3M6B
Crystal Structure of the Ertapenem Pre-isomerized Covalent Adduct with TB B-lactamase
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0005576 | cellular_component | extracellular region |
A | 0005886 | cellular_component | plasma membrane |
A | 0008800 | molecular_function | beta-lactamase activity |
A | 0016787 | molecular_function | hydrolase activity |
A | 0017001 | biological_process | antibiotic catabolic process |
A | 0030655 | biological_process | beta-lactam antibiotic catabolic process |
A | 0042597 | cellular_component | periplasmic space |
A | 0046677 | biological_process | response to antibiotic |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE PO4 A 1 |
Chain | Residue |
A | HOH20 |
A | ARG75 |
A | GLU78 |
A | GLU184 |
A | HOH457 |
A | HOH525 |
A | HOH544 |
site_id | AC2 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE PO4 A 2 |
Chain | Residue |
A | ARG187 |
A | GLU193 |
A | ASP255 |
A | TYR286 |
A | HOH312 |
A | HOH351 |
A | HOH16 |
A | ARG79 |
site_id | AC3 |
Number of Residues | 21 |
Details | BINDING SITE FOR RESIDUE 1RG A 308 |
Chain | Residue |
A | HOH21 |
A | CYS83 |
A | SER84 |
A | LYS87 |
A | ILE117 |
A | SER142 |
A | GLU182 |
A | ASN186 |
A | ARG236 |
A | LYS250 |
A | THR251 |
A | GLY252 |
A | THR253 |
A | GLU289 |
A | PRO290 |
A | GLU292 |
A | 1RG309 |
A | HOH358 |
A | HOH362 |
A | HOH371 |
A | HOH381 |
site_id | AC4 |
Number of Residues | 11 |
Details | BINDING SITE FOR RESIDUE 1RG A 309 |
Chain | Residue |
A | HOH4 |
A | HOH24 |
A | HOH25 |
A | PRO217 |
A | ASP218 |
A | GLU289 |
A | ARG291 |
A | GLU292 |
A | ALA293 |
A | 1RG308 |
A | HOH360 |
Functional Information from PROSITE/UniProt
site_id | PS00146 |
Number of Residues | 16 |
Details | BETA_LACTAMASE_A Beta-lactamase class-A active site. FaFCSTfKaplVAAVL |
Chain | Residue | Details |
A | PHE80-LEU95 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 1 |
Details | Active site: {"description":"Acyl-ester intermediate","evidences":[{"source":"PubMed","id":"19251630","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"20353175","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"20961112","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 1 |
Details | Active site: {"description":"Proton acceptor","evidences":[{"source":"PubMed","id":"20353175","evidenceCode":"ECO:0000303"},{"source":"PubMed","id":"20961112","evidenceCode":"ECO:0000303"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 3 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"19251630","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"20353175","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"20961112","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 1 |
Details | Site: {"description":"Increases nucleophilicity of active site Ser","evidences":[{"source":"PubMed","id":"20353175","evidenceCode":"ECO:0000303"},{"source":"PubMed","id":"20961112","evidenceCode":"ECO:0000303"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI5 |
Number of Residues | 1 |
Details | Site: {"description":"Functions as a gatekeeper residue that regulates substrate accessibility to the enzyme active site","evidences":[{"source":"PubMed","id":"24023821","evidenceCode":"ECO:0000303"}]} |
Chain | Residue | Details |