6H4O
Crystal structure of human KDM4A in complex with compound 18a
Functional Information from PDB Data
| site_id | AC1 |
| Number of Residues | 4 |
| Details | binding site for residue ZN A 401 |
| Chain | Residue |
| A | HIS188 |
| A | GLU190 |
| A | HIS276 |
| A | FQH403 |
| site_id | AC2 |
| Number of Residues | 4 |
| Details | binding site for residue ZN A 402 |
| Chain | Residue |
| A | CYS234 |
| A | HIS240 |
| A | CYS306 |
| A | CYS308 |
| site_id | AC3 |
| Number of Residues | 11 |
| Details | binding site for residue FQH A 403 |
| Chain | Residue |
| A | TYR177 |
| A | PHE185 |
| A | HIS188 |
| A | GLU190 |
| A | ASP191 |
| A | LYS206 |
| A | TRP208 |
| A | HIS276 |
| A | ZN401 |
| A | HOH576 |
| A | TYR132 |
| site_id | AC4 |
| Number of Residues | 11 |
| Details | binding site for residue GOL A 404 |
| Chain | Residue |
| A | VAL75 |
| A | THR76 |
| A | GLY77 |
| A | THR126 |
| A | PHE127 |
| A | HOH550 |
| C | VAL75 |
| C | THR76 |
| C | GLY77 |
| C | THR126 |
| C | PHE127 |
| site_id | AC5 |
| Number of Residues | 1 |
| Details | binding site for residue CL A 405 |
| Chain | Residue |
| A | TYR59 |
| site_id | AC6 |
| Number of Residues | 4 |
| Details | binding site for residue ZN B 401 |
| Chain | Residue |
| B | HIS188 |
| B | GLU190 |
| B | HIS276 |
| B | FQH403 |
| site_id | AC7 |
| Number of Residues | 4 |
| Details | binding site for residue ZN B 402 |
| Chain | Residue |
| B | CYS234 |
| B | HIS240 |
| B | CYS306 |
| B | CYS308 |
| site_id | AC8 |
| Number of Residues | 10 |
| Details | binding site for residue FQH B 403 |
| Chain | Residue |
| B | TYR132 |
| B | TYR175 |
| B | TYR177 |
| B | PHE185 |
| B | HIS188 |
| B | GLU190 |
| B | LYS206 |
| B | TRP208 |
| B | HIS276 |
| B | ZN401 |
| site_id | AC9 |
| Number of Residues | 10 |
| Details | binding site for residue GOL B 404 |
| Chain | Residue |
| B | VAL75 |
| B | THR76 |
| B | GLY77 |
| B | THR126 |
| B | PHE127 |
| D | VAL75 |
| D | THR76 |
| D | GLY77 |
| D | THR126 |
| D | PHE127 |
| site_id | AD1 |
| Number of Residues | 5 |
| Details | binding site for residue ZN C 401 |
| Chain | Residue |
| C | HIS188 |
| C | GLU190 |
| C | HIS276 |
| C | FQH403 |
| C | HOH501 |
| site_id | AD2 |
| Number of Residues | 4 |
| Details | binding site for residue ZN C 402 |
| Chain | Residue |
| C | CYS234 |
| C | HIS240 |
| C | CYS306 |
| C | CYS308 |
| site_id | AD3 |
| Number of Residues | 14 |
| Details | binding site for residue FQH C 403 |
| Chain | Residue |
| C | TYR132 |
| C | ASP135 |
| C | GLU169 |
| C | TYR175 |
| C | TYR177 |
| C | PHE185 |
| C | HIS188 |
| C | GLU190 |
| C | ASP191 |
| C | LYS206 |
| C | TRP208 |
| C | HIS276 |
| C | ZN401 |
| C | HOH501 |
| site_id | AD4 |
| Number of Residues | 4 |
| Details | binding site for residue DMS C 404 |
| Chain | Residue |
| C | ALA12 |
| C | ARG13 |
| C | PHE257 |
| C | HOH543 |
| site_id | AD5 |
| Number of Residues | 2 |
| Details | binding site for residue DMS C 405 |
| Chain | Residue |
| C | ARG294 |
| C | PHE324 |
| site_id | AD6 |
| Number of Residues | 1 |
| Details | binding site for residue CL C 406 |
| Chain | Residue |
| C | HOH592 |
| site_id | AD7 |
| Number of Residues | 5 |
| Details | binding site for residue ZN D 401 |
| Chain | Residue |
| D | HIS188 |
| D | GLU190 |
| D | HIS276 |
| D | FQH403 |
| D | HOH506 |
| site_id | AD8 |
| Number of Residues | 4 |
| Details | binding site for residue ZN D 402 |
| Chain | Residue |
| D | CYS234 |
| D | HIS240 |
| D | CYS306 |
| D | CYS308 |
| site_id | AD9 |
| Number of Residues | 11 |
| Details | binding site for residue FQH D 403 |
| Chain | Residue |
| D | ASP135 |
| D | TYR177 |
| D | PHE185 |
| D | HIS188 |
| D | GLU190 |
| D | LYS206 |
| D | TRP208 |
| D | HIS276 |
| D | ZN401 |
| D | HOH506 |
| D | TYR132 |
| site_id | AE1 |
| Number of Residues | 6 |
| Details | binding site for residue DMS D 404 |
| Chain | Residue |
| D | ASP193 |
| D | LYS217 |
| D | TYR273 |
| D | TYR299 |
| D | GLN302 |
| D | HIS343 |
Functional Information from SwissProt/UniProt
| site_id | SWS_FT_FI1 |
| Number of Residues | 168 |
| Details | Domain: {"description":"JmjN","evidences":[{"source":"PROSITE-ProRule","id":"PRU00537","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI2 |
| Number of Residues | 12 |
| Details | Binding site: {"evidences":[{"source":"PubMed","id":"16677698","evidenceCode":"ECO:0000269"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI3 |
| Number of Residues | 8 |
| Details | Binding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU00538","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"16677698","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"26741168","evidenceCode":"ECO:0000305"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI4 |
| Number of Residues | 4 |
| Details | Binding site: {"evidences":[{"source":"PubMed","id":"16677698","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"26741168","evidenceCode":"ECO:0000305"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI5 |
| Number of Residues | 16 |
| Details | Binding site: {"evidences":[{"source":"PDB","id":"5F2W","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F32","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F37","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F39","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F3E","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F3G","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F5I","evidenceCode":"ECO:0007744"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI6 |
| Number of Residues | 4 |
| Details | Binding site: {"evidences":[{"source":"UniProtKB","id":"B2RXH2","evidenceCode":"ECO:0000250"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI7 |
| Number of Residues | 166 |
| Details | Domain: {"description":"JmjC","evidences":[{"source":"PROSITE-ProRule","id":"PRU00538","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
Catalytic Information from CSA
| site_id | MCSA1 |
| Number of Residues | 6 |
| Details | M-CSA 370 |
| Chain | Residue | Details |
| A | GLY170 | hydrogen bond acceptor, steric role |
| A | TYR177 | hydrogen bond donor, steric role |
| A | HIS188 | metal ligand |
| A | GLU190 | attractive charge-charge interaction, hydrogen bond acceptor, metal ligand, steric role |
| A | HIS276 | metal ligand |
| A | SER288 | hydrogen bond donor, steric role |
| site_id | MCSA2 |
| Number of Residues | 6 |
| Details | M-CSA 370 |
| Chain | Residue | Details |
| B | GLY170 | hydrogen bond acceptor, steric role |
| B | TYR177 | hydrogen bond donor, steric role |
| B | HIS188 | metal ligand |
| B | GLU190 | attractive charge-charge interaction, hydrogen bond acceptor, metal ligand, steric role |
| B | HIS276 | metal ligand |
| B | SER288 | hydrogen bond donor, steric role |
| site_id | MCSA3 |
| Number of Residues | 6 |
| Details | M-CSA 370 |
| Chain | Residue | Details |
| C | GLY170 | hydrogen bond acceptor, steric role |
| C | TYR177 | hydrogen bond donor, steric role |
| C | HIS188 | metal ligand |
| C | GLU190 | attractive charge-charge interaction, hydrogen bond acceptor, metal ligand, steric role |
| C | HIS276 | metal ligand |
| C | SER288 | hydrogen bond donor, steric role |
| site_id | MCSA4 |
| Number of Residues | 6 |
| Details | M-CSA 370 |
| Chain | Residue | Details |
| D | GLY170 | hydrogen bond acceptor, steric role |
| D | TYR177 | hydrogen bond donor, steric role |
| D | HIS188 | metal ligand |
| D | GLU190 | attractive charge-charge interaction, hydrogen bond acceptor, metal ligand, steric role |
| D | HIS276 | metal ligand |
| D | SER288 | hydrogen bond donor, steric role |






