7BKG
Co-crystal structure of Human Nicotinamide N-methyltransferase (NNMT) with the tricyclic inhibitor (2)
Functional Information from GO Data
| Chain | GOid | namespace | contents |
| A | 0005737 | cellular_component | cytoplasm |
| A | 0005829 | cellular_component | cytosol |
| A | 0006769 | biological_process | nicotinamide metabolic process |
| A | 0008112 | molecular_function | nicotinamide N-methyltransferase activity |
| A | 0008168 | molecular_function | methyltransferase activity |
| A | 0008757 | molecular_function | S-adenosylmethionine-dependent methyltransferase activity |
| A | 0016740 | molecular_function | transferase activity |
| A | 0019677 | biological_process | NAD+ catabolic process |
| A | 0030760 | molecular_function | pyridine N-methyltransferase activity |
| A | 0032259 | biological_process | methylation |
| A | 0045722 | biological_process | positive regulation of gluconeogenesis |
| A | 0090312 | biological_process | positive regulation of protein deacetylation |
| A | 1901847 | biological_process | nicotinate metabolic process |
| B | 0005737 | cellular_component | cytoplasm |
| B | 0005829 | cellular_component | cytosol |
| B | 0006769 | biological_process | nicotinamide metabolic process |
| B | 0008112 | molecular_function | nicotinamide N-methyltransferase activity |
| B | 0008168 | molecular_function | methyltransferase activity |
| B | 0008757 | molecular_function | S-adenosylmethionine-dependent methyltransferase activity |
| B | 0016740 | molecular_function | transferase activity |
| B | 0019677 | biological_process | NAD+ catabolic process |
| B | 0030760 | molecular_function | pyridine N-methyltransferase activity |
| B | 0032259 | biological_process | methylation |
| B | 0045722 | biological_process | positive regulation of gluconeogenesis |
| B | 0090312 | biological_process | positive regulation of protein deacetylation |
| B | 1901847 | biological_process | nicotinate metabolic process |
| C | 0005737 | cellular_component | cytoplasm |
| C | 0005829 | cellular_component | cytosol |
| C | 0006769 | biological_process | nicotinamide metabolic process |
| C | 0008112 | molecular_function | nicotinamide N-methyltransferase activity |
| C | 0008168 | molecular_function | methyltransferase activity |
| C | 0008757 | molecular_function | S-adenosylmethionine-dependent methyltransferase activity |
| C | 0016740 | molecular_function | transferase activity |
| C | 0019677 | biological_process | NAD+ catabolic process |
| C | 0030760 | molecular_function | pyridine N-methyltransferase activity |
| C | 0032259 | biological_process | methylation |
| C | 0045722 | biological_process | positive regulation of gluconeogenesis |
| C | 0090312 | biological_process | positive regulation of protein deacetylation |
| C | 1901847 | biological_process | nicotinate metabolic process |
| D | 0005737 | cellular_component | cytoplasm |
| D | 0005829 | cellular_component | cytosol |
| D | 0006769 | biological_process | nicotinamide metabolic process |
| D | 0008112 | molecular_function | nicotinamide N-methyltransferase activity |
| D | 0008168 | molecular_function | methyltransferase activity |
| D | 0008757 | molecular_function | S-adenosylmethionine-dependent methyltransferase activity |
| D | 0016740 | molecular_function | transferase activity |
| D | 0019677 | biological_process | NAD+ catabolic process |
| D | 0030760 | molecular_function | pyridine N-methyltransferase activity |
| D | 0032259 | biological_process | methylation |
| D | 0045722 | biological_process | positive regulation of gluconeogenesis |
| D | 0090312 | biological_process | positive regulation of protein deacetylation |
| D | 1901847 | biological_process | nicotinate metabolic process |
Functional Information from PDB Data
| site_id | AC1 |
| Number of Residues | 21 |
| Details | binding site for residue SAH A 4001 |
| Chain | Residue |
| A | TYR11 |
| A | TYR86 |
| A | SER87 |
| A | ASN90 |
| A | ASP142 |
| A | VAL143 |
| A | THR163 |
| A | LEU164 |
| A | CYS165 |
| A | ALA169 |
| A | U0Z4002 |
| A | TYR20 |
| A | HOH4121 |
| A | HOH4189 |
| A | TYR25 |
| A | GLY63 |
| A | SER64 |
| A | GLY65 |
| A | THR67 |
| A | TYR69 |
| A | ASP85 |
| site_id | AC2 |
| Number of Residues | 12 |
| Details | binding site for residue U0Z A 4002 |
| Chain | Residue |
| A | TYR20 |
| A | TYR24 |
| A | LEU164 |
| A | ASP167 |
| A | ASP197 |
| A | ALA198 |
| A | SER201 |
| A | TYR204 |
| A | SER213 |
| A | TYR242 |
| A | ALA247 |
| A | SAH4001 |
| site_id | AC3 |
| Number of Residues | 22 |
| Details | binding site for residue SAH B 4001 |
| Chain | Residue |
| B | TYR11 |
| B | TYR20 |
| B | TYR25 |
| B | GLY63 |
| B | SER64 |
| B | GLY65 |
| B | THR67 |
| B | TYR69 |
| B | GLN70 |
| B | ASP85 |
| B | TYR86 |
| B | ASN90 |
| B | CYS141 |
| B | ASP142 |
| B | VAL143 |
| B | THR163 |
| B | LEU164 |
| B | CYS165 |
| B | ALA169 |
| B | U0Z4002 |
| B | HOH4146 |
| B | HOH4197 |
| site_id | AC4 |
| Number of Residues | 12 |
| Details | binding site for residue U0Z B 4002 |
| Chain | Residue |
| B | TYR20 |
| B | LEU164 |
| B | ASP167 |
| B | ALA168 |
| B | ASP197 |
| B | ALA198 |
| B | SER201 |
| B | TYR204 |
| B | SER213 |
| B | TYR242 |
| B | ALA247 |
| B | SAH4001 |
| site_id | AC5 |
| Number of Residues | 21 |
| Details | binding site for residue SAH C 4001 |
| Chain | Residue |
| C | TYR11 |
| C | TYR20 |
| C | TYR25 |
| C | GLY63 |
| C | SER64 |
| C | GLY65 |
| C | THR67 |
| C | TYR69 |
| C | GLN70 |
| C | ASP85 |
| C | TYR86 |
| C | ASN90 |
| C | CYS141 |
| C | ASP142 |
| C | VAL143 |
| C | THR163 |
| C | LEU164 |
| C | CYS165 |
| C | ALA169 |
| C | U0Z4002 |
| C | HOH4111 |
| site_id | AC6 |
| Number of Residues | 11 |
| Details | binding site for residue U0Z C 4002 |
| Chain | Residue |
| C | TYR20 |
| C | LEU164 |
| C | ASP167 |
| C | ASP197 |
| C | ALA198 |
| C | SER201 |
| C | TYR204 |
| C | SER213 |
| C | TYR242 |
| C | ALA247 |
| C | SAH4001 |
| site_id | AC7 |
| Number of Residues | 22 |
| Details | binding site for residue SAH D 4001 |
| Chain | Residue |
| D | TYR11 |
| D | TYR20 |
| D | TYR25 |
| D | GLY63 |
| D | SER64 |
| D | GLY65 |
| D | THR67 |
| D | TYR69 |
| D | GLN70 |
| D | ASP85 |
| D | TYR86 |
| D | SER87 |
| D | ASN90 |
| D | CYS141 |
| D | ASP142 |
| D | VAL143 |
| D | THR163 |
| D | LEU164 |
| D | CYS165 |
| D | ALA169 |
| D | U0Z4002 |
| D | HOH4135 |
| site_id | AC8 |
| Number of Residues | 10 |
| Details | binding site for residue U0Z D 4002 |
| Chain | Residue |
| D | TYR20 |
| D | LEU164 |
| D | ASP197 |
| D | ALA198 |
| D | SER201 |
| D | TYR204 |
| D | SER213 |
| D | TYR242 |
| D | ALA247 |
| D | SAH4001 |
Functional Information from PROSITE/UniProt
| site_id | PS01100 |
| Number of Residues | 17 |
| Details | NNMT_PNMT_TEMT NNMT/PNMT/TEMT family of methyltransferases signature. LIDIGSGPTIYQLLSAC |
| Chain | Residue | Details |
| A | LEU59-CYS75 |
Functional Information from SwissProt/UniProt
| site_id | SWS_FT_FI1 |
| Number of Residues | 32 |
| Details | Binding site: {"evidences":[{"source":"PubMed","id":"21823666","evidenceCode":"ECO:0000269"},{"source":"Reference","evidenceCode":"ECO:0000269","citation":{"citationType":"submission","publicationDate":"OCT-2006","submissionDatabase":"PDB data bank","title":"The crystal structure of human nicotinamide N-methyltransferase in complex with SAH.","authoringGroup":["Structural genomics consortium (SGC)"]}}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI2 |
| Number of Residues | 8 |
| Details | Binding site: {"evidences":[{"source":"PubMed","id":"21823666","evidenceCode":"ECO:0000269"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI3 |
| Number of Residues | 12 |
| Details | Modified residue: {"description":"Citrulline; alternate","evidences":[{"source":"PubMed","id":"30044909","evidenceCode":"ECO:0000269"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI4 |
| Number of Residues | 4 |
| Details | Modified residue: {"description":"N6-acetyllysine","evidences":[{"source":"PubMed","id":"19608861","evidenceCode":"ECO:0007744"}]} |
| Chain | Residue | Details |
