorylase from Escherichia coli. Kinetic properties and mechanism. Biochem. Biophys. Acta. 429:1976;352-358.
-
(1976)
Biochem. Biophys. Acta
, vol.429
, pp. 352-358
-
-
Krenitsky, T.A.1
-
31
-
-
0036014793
-
Metal-ligand geometry relevant to proteins and in proteins: Sodium and potassium
-
Harding M.J. Metal-ligand geometry relevant to proteins and in proteins: sodium and potassium. Acta Crystallog. sect. D. 58:2002;872-874.
-
(2002)
Acta Crystallog. Sect. D
, vol.58
, pp. 872-874
-
-
Harding, M.J.1
-
32
-
-
0028917334
-
[[(Guaninylalkyl)phosphinico]methyl]phosphonic acids. Multisubstrate analogue inhibitors of human erythrocyte purine nucleoside phosphorylase
-
Kelly J.L., McLean E.W., Crouch R.C., Averett D.R., Tuttle J.V. [[(Guaninylalkyl)phosphinico]methyl]phosphonic acids. Multisubstrate analogue inhibitors of human erythrocyte purine nucleoside phosphorylase. J. Med. Chem. 38:1995;1005-1014.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1005-1014
-
-
Kelly, J.L.1
McLean, E.W.2
Crouch, R.C.3
Averett, D.R.4
Tuttle, J.V.5
-
33
-
-
0017331267
-
Uridine phosphorylase from Escherichia coli. Physical and chemical characterization
-
Leer J.C., Hammer-Jespersen K., Schwartz M. Uridine phosphorylase from Escherichia coli. Physical and chemical characterization. Eur. J. Biochem. 75:1977;21.
-
(1977)
Eur. J. Biochem.
, vol.75
, pp. 21
-
-
Leer, J.C.1
Hammer-Jespersen, K.2
Schwartz, M.3
-
34
-
-
0028932756
-
Pre-steady-state transition-state analysis of the hydrolytic reaction catalysed by purine nucleoside phosphorylase
-
Kline P.C., Schramm V.L. Pre-steady-state transition-state analysis of the hydrolytic reaction catalysed by purine nucleoside phosphorylase. Biochemistry. 34:1995;1153-1162.
-
(1995)
Biochemistry
, vol.34
, pp. 1153-1162
-
-
Kline, P.C.1
Schramm, V.L.2
-
35
-
-
0035902542
-
Purine nucleoside phosphorylase from Mycobacterium tuberculosis. Analysis of inhibition by a transition-state analogue and dissection by parts
-
Basso L.A., Santos D.S., Shi W., Furneaux R.H., Tyler P.C., Schramm V.L., Blanchard J.S. Purine nucleoside phosphorylase from Mycobacterium tuberculosis. Analysis of inhibition by a transition-state analogue and dissection by parts. Biochemistry. 40:2001;8196-8203.
-
(2001)
Biochemistry
, vol.40
, pp. 8196-8203
-
-
Basso, L.A.1
Santos, D.S.2
Shi, W.3
Furneaux, R.H.4
Tyler, P.C.5
Schramm, V.L.6
Blanchard, J.S.7
-
36
-
-
2242437134
-
Atomic dissection of the hydrogen bond network for transition-state analogue binding to purine nucleoside phosphorylase
-
Kicska G.A., Tyler P.C., Evans G.B., Furneaux R.H., Shi W., Federov A., et al. Atomic dissection of the hydrogen bond network for transition-state analogue binding to purine nucleoside phosphorylase. Biochemistry. 41:2002;14489-14498.
-
(2002)
Biochemistry
, vol.41
, pp. 14489-14498
-
-
Kicska, G.A.1
Tyler, P.C.2
Evans, G.B.3
Furneaux, R.H.4
Shi, W.5
Federov, A.6
-
37
-
-
0037130281
-
Development of transition state analogues of purine nucleoside phosphorylase as anti-T-cell agents
-
Schramm V.L. Development of transition state analogues of purine nucleoside phosphorylase as anti-T-cell agents. Biochem. Biophys. Acta. 1587:2002;107-117.
-
(2002)
Biochem. Biophys. Acta
, vol.1587
, pp. 107-117
-
-
Schramm, V.L.1
-
38
-
-
0030760959
-
Purine nucleoside phosphorylase. 2. Catalytic mechanism
-
Erion M.D., Stoeckler J.D., Guida W.C., Walter R.L., Ealick S.E. Purine nucleoside phosphorylase. 2. Catalytic mechanism. Biochemistry. 36:1997;11735-11748.
-
(1997)
Biochemistry
, vol.36
, pp. 11735-11748
-
-
Erion, M.D.1
Stoeckler, J.D.2
Guida, W.C.3
Walter, R.L.4
Ealick, S.E.5
-
39
-
-
0030817010
-
Purine nucleoside phosphorylase. 1 Structure-function studies
-
Erion M.D., Takabayashi K., Smith H.B., Kessi J., Wagner S., Hönger S., et al. Purine nucleoside phosphorylase. 1 Structure-function studies. Biochemistry. 36:1997;11725-11734.
-
(1997)
Biochemistry
, vol.36
, pp. 11725-11734
-
-
Erion, M.D.1
Takabayashi, K.2
Smith, H.B.3
Kessi, J.4
Wagner, S.5
Hönger, S.6
-
40
-
-
0030874772
-
Purine nucleoside phosphorylase. 3. Reversal of purine base specificity by site-directed mutagenesis
-
Stoeckler J.D., Poirot A.F., Smith R.M., Parks R.E. Jr, Ealick S.E., Takabayashi K., Erion M.D. Purine nucleoside phosphorylase. 3. Reversal of purine base specificity by site-directed mutagenesis. Biochemistry. 36:1997;11749-11756.
-
(1997)
Biochemistry
, vol.36
, pp. 11749-11756
-
-
Stoeckler, J.D.1
Poirot, A.F.2
Smith, R.M.3
Parks Jr., R.E.4
Ealick, S.E.5
Takabayashi, K.6
Erion, M.D.7
-
41
-
-
0014689979
-
Hartley role of a buried acid group in the mechanism of action of chymotrypsin
-
Blow D.M., Birktoft J.J. Hartley role of a buried acid group in the mechanism of action of chymotrypsin. Nature. 221:1969;337-340.
-
(1969)
Nature
, vol.221
, pp. 337-340
-
-
Blow, D.M.1
Birktoft, J.J.2
-
42
-
-
0020037313
-
5-Benzylacyclouridine and 5-benzyloxybenzylacyclouridine, potent inhibitors of uridine phosphorylase
-
Niedzwicki J.G., Chu S.H., El Kouni M.H., Rowe E.C., Cha S. 5-Benzylacyclouridine and 5-benzyloxybenzylacyclouridine, potent inhibitors of uridine phosphorylase. Biochem. Pharmacol. 31:1982;1857-1861.
-
(1982)
Biochem. Pharmacol.
, vol.31
, pp. 1857-1861
-
-
Niedzwicki, J.G.1
Chu, S.H.2
El Kouni, M.H.3
Rowe, E.C.4
Cha, S.5
-
43
-
-
0034666741
-
5-Phenylthioacyclouridine: A potent and specific inhibitor of uridine phosphorylase
-
el Kouni M.H., Goudgaon N.M., Rafeeq M., Al Safarjalani O.N., Schinazi R.F., Naguib F.N.M. 5-Phenylthioacyclouridine: a potent and specific inhibitor of uridine phosphorylase. Biochem. Pharmacol. 60:2000;851-856.
-
(2000)
Biochem. Pharmacol.
, vol.60
, pp. 851-856
-
-
El Kouni, M.H.1
Goudgaon, N.M.2
Rafeeq, M.3
Al Safarjalani, O.N.4
Schinazi, R.F.5
Naguib, F.N.M.6
-
44
-
-
0038336897
-
Application and limitations of X-ray crystallographic data in structure-based ligand and drug design
-
Davis A.M., Teague S.J., Kleywegt G.J. Application and limitations of X-ray crystallographic data in structure-based ligand and drug design. Angew. Chem. Int. Ed. 42:2003;2718-2736.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 2718-2736
-
-
Davis, A.M.1
Teague, S.J.2
Kleywegt, G.J.3
-
45
-
-
0017833140
-
Uridine nucleosidase from yeast
-
Magni G. Uridine nucleosidase from yeast. Methods Enzymol. 26:1978;290-296.
-
(1978)
Methods Enzymol.
, vol.26
, pp. 290-296
-
-
Magni, G.1
-
46
-
-
1442265846
-
-
HKL Research, Inc., Charlottesville, VA.
-
Minor, W. (1993). XDISPLAYF In The HKL Manual, HKL Research, Inc., Charlottesville, VA.
-
(1993)
XDISPLAYF in the HKL Manual
-
-
Minor, W.1
-
48
-
-
0003076963
-
Recent changes to the MOSFLM package for processing film and image plate data
-
Leslie A.G.W. Recent changes to the MOSFLM package for processing film and image plate data. Joint CCP4 ESF-EAMCB Newsletter Protein Crystallog. 26:1992;7-224.
-
(1992)
Joint CCP4 ESF-EAMCB Newsletter Protein Crystallog.
, vol.26
, pp. 7-224
-
-
Leslie, A.G.W.1
-
50
-
-
0000952473
-
On the treatment of negative intensity observations
-
French G.S., Wilson K.S. On the treatment of negative intensity observations. Acta Crystallog. sect. A. 34:1978;517.
-
(1978)
Acta Crystallog. Sect. a
, vol.34
, pp. 517
-
-
French, G.S.1
Wilson, K.S.2
-
52
-
-
0347696954
-
Chymotrypsinogen: A three-dimensional Fourier synthesis at 5 Å resolution
-
Kraut J., Sieker L.C., High D.F., Freer S.T. Chymotrypsinogen: a three-dimensional Fourier synthesis at 5 Å resolution. Proc. Natl Acad. Sci. USA. 48:1962;1417-1424.
-
(1962)
Proc. Natl Acad. Sci. USA
, vol.48
, pp. 1417-1424
-
-
Kraut, J.1
Sieker, L.C.2
High, D.F.3
Freer, S.T.4
-
54
-
-
0033984628
-
RSPS version 4.0: A semi-interactive vector-search program for solving heavy-atom derivatives
-
Knight S.D. RSPS version 4.0: a semi-interactive vector-search program for solving heavy-atom derivatives. Acta Crystallog. sect. D. 52:2000;42-47.
-
(2000)
Acta Crystallog. Sect. D
, vol.52
, pp. 42-47
-
-
Knight, S.D.1
-
55
-
-
0002583957
-
Dm: An automated procedure for phase improvement by density modification
-
Cowtan K. dm: an automated procedure for phase improvement by density modification. Joint CCP4 ESF-EACBM Newsletter Protein Crystallog. 31:1994;34-38.
-
(1994)
Joint CCP4 ESF-EACBM Newsletter Protein Crystallog.
, vol.31
, pp. 34-38
-
-
Cowtan, K.1
-
56
-
-
0002705842
-
A visual protein crystallographic software system for X11/XView
-
McRee D.E. A visual protein crystallographic software system for X11/XView. J. Mol. Graph. 10:1992;44-46.
-
(1992)
J. Mol. Graph.
, vol.10
, pp. 44-46
-
-
McRee, D.E.1
-
57
-
-
0030924992
-
Refinement of macromolecular structures by the maximum-likelihood method
-
Murshudov G.N., Vagin A.A., Dodson E.J. Refinement of macromolecular structures by the maximum-likelihood method. Acta Crystallog. sect. D. 53:1997;240-255.
-
(1997)
Acta Crystallog. Sect. D
, vol.53
, pp. 240-255
-
-
Murshudov, G.N.1
Vagin, A.A.2
Dodson, E.J.3
-
58
-
-
3543012707
-
Crystallography & NMR System: A new software system for macromolecular structure determination
-
Brunger A.T., Adams P.D., Clore G.M., Delano W.L., Gros P., Grosse-Kunstleve R.W., et al. Crystallography & NMR System: a new software system for macromolecular structure determination. Acta Crystallog. sect. D. 54:1998;905-921.
-
(1998)
Acta Crystallog. Sect. D
, vol.54
, pp. 905-921
-
-
Brunger, A.T.1
Adams, P.D.2
Clore, G.M.3
Delano, W.L.4
Gros, P.5
Grosse-Kunstleve, R.W.6
-
59
-
-
84920325457
-
AMoRe: An automated package for molecular replacement
-
Navaza J. AMoRe: an automated package for molecular replacement. Acta Crystallog. sect. A. 50:1994;157-163.
-
(1994)
Acta Crystallog. Sect. a
, vol.50
, pp. 157-163
-
-
Navaza, J.1
-
60
-
-
0025953405
-
Use of vanadate as protein-phosphotyrosine phosphatase inhibitor
-
Gordon J.A. Use of vanadate as protein-phosphotyrosine phosphatase inhibitor. Methods Enzymol. 201:1991;477-482.
-
(1991)
Methods Enzymol.
, vol.201
, pp. 477-482
-
-
Gordon, J.A.1
-
61
-
-
0029034120
-
Crystal structure of the human cell cycle protein CksHs1: Single domain fold with similarity to kinase N-lode domain
-
Arvai A.S., Bourne Y., Hickey M.J., Tainer J.A. Crystal structure of the human cell cycle protein CksHs1: single domain fold with similarity to kinase N-lode domain. J. Mol. Biol. 249:1995;835-842.
-
(1995)
J. Mol. Biol.
, vol.249
, pp. 835-842
-
-
Arvai, A.S.1
Bourne, Y.2
Hickey, M.J.3
Tainer, J.A.4
-
62
-
-
0032922193
-
SFCHECK: A unified set of procedures for evaluating the quality of macromolecular structure-factor data and their agreement with atomic model
-
Vaguine A.A., Richelle J., Wodak S.J. SFCHECK: a unified set of procedures for evaluating the quality of macromolecular structure-factor data and their agreement with atomic model. Acta Crystallog. sect. D. 55:1999;191-205.
-
(1999)
Acta Crystallog. Sect. D
, vol.55
, pp. 191-205
-
-
Vaguine, A.A.1
Richelle, J.2
Wodak, S.J.3
-
64
-
-
0001099937
-
Traitement statistique des erreurs dans la determination des structures crisallines
-
Luzzati V. Traitement statistique des erreurs dans la determination des structures crisallines. Acta Crystallog. 5:1952;802-810.
-
(1952)
Acta Crystallog.
, vol.5
, pp. 802-810
-
-
Luzzati, V.1
-
65
-
-
84944812409
-
Improved Fourier coefficients for maps using phases from partial structures with errors
-
Read R.J. Improved Fourier coefficients for maps using phases from partial structures with errors. Acta Crystallog. sect. A. 42:1986;140-149.
-
(1986)
Acta Crystallog. Sect. a
, vol.42
, pp. 140-149
-
-
Read, R.J.1
-
66
-
-
0030815133
-
Raster3D: Photorealistic molecular graphics
-
Merritt E.A., Bacon D.J. Raster3D: photorealistic molecular graphics. Methods Enzymol. 277:1997;505-524.
-
(1997)
Methods Enzymol.
, vol.277
, pp. 505-524
-
-
Merritt, E.A.1
Bacon, D.J.2
|