4ONV
Crystal structure of YagE, a KDG aldolase protein in complex with 2-Keto-3-deoxy gluconate
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 | 8 |
| Details | BINDING SITE FOR RESIDUE EDO A 401 |
| Chain | Residue |
| A | LEU54 |
| A | PHE60 |
| A | GLY88 |
| A | THR89 |
| A | GLY90 |
| A | VAL113 |
| A | VAL114 |
| A | ILE115 |
| site_id | AC2 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE GOL A 402 |
| Chain | Residue |
| A | PRO141 |
| A | SER168 |
| A | ASN169 |
| A | THR139 |
| site_id | AC3 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE GOL A 403 |
| Chain | Residue |
| A | GLU271 |
| A | LEU275 |
| A | LYS296 |
| D | ARG73 |
| site_id | AC4 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE GOL A 404 |
| Chain | Residue |
| A | SER123 |
| A | GLU124 |
| site_id | AC5 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE GOL A 405 |
| Chain | Residue |
| A | THR263 |
| B | SER123 |
| B | EDO403 |
| site_id | AC6 |
| Number of Residues | 14 |
| Details | BINDING SITE FOR RESIDUE KDG A 406 |
| Chain | Residue |
| A | PRO20 |
| A | PHE52 |
| A | GLY55 |
| A | SER56 |
| A | GLY57 |
| A | TYR145 |
| A | LYS174 |
| A | THR176 |
| A | GLY202 |
| A | TYR203 |
| A | ILE219 |
| A | SER220 |
| A | ALA221 |
| A | HOH532 |
| site_id | AC7 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE EDO B 401 |
| Chain | Residue |
| B | PHE25 |
| B | GLY29 |
| B | LEU31 |
| B | GLU67 |
| site_id | AC8 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE EDO B 402 |
| Chain | Residue |
| B | LEU54 |
| B | PHE60 |
| B | GLY88 |
| B | GLY90 |
| B | VAL113 |
| B | VAL114 |
| B | ILE115 |
| site_id | AC9 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE EDO B 403 |
| Chain | Residue |
| A | GOL405 |
| B | GLU124 |
| B | ALA125 |
| site_id | BC1 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE EDO B 404 |
| Chain | Residue |
| B | ASP178 |
| B | SER179 |
| D | ASP178 |
| D | SER179 |
| site_id | BC2 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE GOL B 405 |
| Chain | Residue |
| B | GLY64 |
| B | ALA65 |
| B | GLU66 |
| B | GLU67 |
| site_id | BC3 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE GOL B 406 |
| Chain | Residue |
| B | THR15 |
| B | GLY16 |
| B | LEU211 |
| B | ASP216 |
| B | LEU234 |
| B | ARG238 |
| site_id | BC4 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE GOL B 407 |
| Chain | Residue |
| B | GLU66 |
| B | LYS69 |
| B | ALA70 |
| B | ARG73 |
| B | HIS103 |
| site_id | BC5 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE GOL B 408 |
| Chain | Residue |
| B | GLN153 |
| B | ASP154 |
| B | HOH649 |
| site_id | BC6 |
| Number of Residues | 12 |
| Details | BINDING SITE FOR RESIDUE KDG B 409 |
| Chain | Residue |
| B | PRO20 |
| B | PHE52 |
| B | GLY55 |
| B | SER56 |
| B | GLY57 |
| B | TYR145 |
| B | LYS174 |
| B | THR176 |
| B | GLY202 |
| B | SER220 |
| B | ALA221 |
| B | HOH642 |
| site_id | BC7 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE EDO C 401 |
| Chain | Residue |
| C | LEU54 |
| C | PHE60 |
| C | GLY88 |
| C | THR89 |
| C | GLY90 |
| C | VAL113 |
| C | ILE115 |
| C | TYR145 |
| site_id | BC8 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE EDO C 402 |
| Chain | Residue |
| C | SER123 |
| C | GLU124 |
| C | ALA125 |
| C | EDO405 |
| site_id | BC9 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE EDO C 403 |
| Chain | Residue |
| C | GLU124 |
| C | ALA158 |
| C | LEU159 |
| C | THR162 |
| site_id | CC1 |
| Number of Residues | 1 |
| Details | BINDING SITE FOR RESIDUE EDO C 404 |
| Chain | Residue |
| C | SER179 |
| site_id | CC2 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE EDO C 405 |
| Chain | Residue |
| C | SER123 |
| C | EDO402 |
| site_id | CC3 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE GOL C 406 |
| Chain | Residue |
| C | ALA164 |
| C | ASP165 |
| C | SER166 |
| C | ARG167 |
| C | SER168 |
| site_id | CC4 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE EDO C 407 |
| Chain | Residue |
| B | LEU31 |
| B | LYS33 |
| B | PRO34 |
| C | ASP32 |
| site_id | CC5 |
| Number of Residues | 13 |
| Details | BINDING SITE FOR RESIDUE KDG C 408 |
| Chain | Residue |
| C | PRO20 |
| C | PHE52 |
| C | GLY55 |
| C | SER56 |
| C | GLY57 |
| C | TYR145 |
| C | LYS174 |
| C | THR176 |
| C | GLY202 |
| C | ILE219 |
| C | SER220 |
| C | ALA221 |
| C | HOH533 |
| site_id | CC6 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE EDO D 401 |
| Chain | Residue |
| D | GLU66 |
| D | LYS69 |
| site_id | CC7 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE EDO D 402 |
| Chain | Residue |
| C | GLN62 |
| C | PRO287 |
| D | THR92 |
| D | PRO117 |
| D | TYR118 |
| D | TYR119 |
| D | TRP120 |
| site_id | CC8 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE EDO D 403 |
| Chain | Residue |
| D | LEU54 |
| D | PHE60 |
| D | GLY88 |
| D | THR89 |
| D | GLY90 |
| D | VAL113 |
| D | VAL114 |
| D | ILE115 |
| site_id | CC9 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE GOL D 404 |
| Chain | Residue |
| D | ASP42 |
| D | ARG278 |
| D | HOH543 |
| site_id | DC1 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE EDO D 405 |
| Chain | Residue |
| D | SER123 |
| D | GLU124 |
| D | ALA125 |
| site_id | DC2 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE GOL D 406 |
| Chain | Residue |
| A | LYS33 |
| D | ALA164 |
| D | ASP165 |
| D | ARG167 |
| D | SER168 |
| site_id | DC3 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE GOL D 407 |
| Chain | Residue |
| D | THR15 |
| D | ASP216 |
| D | ARG238 |
| site_id | DC4 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE GOL D 408 |
| Chain | Residue |
| A | GLU293 |
| D | LYS69 |
| D | ARG73 |
| D | HIS103 |
| site_id | DC5 |
| Number of Residues | 12 |
| Details | BINDING SITE FOR RESIDUE KDG D 409 |
| Chain | Residue |
| D | PRO20 |
| D | PHE52 |
| D | GLY55 |
| D | SER56 |
| D | GLY57 |
| D | TYR145 |
| D | LYS174 |
| D | THR176 |
| D | GLY202 |
| D | TYR203 |
| D | ALA221 |
| D | HOH518 |
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 |






