6H4P
Crystal structure of human KDM4A in complex with compound 16a
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 | FQ5403 |
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 FQ5 A 403 |
Chain | Residue |
A | TYR177 |
A | PHE185 |
A | HIS188 |
A | GLU190 |
A | LYS206 |
A | TRP208 |
A | LYS241 |
A | HIS276 |
A | ZN401 |
A | HOH509 |
A | TYR132 |
site_id | AC4 |
Number of Residues | 2 |
Details | binding site for residue DMS A 404 |
Chain | Residue |
A | TYR273 |
A | GLN302 |
site_id | AC5 |
Number of Residues | 1 |
Details | binding site for residue DMS A 405 |
Chain | Residue |
A | HIS144 |
site_id | AC6 |
Number of Residues | 2 |
Details | binding site for residue DMS A 406 |
Chain | Residue |
A | GLU23 |
A | PHE353 |
site_id | AC7 |
Number of Residues | 2 |
Details | binding site for residue CL A 407 |
Chain | Residue |
A | ARG98 |
A | HOH661 |
site_id | AC8 |
Number of Residues | 4 |
Details | binding site for residue ZN B 401 |
Chain | Residue |
B | HIS188 |
B | GLU190 |
B | HIS276 |
B | FQ5403 |
site_id | AC9 |
Number of Residues | 4 |
Details | binding site for residue ZN B 402 |
Chain | Residue |
B | CYS234 |
B | HIS240 |
B | CYS306 |
B | CYS308 |
site_id | AD1 |
Number of Residues | 12 |
Details | binding site for residue FQ5 B 403 |
Chain | Residue |
B | TYR132 |
B | ASP135 |
B | TYR177 |
B | PHE185 |
B | HIS188 |
B | GLU190 |
B | LYS206 |
B | TRP208 |
B | HIS276 |
B | VAL313 |
B | ZN401 |
B | HOH605 |
site_id | AD2 |
Number of Residues | 3 |
Details | binding site for residue DMS B 404 |
Chain | Residue |
B | GLU23 |
B | TYR33 |
B | PHE353 |
site_id | AD3 |
Number of Residues | 11 |
Details | binding site for residue GOL B 406 |
Chain | Residue |
B | VAL75 |
B | THR76 |
B | GLY77 |
B | THR126 |
B | PHE127 |
B | HOH571 |
D | VAL75 |
D | THR76 |
D | GLY77 |
D | THR126 |
D | PHE127 |
site_id | AD4 |
Number of Residues | 2 |
Details | binding site for residue CL B 407 |
Chain | Residue |
B | ARG294 |
B | HOH559 |
site_id | AD5 |
Number of Residues | 2 |
Details | binding site for residue CL B 408 |
Chain | Residue |
B | ARG98 |
B | HOH691 |
site_id | AD6 |
Number of Residues | 4 |
Details | binding site for residue ZN C 401 |
Chain | Residue |
C | HIS188 |
C | GLU190 |
C | HIS276 |
C | FQ5403 |
site_id | AD7 |
Number of Residues | 4 |
Details | binding site for residue ZN C 402 |
Chain | Residue |
C | CYS234 |
C | HIS240 |
C | CYS306 |
C | CYS308 |
site_id | AD8 |
Number of Residues | 9 |
Details | binding site for residue FQ5 C 403 |
Chain | Residue |
C | TYR132 |
C | TYR177 |
C | PHE185 |
C | HIS188 |
C | GLU190 |
C | LYS206 |
C | TRP208 |
C | HIS276 |
C | ZN401 |
site_id | AD9 |
Number of Residues | 11 |
Details | binding site for residue GOL C 404 |
Chain | Residue |
A | VAL75 |
A | THR76 |
A | GLY77 |
A | THR126 |
A | PHE127 |
C | VAL75 |
C | THR76 |
C | GLY77 |
C | THR126 |
C | PHE127 |
C | HOH574 |
site_id | AE1 |
Number of Residues | 1 |
Details | binding site for residue CL C 405 |
Chain | Residue |
C | TYR59 |
site_id | AE2 |
Number of Residues | 4 |
Details | binding site for residue ZN D 401 |
Chain | Residue |
D | HIS188 |
D | GLU190 |
D | HIS276 |
D | FQ5403 |
site_id | AE3 |
Number of Residues | 4 |
Details | binding site for residue ZN D 402 |
Chain | Residue |
D | CYS306 |
D | CYS308 |
D | CYS234 |
D | HIS240 |
site_id | AE4 |
Number of Residues | 11 |
Details | binding site for residue FQ5 D 403 |
Chain | Residue |
D | TYR132 |
D | GLU169 |
D | TYR175 |
D | TYR177 |
D | PHE185 |
D | HIS188 |
D | GLU190 |
D | LYS206 |
D | TRP208 |
D | HIS276 |
D | ZN401 |
site_id | AE5 |
Number of Residues | 5 |
Details | binding site for residue DMS D 404 |
Chain | Residue |
D | TYR111 |
D | PHE114 |
D | PRO205 |
D | THR261 |
D | HIS281 |
site_id | AE6 |
Number of Residues | 1 |
Details | binding site for residue DMS D 405 |
Chain | Residue |
D | GLN88 |
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 | 166 |
Details | Domain: {"description":"JmjC","evidences":[{"source":"PROSITE-ProRule","id":"PRU00538","evidenceCode":"ECO:0000255"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 12 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"16677698","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
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_FI5 |
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_FI6 |
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_FI7 |
Number of Residues | 4 |
Details | Binding site: {"evidences":[{"source":"UniProtKB","id":"B2RXH2","evidenceCode":"ECO:0000250"}]} |
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 |