Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0005886 | cellular_component | plasma membrane |
A | 0008658 | molecular_function | penicillin binding |
A | 0008800 | molecular_function | beta-lactamase activity |
A | 0016787 | molecular_function | hydrolase activity |
A | 0017001 | biological_process | antibiotic catabolic process |
A | 0046677 | biological_process | response to antibiotic |
A | 0071555 | biological_process | cell wall organization |
B | 0005886 | cellular_component | plasma membrane |
B | 0008658 | molecular_function | penicillin binding |
B | 0008800 | molecular_function | beta-lactamase activity |
B | 0016787 | molecular_function | hydrolase activity |
B | 0017001 | biological_process | antibiotic catabolic process |
B | 0046677 | biological_process | response to antibiotic |
B | 0071555 | biological_process | cell wall organization |
C | 0005886 | cellular_component | plasma membrane |
C | 0008658 | molecular_function | penicillin binding |
C | 0008800 | molecular_function | beta-lactamase activity |
C | 0016787 | molecular_function | hydrolase activity |
C | 0017001 | biological_process | antibiotic catabolic process |
C | 0046677 | biological_process | response to antibiotic |
C | 0071555 | biological_process | cell wall organization |
D | 0005886 | cellular_component | plasma membrane |
D | 0008658 | molecular_function | penicillin binding |
D | 0008800 | molecular_function | beta-lactamase activity |
D | 0016787 | molecular_function | hydrolase activity |
D | 0017001 | biological_process | antibiotic catabolic process |
D | 0046677 | biological_process | response to antibiotic |
D | 0071555 | biological_process | cell wall organization |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 10 |
Details | binding site for residue IM2 A 301 |
Chain | Residue |
A | ALA69 |
A | HOH487 |
A | SER70 |
A | KCX73 |
A | SER118 |
A | VAL120 |
A | THR209 |
A | GLY210 |
A | TYR211 |
A | ARG250 |
site_id | AC2 |
Number of Residues | 4 |
Details | binding site for residue CL C 302 |
Chain | Residue |
A | ARG206 |
A | HOH566 |
C | ARG206 |
C | HOH553 |
site_id | AC3 |
Number of Residues | 4 |
Details | binding site for residue EDO C 303 |
Chain | Residue |
C | THR167 |
C | ILE170 |
C | SER171 |
C | ARG174 |
site_id | AC4 |
Number of Residues | 2 |
Details | binding site for residue CL D 302 |
Chain | Residue |
D | ARG206 |
D | HOH554 |
site_id | AC5 |
Number of Residues | 14 |
Details | binding site for Di-peptide IM2 B 301 and SER B 70 |
Chain | Residue |
B | PRO68 |
B | ALA69 |
B | THR71 |
B | PHE72 |
B | KCX73 |
B | ILE102 |
B | SER118 |
B | VAL120 |
B | LEU158 |
B | LYS208 |
B | THR209 |
B | GLY210 |
B | TYR211 |
B | ARG250 |
site_id | AC6 |
Number of Residues | 18 |
Details | binding site for Di-peptide IM2 C 301 and SER C 70 |
Chain | Residue |
C | PRO68 |
C | ALA69 |
C | THR71 |
C | PHE72 |
C | KCX73 |
C | SER118 |
C | LEU158 |
C | LYS208 |
C | THR209 |
C | GLY210 |
C | TYR211 |
C | LEU247 |
C | ARG250 |
C | HOH408 |
C | HOH411 |
C | HOH433 |
C | HOH482 |
C | HOH487 |
site_id | AC7 |
Number of Residues | 14 |
Details | binding site for Di-peptide IM2 D 301 and SER D 70 |
Chain | Residue |
D | PRO68 |
D | ALA69 |
D | THR71 |
D | PHE72 |
D | KCX73 |
D | ILE102 |
D | SER118 |
D | VAL120 |
D | LYS208 |
D | THR209 |
D | GLY210 |
D | TYR211 |
D | ARG250 |
D | HOH433 |
Functional Information from PROSITE/UniProt
site_id | PS00337 |
Number of Residues | 11 |
Details | BETA_LACTAMASE_D Beta-lactamase class-D active site. PaSTFKIPnSL |
Chain | Residue | Details |
A | PRO68-LEU78 | |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 4 |
Details | ACT_SITE: Acyl-ester intermediate => ECO:0000255|PIRSR:PIRSR602137-50, ECO:0000269|PubMed:25406838, ECO:0000269|PubMed:26731698, ECO:0000269|PubMed:31358584, ECO:0000269|PubMed:32150407, ECO:0007744|PDB:4WMC, ECO:0007744|PDB:5FAQ, ECO:0007744|PDB:5FAS, ECO:0007744|PDB:6P97, ECO:0007744|PDB:6P98, ECO:0007744|PDB:6P99, ECO:0007744|PDB:6P9C, ECO:0007744|PDB:6V1O |
Chain | Residue | Details |
A | SER70 | |
B | SER70 | |
C | SER70 | |
D | SER70 | |
Chain | Residue | Details |
A | SER70 | |
D | SER70 | |
D | SER118 | |
D | ARG250 | |
A | SER118 | |
A | ARG250 | |
B | SER70 | |
B | SER118 | |
B | ARG250 | |
C | SER70 | |
C | SER118 | |
C | ARG250 | |
Chain | Residue | Details |
A | KCX73 | |
B | KCX73 | |
C | KCX73 | |
D | KCX73 | |
Chain | Residue | Details |
A | KCX73 | |
B | KCX73 | |
C | KCX73 | |
D | KCX73 | |