6M9C
PSEUDOMONAS SERINE-CARBOXYL PROTEINASE (SEDOLISIN) COMPLEXED WITH THE INHIBITOR Pseudotyrostatin
Replaces: 1KE1Functional Information from GO Data
Functional Information from PDB Data
| site_id | AC1 |
| Number of Residues | 6 |
| Details | binding site for residue CA A 401 |
| Chain | Residue |
| A | ASP328 |
| A | VAL329 |
| A | GLY344 |
| A | GLY346 |
| A | ASP348 |
| A | HOH548 |
| site_id | AC2 |
| Number of Residues | 6 |
| Details | binding site for residue SO4 A 402 |
| Chain | Residue |
| A | TYR341 |
| A | HOH510 |
| A | HOH619 |
| A | VAL249 |
| A | SER251 |
| A | GLY340 |
| site_id | AC3 |
| Number of Residues | 5 |
| Details | binding site for residue SO4 A 403 |
| Chain | Residue |
| A | ASN27 |
| A | GLN148 |
| A | ARG152 |
| A | HOH564 |
| A | HOH693 |
| site_id | AC4 |
| Number of Residues | 9 |
| Details | binding site for residue SO4 A 404 |
| Chain | Residue |
| A | SER20 |
| A | ALA22 |
| A | THR24 |
| A | PRO196 |
| A | PRO244 |
| A | TRP246 |
| A | HOH558 |
| A | HOH626 |
| A | HOH715 |
| site_id | AC5 |
| Number of Residues | 4 |
| Details | binding site for residue ACY A 405 |
| Chain | Residue |
| A | THR11 |
| A | SER245 |
| A | VAL249 |
| A | HOH774 |
| site_id | AC6 |
| Number of Residues | 4 |
| Details | binding site for residue ACY A 406 |
| Chain | Residue |
| A | TRP347 |
| A | HOH519 |
| A | HOH653 |
| A | HOH730 |
| site_id | AC7 |
| Number of Residues | 4 |
| Details | binding site for residue ACY A 407 |
| Chain | Residue |
| A | TYR240 |
| A | GLU241 |
| A | HOH501 |
| A | HOH810 |
| site_id | AC8 |
| Number of Residues | 4 |
| Details | binding site for residue ACY A 408 |
| Chain | Residue |
| A | ALA211 |
| A | GLY369 |
| A | HOH508 |
| A | HOH773 |
| site_id | AC9 |
| Number of Residues | 3 |
| Details | binding site for residue ACY A 409 |
| Chain | Residue |
| A | SER39 |
| A | SER72 |
| A | ASP73 |
Functional Information from PROSITE/UniProt
| site_id | PS00138 |
| Number of Residues | 11 |
| Details | SUBTILASE_SER Serine proteases, subtilase family, serine active site. GTSlAsPiFVG |
| Chain | Residue | Details |
| A | GLY285-GLY295 |
Functional Information from SwissProt/UniProt
| site_id | SWS_FT_FI1 |
| Number of Residues | 364 |
| Details | Domain: {"description":"Peptidase S53","evidences":[{"source":"PROSITE-ProRule","id":"PRU01032","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI2 |
| Number of Residues | 19 |
| Details | Region: {"description":"Disordered","evidences":[{"source":"SAM","id":"MobiDB-lite","evidenceCode":"ECO:0000256"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI3 |
| Number of Residues | 3 |
| Details | Active site: {"description":"Charge relay system","evidences":[{"source":"PubMed","id":"11323721","evidenceCode":"ECO:0000305"},{"source":"PubMed","id":"11747435","evidenceCode":"ECO:0000305"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI4 |
| Number of Residues | 5 |
| Details | Binding site: {"evidences":[{"source":"PubMed","id":"11323721","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"11747435","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1GA4","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1GA6","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1NLU","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6M8W","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6M8Y","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6M9C","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6M9D","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6M9F","evidenceCode":"ECO:0007744"}]} |
| Chain | Residue | Details |
Catalytic Information from CSA
| site_id | MCSA1 |
| Number of Residues | 4 |
| Details | M-CSA 380 |
| Chain | Residue | Details |
| A | GLU80 | proton shuttle (general acid/base) |
| A | ASP84 | proton shuttle (general acid/base) |
| A | ASP170 | electrostatic stabiliser |
| A | SER287 | covalent catalysis |






