2BFM
Leishmania major pteridine reductase 1 in complex with NADP and trimethoprim
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004155 | molecular_function | 6,7-dihydropteridine reductase activity |
A | 0005829 | cellular_component | cytosol |
A | 0006729 | biological_process | tetrahydrobiopterin biosynthetic process |
A | 0016491 | molecular_function | oxidoreductase activity |
A | 0031427 | biological_process | response to methotrexate |
A | 0047040 | molecular_function | pteridine reductase activity |
B | 0004155 | molecular_function | 6,7-dihydropteridine reductase activity |
B | 0005829 | cellular_component | cytosol |
B | 0006729 | biological_process | tetrahydrobiopterin biosynthetic process |
B | 0016491 | molecular_function | oxidoreductase activity |
B | 0031427 | biological_process | response to methotrexate |
B | 0047040 | molecular_function | pteridine reductase activity |
C | 0004155 | molecular_function | 6,7-dihydropteridine reductase activity |
C | 0005829 | cellular_component | cytosol |
C | 0006729 | biological_process | tetrahydrobiopterin biosynthetic process |
C | 0016491 | molecular_function | oxidoreductase activity |
C | 0031427 | biological_process | response to methotrexate |
C | 0047040 | molecular_function | pteridine reductase activity |
D | 0004155 | molecular_function | 6,7-dihydropteridine reductase activity |
D | 0005829 | cellular_component | cytosol |
D | 0006729 | biological_process | tetrahydrobiopterin biosynthetic process |
D | 0016491 | molecular_function | oxidoreductase activity |
D | 0031427 | biological_process | response to methotrexate |
D | 0047040 | molecular_function | pteridine reductase activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 29 |
Details | BINDING SITE FOR RESIDUE NDP A1289 |
Chain | Residue |
A | ARG17 |
A | ASN109 |
A | ALA110 |
A | SER111 |
A | SER112 |
A | ASP142 |
A | MET179 |
A | VAL180 |
A | ASP181 |
A | TYR194 |
A | LYS198 |
A | LEU18 |
A | PRO224 |
A | GLY225 |
A | LEU226 |
A | SER227 |
A | TOP1290 |
A | HOH2023 |
A | HOH2057 |
A | HOH2058 |
A | HOH2059 |
A | HOH2060 |
A | TYR37 |
A | HIS38 |
A | ARG39 |
A | SER40 |
A | ALA64 |
A | ASP65 |
A | LEU66 |
site_id | AC2 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE TOP A1290 |
Chain | Residue |
A | PHE113 |
A | ASP181 |
A | LEU188 |
A | TYR194 |
A | LEU226 |
A | HIS241 |
A | TYR283 |
A | NDP1289 |
D | ARG287 |
site_id | AC3 |
Number of Residues | 27 |
Details | BINDING SITE FOR RESIDUE NDP B1289 |
Chain | Residue |
B | ARG17 |
B | LEU18 |
B | HIS38 |
B | ARG39 |
B | SER40 |
B | ALA64 |
B | ASP65 |
B | LEU66 |
B | ASN109 |
B | ALA110 |
B | SER111 |
B | SER112 |
B | ASP142 |
B | MET179 |
B | VAL180 |
B | ASP181 |
B | TYR194 |
B | LYS198 |
B | PRO224 |
B | GLY225 |
B | LEU226 |
B | SER227 |
B | TOP1290 |
B | HOH2001 |
B | HOH2015 |
B | HOH2043 |
B | HOH2044 |
site_id | AC4 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE TOP B1290 |
Chain | Residue |
B | PHE113 |
B | ASP181 |
B | LEU188 |
B | TYR191 |
B | TYR194 |
B | LEU226 |
B | HIS241 |
B | NDP1289 |
B | HOH2045 |
site_id | AC5 |
Number of Residues | 25 |
Details | BINDING SITE FOR RESIDUE NDP C1289 |
Chain | Residue |
C | ARG17 |
C | LEU18 |
C | TYR37 |
C | HIS38 |
C | ARG39 |
C | SER40 |
C | ALA64 |
C | ASP65 |
C | LEU66 |
C | ASN109 |
C | ALA110 |
C | SER111 |
C | ASP142 |
C | MET179 |
C | VAL180 |
C | ASP181 |
C | TYR194 |
C | LYS198 |
C | PRO224 |
C | GLY225 |
C | LEU226 |
C | SER227 |
C | HOH2001 |
C | HOH2043 |
C | HOH2044 |
site_id | AC6 |
Number of Residues | 23 |
Details | BINDING SITE FOR RESIDUE NDP D1289 |
Chain | Residue |
D | ARG17 |
D | LEU18 |
D | HIS38 |
D | ARG39 |
D | SER40 |
D | ALA64 |
D | ASP65 |
D | LEU66 |
D | ASN109 |
D | ALA110 |
D | SER111 |
D | SER112 |
D | ASP142 |
D | MET179 |
D | VAL180 |
D | ASP181 |
D | TYR194 |
D | LYS198 |
D | PRO224 |
D | GLY225 |
D | LEU226 |
D | SER227 |
D | HOH2036 |
Functional Information from PROSITE/UniProt
site_id | PS00061 |
Number of Residues | 29 |
Details | ADH_SHORT Short-chain dehydrogenases/reductases family signature. DamtnqpllgYtiYTMAKGALeGLTrSAA |
Chain | Residue | Details |
A | ASP181-ALA209 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 4 |
Details | ACT_SITE: Proton acceptor |
Chain | Residue | Details |
A | TYR194 | |
B | TYR194 | |
C | TYR194 | |
D | TYR194 |
site_id | SWS_FT_FI2 |
Number of Residues | 4 |
Details | BINDING: BINDING => ECO:0000250 |
Chain | Residue | Details |
A | ARG17 | |
B | ARG17 | |
C | ARG17 | |
D | ARG17 |
site_id | SWS_FT_FI3 |
Number of Residues | 4 |
Details | BINDING: BINDING => ECO:0000269|PubMed:11373620 |
Chain | Residue | Details |
A | SER175 | |
B | SER175 | |
C | SER175 | |
D | SER175 |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1qsg |
Chain | Residue | Details |
A | LYS198 | |
A | TYR191 |
site_id | CSA2 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1qsg |
Chain | Residue | Details |
B | LYS198 | |
B | TYR191 |
site_id | CSA3 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1qsg |
Chain | Residue | Details |
C | LYS198 | |
C | TYR191 |
site_id | CSA4 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1qsg |
Chain | Residue | Details |
D | LYS198 | |
D | TYR191 |
site_id | CSA5 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1qsg |
Chain | Residue | Details |
A | LYS198 | |
A | TYR194 |
site_id | CSA6 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1qsg |
Chain | Residue | Details |
B | LYS198 | |
B | TYR194 |
site_id | CSA7 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1qsg |
Chain | Residue | Details |
C | LYS198 | |
C | TYR194 |
site_id | CSA8 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1qsg |
Chain | Residue | Details |
D | LYS198 | |
D | TYR194 |