1NDY
Crystal Structure of Adenosine Deaminase Complexed with FR230513
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004000 | molecular_function | adenosine deaminase activity |
A | 0005515 | molecular_function | protein binding |
A | 0005737 | cellular_component | cytoplasm |
A | 0005764 | cellular_component | lysosome |
A | 0005829 | cellular_component | cytosol |
A | 0005886 | cellular_component | plasma membrane |
A | 0006154 | biological_process | adenosine catabolic process |
A | 0007155 | biological_process | cell adhesion |
A | 0008270 | molecular_function | zinc ion binding |
A | 0009117 | biological_process | nucleotide metabolic process |
A | 0009168 | biological_process | purine ribonucleoside monophosphate biosynthetic process |
A | 0009897 | cellular_component | external side of plasma membrane |
A | 0016787 | molecular_function | hydrolase activity |
A | 0019239 | molecular_function | deaminase activity |
A | 0031410 | cellular_component | cytoplasmic vesicle |
A | 0042110 | biological_process | T cell activation |
A | 0043103 | biological_process | hypoxanthine salvage |
A | 0046103 | biological_process | inosine biosynthetic process |
A | 0046872 | molecular_function | metal ion binding |
A | 0046936 | molecular_function | 2'-deoxyadenosine deaminase activity |
A | 0060169 | biological_process | negative regulation of adenosine receptor signaling pathway |
A | 0060205 | cellular_component | cytoplasmic vesicle lumen |
A | 0070161 | cellular_component | anchoring junction |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE ZN A 400 |
Chain | Residue |
A | HIS15 |
A | HIS17 |
A | HIS214 |
A | ASP295 |
A | HOH1195 |
site_id | AC2 |
Number of Residues | 14 |
Details | BINDING SITE FOR RESIDUE FR3 A 1001 |
Chain | Residue |
A | TYR102 |
A | LEU106 |
A | MET155 |
A | HIS157 |
A | GLY184 |
A | ASP185 |
A | ASP296 |
A | HOH1044 |
A | HOH1128 |
A | HOH1228 |
A | HIS17 |
A | ASP19 |
A | LEU62 |
A | PHE65 |
Functional Information from PROSITE/UniProt
site_id | PS00485 |
Number of Residues | 7 |
Details | A_DEAMINASE Adenosine and AMP deaminase signature. SLNTDDP |
Chain | Residue | Details |
A | SER291-PRO297 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 1 |
Details | ACT_SITE: Proton donor => ECO:0000250|UniProtKB:P03958 |
Chain | Residue | Details |
A | VAL218 |
site_id | SWS_FT_FI2 |
Number of Residues | 4 |
Details | BINDING: BINDING => ECO:0000269|PubMed:12554940, ECO:0000269|PubMed:14709046, ECO:0000269|PubMed:15139750, ECO:0000269|PubMed:15213224, ECO:0000269|PubMed:15239652, ECO:0000269|PubMed:15695814, ECO:0000269|PubMed:16033254, ECO:0000269|PubMed:16060665, ECO:0000269|PubMed:18549808, ECO:0007744|PDB:1KRM, ECO:0007744|PDB:1NDV, ECO:0007744|PDB:1NDW, ECO:0007744|PDB:1NDY, ECO:0007744|PDB:1NDZ, ECO:0007744|PDB:1O5R, ECO:0007744|PDB:1QXL, ECO:0007744|PDB:1VFL |
Chain | Residue | Details |
A | VAL16 | |
A | LEU18 | |
A | ALA215 | |
A | ASP296 |
site_id | SWS_FT_FI3 |
Number of Residues | 1 |
Details | BINDING: BINDING => ECO:0000269|PubMed:12554940, ECO:0000269|PubMed:14709046, ECO:0000269|PubMed:15139750, ECO:0000269|PubMed:15239652, ECO:0000269|PubMed:16033254, ECO:0000269|PubMed:16060665, ECO:0000269|PubMed:18549808, ECO:0007744|PDB:1NDW, ECO:0007744|PDB:1NDY, ECO:0007744|PDB:1NDZ, ECO:0007744|PDB:1O5R, ECO:0007744|PDB:1QXL |
Chain | Residue | Details |
A | GLY20 |
site_id | SWS_FT_FI4 |
Number of Residues | 1 |
Details | BINDING: BINDING => ECO:0000269|PubMed:14709046, ECO:0000269|PubMed:16060665, ECO:0007744|PDB:1NDY, ECO:0007744|PDB:1WXY |
Chain | Residue | Details |
A | ASP185 |
site_id | SWS_FT_FI5 |
Number of Residues | 1 |
Details | BINDING: BINDING => ECO:0000269|PubMed:12554940, ECO:0000269|PubMed:14709046, ECO:0000269|PubMed:15139750, ECO:0000269|PubMed:15239652, ECO:0000269|PubMed:16033254, ECO:0000269|PubMed:18549808, ECO:0007744|PDB:1NDW, ECO:0007744|PDB:1NDY, ECO:0007744|PDB:1NDZ, ECO:0007744|PDB:1O5R, ECO:0007744|PDB:1QXL |
Chain | Residue | Details |
A | PRO297 |
site_id | SWS_FT_FI6 |
Number of Residues | 2 |
Details | SITE: Important for interaction with adenosine receptors and increasing their affinity for agonists => ECO:0000250|UniProtKB:P00813 |
Chain | Residue | Details |
A | PRO59 | |
A | ALA63 |
site_id | SWS_FT_FI7 |
Number of Residues | 1 |
Details | SITE: Important for catalytic activity => ECO:0000250|UniProtKB:P03958 |
Chain | Residue | Details |
A | GLY239 |
site_id | SWS_FT_FI8 |
Number of Residues | 1 |
Details | MOD_RES: N-acetylalanine => ECO:0000250|UniProtKB:P00813 |
Chain | Residue | Details |
A | GLN3 |
site_id | SWS_FT_FI9 |
Number of Residues | 2 |
Details | MOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:P00813 |
Chain | Residue | Details |
A | PRO55 | |
A | THR233 |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 4 |
Details | Annotated By Reference To The Literature 1a4l |
Chain | Residue | Details |
A | HIS238 | |
A | TYR240 | |
A | GLU217 | |
A | ASP295 |