1C29
CRYSTAL STRUCTURE OF THE COMPLEX OF BACTERIAL TRYPTOPHAN SYNTHASE WITH THE TRANSITION STATE ANALOGUE INHIBITOR 4-(2-HYDROXYPHENYLTHIO)-1-BUTENYLPHOSPHONIC ACID
Functional Information from GO Data
| Chain | GOid | namespace | contents | 
| A | 0000162 | biological_process | L-tryptophan biosynthetic process | 
| A | 0003824 | molecular_function | catalytic activity | 
| A | 0004834 | molecular_function | tryptophan synthase activity | 
| A | 0005515 | molecular_function | protein binding | 
| A | 0005829 | cellular_component | cytosol | 
| A | 0006568 | biological_process | L-tryptophan metabolic process | 
| A | 0008652 | biological_process | amino acid biosynthetic process | 
| A | 0009073 | biological_process | aromatic amino acid family biosynthetic process | 
| A | 0016829 | molecular_function | lyase activity | 
| B | 0000162 | biological_process | L-tryptophan biosynthetic process | 
| B | 0004834 | molecular_function | tryptophan synthase activity | 
| B | 0005515 | molecular_function | protein binding | 
| B | 0005737 | cellular_component | cytoplasm | 
| B | 0006568 | biological_process | L-tryptophan metabolic process | 
| B | 0008652 | biological_process | amino acid biosynthetic process | 
| B | 0009073 | biological_process | aromatic amino acid family biosynthetic process | 
| B | 0016829 | molecular_function | lyase activity | 
| B | 0042802 | molecular_function | identical protein binding | 
Functional Information from PDB Data
| site_id | AC1 | 
| Number of Residues | 5 | 
| Details | BINDING SITE FOR RESIDUE NA B 1168 | 
| Chain | Residue | 
| B | GLY232 | 
| B | PHE306 | 
| B | SER308 | 
| B | HOH1028 | 
| B | HOH1116 | 
| site_id | AC2 | 
| Number of Residues | 14 | 
| Details | BINDING SITE FOR RESIDUE PLP B 900 | 
| Chain | Residue | 
| B | GLY232 | 
| B | GLY233 | 
| B | GLY234 | 
| B | SER235 | 
| B | ASN236 | 
| B | GLY303 | 
| B | GLU350 | 
| B | SER377 | 
| B | GLY378 | 
| B | HOH1026 | 
| B | HIS86 | 
| B | LYS87 | 
| B | GLN114 | 
| B | THR190 | 
| site_id | AC3 | 
| Number of Residues | 12 | 
| Details | BINDING SITE FOR RESIDUE HE1 A 270 | 
| Chain | Residue | 
| A | PHE22 | 
| A | ASP60 | 
| A | LEU100 | 
| A | TYR175 | 
| A | THR183 | 
| A | GLY184 | 
| A | PHE212 | 
| A | GLY213 | 
| A | GLY234 | 
| A | SER235 | 
| A | HOH1024 | 
| A | HOH1063 | 
Functional Information from PROSITE/UniProt
| site_id | PS00167 | 
| Number of Residues | 14 | 
| Details | TRP_SYNTHASE_ALPHA Tryptophan synthase alpha chain signature. LELGvPFSDPLADG | 
| Chain | Residue | Details | 
| A | LEU48-GLY61 | 
| site_id | PS00168 | 
| Number of Residues | 15 | 
| Details | TRP_SYNTHASE_BETA Tryptophan synthase beta chain pyridoxal-phosphate attachment site. LlHgGAHKtNqvLgQ | 
| Chain | Residue | Details | 
| B | LEU80-GLN94 | 
Functional Information from SwissProt/UniProt
| site_id | SWS_FT_FI1 | 
| Number of Residues | 2 | 
| Details | Active site: {"description":"Proton acceptor"} | 
| Chain | Residue | Details | 
| site_id | SWS_FT_FI2 | 
| Number of Residues | 1 | 
| Details | Modified residue: {"description":"N6-(pyridoxal phosphate)lysine"} | 
| Chain | Residue | Details | 
Catalytic Information from CSA
| site_id | CSA1 | 
| Number of Residues | 4 | 
| Details | Annotated By Reference To The Literature 1a50 | 
| Chain | Residue | Details | 
| B | HIS86 | |
| B | LYS87 | |
| B | LYS167 | |
| B | ASP305 | 
| site_id | CSA2 | 
| Number of Residues | 1 | 
| Details | Annotated By Reference To The Literature 1a50 | 
| Chain | Residue | Details | 
| B | LYS87 | 
| site_id | CSA3 | 
| Number of Residues | 2 | 
| Details | Annotated By Reference To The Literature 1a50 | 
| Chain | Residue | Details | 
| B | SER377 | |
| B | LYS87 | 
| site_id | CSA4 | 
| Number of Residues | 3 | 
| Details | Annotated By Reference To The Literature 1a50 | 
| Chain | Residue | Details | 
| A | TYR175 | |
| A | GLU49 | |
| A | ASP60 | 
| site_id | MCSA1 | 
| Number of Residues | 3 | 
| Details | M-CSA 383 | 
| Chain | Residue | Details | 
| B | LYS87 | electron pair acceptor, electron pair donor, nucleofuge, nucleophile, proton acceptor, proton donor | 
| B | GLU109 | |
| B | SER377 | hydrogen bond donor | 











