2X1C
The crystal structure of precursor acyl coenzyme A:isopenicillin N acyltransferase from Penicillium chrysogenum
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0005777 | cellular_component | peroxisome |
A | 0005782 | cellular_component | peroxisomal matrix |
A | 0016740 | molecular_function | transferase activity |
A | 0016746 | molecular_function | acyltransferase activity |
A | 0017000 | biological_process | antibiotic biosynthetic process |
A | 0042318 | biological_process | penicillin biosynthetic process |
A | 0050640 | molecular_function | isopenicillin-N N-acyltransferase activity |
B | 0005777 | cellular_component | peroxisome |
B | 0005782 | cellular_component | peroxisomal matrix |
B | 0016740 | molecular_function | transferase activity |
B | 0016746 | molecular_function | acyltransferase activity |
B | 0017000 | biological_process | antibiotic biosynthetic process |
B | 0042318 | biological_process | penicillin biosynthetic process |
B | 0050640 | molecular_function | isopenicillin-N N-acyltransferase activity |
C | 0005777 | cellular_component | peroxisome |
C | 0005782 | cellular_component | peroxisomal matrix |
C | 0016740 | molecular_function | transferase activity |
C | 0016746 | molecular_function | acyltransferase activity |
C | 0017000 | biological_process | antibiotic biosynthetic process |
C | 0042318 | biological_process | penicillin biosynthetic process |
C | 0050640 | molecular_function | isopenicillin-N N-acyltransferase activity |
D | 0005777 | cellular_component | peroxisome |
D | 0005782 | cellular_component | peroxisomal matrix |
D | 0016740 | molecular_function | transferase activity |
D | 0016746 | molecular_function | acyltransferase activity |
D | 0017000 | biological_process | antibiotic biosynthetic process |
D | 0042318 | biological_process | penicillin biosynthetic process |
D | 0050640 | molecular_function | isopenicillin-N N-acyltransferase activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE SO4 A 1356 |
Chain | Residue |
A | ARG132 |
A | LYS144 |
A | VAL341 |
A | MET342 |
A | ARG343 |
A | GOL1360 |
A | HOH2155 |
A | HOH2160 |
site_id | AC2 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE SO4 B 1357 |
Chain | Residue |
B | LYS144 |
B | VAL341 |
B | MET342 |
B | ARG343 |
B | HOH2210 |
B | HOH2211 |
B | ARG132 |
site_id | AC3 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE SO4 A 1357 |
Chain | Residue |
A | LEU262 |
A | ARG302 |
A | LYS308 |
A | SER309 |
A | ARG310 |
A | HOH2137 |
site_id | AC4 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE SO4 D 1356 |
Chain | Residue |
D | ARG132 |
D | LYS144 |
D | VAL341 |
D | MET342 |
D | ARG343 |
D | HOH2062 |
D | HOH2065 |
site_id | AC5 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE SO4 A 1358 |
Chain | Residue |
A | ARG232 |
A | LEU250 |
A | GLN251 |
A | HOH2161 |
site_id | AC6 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE SO4 B 1358 |
Chain | Residue |
B | ARG232 |
B | LEU250 |
B | GLN251 |
site_id | AC7 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE SO4 A 1359 |
Chain | Residue |
A | LYS48 |
A | ASP79 |
A | VAL80 |
A | SER81 |
site_id | AC8 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE GOL C 1356 |
Chain | Residue |
B | GLN7 |
B | GLU12 |
B | GLU16 |
B | HOH2008 |
C | MET1 |
C | ARG132 |
C | GLU338 |
C | PHE340 |
C | HOH2129 |
site_id | AC9 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE GOL B 1359 |
Chain | Residue |
B | ASP79 |
B | VAL80 |
B | SER81 |
B | HOH2063 |
site_id | BC1 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE GOL B 1360 |
Chain | Residue |
B | TYR94 |
B | GLY95 |
B | LEU96 |
B | ARG100 |
B | HIS170 |
B | LEU171 |
B | HOH2070 |
B | HOH2074 |
site_id | BC2 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE GOL B 1361 |
Chain | Residue |
B | GLU16 |
B | HOH2221 |
C | ARG132 |
C | LYS144 |
C | VAL341 |
C | MET342 |
C | ARG343 |
site_id | BC3 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE GOL C 1357 |
Chain | Residue |
C | ARG175 |
C | PRO176 |
C | THR177 |
D | ARG175 |
site_id | BC4 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE GOL A 1360 |
Chain | Residue |
A | HIS3 |
A | THR134 |
A | ARG136 |
A | LYS144 |
A | ASP345 |
A | ASP348 |
A | SO41356 |
A | HOH2155 |
site_id | BC5 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE CL B 1362 |
Chain | Residue |
B | PHE340 |
B | VAL341 |
B | VAL341 |
B | HOH2209 |
site_id | BC6 |
Number of Residues | 1 |
Details | BINDING SITE FOR RESIDUE CL B 1363 |
Chain | Residue |
B | ARG343 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 8 |
Details | BINDING: BINDING => ECO:0000269|PubMed:20223213, ECO:0007744|PDB:2X1E |
Chain | Residue | Details |
A | ASP121 | |
A | ARG310 | |
B | ASP121 | |
B | ARG310 | |
C | ASP121 | |
C | ARG310 | |
D | ASP121 | |
D | ARG310 |