Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004672 | molecular_function | protein kinase activity |
A | 0004674 | molecular_function | protein serine/threonine kinase activity |
A | 0005524 | molecular_function | ATP binding |
A | 0006468 | biological_process | protein phosphorylation |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE 3RC A 0 |
Chain | Residue |
A | SER94 |
A | ALA109 |
A | LYS111 |
A | SER160 |
A | TYR161 |
A | ALA162 |
A | LEU212 |
A | THR222 |
A | HOH448 |
Functional Information from PROSITE/UniProt
site_id | PS00107 |
Number of Residues | 24 |
Details | PROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. LGEGSFSTVVlArelatsre..........YAIK |
Chain | Residue | Details |
A | LEU88-LYS111 | |
site_id | PS00108 |
Number of Residues | 13 |
Details | PROTEIN_KINASE_ST Serine/Threonine protein kinases active-site signature. IiHrDLKpeNILL |
Chain | Residue | Details |
A | ILE201-LEU213 | |
Functional Information from SwissProt/UniProt
Chain | Residue | Details |
A | ASP205 | |
Chain | Residue | Details |
A | SER92 | |
A | LYS111 | |
A | SER160 | |
A | GLU166 | |
A | ASP223 | |
Chain | Residue | Details |
A | GLU209 | |
Chain | Residue | Details |
A | SEP241 | |
Chain | Residue | Details |
A | LYS304 | |
Chain | Residue | Details |
A | THR354 | |