3CMC
Thioacylenzyme intermediate of Bacillus stearothermophilus phosphorylating GAPDH
Functional Information from GO Data
| Chain | GOid | namespace | contents |
| O | 0000166 | molecular_function | nucleotide binding |
| O | 0004365 | molecular_function | glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity |
| O | 0005737 | cellular_component | cytoplasm |
| O | 0006006 | biological_process | glucose metabolic process |
| O | 0006096 | biological_process | glycolytic process |
| O | 0016491 | molecular_function | oxidoreductase activity |
| O | 0016620 | molecular_function | oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor |
| O | 0030554 | molecular_function | adenyl nucleotide binding |
| O | 0050661 | molecular_function | NADP binding |
| O | 0051287 | molecular_function | NAD binding |
| P | 0000166 | molecular_function | nucleotide binding |
| P | 0004365 | molecular_function | glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity |
| P | 0005737 | cellular_component | cytoplasm |
| P | 0006006 | biological_process | glucose metabolic process |
| P | 0006096 | biological_process | glycolytic process |
| P | 0016491 | molecular_function | oxidoreductase activity |
| P | 0016620 | molecular_function | oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor |
| P | 0030554 | molecular_function | adenyl nucleotide binding |
| P | 0050661 | molecular_function | NADP binding |
| P | 0051287 | molecular_function | NAD binding |
| Q | 0000166 | molecular_function | nucleotide binding |
| Q | 0004365 | molecular_function | glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity |
| Q | 0005737 | cellular_component | cytoplasm |
| Q | 0006006 | biological_process | glucose metabolic process |
| Q | 0006096 | biological_process | glycolytic process |
| Q | 0016491 | molecular_function | oxidoreductase activity |
| Q | 0016620 | molecular_function | oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor |
| Q | 0030554 | molecular_function | adenyl nucleotide binding |
| Q | 0050661 | molecular_function | NADP binding |
| Q | 0051287 | molecular_function | NAD binding |
| R | 0000166 | molecular_function | nucleotide binding |
| R | 0004365 | molecular_function | glyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity |
| R | 0005737 | cellular_component | cytoplasm |
| R | 0006006 | biological_process | glucose metabolic process |
| R | 0006096 | biological_process | glycolytic process |
| R | 0016491 | molecular_function | oxidoreductase activity |
| R | 0016620 | molecular_function | oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor |
| R | 0030554 | molecular_function | adenyl nucleotide binding |
| R | 0050661 | molecular_function | NADP binding |
| R | 0051287 | molecular_function | NAD binding |
Functional Information from PDB Data
| site_id | AC1 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE SO4 O 401 |
| Chain | Residue |
| O | SER148 |
| O | THR207 |
| O | THR208 |
| O | GLY209 |
| O | ALA210 |
| site_id | AC2 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE SO4 P 401 |
| Chain | Residue |
| P | GLY209 |
| P | ALA210 |
| P | PRO121 |
| P | SER148 |
| P | THR207 |
| P | THR208 |
| site_id | AC3 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE SO4 Q 401 |
| Chain | Residue |
| Q | PRO121 |
| Q | SER148 |
| Q | THR207 |
| Q | THR208 |
| Q | GLY209 |
| Q | ALA210 |
| site_id | AC4 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE SO4 R 401 |
| Chain | Residue |
| R | SER148 |
| R | THR207 |
| R | THR208 |
| R | GLY209 |
| R | ALA210 |
| site_id | AC5 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE SO4 O 402 |
| Chain | Residue |
| O | THR179 |
| O | ASP181 |
| O | ARG195 |
| O | ARG231 |
| site_id | AC6 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE SO4 P 402 |
| Chain | Residue |
| P | THR179 |
| P | ASP181 |
| P | ARG195 |
| P | ARG231 |
| site_id | AC7 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE SO4 Q 402 |
| Chain | Residue |
| Q | THR179 |
| Q | ASP181 |
| Q | ARG195 |
| Q | ARG231 |
| site_id | AC8 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE SO4 R 402 |
| Chain | Residue |
| R | THR179 |
| R | ASP181 |
| R | ARG195 |
| R | ARG231 |
| site_id | AC9 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE SO4 O 403 |
| Chain | Residue |
| O | ARG169 |
| P | LYS303 |
| site_id | BC1 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE SO4 O 404 |
| Chain | Residue |
| O | ARG183 |
| O | HIS190 |
| O | LYS191 |
| site_id | BC2 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE SO4 R 403 |
| Chain | Residue |
| Q | LYS303 |
| R | ARG169 |
| site_id | BC3 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE SO4 Q 403 |
| Chain | Residue |
| Q | ARG183 |
| Q | PRO188 |
| Q | HIS190 |
| Q | LYS191 |
| site_id | BC4 |
| Number of Residues | 1 |
| Details | BINDING SITE FOR RESIDUE SO4 R 404 |
| Chain | Residue |
| R | ARG52 |
| site_id | BC5 |
| Number of Residues | 1 |
| Details | BINDING SITE FOR RESIDUE SO4 R 405 |
| Chain | Residue |
| R | SER58 |
| site_id | BC6 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE SO4 O 405 |
| Chain | Residue |
| O | ASN62 |
| O | ASN63 |
| site_id | BC7 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE SO4 R 406 |
| Chain | Residue |
| R | ARG183 |
| R | HIS190 |
| R | LYS191 |
| site_id | BC8 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE SO4 R 407 |
| Chain | Residue |
| P | ASP138 |
| P | LYS139 |
| R | LEU109 |
| R | GLY112 |
| R | ALA113 |
| R | LYS114 |
| site_id | BC9 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE SO4 O 406 |
| Chain | Residue |
| O | GLY85 |
| O | ALA111 |
| O | GLY112 |
| site_id | CC1 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE G3H O 400 |
| Chain | Residue |
| O | SER148 |
| O | CYS149 |
| O | THR150 |
| O | HIS176 |
| O | THR179 |
| O | THR208 |
| O | GLY209 |
| O | ARG231 |
| site_id | CC2 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE G3H P 400 |
| Chain | Residue |
| P | SER148 |
| P | CYS149 |
| P | THR150 |
| P | HIS176 |
| P | THR208 |
| P | GLY209 |
| P | ARG231 |
| site_id | CC3 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE G3H Q 400 |
| Chain | Residue |
| Q | SER148 |
| Q | CYS149 |
| Q | THR150 |
| Q | HIS176 |
| Q | THR179 |
| Q | THR208 |
| Q | GLY209 |
| Q | ARG231 |
| site_id | CC4 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE G3H R 400 |
| Chain | Residue |
| R | SER148 |
| R | CYS149 |
| R | THR150 |
| R | HIS176 |
| R | THR179 |
| R | THR208 |
| R | GLY209 |
| R | ARG231 |
| site_id | CC5 |
| Number of Residues | 19 |
| Details | BINDING SITE FOR RESIDUE NAD O 407 |
| Chain | Residue |
| O | ILE11 |
| O | ASN31 |
| O | ASP32 |
| O | LEU33 |
| O | ARG77 |
| O | SER95 |
| O | THR96 |
| O | GLY97 |
| O | ARG98 |
| O | PHE99 |
| O | SER119 |
| O | ALA120 |
| O | ASN180 |
| O | ASN313 |
| O | TYR317 |
| R | LEU187 |
| O | GLY7 |
| O | GLY9 |
| O | ARG10 |
| site_id | CC6 |
| Number of Residues | 16 |
| Details | BINDING SITE FOR RESIDUE NAD P 403 |
| Chain | Residue |
| P | GLY7 |
| P | GLY9 |
| P | ARG10 |
| P | ILE11 |
| P | ASN31 |
| P | ASP32 |
| P | LEU33 |
| P | ARG77 |
| P | SER95 |
| P | THR96 |
| P | GLY97 |
| P | SER119 |
| P | ALA120 |
| P | ASN180 |
| P | ASN313 |
| P | TYR317 |
| site_id | CC7 |
| Number of Residues | 18 |
| Details | BINDING SITE FOR RESIDUE NAD Q 404 |
| Chain | Residue |
| Q | GLY7 |
| Q | GLY9 |
| Q | ARG10 |
| Q | ILE11 |
| Q | ASN31 |
| Q | ASP32 |
| Q | LEU33 |
| Q | ARG77 |
| Q | SER95 |
| Q | THR96 |
| Q | GLY97 |
| Q | ARG98 |
| Q | PHE99 |
| Q | SER119 |
| Q | ALA120 |
| Q | ASN180 |
| Q | ASN313 |
| Q | TYR317 |
| site_id | CC8 |
| Number of Residues | 18 |
| Details | BINDING SITE FOR RESIDUE NAD R 408 |
| Chain | Residue |
| R | GLY7 |
| R | GLY9 |
| R | ARG10 |
| R | ILE11 |
| R | ASN31 |
| R | ASP32 |
| R | LEU33 |
| R | ARG77 |
| R | SER95 |
| R | THR96 |
| R | GLY97 |
| R | ARG98 |
| R | PHE99 |
| R | SER119 |
| R | ALA120 |
| R | ASN180 |
| R | ASN313 |
| R | TYR317 |
| site_id | CC9 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE EDO Q 405 |
| Chain | Residue |
| Q | GLN134 |
| Q | ASP135 |
| Q | LYS159 |
| site_id | DC1 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE GOL R 409 |
| Chain | Residue |
| Q | ARG169 |
| R | LYS303 |
| site_id | DC2 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE GOL P 404 |
| Chain | Residue |
| P | GLY131 |
| P | GLN134 |
| P | ASP135 |
| P | LYS159 |
| site_id | DC3 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE GOL P 405 |
| Chain | Residue |
| P | ASP181 |
| P | ARG183 |
| P | PRO188 |
| P | HIS190 |
| P | LYS191 |
| site_id | DC4 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE GOL O 408 |
| Chain | Residue |
| O | LYS303 |
| P | ARG169 |
| site_id | DC5 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE GOL R 410 |
| Chain | Residue |
| R | GLN134 |
| R | ASP135 |
| site_id | DC6 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE GOL P 406 |
| Chain | Residue |
| P | LYS212 |
| P | ALA215 |
| P | GLY223 |
| site_id | DC7 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE GOL Q 406 |
| Chain | Residue |
| Q | ASN14 |
| Q | ARG17 |
| Q | HIS50 |
| Q | THR315 |
| site_id | DC8 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE GOL P 407 |
| Chain | Residue |
| P | HIS50 |
| P | GLY51 |
| R | ARG281 |
Functional Information from PROSITE/UniProt
| site_id | PS00071 |
| Number of Residues | 8 |
| Details | GAPDH Glyceraldehyde 3-phosphate dehydrogenase active site. ASCTTNcL |
| Chain | Residue | Details |
| O | ALA147-LEU154 |
Functional Information from SwissProt/UniProt
| site_id | SWS_FT_FI1 |
| Number of Residues | 4 |
| Details | Active site: {"description":"Nucleophile","evidences":[{"source":"PubMed","id":"18480053","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"12569100","evidenceCode":"ECO:0000305"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI2 |
| Number of Residues | 24 |
| Details | Binding site: {"evidences":[{"source":"PubMed","id":"12569100","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"18480053","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"3586018","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9175858","evidenceCode":"ECO:0000269"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI3 |
| Number of Residues | 16 |
| Details | Binding site: {"evidences":[{"source":"PubMed","id":"12569100","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"18480053","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"3210237","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"3586018","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9175858","evidenceCode":"ECO:0000269"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI4 |
| Number of Residues | 4 |
| Details | Binding site: {"evidences":[{"source":"PubMed","id":"12569100","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"18480053","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9175858","evidenceCode":"ECO:0000269"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI5 |
| Number of Residues | 4 |
| Details | Binding site: {"evidences":[{"source":"PubMed","id":"18480053","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"3210237","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"3586018","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9175858","evidenceCode":"ECO:0000269"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI6 |
| Number of Residues | 4 |
| Details | Site: {"description":"Activates thiol group during catalysis","evidences":[{"source":"UniProtKB","id":"Q6GIL8","evidenceCode":"ECO:0000250"}]} |
| Chain | Residue | Details |
Catalytic Information from CSA
| site_id | CSA1 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1szj |
| Chain | Residue | Details |
| O | CYS149 | |
| O | HIS176 |
| site_id | CSA2 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1szj |
| Chain | Residue | Details |
| P | CYS149 | |
| P | HIS176 |
| site_id | CSA3 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1szj |
| Chain | Residue | Details |
| Q | CYS149 | |
| Q | HIS176 |
| site_id | CSA4 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1szj |
| Chain | Residue | Details |
| R | CYS149 | |
| R | HIS176 |






