58
|
192
|
4hofA |
Candida albicans dihydrofolate reductase complexed with nadph and 5-[3-(2-methoxy-4-phenylphenyl)but-1-yn-1-yl]-6-methylpyrimidine-2,4-diamine (ucp111h) |
51
|
189
|
4h95A |
Candida albicans dihydrofolate reductase complexed with nadph and 6-ethyl-5-{3-[3-methoxy-5-(pyridin-4-yl)phenyl]but-1-yn-1-yl}pyrimidine-2,4-diamine (ucp1006) |
58
|
235
|
4ha9A |
Structural insights into the reduction mechanism of saccharomyces cerevisia riboflavin biosynthesis reductase rib7 |
58
|
224
|
4h98A |
Candida glabrata dihydrofolate reductase complexed with nadph and 5-{3-[3-(2,3-dihydro-1,4-benzodioxin-6-yl)-5-methoxyphenyl]prop-1-yn-1-yl}-6-ethylpyrimidine-2,4-diamine (ucp1018) |
46
|
189
|
4h96A |
Candida albicans dihydrofolate reductase complexed with nadph and 5-{3-[3-(2,3-dihydro-1,4-benzodioxin-6-yl)-5-methoxyphenyl]prop-1-yn-1-yl}-6-ethylpyrimidine-2,4-diamine (ucp1018) |
60
|
235
|
4ha7A |
Structural insights into the reduction mechanism of saccharomyces cerevisia riboflavin biosynthesis reductase rib7 |
54
|
190
|
4h97A |
Candida albicans dihydrofolate reductase complexed with nadph and 5-{3-[3-methoxy-5-(4-methylphenyl)phenyl]but-1-yn-1-yl}-6-methylpyrimidine-2,4-diamine (ucp111d4m) |
110
|
361
|
4g3mA |
Complex structure of bacillus subtilis ribg: the deamination process in riboflavin biosynthesis |
56
|
204
|
4g8zX |
Pcdhfr k37s/f69n double mutant tmp nadph ternary complex |
45
|
162
|
4gh8A |
Crystal structure of a 'humanized' e. coli dihydrofolate reductase |
55
|
186
|
4g95A |
Hdhfr-oag binary complex |
43
|
163
|
4fggA |
S. aureus dihydrofolate reductase co-crystallized with propyl-dap isobutenyl-dihydrophthalazine inhibitor |
41
|
159
|
4fhbA |
Enhancing dhfr catalysis by binding of an allosteric regulator nanobody (nb179) |
44
|
159
|
3r33A |
Evidence for dynamic motion in proteins as a mechanism for ligand dissociation |
40
|
163
|
4fghA |
S. aureus dihydrofolate reductase co-crystallized with ethyl-dap isobutenyl-dihydrophthalazine inhibitor |
45
|
159
|
3qyoA |
Sensitivity of receptor internal motions to ligand binding affinity and kinetic off-rate |
173
|
608
|
3qg2A |
Plasmodium falciparum dhfr-ts qradruple mutant (n51i+c59r+s108n+i164l, v1/s) pyrimethamine complex |
46
|
159
|
3ql3A |
Re-refined coordinates for pdb entry 1rx2 |
59
|
192
|
3qlrA |
Candida albicans dihydrofolate reductase complexed with nadph and 6-methyl-5-[(3r)-3-(3,4,5-trimethoxyphenyl)pent-1-yn-1-yl]pyrimidine-2,4-diamine (ucp112a) |
63
|
225
|
3qlzA |
Candida glabrata dihydrofolate reductase complexed with nadph and 5-[3-(2,5-dimethoxyphenyl)prop-1-yn-1-yl]-6-propylpyrimidine-2,4-diamine (ucp130b) |
58
|
219
|
3qfxA |
Trypanosoma brucei dihydrofolate reductase pyrimethamine complex |
43
|
160
|
3ql0A |
Crystal structure of n23pp/s148a mutant of e. coli dihydrofolate reductase |
177
|
608
|
3qgtA |
Crystal structure of wild-type pfdhfr-ts complexed with nadph, dump and pyrimethamine |
61
|
225
|
3qlxA |
Candida glabrata dihydrofolate reductase complexed with nadph and 6-methyl-5-[(3r)-3-(3,4,5-trimethoxyphenyl)pent-1-yn-1-yl]pyrimidine-2,4-diamine (ucp112a) |
56
|
192
|
3qlsA |
Candida albicans dihydrofolate reductase complexed with nadph and 6-methyl-5-[3-methyl-3-(3,4,5-trimethoxyphenyl)but-1-yn-1-yl]pyrimidine-2,4-diamine (ucp115a) |
53
|
190
|
3qlwA |
Candida albicans dihydrofolate reductase complexed with nadph and 5-[3-(2,5-dimethoxyphenyl)prop-1-yn-1-yl]-6-ethylpyrimidine-2,4-diamine (ucp120b) |
61
|
225
|
3qlyA |
Candida glabrata dihydrofolate reductase complexed with nadph and 6-methyl-5-[3-methyl-3-(3,4,5-trimethoxyphenyl)but-1-yn-1-yl]pyrimidine-2,4-diamine (ucp115a) |
46
|
159
|
3qylA |
Sensitivity of receptor internal motions to ligand binding affinity and kinetic off-rate |
40
|
161
|
3q1hA |
Crystal structure of dihydrofolate reductase from yersinia pestis |
59
|
186
|
3nzdA |
Structural analysis of pneumocystis carinii and human dhfr complexes with nadph and a series of five 5-(omega-carboxy(alkyloxy(pyrido[2,3-d]pyrimidine derivatives |
57
|
186
|
3nxvA |
Preferential selection of isomer binding from chiral mixtures: alternate binding modes observed for the e- and z-isomers of a series of 5-substituted 2,4-diaminofuro[2,3-d]pyrimidines as ternary complexes with nadph and human dihydrofolate reductase |
58
|
186
|
3nxxA |
Preferential selection of isomer binding from chiral mixtures: alternate binding modes observed for the e- and z-isomers of a series of 5-substituted 2,4-diaminofuro-2,3-d]pyrimidines as ternary complexes with nadph and human dihydrofolate reductase |
57
|
206
|
3nzbX |
Structural analysis of pneumocystis carinii and human dhfr complexes with nadph and a series of potent 5-(omega-carboxyl(alkyloxy)pyrido[2,-d]pyrimidine derivatives |
59
|
206
|
3nzcX |
Structural analysis of pneumocystis carinii and human dhfr complexes with nadph and a series of five potent 5-(omega-carboxy(alkyloxy)pyrido[2,3-d]pyridine derivativea |
54
|
186
|
3oafA |
Structural and kinetic data for antifolate interactions against pneumocystis jirovecii, pneumocystis carinii and human dihydrofolate reductase and thier active site mutants |
59
|
206
|
3nz9X |
Structural analysis of pneumocystis carinii and human dhfr complexes with nadph and a series of five potent 5-(omega-carboxy(alkyloxy)pyrido[2,3-d]pyrimidine derivatives |
44
|
159
|
3ochA |
Chemically self-assembled antibody nanorings (csans): design and characterization of an anti-cd3 igm biomimetic |
59
|
206
|
3nzaX |
Structural analysis of pneumocystis carinii and human dhfr complexes with nadph and a series of five potent 5-(omega-carboxy(alkyloxy)pyrido[2,3-d]pyrimidine derivatives |
55
|
186
|
3nxtA |
Preferential selection of isomer binding from chiral mixtures: alternate binding modes observed for the e-and z-isomers of a series of 5-substituted 2,4-diaminofuro[2m,3-d]pyrimidines as ternary complexes with nadph and human dihydrofolate reductase |
53
|
186
|
3nxyA |
Preferential selection of isomer binding from chiral mixtures: alernate binding modes observed fro the e- and z-isomers of a series of 5-substituted 2,4-diaminofuro[2,3-d]pyrimidines as ternary complexes with nadph and human dihydrofolate reductase |
162
|
509
|
3nrrA |
Co-crystal structure of dihydrofolate reductase-thymidylate synthase from babesia bovis with dump, raltitrexed and nadp |
54
|
186
|
3nxoA |
Perferential selection of isomer binding from chiral mixtures: alternate binding modes observed for the e- and z-isomers of a series of 5-substituted 2,4-diaminofuro[2,3-d]pyrimidines as ternary complexes with nadph and human dihydrofolate reductase |
54
|
186
|
3ntzA |
Design, synthesis, biological evaluation and x-ray crystal structures of novel classical 6,5,6-tricyclicbenzo[4,5]thieno[2,3-d]pyrimidines as dual thymidylate synthase and dihydrofolate reductase inhibitors |
57
|
186
|
3nxrA |
Perferential selection of isomer binding from chiral mixtures: alternate binding modes observed for the e- and z-isomers of a series of 5-substituted 2,4-diaminofuro[2,3-d]pyrimidines as ternary complexes with nadph and human dihydrofolate reductase |
48
|
206
|
3nz6X |
Structural analysis of pneumocystis carinii and human dhfr complexes with nadph and a series of five potent 5-(omega-carboxy(alkyloxy)pyrido[2,3-d]pyrimidine derivatives |
55
|
186
|
3nu0A |
Design, synthesis, biological evaluation and x-ray crystal structure of novel classical 6,5,6-tricyclicbenzo[4,5]thieno[2,3-d]pyrimidines as dual thymidylate synthase and dihydrofolate reductase inhibitors |
52
|
186
|
3n0hA |
Hdhfr double mutant q35s/n64f trimethoprim binary complex |
41
|
161
|
3m09A |
F98y tmp-resistant dihydrofolate reductase from staphylococcus aureus with inhibitor rab1 |
40
|
161
|
3m08A |
Wild type dihydrofolate reductase from staphylococcus aureus with inhibitor rab1 |
39
|
157
|
3lg4A |
Staphylococcus aureus v31y, f92i mutant dihydrofolate reductase complexed with nadph and 5-[(3s)-3-(5-methoxy-2',6'-dimethylbiphenyl-3-yl)but-1-yn-1-yl]-6-methylpyrimidine-2,4-diamine |