7MYM
Crystal structure of Escherichia coli dihydrofolate reductase in complex with TRIMETHOPRIM and NADPH
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004146 | molecular_function | dihydrofolate reductase activity |
A | 0005515 | molecular_function | protein binding |
A | 0005542 | molecular_function | folic acid binding |
A | 0005829 | cellular_component | cytosol |
A | 0006730 | biological_process | one-carbon metabolic process |
A | 0009257 | biological_process | 10-formyltetrahydrofolate biosynthetic process |
A | 0009410 | biological_process | response to xenobiotic stimulus |
A | 0016491 | molecular_function | oxidoreductase activity |
A | 0031427 | biological_process | response to methotrexate |
A | 0046452 | biological_process | dihydrofolate metabolic process |
A | 0046654 | biological_process | tetrahydrofolate biosynthetic process |
A | 0046655 | biological_process | folic acid metabolic process |
A | 0046656 | biological_process | folic acid biosynthetic process |
A | 0046677 | biological_process | response to antibiotic |
A | 0050661 | molecular_function | NADP binding |
A | 0051870 | molecular_function | methotrexate binding |
A | 0051871 | molecular_function | dihydrofolic acid binding |
A | 0070401 | molecular_function | NADP+ binding |
A | 0070402 | molecular_function | NADPH binding |
B | 0004146 | molecular_function | dihydrofolate reductase activity |
B | 0005515 | molecular_function | protein binding |
B | 0005542 | molecular_function | folic acid binding |
B | 0005829 | cellular_component | cytosol |
B | 0006730 | biological_process | one-carbon metabolic process |
B | 0009257 | biological_process | 10-formyltetrahydrofolate biosynthetic process |
B | 0009410 | biological_process | response to xenobiotic stimulus |
B | 0016491 | molecular_function | oxidoreductase activity |
B | 0031427 | biological_process | response to methotrexate |
B | 0046452 | biological_process | dihydrofolate metabolic process |
B | 0046654 | biological_process | tetrahydrofolate biosynthetic process |
B | 0046655 | biological_process | folic acid metabolic process |
B | 0046656 | biological_process | folic acid biosynthetic process |
B | 0046677 | biological_process | response to antibiotic |
B | 0050661 | molecular_function | NADP binding |
B | 0051870 | molecular_function | methotrexate binding |
B | 0051871 | molecular_function | dihydrofolic acid binding |
B | 0070401 | molecular_function | NADP+ binding |
B | 0070402 | molecular_function | NADPH binding |
C | 0004146 | molecular_function | dihydrofolate reductase activity |
C | 0005515 | molecular_function | protein binding |
C | 0005542 | molecular_function | folic acid binding |
C | 0005829 | cellular_component | cytosol |
C | 0006730 | biological_process | one-carbon metabolic process |
C | 0009257 | biological_process | 10-formyltetrahydrofolate biosynthetic process |
C | 0009410 | biological_process | response to xenobiotic stimulus |
C | 0016491 | molecular_function | oxidoreductase activity |
C | 0031427 | biological_process | response to methotrexate |
C | 0046452 | biological_process | dihydrofolate metabolic process |
C | 0046654 | biological_process | tetrahydrofolate biosynthetic process |
C | 0046655 | biological_process | folic acid metabolic process |
C | 0046656 | biological_process | folic acid biosynthetic process |
C | 0046677 | biological_process | response to antibiotic |
C | 0050661 | molecular_function | NADP binding |
C | 0051870 | molecular_function | methotrexate binding |
C | 0051871 | molecular_function | dihydrofolic acid binding |
C | 0070401 | molecular_function | NADP+ binding |
C | 0070402 | molecular_function | NADPH binding |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 6 |
Details | binding site for residue ARG A 201 |
Chain | Residue |
A | PRO130 |
A | ASP131 |
A | ASP132 |
A | TRP133 |
A | GLU134 |
A | ARG158 |
site_id | AC2 |
Number of Residues | 24 |
Details | binding site for residue NAP A 202 |
Chain | Residue |
A | ASN18 |
A | ALA19 |
A | MET20 |
A | GLY43 |
A | ARG44 |
A | HIS45 |
A | THR46 |
A | SER49 |
A | LEU62 |
A | SER63 |
A | SER64 |
A | LYS76 |
A | ILE94 |
A | GLY96 |
A | GLY97 |
A | ARG98 |
A | VAL99 |
A | TYR100 |
A | GLN102 |
A | THR123 |
A | TOP203 |
A | ALA7 |
A | ILE14 |
A | GLY15 |
site_id | AC3 |
Number of Residues | 12 |
Details | binding site for residue TOP A 203 |
Chain | Residue |
A | ILE5 |
A | ALA6 |
A | ALA7 |
A | MET20 |
A | ASP27 |
A | LEU28 |
A | PHE31 |
A | SER49 |
A | ILE94 |
A | TYR100 |
A | THR113 |
A | NAP202 |
site_id | AC4 |
Number of Residues | 6 |
Details | binding site for residue SO4 A 204 |
Chain | Residue |
A | LEU104 |
A | TYR128 |
A | GLU129 |
A | ASP132 |
A | TRP133 |
A | ARG158 |
site_id | AC5 |
Number of Residues | 5 |
Details | binding site for residue SO4 A 205 |
Chain | Residue |
A | LYS32 |
A | ARG52 |
A | LEU54 |
A | PRO55 |
A | ARG57 |
site_id | AC6 |
Number of Residues | 5 |
Details | binding site for residue ARG C 201 |
Chain | Residue |
C | ASP131 |
C | ASP132 |
C | TRP133 |
C | GLU134 |
C | ARG158 |
site_id | AC7 |
Number of Residues | 23 |
Details | binding site for residue NAP C 202 |
Chain | Residue |
C | ALA6 |
C | ALA7 |
C | ILE14 |
C | ASN18 |
C | ALA19 |
C | MET20 |
C | GLY43 |
C | ARG44 |
C | HIS45 |
C | THR46 |
C | LEU62 |
C | SER63 |
C | SER64 |
C | LYS76 |
C | ILE94 |
C | GLY96 |
C | GLY97 |
C | ARG98 |
C | VAL99 |
C | TYR100 |
C | GLN102 |
C | THR123 |
C | TOP203 |
site_id | AC8 |
Number of Residues | 11 |
Details | binding site for residue TOP C 203 |
Chain | Residue |
C | ILE5 |
C | ALA6 |
C | MET20 |
C | ASP27 |
C | PHE31 |
C | SER49 |
C | ILE50 |
C | ILE94 |
C | TYR100 |
C | THR113 |
C | NAP202 |
site_id | AC9 |
Number of Residues | 5 |
Details | binding site for residue SO4 C 204 |
Chain | Residue |
C | LYS32 |
C | ARG52 |
C | LEU54 |
C | PRO55 |
C | ARG57 |
site_id | AD1 |
Number of Residues | 26 |
Details | binding site for residue NAP B 201 |
Chain | Residue |
B | GLY15 |
B | MET16 |
B | ASN18 |
B | ALA19 |
B | MET20 |
B | GLY43 |
B | ARG44 |
B | HIS45 |
B | THR46 |
B | SER49 |
B | LEU62 |
B | SER63 |
B | SER64 |
B | LYS76 |
B | ILE94 |
B | GLY95 |
B | GLY96 |
B | GLY97 |
B | ARG98 |
B | VAL99 |
B | TYR100 |
B | GLN102 |
B | THR123 |
B | TOP202 |
B | ALA7 |
B | ILE14 |
site_id | AD2 |
Number of Residues | 12 |
Details | binding site for residue TOP B 202 |
Chain | Residue |
B | ILE5 |
B | ALA6 |
B | MET20 |
B | ASP27 |
B | LEU28 |
B | PHE31 |
B | SER49 |
B | ILE50 |
B | ILE94 |
B | TYR100 |
B | THR113 |
B | NAP201 |
site_id | AD3 |
Number of Residues | 4 |
Details | binding site for residue SO4 B 203 |
Chain | Residue |
B | LYS32 |
B | ARG52 |
B | PRO55 |
B | ARG57 |
Functional Information from PROSITE/UniProt
site_id | PS00075 |
Number of Residues | 23 |
Details | DHFR_1 Dihydrofolate reductase (DHFR) domain signature. VIGmenaMPWnlpa.DlawFkrnT |
Chain | Residue | Details |
A | VAL13-THR35 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 15 |
Details | BINDING: BINDING => ECO:0000305|PubMed:9012674 |
Chain | Residue | Details |
A | ILE5 | |
C | THR113 | |
B | ILE5 | |
B | ASP27 | |
B | ARG52 | |
B | ARG57 | |
B | THR113 | |
A | ASP27 | |
A | ARG52 | |
A | ARG57 | |
A | THR113 | |
C | ILE5 | |
C | ASP27 | |
C | ARG52 | |
C | ARG57 |
site_id | SWS_FT_FI2 |
Number of Residues | 18 |
Details | BINDING: BINDING => ECO:0000269|PubMed:19374017 |
Chain | Residue | Details |
A | ALA7 | |
C | SER63 | |
C | LYS76 | |
C | GLY95 | |
B | ALA7 | |
B | VAL13 | |
B | HIS45 | |
B | SER63 | |
B | LYS76 | |
B | GLY95 | |
A | VAL13 | |
A | HIS45 | |
A | SER63 | |
A | LYS76 | |
A | GLY95 | |
C | ALA7 | |
C | VAL13 | |
C | HIS45 |