5QAD
OXA-48 IN COMPLEX WITH COMPOUND 8a
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 | 5 |
| Details | binding site for residue WVV A 301 |
| Chain | Residue |
| A | TYR117 |
| A | ARG250 |
| A | EDO307 |
| A | HOH402 |
| A | HOH405 |
| site_id | AC2 |
| Number of Residues | 6 |
| Details | binding site for residue EDO A 302 |
| Chain | Residue |
| A | HOH432 |
| A | HOH485 |
| A | SER40 |
| A | ASP240 |
| A | MET241 |
| A | PRO242 |
| site_id | AC3 |
| Number of Residues | 2 |
| Details | binding site for residue EDO A 303 |
| Chain | Residue |
| A | HIS38 |
| A | GLU256 |
| site_id | AC4 |
| Number of Residues | 5 |
| Details | binding site for residue EDO A 304 |
| Chain | Residue |
| A | LEU81 |
| A | SER184 |
| A | ARG186 |
| A | SER187 |
| A | HOH501 |
| site_id | AC5 |
| Number of Residues | 4 |
| Details | binding site for residue EDO A 305 |
| Chain | Residue |
| A | VAL92 |
| A | ASN110 |
| C | ASP229 |
| C | ASP230 |
| site_id | AC6 |
| Number of Residues | 6 |
| Details | binding site for residue EDO A 306 |
| Chain | Residue |
| A | LYS94 |
| A | TRP95 |
| A | ASP96 |
| A | VAL122 |
| A | HOH466 |
| A | HOH586 |
| site_id | AC7 |
| Number of Residues | 4 |
| Details | binding site for residue EDO A 307 |
| Chain | Residue |
| A | ASP101 |
| A | WVV301 |
| A | HOH420 |
| A | HOH438 |
| site_id | AC8 |
| Number of Residues | 2 |
| Details | binding site for residue EDO A 308 |
| Chain | Residue |
| A | ARG100 |
| C | HOH416 |
| site_id | AC9 |
| Number of Residues | 4 |
| Details | binding site for residue EDO A 309 |
| Chain | Residue |
| A | GLU198 |
| A | ASN200 |
| C | GLU198 |
| C | ALA199 |
| site_id | AD1 |
| Number of Residues | 5 |
| Details | binding site for residue WVV B 301 |
| Chain | Residue |
| B | TYR117 |
| B | ARG250 |
| B | HOH403 |
| B | HOH407 |
| B | HOH580 |
| site_id | AD2 |
| Number of Residues | 1 |
| Details | binding site for residue CL B 302 |
| Chain | Residue |
| B | ARG206 |
| site_id | AD3 |
| Number of Residues | 2 |
| Details | binding site for residue EDO B 303 |
| Chain | Residue |
| B | HOH517 |
| B | HOH540 |
| site_id | AD4 |
| Number of Residues | 6 |
| Details | binding site for residue EDO B 304 |
| Chain | Residue |
| B | SER40 |
| B | ASP240 |
| B | MET241 |
| B | PRO242 |
| B | HOH420 |
| B | HOH450 |
| site_id | AD5 |
| Number of Residues | 5 |
| Details | binding site for residue EDO B 305 |
| Chain | Residue |
| B | LYS94 |
| B | TRP95 |
| B | ASP96 |
| B | HOH453 |
| B | HOH544 |
| site_id | AD6 |
| Number of Residues | 5 |
| Details | binding site for residue EDO B 306 |
| Chain | Residue |
| B | SER184 |
| B | ARG186 |
| B | SER187 |
| B | HOH462 |
| B | HOH474 |
| site_id | AD7 |
| Number of Residues | 5 |
| Details | binding site for residue EDO B 307 |
| Chain | Residue |
| A | ARG214 |
| B | ARG100 |
| B | HOH425 |
| B | HOH564 |
| B | HOH579 |
| site_id | AD8 |
| Number of Residues | 5 |
| Details | binding site for residue WVV C 301 |
| Chain | Residue |
| C | TYR117 |
| C | SER118 |
| C | ARG250 |
| C | HOH401 |
| C | HOH436 |
| site_id | AD9 |
| Number of Residues | 3 |
| Details | binding site for residue CL C 302 |
| Chain | Residue |
| A | ARG206 |
| A | HOH665 |
| C | ARG206 |
| site_id | AE1 |
| Number of Residues | 4 |
| Details | binding site for residue EDO C 303 |
| Chain | Residue |
| A | ASP229 |
| A | ASP230 |
| C | ASN110 |
| C | HOH450 |
| site_id | AE2 |
| Number of Residues | 3 |
| Details | binding site for residue EDO C 304 |
| Chain | Residue |
| C | ARG100 |
| C | ASP101 |
| C | HOH512 |
| site_id | AE3 |
| Number of Residues | 7 |
| Details | binding site for residue EDO C 305 |
| Chain | Residue |
| A | HIS90 |
| C | TYR177 |
| C | GLU227 |
| C | VAL232 |
| C | HOH426 |
| C | HOH452 |
| C | HOH520 |
| site_id | AE4 |
| Number of Residues | 4 |
| Details | binding site for residue EDO C 306 |
| Chain | Residue |
| C | TRP25 |
| C | THR167 |
| C | SER171 |
| C | ARG174 |
| site_id | AE5 |
| Number of Residues | 5 |
| Details | binding site for residue EDO C 307 |
| Chain | Residue |
| C | LEU81 |
| C | SER184 |
| C | ARG186 |
| C | SER187 |
| C | HOH439 |
| site_id | AE6 |
| Number of Residues | 5 |
| Details | binding site for residue WVV D 301 |
| Chain | Residue |
| D | ARG250 |
| D | HOH411 |
| D | HOH415 |
| D | HOH440 |
| D | THR209 |
| site_id | AE7 |
| Number of Residues | 2 |
| Details | binding site for residue EDO D 302 |
| Chain | Residue |
| D | ASN110 |
| D | HOH527 |
| site_id | AE8 |
| Number of Residues | 3 |
| Details | binding site for residue EDO D 303 |
| Chain | Residue |
| D | LYS116 |
| D | HOH418 |
| D | HOH419 |
| site_id | AE9 |
| Number of Residues | 6 |
| Details | binding site for residue EDO D 304 |
| Chain | Residue |
| D | TYR177 |
| D | GLU227 |
| D | VAL232 |
| D | HOH423 |
| D | HOH470 |
| D | HOH504 |
| site_id | AF1 |
| Number of Residues | 5 |
| Details | binding site for residue EDO D 305 |
| Chain | Residue |
| D | LEU81 |
| D | SER184 |
| D | ARG186 |
| D | SER187 |
| D | HOH435 |
| site_id | AF2 |
| Number of Residues | 2 |
| Details | binding site for residue EDO D 306 |
| Chain | Residue |
| D | ARG100 |
| D | ASP101 |
| site_id | AF3 |
| Number of Residues | 4 |
| Details | binding site for residue EDO D 307 |
| Chain | Residue |
| D | THR167 |
| D | ILE170 |
| D | SER171 |
| D | ARG174 |
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 | 12 |
| Details | Binding site: {"evidences":[{"source":"UniProtKB","id":"Q8RLA6","evidenceCode":"ECO:0000250"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI3 |
| Number of Residues | 4 |
| Details | Binding site: {"evidences":[{"source":"UniProtKB","id":"P13661","evidenceCode":"ECO:0000250"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI4 |
| 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 |






