3MO5
Human G9a-like (GLP, also known as EHMT1) in complex with inhibitor E72
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0002039 | molecular_function | p53 binding |
A | 0005634 | cellular_component | nucleus |
A | 0008270 | molecular_function | zinc ion binding |
A | 0016279 | molecular_function | protein-lysine N-methyltransferase activity |
A | 0042054 | molecular_function | histone methyltransferase activity |
A | 0046974 | molecular_function | histone H3K9 methyltransferase activity |
B | 0002039 | molecular_function | p53 binding |
B | 0005634 | cellular_component | nucleus |
B | 0008270 | molecular_function | zinc ion binding |
B | 0016279 | molecular_function | protein-lysine N-methyltransferase activity |
B | 0042054 | molecular_function | histone methyltransferase activity |
B | 0046974 | molecular_function | histone H3K9 methyltransferase activity |
C | 0002039 | molecular_function | p53 binding |
C | 0005634 | cellular_component | nucleus |
C | 0008270 | molecular_function | zinc ion binding |
C | 0016279 | molecular_function | protein-lysine N-methyltransferase activity |
C | 0042054 | molecular_function | histone methyltransferase activity |
C | 0046974 | molecular_function | histone H3K9 methyltransferase activity |
D | 0002039 | molecular_function | p53 binding |
D | 0005634 | cellular_component | nucleus |
D | 0008270 | molecular_function | zinc ion binding |
D | 0016279 | molecular_function | protein-lysine N-methyltransferase activity |
D | 0042054 | molecular_function | histone methyltransferase activity |
D | 0046974 | molecular_function | histone H3K9 methyltransferase activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ZN A 1 |
Chain | Residue |
A | CYS1031 |
A | CYS1044 |
A | CYS1074 |
A | CYS1078 |
site_id | AC2 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE ZN A 2 |
Chain | Residue |
A | ZN3 |
A | CYS1037 |
A | CYS1074 |
A | CYS1080 |
A | CYS1084 |
site_id | AC3 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE ZN A 3 |
Chain | Residue |
A | ZN2 |
A | CYS1031 |
A | CYS1033 |
A | CYS1037 |
A | CYS1042 |
site_id | AC4 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ZN A 4 |
Chain | Residue |
A | CYS1172 |
A | CYS1225 |
A | CYS1227 |
A | CYS1232 |
site_id | AC5 |
Number of Residues | 16 |
Details | BINDING SITE FOR RESIDUE E72 A 1236 |
Chain | Residue |
A | HOH245 |
A | HOH672 |
A | HOH674 |
A | TYR1124 |
A | ASP1131 |
A | ALA1134 |
A | ASP1135 |
A | ARG1137 |
A | ASP1140 |
A | SER1141 |
A | LEU1143 |
A | ASP1145 |
A | TYR1211 |
A | ARG1214 |
A | PHE1215 |
A | LYS1219 |
site_id | AC6 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE ZN B 5 |
Chain | Residue |
B | ZN7 |
B | CYS1031 |
B | CYS1044 |
B | CYS1074 |
B | CYS1078 |
site_id | AC7 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ZN B 6 |
Chain | Residue |
B | CYS1037 |
B | CYS1074 |
B | CYS1080 |
B | CYS1084 |
site_id | AC8 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE ZN B 7 |
Chain | Residue |
B | ZN5 |
B | CYS1031 |
B | CYS1033 |
B | CYS1037 |
B | CYS1042 |
site_id | AC9 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ZN B 8 |
Chain | Residue |
B | CYS1172 |
B | CYS1225 |
B | CYS1227 |
B | CYS1232 |
site_id | BC1 |
Number of Residues | 19 |
Details | BINDING SITE FOR RESIDUE E72 B 2 |
Chain | Residue |
B | HOH86 |
B | HOH197 |
B | ASP1131 |
B | ALA1134 |
B | ASP1135 |
B | VAL1136 |
B | ARG1137 |
B | ASP1140 |
B | SER1141 |
B | LEU1143 |
B | ASP1145 |
B | TYR1211 |
B | ARG1214 |
B | PHE1215 |
B | ILE1218 |
B | LYS1219 |
D | HOH153 |
D | ASP1022 |
D | ARG1189 |
site_id | BC2 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE ZN C 1 |
Chain | Residue |
C | ZN2 |
C | CYS1031 |
C | CYS1044 |
C | CYS1074 |
C | CYS1078 |
site_id | BC3 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE ZN C 2 |
Chain | Residue |
C | ZN1 |
C | CYS1037 |
C | CYS1074 |
C | CYS1080 |
C | CYS1084 |
site_id | BC4 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ZN C 3 |
Chain | Residue |
C | CYS1031 |
C | CYS1033 |
C | CYS1037 |
C | CYS1042 |
site_id | BC5 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ZN C 4 |
Chain | Residue |
C | CYS1172 |
C | CYS1225 |
C | CYS1227 |
C | CYS1232 |
site_id | BC6 |
Number of Residues | 12 |
Details | BINDING SITE FOR RESIDUE SAH C 103 |
Chain | Residue |
C | ARG1226 |
C | CYS1227 |
C | HOH362 |
C | MET1105 |
C | GLY1106 |
C | TRP1107 |
C | TYR1142 |
C | ARG1166 |
C | ASN1169 |
C | HIS1170 |
C | TYR1211 |
C | CYS1225 |
site_id | BC7 |
Number of Residues | 19 |
Details | BINDING SITE FOR RESIDUE E72 C 1236 |
Chain | Residue |
A | HOH132 |
A | HOH244 |
A | ASP1022 |
A | GLU1152 |
A | ASP1187 |
A | ARG1189 |
C | HOH172 |
C | HOH398 |
C | ASP1131 |
C | ALA1134 |
C | ASP1135 |
C | ASP1140 |
C | SER1141 |
C | LEU1143 |
C | ASP1145 |
C | TYR1211 |
C | ARG1214 |
C | PHE1215 |
C | LYS1219 |
site_id | BC8 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE ZN D 5 |
Chain | Residue |
D | HOH548 |
D | CYS1031 |
D | CYS1044 |
D | CYS1074 |
D | CYS1078 |
site_id | BC9 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE ZN D 6 |
Chain | Residue |
D | HOH548 |
D | CYS1037 |
D | CYS1074 |
D | CYS1080 |
D | CYS1084 |
site_id | CC1 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ZN D 7 |
Chain | Residue |
D | CYS1031 |
D | CYS1033 |
D | CYS1037 |
D | CYS1042 |
site_id | CC2 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ZN D 8 |
Chain | Residue |
D | CYS1172 |
D | CYS1225 |
D | CYS1227 |
D | CYS1232 |
site_id | CC3 |
Number of Residues | 12 |
Details | BINDING SITE FOR RESIDUE SAH D 104 |
Chain | Residue |
D | MET1105 |
D | GLY1106 |
D | TRP1107 |
D | TYR1142 |
D | ARG1166 |
D | ASN1169 |
D | HIS1170 |
D | TYR1211 |
D | PHE1215 |
D | PHE1223 |
D | CYS1225 |
D | ARG1226 |
site_id | CC4 |
Number of Residues | 14 |
Details | BINDING SITE FOR RESIDUE E72 D 4 |
Chain | Residue |
D | HOH453 |
D | ASP1131 |
D | ALA1134 |
D | ASP1135 |
D | VAL1136 |
D | ARG1137 |
D | ASP1140 |
D | SER1141 |
D | LEU1143 |
D | ASP1145 |
D | TYR1211 |
D | ARG1214 |
D | PHE1215 |
D | ILE1218 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 252 |
Details | Domain: {"description":"Pre-SET","evidences":[{"source":"PROSITE-ProRule","id":"PRU00157","evidenceCode":"ECO:0000255"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 12 |
Details | Region: {"description":"Interaction with histone H3"} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 72 |
Details | Binding site: {} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 4 |
Details | Site: {"description":"Histone H3K9me binding","evidences":[{"source":"PubMed","id":"18264113","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"20084102","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI5 |
Number of Residues | 4 |
Details | Modified residue: {"description":"Phosphoserine","evidences":[{"source":"PubMed","id":"23186163","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |