1N20
(+)-Bornyl Diphosphate Synthase: Complex with Mg and 3-aza-2,3-dihydrogeranyl diphosphate
Functional Information from GO Data
| Chain | GOid | namespace | contents |
| A | 0000287 | molecular_function | magnesium ion binding |
| A | 0003824 | molecular_function | catalytic activity |
| A | 0009507 | cellular_component | chloroplast |
| A | 0010333 | molecular_function | terpene synthase activity |
| A | 0016102 | biological_process | diterpenoid biosynthetic process |
| A | 0016829 | molecular_function | lyase activity |
| A | 0016853 | molecular_function | isomerase activity |
| A | 0042803 | molecular_function | protein homodimerization activity |
| A | 0046211 | biological_process | (+)-camphor biosynthetic process |
| A | 0046872 | molecular_function | metal ion binding |
| A | 0047926 | molecular_function | geranyl-diphosphate cyclase activity |
| A | 0102703 | molecular_function | camphene synthase activity |
| B | 0000287 | molecular_function | magnesium ion binding |
| B | 0003824 | molecular_function | catalytic activity |
| B | 0009507 | cellular_component | chloroplast |
| B | 0010333 | molecular_function | terpene synthase activity |
| B | 0016102 | biological_process | diterpenoid biosynthetic process |
| B | 0016829 | molecular_function | lyase activity |
| B | 0016853 | molecular_function | isomerase activity |
| B | 0042803 | molecular_function | protein homodimerization activity |
| B | 0046211 | biological_process | (+)-camphor biosynthetic process |
| B | 0046872 | molecular_function | metal ion binding |
| B | 0047926 | molecular_function | geranyl-diphosphate cyclase activity |
| B | 0102703 | molecular_function | camphene synthase activity |
Functional Information from PDB Data
| site_id | AC1 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE MG A 701 |
| Chain | Residue |
| A | ASP351 |
| A | ASP355 |
| A | MG702 |
| A | 3AG900 |
| A | HOH977 |
| A | HOH978 |
| A | HOH979 |
| site_id | AC2 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE MG A 702 |
| Chain | Residue |
| A | MG701 |
| A | 3AG900 |
| A | HOH975 |
| A | HOH976 |
| A | ASP351 |
| A | ASP355 |
| site_id | AC3 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE MG A 703 |
| Chain | Residue |
| A | ASP496 |
| A | THR500 |
| A | GLU504 |
| A | 3AG900 |
| A | HOH980 |
| site_id | AC4 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE MG B 704 |
| Chain | Residue |
| B | ASP496 |
| B | THR500 |
| B | GLU504 |
| B | 3AG901 |
| B | HOH965 |
| site_id | AC5 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE MG B 705 |
| Chain | Residue |
| B | ASP351 |
| B | ASP355 |
| B | MG706 |
| B | 3AG901 |
| B | HOH966 |
| B | HOH967 |
| site_id | AC6 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE MG B 706 |
| Chain | Residue |
| B | ASP351 |
| B | ASP355 |
| B | MG705 |
| B | 3AG901 |
| B | HOH968 |
| B | HOH969 |
| B | HOH970 |
| site_id | AC7 |
| Number of Residues | 25 |
| Details | BINDING SITE FOR RESIDUE 3AG A 900 |
| Chain | Residue |
| A | ARG314 |
| A | ILE344 |
| A | THR348 |
| A | ASP351 |
| A | ASP355 |
| A | VAL452 |
| A | ILE457 |
| A | LEU492 |
| A | ARG493 |
| A | ASP496 |
| A | THR500 |
| A | GLU504 |
| A | LYS512 |
| A | TYR572 |
| A | PHE578 |
| A | MG701 |
| A | MG702 |
| A | MG703 |
| A | HOH952 |
| A | HOH975 |
| A | HOH976 |
| A | HOH979 |
| A | HOH980 |
| A | HOH1036 |
| A | HOH1037 |
| site_id | AC8 |
| Number of Residues | 23 |
| Details | BINDING SITE FOR RESIDUE 3AG B 901 |
| Chain | Residue |
| B | ARG314 |
| B | ILE344 |
| B | ASP351 |
| B | ASP355 |
| B | VAL452 |
| B | ILE457 |
| B | LEU492 |
| B | ARG493 |
| B | ASP496 |
| B | THR500 |
| B | GLU504 |
| B | LYS512 |
| B | TYR572 |
| B | PHE578 |
| B | MG704 |
| B | MG705 |
| B | MG706 |
| B | HOH916 |
| B | HOH965 |
| B | HOH966 |
| B | HOH967 |
| B | HOH970 |
| B | HOH1024 |
Functional Information from SwissProt/UniProt
| site_id | SWS_FT_FI1 |
| Number of Residues | 16 |
| Details | BINDING: BINDING => ECO:0000269|PubMed:12432096, ECO:0007744|PDB:1N1Z |
| Chain | Residue | Details |
| A | ARG314 | |
| B | ASP351 | |
| B | ASP355 | |
| B | ARG493 | |
| B | ASP496 | |
| B | THR500 | |
| B | GLU504 | |
| B | LYS512 | |
| A | ASP351 | |
| A | ASP355 | |
| A | ARG493 | |
| A | ASP496 | |
| A | THR500 | |
| A | GLU504 | |
| A | LYS512 | |
| B | ARG314 |
Catalytic Information from CSA
| site_id | CSA1 |
| Number of Residues | 2 |
| Details | a catalytic site defined by CSA, PubMed 12432096 |
| Chain | Residue | Details |
| A | PHE578 | |
| A | TRP323 |
| site_id | CSA2 |
| Number of Residues | 2 |
| Details | a catalytic site defined by CSA, PubMed 12432096 |
| Chain | Residue | Details |
| B | PHE578 | |
| B | TRP323 |
| site_id | MCSA1 |
| Number of Residues | 9 |
| Details | M-CSA 259 |
| Chain | Residue | Details |
| A | TRP323 | electrostatic stabiliser, polar/non-polar interaction, steric role, van der waals interaction |
| A | ILE344 | steric role, van der waals interaction |
| A | ASP351 | metal ligand |
| A | ASP355 | metal ligand |
| A | VAL452 | steric role, van der waals interaction |
| A | ASP496 | metal ligand |
| A | THR500 | metal ligand |
| A | GLU504 | metal ligand |
| A | PHE578 | electrostatic stabiliser, polar/non-polar interaction, steric role, van der waals interaction |
| site_id | MCSA2 |
| Number of Residues | 9 |
| Details | M-CSA 259 |
| Chain | Residue | Details |
| B | TRP323 | electrostatic stabiliser, polar/non-polar interaction, steric role, van der waals interaction |
| B | ILE344 | steric role, van der waals interaction |
| B | ASP351 | metal ligand |
| B | ASP355 | metal ligand |
| B | VAL452 | steric role, van der waals interaction |
| B | ASP496 | metal ligand |
| B | THR500 | metal ligand |
| B | GLU504 | metal ligand |
| B | PHE578 | electrostatic stabiliser, polar/non-polar interaction, steric role, van der waals interaction |
