1H1W
High resolution crystal structure of the human PDK1 catalytic domain
Functional Information from GO Data
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE SO4 A 1368 |
Chain | Residue |
A | LYS76 |
A | ARG131 |
A | THR148 |
A | PHE149 |
A | GLN150 |
A | HOH2043 |
site_id | AC2 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE SO4 A 1369 |
Chain | Residue |
A | GOL1363 |
A | HOH2194 |
A | HOH2195 |
A | TYR146 |
A | SER160 |
A | GLN220 |
site_id | AC3 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE SO4 A 1370 |
Chain | Residue |
A | ARG106 |
A | PRO140 |
A | GOL1363 |
A | GOL1365 |
A | HOH2195 |
site_id | AC4 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE SO4 A 1371 |
Chain | Residue |
A | LYS83 |
A | THR346 |
A | TRP347 |
A | GLU348 |
site_id | AC5 |
Number of Residues | 3 |
Details | BINDING SITE FOR RESIDUE SO4 A 1372 |
Chain | Residue |
A | ARG75 |
A | ARG136 |
A | LYS199 |
site_id | AC6 |
Number of Residues | 18 |
Details | BINDING SITE FOR RESIDUE ATP A 1373 |
Chain | Residue |
A | GLY89 |
A | GLY91 |
A | SER92 |
A | SER94 |
A | VAL96 |
A | ALA109 |
A | LYS111 |
A | SER160 |
A | ALA162 |
A | GLU166 |
A | LEU212 |
A | GOL1366 |
A | HOH2104 |
A | HOH2196 |
A | HOH2197 |
A | HOH2198 |
A | HOH2199 |
A | HOH2200 |
site_id | AC7 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE GOL A 1360 |
Chain | Residue |
A | PHE84 |
A | LYS154 |
A | TYR156 |
A | GLU328 |
A | GLU331 |
A | GLY332 |
A | HOH2187 |
site_id | AC8 |
Number of Residues | 10 |
Details | BINDING SITE FOR RESIDUE GOL A 1361 |
Chain | Residue |
A | ALA103 |
A | THR104 |
A | SER105 |
A | HIS139 |
A | SER191 |
A | TRP347 |
A | GLU348 |
A | ASN349 |
A | LEU350 |
A | HIS351 |
site_id | AC9 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE GOL A 1362 |
Chain | Residue |
A | PHE82 |
A | LYS83 |
A | PHE84 |
A | GLU194 |
A | GLY334 |
A | LYS337 |
A | HOH2187 |
A | HOH2189 |
site_id | BC1 |
Number of Residues | 9 |
Details | BINDING SITE FOR RESIDUE GOL A 1363 |
Chain | Residue |
A | ARG106 |
A | GLU107 |
A | TYR108 |
A | SER160 |
A | TYR161 |
A | GOL1365 |
A | SO41369 |
A | SO41370 |
A | HOH2069 |
site_id | BC2 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE GOL A 1364 |
Chain | Residue |
A | LYS315 |
A | MET330 |
A | HOH2010 |
A | HOH2153 |
A | HOH2191 |
A | HOH2192 |
A | HOH2193 |
site_id | BC3 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE GOL A 1365 |
Chain | Residue |
A | SER105 |
A | ARG106 |
A | GLU107 |
A | HIS351 |
A | GLN352 |
A | GOL1363 |
A | SO41370 |
site_id | BC4 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE GOL A 1366 |
Chain | Residue |
A | SER94 |
A | LYS111 |
A | GLU130 |
A | ATP1373 |
A | HOH2111 |
A | HOH2200 |
site_id | BC5 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE GOL A 1367 |
Chain | Residue |
A | HOH2143 |
A | LEU297 |
A | TYR299 |
A | PHE301 |
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
site_id | SWS_FT_FI1 |
Number of Residues | 44 |
Details | Region: {"description":"PIF-pocket","evidences":[{"source":"PubMed","id":"22999883","evidenceCode":"ECO:0000305"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 1 |
Details | Active site: {"description":"Proton acceptor","evidences":[{"source":"PROSITE-ProRule","id":"PRU00159","evidenceCode":"ECO:0000255"},{"source":"PROSITE-ProRule","id":"PRU10027","evidenceCode":"ECO:0000255"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 7 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"12169624","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"15741170","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"22999883","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 1 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"22999883","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI5 |
Number of Residues | 1 |
Details | Modified residue: {"description":"Phosphoserine; by autocatalysis","evidences":[{"source":"PubMed","id":"10455013","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"11481331","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"15772071","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"16780920","evidenceCode":"ECO:0000269"},{"source":"Reference","evidenceCode":"ECO:0000269","citation":{"citationType":"submission","publicationDate":"MAR-2009","submissionDatabase":"UniProtKB","authors":["Bienvenut W.V.","Waridel P.","Quadroni M."]}}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI6 |
Number of Residues | 1 |
Details | Modified residue: {"description":"N6-acetyllysine","evidences":[{"source":"UniProtKB","id":"Q9Z2A0","evidenceCode":"ECO:0000250"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI7 |
Number of Residues | 1 |
Details | Modified residue: {"description":"Phosphothreonine; by MELK","evidences":[{"source":"PubMed","id":"22544756","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1ir3 |
Chain | Residue | Details |
A | GLU209 | |
A | ASP205 |
site_id | CSA2 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1ir3 |
Chain | Residue | Details |
A | LYS207 | |
A | ASP205 |
site_id | CSA3 |
Number of Residues | 3 |
Details | Annotated By Reference To The Literature 1ir3 |
Chain | Residue | Details |
A | LYS207 | |
A | THR245 | |
A | ASP205 |
site_id | CSA4 |
Number of Residues | 3 |
Details | Annotated By Reference To The Literature 1ir3 |
Chain | Residue | Details |
A | LYS207 | |
A | ASN210 | |
A | ASP205 |