6PK0
Crystal Structure of OXA-48 with Hydrolyzed Imipenem
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 | 14 | 
| Details | binding site for residue HIW A 301 | 
| Chain | Residue | 
| A | ALA69 | 
| A | GLY210 | 
| A | TYR211 | 
| A | SER244 | 
| A | ARG250 | 
| A | HOH402 | 
| A | SER70 | 
| A | KCX73 | 
| A | ILE102 | 
| A | TRP105 | 
| A | SER118 | 
| A | VAL120 | 
| A | LEU158 | 
| A | THR209 | 
| site_id | AC2 | 
| Number of Residues | 7 | 
| Details | binding site for residue HIW A 302 | 
| Chain | Residue | 
| A | SER184 | 
| A | GLU185 | 
| A | ARG186 | 
| A | HOH464 | 
| C | ASP82 | 
| C | HIS140 | 
| C | HIS182 | 
| site_id | AC3 | 
| Number of Residues | 3 | 
| Details | binding site for residue CL A 303 | 
| Chain | Residue | 
| A | ARG206 | 
| A | HOH572 | 
| B | ARG206 | 
| site_id | AC4 | 
| Number of Residues | 8 | 
| Details | binding site for residue GOL A 304 | 
| Chain | Residue | 
| A | LYS94 | 
| A | TRP95 | 
| A | ASP96 | 
| A | PRO121 | 
| A | HOH449 | 
| A | HOH461 | 
| A | HOH486 | 
| A | HOH519 | 
| site_id | AC5 | 
| Number of Residues | 7 | 
| Details | binding site for residue GOL A 305 | 
| Chain | Residue | 
| A | PHE22 | 
| A | TRP25 | 
| A | TRP47 | 
| A | THR167 | 
| A | ILE170 | 
| A | SER171 | 
| A | ARG174 | 
| site_id | AC6 | 
| Number of Residues | 14 | 
| Details | binding site for residue HIW B 301 | 
| Chain | Residue | 
| B | ALA69 | 
| B | SER70 | 
| B | KCX73 | 
| B | TRP105 | 
| B | TYR117 | 
| B | SER118 | 
| B | VAL120 | 
| B | LEU158 | 
| B | THR209 | 
| B | GLY210 | 
| B | TYR211 | 
| B | ARG250 | 
| B | HOH443 | 
| B | HOH575 | 
| site_id | AC7 | 
| Number of Residues | 4 | 
| Details | binding site for residue GOL B 302 | 
| Chain | Residue | 
| B | ARG100 | 
| B | ASP101 | 
| B | ILE102 | 
| B | HOH557 | 
| site_id | AC8 | 
| Number of Residues | 5 | 
| Details | binding site for residue GOL B 303 | 
| Chain | Residue | 
| B | TRP25 | 
| B | THR167 | 
| B | SER171 | 
| B | ARG174 | 
| B | HOH545 | 
| site_id | AC9 | 
| Number of Residues | 4 | 
| Details | binding site for residue GOL B 304 | 
| Chain | Residue | 
| A | VAL92 | 
| A | ASP108 | 
| A | THR113 | 
| B | ASP229 | 
| site_id | AD1 | 
| Number of Residues | 16 | 
| Details | binding site for residue HIW C 301 | 
| Chain | Residue | 
| C | ALA69 | 
| C | SER70 | 
| C | KCX73 | 
| C | ILE102 | 
| C | THR104 | 
| C | TYR117 | 
| C | SER118 | 
| C | VAL120 | 
| C | LEU158 | 
| C | THR209 | 
| C | GLY210 | 
| C | TYR211 | 
| C | ARG250 | 
| C | HOH470 | 
| C | HOH505 | 
| C | HOH507 | 
| site_id | AD2 | 
| Number of Residues | 2 | 
| Details | binding site for residue CL C 302 | 
| Chain | Residue | 
| C | ARG206 | 
| D | ARG206 | 
| site_id | AD3 | 
| Number of Residues | 7 | 
| Details | binding site for residue GOL C 303 | 
| Chain | Residue | 
| C | LYS94 | 
| C | TRP95 | 
| C | ASP96 | 
| C | PRO121 | 
| C | HOH436 | 
| C | HOH448 | 
| C | HOH534 | 
| site_id | AD4 | 
| Number of Residues | 12 | 
| Details | binding site for residue HIW D 301 | 
| Chain | Residue | 
| D | GLY210 | 
| D | TYR211 | 
| D | ARG250 | 
| D | HOH407 | 
| D | ALA69 | 
| D | SER70 | 
| D | KCX73 | 
| D | SER118 | 
| D | VAL120 | 
| D | LEU158 | 
| D | LYS208 | 
| D | THR209 | 
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 | Active site: {"description":"Acyl-ester intermediate","evidences":[{"source":"PIRSR","id":"PIRSR602137-50","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"25406838","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"26731698","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"31358584","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"32150407","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"4WMC","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5FAQ","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5FAS","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6P97","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6P98","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6P99","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6P9C","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6V1O","evidenceCode":"ECO:0007744"}]} | 
| Chain | Residue | Details | 
| site_id | SWS_FT_FI2 | 
| Number of Residues | 4 | 
| Details | Modified residue: {"description":"N6-carboxylysine","evidences":[{"source":"PIRSR","id":"PIRSR602137-50","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"19477418","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"25406838","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"3HBR","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4WMC","evidenceCode":"ECO:0007744"}]} | 
| Chain | Residue | Details | 
| site_id | SWS_FT_FI3 | 
| Number of Residues | 12 | 
| Details | Binding site: {"evidences":[{"source":"UniProtKB","id":"Q8RLA6","evidenceCode":"ECO:0000250"}]} | 
| Chain | Residue | Details | 
| site_id | SWS_FT_FI4 | 
| Number of Residues | 4 | 
| Details | Binding site: {"evidences":[{"source":"UniProtKB","id":"P13661","evidenceCode":"ECO:0000250"}]} | 
| Chain | Residue | Details | 











