4O1B
The crystal structure of a mutant NAMPT (G217R) in complex with an inhibitor APO866
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0005125 | molecular_function | cytokine activity |
A | 0005515 | molecular_function | protein binding |
A | 0005576 | cellular_component | extracellular region |
A | 0005615 | cellular_component | extracellular space |
A | 0005634 | cellular_component | nucleus |
A | 0005737 | cellular_component | cytoplasm |
A | 0005829 | cellular_component | cytosol |
A | 0007165 | biological_process | signal transduction |
A | 0007267 | biological_process | cell-cell signaling |
A | 0007623 | biological_process | circadian rhythm |
A | 0008284 | biological_process | positive regulation of cell population proliferation |
A | 0008286 | biological_process | insulin receptor signaling pathway |
A | 0009435 | biological_process | NAD biosynthetic process |
A | 0016607 | cellular_component | nuclear speck |
A | 0016757 | molecular_function | glycosyltransferase activity |
A | 0019363 | biological_process | pyridine nucleotide biosynthetic process |
A | 0030054 | cellular_component | cell junction |
A | 0032922 | biological_process | circadian regulation of gene expression |
A | 0034356 | biological_process | NAD biosynthesis via nicotinamide riboside salvage pathway |
A | 0042802 | molecular_function | identical protein binding |
A | 0045944 | biological_process | positive regulation of transcription by RNA polymerase II |
A | 0047280 | molecular_function | nicotinamide phosphoribosyltransferase activity |
A | 0048511 | biological_process | rhythmic process |
A | 0051770 | biological_process | positive regulation of nitric-oxide synthase biosynthetic process |
A | 0060612 | biological_process | adipose tissue development |
A | 0070062 | cellular_component | extracellular exosome |
B | 0005125 | molecular_function | cytokine activity |
B | 0005515 | molecular_function | protein binding |
B | 0005576 | cellular_component | extracellular region |
B | 0005615 | cellular_component | extracellular space |
B | 0005634 | cellular_component | nucleus |
B | 0005737 | cellular_component | cytoplasm |
B | 0005829 | cellular_component | cytosol |
B | 0007165 | biological_process | signal transduction |
B | 0007267 | biological_process | cell-cell signaling |
B | 0007623 | biological_process | circadian rhythm |
B | 0008284 | biological_process | positive regulation of cell population proliferation |
B | 0008286 | biological_process | insulin receptor signaling pathway |
B | 0009435 | biological_process | NAD biosynthetic process |
B | 0016607 | cellular_component | nuclear speck |
B | 0016757 | molecular_function | glycosyltransferase activity |
B | 0019363 | biological_process | pyridine nucleotide biosynthetic process |
B | 0030054 | cellular_component | cell junction |
B | 0032922 | biological_process | circadian regulation of gene expression |
B | 0034356 | biological_process | NAD biosynthesis via nicotinamide riboside salvage pathway |
B | 0042802 | molecular_function | identical protein binding |
B | 0045944 | biological_process | positive regulation of transcription by RNA polymerase II |
B | 0047280 | molecular_function | nicotinamide phosphoribosyltransferase activity |
B | 0048511 | biological_process | rhythmic process |
B | 0051770 | biological_process | positive regulation of nitric-oxide synthase biosynthetic process |
B | 0060612 | biological_process | adipose tissue development |
B | 0070062 | cellular_component | extracellular exosome |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 15 |
Details | BINDING SITE FOR RESIDUE DGB A 601 |
Chain | Residue |
A | GLY185 |
A | ARG311 |
A | ILE378 |
A | ALA379 |
A | HOH754 |
A | HOH893 |
B | TYR18 |
A | LYS189 |
A | PHE193 |
A | ARG196 |
A | ARG217 |
A | ASP219 |
A | VAL242 |
A | ALA244 |
A | SER275 |
site_id | AC2 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE PO4 A 602 |
Chain | Residue |
A | ARG392 |
A | SER398 |
A | LYS400 |
A | EDO606 |
A | HOH744 |
A | HOH763 |
A | HOH767 |
A | HOH1086 |
B | ARG196 |
site_id | AC3 |
Number of Residues | 10 |
Details | BINDING SITE FOR RESIDUE PO4 A 603 |
Chain | Residue |
A | ARG196 |
A | GLU246 |
A | HIS247 |
A | ARG311 |
A | ASP313 |
A | HOH824 |
A | HOH917 |
B | TYR18 |
B | HOH738 |
B | HOH823 |
site_id | AC4 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE EDO A 604 |
Chain | Residue |
A | ASP354 |
A | GLY355 |
A | GLY383 |
A | GLY384 |
A | HOH829 |
A | HOH847 |
A | HOH944 |
A | HOH1001 |
A | HOH1122 |
site_id | AC5 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE EDO A 605 |
Chain | Residue |
A | GLY315 |
A | PRO317 |
A | ASP354 |
A | HOH1137 |
B | HOH934 |
site_id | AC6 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE EDO A 606 |
Chain | Residue |
A | ARG40 |
A | ARG392 |
A | ASP393 |
A | ASN396 |
A | CYS397 |
A | SER398 |
A | PO4602 |
A | HOH1056 |
site_id | AC7 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE EDO A 607 |
Chain | Residue |
A | PHE123 |
A | VAL124 |
A | ARG434 |
A | ASN479 |
site_id | AC8 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE EDO A 608 |
Chain | Residue |
A | GLY181 |
A | ASN182 |
site_id | AC9 |
Number of Residues | 13 |
Details | BINDING SITE FOR RESIDUE DGB B 601 |
Chain | Residue |
A | TYR18 |
B | GLY185 |
B | LYS189 |
B | PHE193 |
B | ARG196 |
B | ASP219 |
B | ALA244 |
B | SER275 |
B | ARG311 |
B | ILE378 |
B | ALA379 |
B | HOH735 |
B | HOH898 |
site_id | BC1 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE PO4 B 602 |
Chain | Residue |
A | ARG196 |
A | HOH917 |
B | ARG392 |
B | SER398 |
B | LYS400 |
B | EDO604 |
B | HOH728 |
B | HOH823 |
B | HOH1037 |
site_id | BC2 |
Number of Residues | 10 |
Details | BINDING SITE FOR RESIDUE PO4 B 603 |
Chain | Residue |
A | TYR18 |
A | HOH741 |
A | HOH763 |
B | ARG196 |
B | GLU246 |
B | HIS247 |
B | ARG311 |
B | ASP313 |
B | HOH766 |
B | HOH851 |
site_id | BC3 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE EDO B 604 |
Chain | Residue |
B | SER398 |
B | PO4602 |
B | ARG40 |
B | ARG392 |
B | ASP393 |
B | ASN396 |
B | CYS397 |
site_id | BC4 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE EDO B 605 |
Chain | Residue |
A | LYS400 |
A | CYS401 |
A | PHE414 |
B | HIS247 |
B | SER248 |
B | THR251 |
B | HOH727 |
site_id | BC5 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE EDO B 606 |
Chain | Residue |
A | HOH948 |
B | GLY315 |
B | ASP354 |
B | GLY355 |
B | HOH958 |
B | HOH1167 |
B | HOH1223 |
site_id | BC6 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE EDO B 607 |
Chain | Residue |
B | ARG217 |
B | TYR240 |
B | SER241 |
site_id | BC7 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE EDO B 608 |
Chain | Residue |
A | HOH1262 |
B | SER382 |
B | GLY383 |
B | GLY384 |
B | HOH840 |
B | HOH848 |
B | HOH1105 |
B | HOH1132 |
site_id | BC8 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE EDO B 609 |
Chain | Residue |
B | LYS117 |
B | ASP456 |
B | LEU458 |
B | HOH774 |
B | HOH906 |
B | HOH991 |
B | HOH1219 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 14 |
Details | BINDING: |
Chain | Residue | Details |
A | ARG196 | |
B | HIS247 | |
B | ARG311 | |
B | GLY353 | |
B | GLY384 | |
B | ARG392 | |
A | ASP219 | |
A | HIS247 | |
A | ARG311 | |
A | GLY353 | |
A | GLY384 | |
A | ARG392 | |
B | ARG196 | |
B | ASP219 |
site_id | SWS_FT_FI2 |
Number of Residues | 2 |
Details | MOD_RES: N-acetylmethionine => ECO:0007744|PubMed:22223895 |
Chain | Residue | Details |
A | MET1 | |
B | MET1 |
site_id | SWS_FT_FI3 |
Number of Residues | 2 |
Details | MOD_RES: Phosphotyrosine => ECO:0007744|PubMed:15592455 |
Chain | Residue | Details |
A | TYR188 | |
B | TYR188 |
site_id | SWS_FT_FI4 |
Number of Residues | 2 |
Details | MOD_RES: Phosphoserine => ECO:0007744|PubMed:23186163 |
Chain | Residue | Details |
A | SER472 | |
B | SER472 |