2CCJ
Crystal structure of S. aureus thymidylate kinase complexed with thymidine monophosphate
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004798 | molecular_function | thymidylate kinase activity |
A | 0005524 | molecular_function | ATP binding |
A | 0005737 | cellular_component | cytoplasm |
A | 0005829 | cellular_component | cytosol |
A | 0006227 | biological_process | dUDP biosynthetic process |
A | 0006233 | biological_process | dTDP biosynthetic process |
A | 0006235 | biological_process | dTTP biosynthetic process |
A | 0009165 | biological_process | nucleotide biosynthetic process |
A | 0016301 | molecular_function | kinase activity |
A | 0046940 | biological_process | nucleoside monophosphate phosphorylation |
B | 0004798 | molecular_function | thymidylate kinase activity |
B | 0005524 | molecular_function | ATP binding |
B | 0005737 | cellular_component | cytoplasm |
B | 0005829 | cellular_component | cytosol |
B | 0006227 | biological_process | dUDP biosynthetic process |
B | 0006233 | biological_process | dTDP biosynthetic process |
B | 0006235 | biological_process | dTTP biosynthetic process |
B | 0009165 | biological_process | nucleotide biosynthetic process |
B | 0016301 | molecular_function | kinase activity |
B | 0046940 | biological_process | nucleoside monophosphate phosphorylation |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE CL A1206 |
Chain | Residue |
A | ASN132 |
A | ASN182 |
B | HOH2080 |
site_id | AC2 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE CL A1207 |
Chain | Residue |
A | ARG36 |
A | GLY39 |
A | LYS77 |
A | HOH2015 |
site_id | AC3 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE CL A1208 |
Chain | Residue |
A | LEU187 |
B | HOH2142 |
site_id | AC4 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE CL B1206 |
Chain | Residue |
A | HOH2149 |
B | LEU187 |
site_id | AC5 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE CL B1207 |
Chain | Residue |
A | GLU53 |
B | ASN132 |
B | VAL181 |
B | ASN182 |
B | HOH2170 |
site_id | AC6 |
Number of Residues | 12 |
Details | BINDING SITE FOR RESIDUE TMP A1209 |
Chain | Residue |
A | LYS15 |
A | GLU37 |
A | PHE66 |
A | ARG70 |
A | ARG92 |
A | SER97 |
A | TYR100 |
A | GLN101 |
A | HOH2102 |
A | HOH2105 |
A | HOH2109 |
A | HOH2216 |
site_id | AC7 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE EDO A1210 |
Chain | Residue |
A | ARG71 |
A | LEU74 |
A | ILE120 |
A | ASN121 |
site_id | AC8 |
Number of Residues | 14 |
Details | BINDING SITE FOR RESIDUE TMP B1208 |
Chain | Residue |
B | GLU11 |
B | LYS15 |
B | ARG36 |
B | ARG70 |
B | ARG92 |
B | SER96 |
B | SER97 |
B | TYR100 |
B | GLN101 |
B | TMP1209 |
B | HOH2011 |
B | HOH2115 |
B | HOH2194 |
B | HOH2195 |
site_id | AC9 |
Number of Residues | 10 |
Details | BINDING SITE FOR RESIDUE TMP B1209 |
Chain | Residue |
B | ALA63 |
B | PHE66 |
B | GLN101 |
B | ARG105 |
B | TMP1208 |
B | HOH2066 |
B | HOH2092 |
B | HOH2115 |
B | HOH2195 |
B | HOH2197 |
site_id | BC1 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE EDO B1210 |
Chain | Residue |
B | ARG71 |
B | ILE120 |
B | ASN121 |
site_id | BC2 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE EDO B1211 |
Chain | Residue |
B | GLU37 |
B | ARG48 |
B | PHE66 |
B | SER69 |
B | ARG70 |
Functional Information from PROSITE/UniProt
site_id | PS01331 |
Number of Residues | 13 |
Details | THYMIDYLATE_KINASE Thymidylate kinase signature. LCDRYidSSlAYQ |
Chain | Residue | Details |
A | LEU89-GLN101 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 2 |
Details | BINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00165 |
Chain | Residue | Details |
A | GLY9 | |
B | GLY9 |