6MWJ
Crystal structure of 2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase (IspF) Burkholderia pseudomallei in complex with ligand HGN-0863
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0008299 | biological_process | isoprenoid biosynthetic process |
A | 0008685 | molecular_function | 2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase activity |
A | 0016114 | biological_process | terpenoid biosynthetic process |
A | 0016829 | molecular_function | lyase activity |
A | 0019288 | biological_process | isopentenyl diphosphate biosynthetic process, methylerythritol 4-phosphate pathway |
A | 0046872 | molecular_function | metal ion binding |
B | 0008299 | biological_process | isoprenoid biosynthetic process |
B | 0008685 | molecular_function | 2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase activity |
B | 0016114 | biological_process | terpenoid biosynthetic process |
B | 0016829 | molecular_function | lyase activity |
B | 0019288 | biological_process | isopentenyl diphosphate biosynthetic process, methylerythritol 4-phosphate pathway |
B | 0046872 | molecular_function | metal ion binding |
C | 0008299 | biological_process | isoprenoid biosynthetic process |
C | 0008685 | molecular_function | 2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase activity |
C | 0016114 | biological_process | terpenoid biosynthetic process |
C | 0016829 | molecular_function | lyase activity |
C | 0019288 | biological_process | isopentenyl diphosphate biosynthetic process, methylerythritol 4-phosphate pathway |
C | 0046872 | molecular_function | metal ion binding |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 4 |
Details | binding site for residue ZN A 200 |
Chain | Residue |
A | ASP10 |
A | HIS12 |
A | HIS44 |
A | AZM201 |
site_id | AC2 |
Number of Residues | 12 |
Details | binding site for residue AZM A 201 |
Chain | Residue |
A | GLY60 |
A | PHE63 |
A | ASP65 |
A | PHE70 |
A | LEU78 |
A | ZN200 |
B | LYS134 |
A | ASP10 |
A | HIS12 |
A | SER37 |
A | HIS44 |
A | ILE59 |
site_id | AC3 |
Number of Residues | 8 |
Details | binding site for residue DMS A 202 |
Chain | Residue |
A | ALA102 |
A | GLN103 |
A | PRO105 |
A | LYS106 |
A | LEU107 |
A | LYS134 |
A | THR135 |
A | HOH313 |
site_id | AC4 |
Number of Residues | 4 |
Details | binding site for residue ZN B 201 |
Chain | Residue |
B | ASP10 |
B | HIS12 |
B | HIS44 |
B | HOH347 |
site_id | AC5 |
Number of Residues | 5 |
Details | binding site for residue DMS B 202 |
Chain | Residue |
B | ALA102 |
B | PRO105 |
B | LYS106 |
B | LEU107 |
B | HOH313 |
site_id | AC6 |
Number of Residues | 5 |
Details | binding site for residue ZN C 201 |
Chain | Residue |
C | ASP10 |
C | HIS12 |
C | HIS44 |
C | HOH309 |
C | HOH359 |
site_id | AC7 |
Number of Residues | 6 |
Details | binding site for residue DMS C 202 |
Chain | Residue |
C | ALA102 |
C | PRO105 |
C | LYS106 |
C | LEU107 |
C | ALA133 |
C | LYS134 |
Functional Information from PROSITE/UniProt
site_id | PS01350 |
Number of Residues | 16 |
Details | ISPF 2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase signature. SDADVLlHAitDAlfG |
Chain | Residue | Details |
A | SER37-GLY52 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 35 |
Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_00107","evidenceCode":"ECO:0000255"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 54 |
Details | Binding site: {} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 6 |
Details | Site: {"description":"Transition state stabilizer","evidences":[{"source":"HAMAP-Rule","id":"MF_00107","evidenceCode":"ECO:0000255"}]} |
Chain | Residue | Details |