5BTR
Crystal structure of SIRT1 in complex with resveratrol and an AMC-containing peptide
Functional Information from GO Data
Functional Information from PDB Data
| site_id | AC1 |
| Number of Residues | 4 |
| Details | binding site for residue ZN A 701 |
| Chain | Residue |
| A | CYS371 |
| A | CYS374 |
| A | CYS395 |
| A | CYS398 |
| site_id | AC2 |
| Number of Residues | 10 |
| Details | binding site for residue STL A 702 |
| Chain | Residue |
| A | ASP298 |
| A | PHE414 |
| A | LYS444 |
| D | FDL4 |
| D | STL102 |
| A | THR209 |
| A | PRO212 |
| A | ASP292 |
| A | GLN294 |
| A | ALA295 |
| site_id | AC3 |
| Number of Residues | 4 |
| Details | binding site for residue ZN B 701 |
| Chain | Residue |
| B | CYS371 |
| B | CYS374 |
| B | CYS395 |
| B | CYS398 |
| site_id | AC4 |
| Number of Residues | 9 |
| Details | binding site for residue STL B 702 |
| Chain | Residue |
| B | ARG274 |
| B | ASP292 |
| B | GLN294 |
| B | ALA295 |
| B | ASP298 |
| B | PHE414 |
| B | LYS444 |
| B | STL703 |
| E | FDL4 |
| site_id | AC5 |
| Number of Residues | 11 |
| Details | binding site for residue STL B 703 |
| Chain | Residue |
| B | PRO212 |
| B | LEU215 |
| B | GLN222 |
| B | ASN226 |
| B | ASP298 |
| B | PHE414 |
| B | GLY415 |
| B | STL702 |
| E | ARG1 |
| E | LYS3 |
| E | FDL4 |
| site_id | AC6 |
| Number of Residues | 5 |
| Details | binding site for residue ZN C 701 |
| Chain | Residue |
| C | CYS371 |
| C | ILE373 |
| C | CYS374 |
| C | CYS395 |
| C | ALA405 |
| site_id | AC7 |
| Number of Residues | 7 |
| Details | binding site for residue STL C 702 |
| Chain | Residue |
| C | PRO212 |
| C | ASP292 |
| C | GLN294 |
| C | ASP298 |
| C | LYS444 |
| C | STL703 |
| F | FDL4 |
| site_id | AC8 |
| Number of Residues | 12 |
| Details | binding site for residue STL C 703 |
| Chain | Residue |
| C | PRO212 |
| C | LEU215 |
| C | THR219 |
| C | GLN222 |
| C | ILE223 |
| C | ASN226 |
| C | PHE414 |
| C | GLY415 |
| C | STL702 |
| F | ARG1 |
| F | LYS3 |
| F | FDL4 |
| site_id | AC9 |
| Number of Residues | 11 |
| Details | binding site for residue STL D 101 |
| Chain | Residue |
| A | LEU206 |
| A | PRO211 |
| A | ILE223 |
| A | ASN226 |
| A | GLU230 |
| A | ARG446 |
| A | PRO447 |
| A | LEU450 |
| D | HIS2 |
| D | LYS3 |
| D | FDL4 |
| site_id | AD1 |
| Number of Residues | 11 |
| Details | binding site for residue STL D 102 |
| Chain | Residue |
| A | LEU215 |
| A | GLN222 |
| A | ASN226 |
| A | ASP298 |
| A | GLU300 |
| A | PHE414 |
| A | GLY415 |
| A | STL702 |
| D | ARG1 |
| D | LYS3 |
| D | FDL4 |
| site_id | AD2 |
| Number of Residues | 9 |
| Details | binding site for residue STL E 101 |
| Chain | Residue |
| B | LEU206 |
| B | PRO211 |
| B | ILE223 |
| B | ASN226 |
| B | GLU230 |
| B | PRO447 |
| E | HIS2 |
| E | LYS3 |
| E | FDL4 |
| site_id | AD3 |
| Number of Residues | 11 |
| Details | binding site for residue STL F 101 |
| Chain | Residue |
| C | PRO447 |
| C | LEU450 |
| F | HIS2 |
| F | LYS3 |
| F | FDL4 |
| C | LEU206 |
| C | PRO211 |
| C | ILE223 |
| C | ASN226 |
| C | GLU230 |
| C | ARG446 |
| site_id | AD4 |
| Number of Residues | 7 |
| Details | binding site for Di-peptide ACE D 0 and ARG D 1 |
| Chain | Residue |
| A | ASN226 |
| C | PHE148 |
| C | ASP150 |
| C | PRO180 |
| D | HIS2 |
| D | LYS3 |
| D | STL102 |
| site_id | AD5 |
| Number of Residues | 18 |
| Details | binding site for Di-peptide LYS D 3 and FDL D 4 |
| Chain | Residue |
| A | LEU206 |
| A | THR209 |
| A | ARG274 |
| A | PHE297 |
| A | HIS363 |
| A | VAL412 |
| A | PHE414 |
| A | GLY415 |
| A | GLU416 |
| A | ASN417 |
| A | LEU418 |
| A | ARG446 |
| A | STL702 |
| D | ACE0 |
| D | ARG1 |
| D | HIS2 |
| D | STL101 |
| D | STL102 |
| site_id | AD6 |
| Number of Residues | 7 |
| Details | binding site for Di-peptide ACE E 0 and ARG E 1 |
| Chain | Residue |
| A | PHE148 |
| A | ASP150 |
| A | PRO180 |
| B | ASN226 |
| B | STL703 |
| E | HIS2 |
| E | LYS3 |
| site_id | AD7 |
| Number of Residues | 15 |
| Details | binding site for Di-peptide LYS E 3 and FDL E 4 |
| Chain | Residue |
| B | LEU206 |
| B | HIS363 |
| B | VAL412 |
| B | PHE414 |
| B | GLY415 |
| B | GLU416 |
| B | ASN417 |
| B | LEU418 |
| B | ARG446 |
| B | STL702 |
| B | STL703 |
| E | ACE0 |
| E | ARG1 |
| E | HIS2 |
| E | STL101 |
| site_id | AD8 |
| Number of Residues | 7 |
| Details | binding site for Di-peptide ACE F 0 and ARG F 1 |
| Chain | Residue |
| B | ASP150 |
| B | PRO180 |
| C | TYR185 |
| C | ASN226 |
| C | STL703 |
| F | HIS2 |
| F | LYS3 |
| site_id | AD9 |
| Number of Residues | 19 |
| Details | binding site for Di-peptide LYS F 3 and FDL F 4 |
| Chain | Residue |
| C | LEU206 |
| C | THR209 |
| C | PHE297 |
| C | HIS363 |
| C | VAL412 |
| C | PHE413 |
| C | PHE414 |
| C | GLY415 |
| C | GLU416 |
| C | ASN417 |
| C | LYS444 |
| C | ARG446 |
| C | PRO447 |
| C | STL702 |
| C | STL703 |
| F | ACE0 |
| F | ARG1 |
| F | HIS2 |
| F | STL101 |
Functional Information from SwissProt/UniProt
| site_id | SWS_FT_FI1 |
| Number of Residues | 520 |
| Details | Domain: {"description":"Deacetylase sirtuin-type","evidences":[{"source":"PROSITE-ProRule","id":"PRU00236","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI2 |
| Number of Residues | 9 |
| Details | Region: {"description":"Required for interaction with the sumoylated form of CCAR2","evidences":[{"source":"PubMed","id":"25406032","evidenceCode":"ECO:0000269"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI3 |
| Number of Residues | 21 |
| Details | Motif: {"description":"Nuclear localization signal","evidences":[{"evidenceCode":"ECO:0000250"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI4 |
| Number of Residues | 18 |
| Details | Motif: {"description":"Nuclear export signal","evidences":[{"evidenceCode":"ECO:0000250"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI5 |
| Number of Residues | 3 |
| Details | Active site: {"description":"Proton acceptor","evidences":[{"source":"PROSITE-ProRule","id":"PRU00236","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"11672523","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"12006491","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"12535671","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17290224","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"18004385","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"18235501","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"18485871","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19934257","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"25406032","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"28497810","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"38512451","evidenceCode":"ECO:0000269"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI6 |
| Number of Residues | 59 |
| Details | Binding site: {"evidences":[{"source":"UniProtKB","id":"Q8IXJ6","evidenceCode":"ECO:0000250"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI7 |
| Number of Residues | 11 |
| Details | Binding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU00236","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI8 |
| Number of Residues | 3 |
| Details | Binding site: {"evidences":[{"evidenceCode":"ECO:0000250"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI9 |
| Number of Residues | 11 |
| Details | Modified residue: {"description":"N6-acetyllysine","evidences":[{"source":"UniProtKB","id":"Q923E4","evidenceCode":"ECO:0000250"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI10 |
| Number of Residues | 5 |
| Details | Modified residue: {"description":"S-nitrosocysteine","evidences":[{"source":"UniProtKB","id":"Q923E4","evidenceCode":"ECO:0000250"}]} |
| Chain | Residue | Details |






