7CU1
CRYSTAL STRUCTURE OF STREPTOMYCES ALBOGRISEOLUS FLAVIN-DEPENDENT TRYPTOPHAN 6-HALOGENASE (THAL) IN COMPLEX WITH FAD and AMP
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0000166 | molecular_function | nucleotide binding |
A | 0004497 | molecular_function | monooxygenase activity |
A | 0016491 | molecular_function | oxidoreductase activity |
B | 0000166 | molecular_function | nucleotide binding |
B | 0004497 | molecular_function | monooxygenase activity |
B | 0016491 | molecular_function | oxidoreductase activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 42 |
Details | binding site for residue FAD A 601 |
Chain | Residue |
A | LEU11 |
A | ARG44 |
A | ILE45 |
A | VAL47 |
A | GLY48 |
A | GLU49 |
A | ALA50 |
A | ASP196 |
A | GLU197 |
A | MET198 |
A | CYS228 |
A | GLY12 |
A | SER229 |
A | GLY230 |
A | LEU234 |
A | ALA256 |
A | GLY348 |
A | LEU349 |
A | PHE353 |
A | PRO356 |
A | SER359 |
A | GLY361 |
A | GLY13 |
A | ILE362 |
A | ILE365 |
A | HOH732 |
A | HOH737 |
A | HOH757 |
A | HOH769 |
A | HOH771 |
A | HOH772 |
A | HOH774 |
A | HOH776 |
A | GLY14 |
A | HOH812 |
A | HOH878 |
A | HOH951 |
A | THR15 |
A | ALA16 |
A | GLU38 |
A | ALA39 |
A | ILE42 |
site_id | AC2 |
Number of Residues | 15 |
Details | binding site for residue AMP B 601 |
Chain | Residue |
A | ASN323 |
B | LEU11 |
B | GLY12 |
B | GLY13 |
B | GLU38 |
B | ALA39 |
B | THR41 |
B | MET198 |
B | CYS228 |
B | SER229 |
B | GLY230 |
B | ARG232 |
B | LEU234 |
B | HOH714 |
B | HOH846 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 2 |
Details | ACT_SITE: ACT_SITE => ECO:0000305|PubMed:30559288, ECO:0000305|PubMed:33465708 |
Chain | Residue | Details |
A | LYS79 | |
B | LYS79 |
site_id | SWS_FT_FI2 |
Number of Residues | 16 |
Details | BINDING: BINDING => ECO:0000269|PubMed:31589794, ECO:0000269|PubMed:33465708, ECO:0007744|PDB:6SLS, ECO:0007744|PDB:6SLT, ECO:0007744|PDB:7CU1 |
Chain | Residue | Details |
A | GLY13 | |
B | ALA16 | |
B | ILE42 | |
B | ILE45 | |
B | ALA50 | |
B | MET198 | |
B | LEU349 | |
B | ILE362 | |
A | ALA16 | |
A | ILE42 | |
A | ILE45 | |
A | ALA50 | |
A | MET198 | |
A | LEU349 | |
A | ILE362 | |
B | GLY13 |
site_id | SWS_FT_FI3 |
Number of Residues | 2 |
Details | BINDING: BINDING => ECO:0000269|PubMed:33465708, ECO:0007744|PDB:7CU1 |
Chain | Residue | Details |
A | THR15 | |
B | THR15 |
site_id | SWS_FT_FI4 |
Number of Residues | 2 |
Details | BINDING: BINDING => ECO:0000269|PubMed:31589794, ECO:0007744|PDB:6SLS |
Chain | Residue | Details |
A | ALA39 | |
B | ALA39 |
site_id | SWS_FT_FI5 |
Number of Residues | 2 |
Details | BINDING: BINDING => ECO:0000269|PubMed:31589794, ECO:0007744|PDB:6SLS, ECO:0007744|PDB:6SLT |
Chain | Residue | Details |
A | VAL47 | |
B | VAL47 |
site_id | SWS_FT_FI6 |
Number of Residues | 10 |
Details | BINDING: BINDING => ECO:0000269|PubMed:30559288, ECO:0000269|PubMed:31589794, ECO:0000269|PubMed:33465708, ECO:0007744|PDB:6H44, ECO:0007744|PDB:6SLT, ECO:0007744|PDB:7CU0 |
Chain | Residue | Details |
A | PRO111 | |
B | PHE465 | |
A | TYR454 | |
A | TYR455 | |
A | GLU461 | |
A | PHE465 | |
B | PRO111 | |
B | TYR454 | |
B | TYR455 | |
B | GLU461 |
site_id | SWS_FT_FI7 |
Number of Residues | 4 |
Details | BINDING: BINDING => ECO:0000250|UniProtKB:E9P162 |
Chain | Residue | Details |
A | SER360 | |
A | GLY361 | |
B | SER360 | |
B | GLY361 |
site_id | SWS_FT_FI8 |
Number of Residues | 2 |
Details | SITE: Important for activity => ECO:0000250|UniProtKB:P95480 |
Chain | Residue | Details |
A | GLU358 | |
B | GLU358 |