4PTN
Crystal Structure of YagE, a KDG aldolase protein in complex with Magnesium cation coordinated L-glyceraldehyde
Functional Information from GO Data
| Chain | GOid | namespace | contents |
| A | 0005737 | cellular_component | cytoplasm |
| A | 0005829 | cellular_component | cytosol |
| A | 0016829 | molecular_function | lyase activity |
| A | 0042802 | molecular_function | identical protein binding |
| A | 0046176 | biological_process | aldonic acid catabolic process |
| A | 0047440 | molecular_function | 2-dehydro-3-deoxy-D-pentonate aldolase activity |
| A | 0061677 | molecular_function | 2-dehydro-3-deoxy-D-gluconate aldolase activity |
| B | 0005737 | cellular_component | cytoplasm |
| B | 0005829 | cellular_component | cytosol |
| B | 0016829 | molecular_function | lyase activity |
| B | 0042802 | molecular_function | identical protein binding |
| B | 0046176 | biological_process | aldonic acid catabolic process |
| B | 0047440 | molecular_function | 2-dehydro-3-deoxy-D-pentonate aldolase activity |
| B | 0061677 | molecular_function | 2-dehydro-3-deoxy-D-gluconate aldolase activity |
| C | 0005737 | cellular_component | cytoplasm |
| C | 0005829 | cellular_component | cytosol |
| C | 0016829 | molecular_function | lyase activity |
| C | 0042802 | molecular_function | identical protein binding |
| C | 0046176 | biological_process | aldonic acid catabolic process |
| C | 0047440 | molecular_function | 2-dehydro-3-deoxy-D-pentonate aldolase activity |
| C | 0061677 | molecular_function | 2-dehydro-3-deoxy-D-gluconate aldolase activity |
| D | 0005737 | cellular_component | cytoplasm |
| D | 0005829 | cellular_component | cytosol |
| D | 0016829 | molecular_function | lyase activity |
| D | 0042802 | molecular_function | identical protein binding |
| D | 0046176 | biological_process | aldonic acid catabolic process |
| D | 0047440 | molecular_function | 2-dehydro-3-deoxy-D-pentonate aldolase activity |
| D | 0061677 | molecular_function | 2-dehydro-3-deoxy-D-gluconate aldolase activity |
Functional Information from PDB Data
| site_id | AC1 |
| Number of Residues | 10 |
| Details | BINDING SITE FOR RESIDUE EDO A 401 |
| Chain | Residue |
| A | PHE52 |
| A | TYR145 |
| A | LEU54 |
| A | GLY55 |
| A | PHE60 |
| A | GLY88 |
| A | GLY90 |
| A | VAL113 |
| A | VAL114 |
| A | ILE115 |
| site_id | AC2 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE EDO A 402 |
| Chain | Residue |
| A | ASP178 |
| A | TYR203 |
| A | ASP205 |
| A | HIS206 |
| C | ALA181 |
| C | ARG184 |
| site_id | AC3 |
| Number of Residues | 11 |
| Details | BINDING SITE FOR RESIDUE GXV A 403 |
| Chain | Residue |
| A | LYS174 |
| A | THR176 |
| A | GLY202 |
| A | TYR203 |
| A | ILE219 |
| A | SER220 |
| A | ALA221 |
| A | PHE265 |
| A | MG404 |
| A | HOH524 |
| A | HOH532 |
| site_id | AC4 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE MG A 404 |
| Chain | Residue |
| A | PRO20 |
| A | GLY57 |
| A | GXV403 |
| A | HOH524 |
| A | HOH532 |
| site_id | AC5 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE EDO B 401 |
| Chain | Residue |
| B | LEU54 |
| B | PHE60 |
| B | GLY88 |
| B | GLY90 |
| B | VAL113 |
| B | VAL114 |
| B | ILE115 |
| B | TYR145 |
| site_id | AC6 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE EDO B 402 |
| Chain | Residue |
| B | ASP178 |
| B | TYR203 |
| B | ASP205 |
| B | HIS206 |
| B | PRO256 |
| D | ARG184 |
| site_id | AC7 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE EDO B 403 |
| Chain | Residue |
| B | TYR248 |
| B | THR251 |
| B | LEU306 |
| site_id | AC8 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE EDO B 404 |
| Chain | Residue |
| B | PHE147 |
| B | ALA149 |
| B | ASP178 |
| B | TYR203 |
| B | HOH511 |
| site_id | AC9 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE GOL B 405 |
| Chain | Residue |
| B | ASP178 |
| D | ASP178 |
| site_id | BC1 |
| Number of Residues | 12 |
| Details | BINDING SITE FOR RESIDUE GXV B 406 |
| Chain | Residue |
| B | PRO20 |
| B | LYS174 |
| B | THR176 |
| B | GLY202 |
| B | TYR203 |
| B | ILE219 |
| B | SER220 |
| B | ALA221 |
| B | PHE265 |
| B | MG407 |
| B | HOH508 |
| B | HOH634 |
| site_id | BC2 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE MG B 407 |
| Chain | Residue |
| B | PRO20 |
| B | SER56 |
| B | GLY57 |
| B | GXV406 |
| B | HOH508 |
| site_id | BC3 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE PYR B 408 |
| Chain | Residue |
| A | ALA125 |
| B | ASP262 |
| B | SER289 |
| B | PRO290 |
| B | ASP292 |
| B | HOH539 |
| B | HOH600 |
| site_id | BC4 |
| Number of Residues | 9 |
| Details | BINDING SITE FOR RESIDUE EDO C 401 |
| Chain | Residue |
| C | LEU54 |
| C | PHE60 |
| C | ARG68 |
| C | GLY88 |
| C | THR89 |
| C | GLY90 |
| C | VAL113 |
| C | VAL114 |
| C | ILE115 |
| site_id | BC5 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE EDO C 402 |
| Chain | Residue |
| A | ALA181 |
| A | ARG184 |
| C | ASP178 |
| C | TYR203 |
| C | ASP205 |
| C | HIS206 |
| site_id | BC6 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE EDO C 403 |
| Chain | Residue |
| C | HOH609 |
| C | HOH625 |
| C | GLY64 |
| C | ALA65 |
| C | GLU66 |
| C | GLU67 |
| site_id | BC7 |
| Number of Residues | 11 |
| Details | BINDING SITE FOR RESIDUE GXV C 404 |
| Chain | Residue |
| C | LYS174 |
| C | THR176 |
| C | GLY202 |
| C | TYR203 |
| C | ILE219 |
| C | SER220 |
| C | ALA221 |
| C | PHE265 |
| C | MG405 |
| C | HOH528 |
| C | HOH603 |
| site_id | BC8 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE MG C 405 |
| Chain | Residue |
| C | PRO20 |
| C | GLY57 |
| C | GXV404 |
| C | HOH528 |
| site_id | BC9 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE EDO D 401 |
| Chain | Residue |
| B | ALA181 |
| B | ARG184 |
| D | ASP178 |
| D | TYR203 |
| D | ASP205 |
| D | HIS206 |
| D | PRO256 |
| site_id | CC1 |
| Number of Residues | 11 |
| Details | BINDING SITE FOR RESIDUE EDO D 402 |
| Chain | Residue |
| D | PHE52 |
| D | LEU54 |
| D | PHE60 |
| D | ARG68 |
| D | GLY88 |
| D | THR89 |
| D | GLY90 |
| D | VAL113 |
| D | VAL114 |
| D | ILE115 |
| D | TYR145 |
| site_id | CC2 |
| Number of Residues | 10 |
| Details | BINDING SITE FOR RESIDUE GXV D 403 |
| Chain | Residue |
| D | LYS174 |
| D | GLY202 |
| D | TYR203 |
| D | ILE219 |
| D | SER220 |
| D | ALA221 |
| D | PHE265 |
| D | MG404 |
| D | HOH528 |
| D | HOH643 |
| site_id | CC3 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE MG D 404 |
| Chain | Residue |
| D | PRO20 |
| D | SER56 |
| D | GLY57 |
| D | GXV403 |
| D | HOH528 |
| site_id | CC4 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE PYR D 405 |
| Chain | Residue |
| D | ASP262 |
| D | SER289 |
| D | PRO290 |
| D | ASP292 |
| D | HOH533 |
| D | HOH586 |
| D | HOH609 |
Functional Information from PROSITE/UniProt
Functional Information from SwissProt/UniProt
| site_id | SWS_FT_FI1 |
| Number of Residues | 8 |
| Details | Active site: {"description":"Charge relay system","evidences":[{"source":"PubMed","id":"21294156","evidenceCode":"ECO:0000305"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI2 |
| Number of Residues | 4 |
| Details | Active site: {"description":"Proton donor","evidences":[{"source":"PubMed","id":"21294156","evidenceCode":"ECO:0000305"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI3 |
| Number of Residues | 4 |
| Details | Active site: {"description":"Schiff-base intermediate with substrate","evidences":[{"source":"PubMed","id":"21294156","evidenceCode":"ECO:0000305"}]} |
| Chain | Residue | Details |






