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1H1W

High resolution crystal structure of the human PDK1 catalytic domain

Functional Information from GO Data
ChainGOidnamespacecontents
A0004672molecular_functionprotein kinase activity
A0004674molecular_functionprotein serine/threonine kinase activity
A0005524molecular_functionATP binding
A0006468biological_processprotein phosphorylation
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 A 1368
ChainResidue
ALYS76
AARG131
ATHR148
APHE149
AGLN150
AHOH2043

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 A 1369
ChainResidue
AGOL1363
AHOH2194
AHOH2195
ATYR146
ASER160
AGLN220

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 1370
ChainResidue
AARG106
APRO140
AGOL1363
AGOL1365
AHOH2195

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 1371
ChainResidue
ALYS83
ATHR346
ATRP347
AGLU348

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 1372
ChainResidue
AARG75
AARG136
ALYS199

site_idAC6
Number of Residues18
DetailsBINDING SITE FOR RESIDUE ATP A 1373
ChainResidue
AGLY89
AGLY91
ASER92
ASER94
AVAL96
AALA109
ALYS111
ASER160
AALA162
AGLU166
ALEU212
AGOL1366
AHOH2104
AHOH2196
AHOH2197
AHOH2198
AHOH2199
AHOH2200

site_idAC7
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL A 1360
ChainResidue
APHE84
ALYS154
ATYR156
AGLU328
AGLU331
AGLY332
AHOH2187

site_idAC8
Number of Residues10
DetailsBINDING SITE FOR RESIDUE GOL A 1361
ChainResidue
AALA103
ATHR104
ASER105
AHIS139
ASER191
ATRP347
AGLU348
AASN349
ALEU350
AHIS351

site_idAC9
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 1362
ChainResidue
APHE82
ALYS83
APHE84
AGLU194
AGLY334
ALYS337
AHOH2187
AHOH2189

site_idBC1
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL A 1363
ChainResidue
AARG106
AGLU107
ATYR108
ASER160
ATYR161
AGOL1365
ASO41369
ASO41370
AHOH2069

site_idBC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL A 1364
ChainResidue
ALYS315
AMET330
AHOH2010
AHOH2153
AHOH2191
AHOH2192
AHOH2193

site_idBC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL A 1365
ChainResidue
ASER105
AARG106
AGLU107
AHIS351
AGLN352
AGOL1363
ASO41370

site_idBC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL A 1366
ChainResidue
ASER94
ALYS111
AGLU130
AATP1373
AHOH2111
AHOH2200

site_idBC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 1367
ChainResidue
AHOH2143
ALEU297
ATYR299
APHE301

Functional Information from PROSITE/UniProt
site_idPS00107
Number of Residues24
DetailsPROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. LGEGSFSTVVlArelatsre..........YAIK
ChainResidueDetails
ALEU88-LYS111

site_idPS00108
Number of Residues13
DetailsPROTEIN_KINASE_ST Serine/Threonine protein kinases active-site signature. IiHrDLKpeNILL
ChainResidueDetails
AILE201-LEU213

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues44
DetailsRegion: {"description":"PIF-pocket","evidences":[{"source":"PubMed","id":"22999883","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues1
DetailsActive site: {"description":"Proton acceptor","evidences":[{"source":"PROSITE-ProRule","id":"PRU00159","evidenceCode":"ECO:0000255"},{"source":"PROSITE-ProRule","id":"PRU10027","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues7
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"12169624","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"15741170","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"22999883","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues1
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"22999883","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues1
DetailsModified 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."]}}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues1
DetailsModified residue: {"description":"N6-acetyllysine","evidences":[{"source":"UniProtKB","id":"Q9Z2A0","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues1
DetailsModified residue: {"description":"Phosphothreonine; by MELK","evidences":[{"source":"PubMed","id":"22544756","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
AGLU209
AASP205

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
ALYS207
AASP205

site_idCSA3
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
ALYS207
ATHR245
AASP205

site_idCSA4
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
ALYS207
AASN210
AASP205

239803

PDB entries from 2025-08-06

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