3C61
Crystal structure of dihydroorotate dehydrogenase from Leishmania donovani
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0000166 | molecular_function | nucleotide binding |
A | 0004152 | molecular_function | dihydroorotate dehydrogenase activity |
A | 0005737 | cellular_component | cytoplasm |
A | 0006207 | biological_process | 'de novo' pyrimidine nucleobase biosynthetic process |
A | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
A | 0006222 | biological_process | UMP biosynthetic process |
A | 0016491 | molecular_function | oxidoreductase activity |
A | 0016627 | molecular_function | oxidoreductase activity, acting on the CH-CH group of donors |
A | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
A | 1990663 | molecular_function | dihydroorotate dehydrogenase (fumarate) activity |
B | 0000166 | molecular_function | nucleotide binding |
B | 0004152 | molecular_function | dihydroorotate dehydrogenase activity |
B | 0005737 | cellular_component | cytoplasm |
B | 0006207 | biological_process | 'de novo' pyrimidine nucleobase biosynthetic process |
B | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
B | 0006222 | biological_process | UMP biosynthetic process |
B | 0016491 | molecular_function | oxidoreductase activity |
B | 0016627 | molecular_function | oxidoreductase activity, acting on the CH-CH group of donors |
B | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
B | 1990663 | molecular_function | dihydroorotate dehydrogenase (fumarate) activity |
C | 0000166 | molecular_function | nucleotide binding |
C | 0004152 | molecular_function | dihydroorotate dehydrogenase activity |
C | 0005737 | cellular_component | cytoplasm |
C | 0006207 | biological_process | 'de novo' pyrimidine nucleobase biosynthetic process |
C | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
C | 0006222 | biological_process | UMP biosynthetic process |
C | 0016491 | molecular_function | oxidoreductase activity |
C | 0016627 | molecular_function | oxidoreductase activity, acting on the CH-CH group of donors |
C | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
C | 1990663 | molecular_function | dihydroorotate dehydrogenase (fumarate) activity |
D | 0000166 | molecular_function | nucleotide binding |
D | 0004152 | molecular_function | dihydroorotate dehydrogenase activity |
D | 0005737 | cellular_component | cytoplasm |
D | 0006207 | biological_process | 'de novo' pyrimidine nucleobase biosynthetic process |
D | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
D | 0006222 | biological_process | UMP biosynthetic process |
D | 0016491 | molecular_function | oxidoreductase activity |
D | 0016627 | molecular_function | oxidoreductase activity, acting on the CH-CH group of donors |
D | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
D | 1990663 | molecular_function | dihydroorotate dehydrogenase (fumarate) activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE CL D 314 |
Chain | Residue |
D | PRO57 |
D | ARG58 |
D | TYR59 |
site_id | AC2 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE CL A 314 |
Chain | Residue |
A | PRO57 |
A | ARG58 |
A | TYR59 |
site_id | AC3 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE CL B 314 |
Chain | Residue |
B | GLY272 |
B | THR273 |
B | ALA274 |
site_id | AC4 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE CL B 315 |
Chain | Residue |
B | PRO57 |
B | ARG58 |
site_id | AC5 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE CL C 314 |
Chain | Residue |
C | PRO57 |
C | ARG58 |
site_id | AC6 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE CL A 315 |
Chain | Residue |
A | THR34 |
A | TYR83 |
A | ASP89 |
site_id | AC7 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE CL C 315 |
Chain | Residue |
C | THR34 |
C | TYR83 |
C | ASP89 |
site_id | AC8 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE CL D 315 |
Chain | Residue |
D | THR34 |
D | TYR83 |
D | ASP89 |
site_id | AC9 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE CL C 316 |
Chain | Residue |
C | THR254 |
C | GLY255 |
C | GLU256 |
C | GLU289 |
site_id | BC1 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE CL B 317 |
Chain | Residue |
B | THR34 |
B | TYR83 |
B | ASP89 |
site_id | BC2 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE AZI A 317 |
Chain | Residue |
A | ALA115 |
A | THR119 |
C | ARG224 |
C | TYR253 |
site_id | BC3 |
Number of Residues | 18 |
Details | BINDING SITE FOR RESIDUE FMN A 401 |
Chain | Residue |
A | ALA19 |
A | ALA20 |
A | GLY21 |
A | LYS44 |
A | SER45 |
A | ASN68 |
A | MET70 |
A | ASN128 |
A | LYS165 |
A | ILE194 |
A | ASN195 |
A | SER196 |
A | GLY223 |
A | CYS249 |
A | GLY250 |
A | GLY251 |
A | GLY272 |
A | THR273 |
site_id | BC4 |
Number of Residues | 11 |
Details | BINDING SITE FOR RESIDUE ORO A 501 |
Chain | Residue |
A | LYS44 |
A | ASN68 |
A | MET70 |
A | GLY71 |
A | LEU72 |
A | ASN128 |
A | CYS131 |
A | PRO132 |
A | ASN133 |
A | ASN195 |
A | SER196 |
site_id | BC5 |
Number of Residues | 18 |
Details | BINDING SITE FOR RESIDUE FMN B 401 |
Chain | Residue |
B | ALA19 |
B | ALA20 |
B | GLY21 |
B | SER45 |
B | TYR59 |
B | ASN68 |
B | MET70 |
B | ASN128 |
B | LYS165 |
B | ILE194 |
B | ASN195 |
B | SER196 |
B | GLY223 |
B | CYS249 |
B | GLY250 |
B | GLY251 |
B | GLY272 |
B | THR273 |
site_id | BC6 |
Number of Residues | 11 |
Details | BINDING SITE FOR RESIDUE ORO B 501 |
Chain | Residue |
B | ASN68 |
B | MET70 |
B | GLY71 |
B | LEU72 |
B | PRO73 |
B | ASN128 |
B | CYS131 |
B | PRO132 |
B | ASN133 |
B | ASN195 |
B | SER196 |
site_id | BC7 |
Number of Residues | 19 |
Details | BINDING SITE FOR RESIDUE FMN C 401 |
Chain | Residue |
C | ASN128 |
C | LYS165 |
C | ILE194 |
C | ASN195 |
C | SER196 |
C | GLY223 |
C | CYS249 |
C | GLY250 |
C | GLY251 |
C | GLY272 |
C | THR273 |
C | ALA19 |
C | ALA20 |
C | GLY21 |
C | LYS44 |
C | SER45 |
C | TYR59 |
C | ASN68 |
C | MET70 |
site_id | BC8 |
Number of Residues | 12 |
Details | BINDING SITE FOR RESIDUE ORO C 501 |
Chain | Residue |
C | LYS44 |
C | ASN68 |
C | MET70 |
C | GLY71 |
C | LEU72 |
C | PRO73 |
C | ASN128 |
C | CYS131 |
C | PRO132 |
C | ASN133 |
C | ASN195 |
C | SER196 |
site_id | BC9 |
Number of Residues | 18 |
Details | BINDING SITE FOR RESIDUE FMN D 401 |
Chain | Residue |
D | ALA19 |
D | ALA20 |
D | GLY21 |
D | LYS44 |
D | SER45 |
D | ASN68 |
D | MET70 |
D | ASN128 |
D | LYS165 |
D | ILE194 |
D | ASN195 |
D | SER196 |
D | GLY223 |
D | CYS249 |
D | GLY250 |
D | GLY251 |
D | GLY272 |
D | THR273 |
site_id | CC1 |
Number of Residues | 11 |
Details | BINDING SITE FOR RESIDUE ORO D 501 |
Chain | Residue |
D | LYS44 |
D | ASN68 |
D | MET70 |
D | GLY71 |
D | LEU72 |
D | ASN128 |
D | CYS131 |
D | PRO132 |
D | ASN133 |
D | ASN195 |
D | SER196 |
site_id | CC2 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE DTU D 502 |
Chain | Residue |
C | TYR169 |
C | PHE170 |
C | ASP171 |
C | HIS174 |
D | TYR142 |
D | TYR169 |
D | PHE170 |
D | ASP171 |
D | HIS174 |
site_id | CC3 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE DTU A 502 |
Chain | Residue |
A | TYR142 |
A | PHE170 |
A | ASP171 |
A | HIS174 |
B | TYR142 |
B | PHE170 |
B | ASP171 |
B | HIS174 |
site_id | CC4 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE GOL B 1002 |
Chain | Residue |
A | LEU227 |
A | PRO228 |
A | LEU231 |
B | ILE203 |
B | TYR225 |
D | GLU156 |
site_id | CC5 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE GOL C 1001 |
Chain | Residue |
A | GLU156 |
C | ILE203 |
C | TYR225 |
D | LEU227 |
D | PRO228 |
D | LEU231 |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 2dor |
Chain | Residue | Details |
A | LYS44 | |
A | CYS131 |
site_id | CSA2 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 2dor |
Chain | Residue | Details |
B | LYS44 | |
B | CYS131 |
site_id | CSA3 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 2dor |
Chain | Residue | Details |
C | LYS44 | |
C | CYS131 |
site_id | CSA4 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 2dor |
Chain | Residue | Details |
D | LYS44 | |
D | CYS131 |
site_id | CSA5 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 2dor |
Chain | Residue | Details |
A | CYS131 |
site_id | CSA6 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 2dor |
Chain | Residue | Details |
B | CYS131 |
site_id | CSA7 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 2dor |
Chain | Residue | Details |
C | CYS131 |
site_id | CSA8 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 2dor |
Chain | Residue | Details |
D | CYS131 |