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4HPU

Crystal structure of the catalytic subunit of cAMP-dependent protein kinase displaying partial phosphoryl transfer of AMP-PNP onto a substrate peptide

Functional Information from GO Data
ChainGOidnamespacecontents
E0000122biological_processnegative regulation of transcription by RNA polymerase II
E0000287molecular_functionmagnesium ion binding
E0001669cellular_componentacrosomal vesicle
E0001707biological_processmesoderm formation
E0001843biological_processneural tube closure
E0004672molecular_functionprotein kinase activity
E0004674molecular_functionprotein serine/threonine kinase activity
E0004691molecular_functioncAMP-dependent protein kinase activity
E0004712molecular_functionprotein serine/threonine/tyrosine kinase activity
E0005515molecular_functionprotein binding
E0005524molecular_functionATP binding
E0005634cellular_componentnucleus
E0005654cellular_componentnucleoplasm
E0005737cellular_componentcytoplasm
E0005739cellular_componentmitochondrion
E0005813cellular_componentcentrosome
E0005829cellular_componentcytosol
E0005886cellular_componentplasma membrane
E0005930cellular_componentaxoneme
E0005952cellular_componentcAMP-dependent protein kinase complex
E0006397biological_processmRNA processing
E0006468biological_processprotein phosphorylation
E0006611biological_processprotein export from nucleus
E0007189biological_processadenylate cyclase-activating G protein-coupled receptor signaling pathway
E0007193biological_processadenylate cyclase-inhibiting G protein-coupled receptor signaling pathway
E0016607cellular_componentnuclear speck
E0018105biological_processpeptidyl-serine phosphorylation
E0019901molecular_functionprotein kinase binding
E0019904molecular_functionprotein domain specific binding
E0030145molecular_functionmanganese ion binding
E0031410cellular_componentcytoplasmic vesicle
E0031514cellular_componentmotile cilium
E0031594cellular_componentneuromuscular junction
E0031625molecular_functionubiquitin protein ligase binding
E0032024biological_processpositive regulation of insulin secretion
E0034237molecular_functionprotein kinase A regulatory subunit binding
E0034605biological_processcellular response to heat
E0036126cellular_componentsperm flagellum
E0044853cellular_componentplasma membrane raft
E0045542biological_processpositive regulation of cholesterol biosynthetic process
E0045667biological_processregulation of osteoblast differentiation
E0045722biological_processpositive regulation of gluconeogenesis
E0045879biological_processnegative regulation of smoothened signaling pathway
E0046827biological_processpositive regulation of protein export from nucleus
E0048240biological_processsperm capacitation
E0048471cellular_componentperinuclear region of cytoplasm
E0050804biological_processmodulation of chemical synaptic transmission
E0051726biological_processregulation of cell cycle
E0061136biological_processregulation of proteasomal protein catabolic process
E0070417biological_processcellular response to cold
E0070613biological_processregulation of protein processing
E0071333biological_processcellular response to glucose stimulus
E0071374biological_processcellular response to parathyroid hormone stimulus
E0071377biological_processcellular response to glucagon stimulus
E0097546cellular_componentciliary base
E0098794cellular_componentpostsynapse
E0098978cellular_componentglutamatergic synapse
E0099170biological_processpostsynaptic modulation of chemical synaptic transmission
E0106310molecular_functionprotein serine kinase activity
E0141156biological_processcAMP/PKA signal transduction
E1904262biological_processnegative regulation of TORC1 signaling
E1904539biological_processnegative regulation of glycolytic process through fructose-6-phosphate
E1990044biological_processprotein localization to lipid droplet
E2000810biological_processregulation of bicellular tight junction assembly
I0004862molecular_functioncAMP-dependent protein kinase inhibitor activity
I0006469biological_processnegative regulation of protein kinase activity
Functional Information from PDB Data
site_idAC1
Number of Residues2
DetailsBINDING SITE FOR RESIDUE MYR E 401
ChainResidue
ELEU152
EGLU155

site_idAC2
Number of Residues23
DetailsBINDING SITE FOR RESIDUE ANP E 402
ChainResidue
EVAL123
EGLU127
EGLU170
EASN171
ELEU173
ETHR183
EASP184
EPHE327
EMG403
EMG404
EHOH521
EHOH596
EHOH740
IARG18
ISEP21
IHOH714
EVAL57
EALA70
ELYS72
EVAL104
EMET120
EGLU121
ETYR122

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG E 403
ChainResidue
EASP184
EANP402
EHOH595
ISEP21
IANP600
IHOH714

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG E 404
ChainResidue
EASN171
EASP184
EANP402
EHOH596
IANP600
IHOH747

site_idAC5
Number of Residues31
DetailsBINDING SITE FOR RESIDUE ANP I 600
ChainResidue
ELEU49
EGLY50
EGLY52
EVAL57
EALA70
ELYS72
EVAL104
EMET120
EGLU121
EVAL123
EGLU127
ELYS168
EGLU170
EASN171
ELEU173
ETHR183
EASP184
EPHE327
EMG403
EMG404
EHOH521
EHOH595
EHOH596
IARG18
IALA20
ISEP21
IHOH702
IHOH714
IHOH729
IHOH747
IHOH750

site_idAC6
Number of Residues77
DetailsBINDING SITE FOR CHAIN I OF CAMP-DEPENDENT PROTEIN KINASE INHIBITOR ALPHA
ChainResidue
ETYR330
EGLU349
EANP402
EMG403
EHOH514
EHOH518
EHOH592
EHOH595
EHOH728
EHOH882
IANP600
IHOH701
IHOH703
IHOH704
IHOH705
IHOH706
IHOH707
IHOH708
IHOH709
IHOH710
IHOH711
IHOH712
IHOH713
IHOH714
IHOH715
IHOH716
IHOH717
IHOH718
IHOH719
IHOH720
IHOH721
IHOH723
IHOH726
IHOH729
IHOH731
IHOH732
IHOH735
IHOH737
IHOH740
IHOH742
IHOH744
IHOH746
IHOH747
IHOH748
IHOH749
IHOH750
ETHR51
ESER53
ELEU82
EGLN84
EGLU86
ELEU89
EARG93
EGLU127
EPHE129
EARG133
ELYS168
EPRO169
EGLU170
EASP184
EPHE187
ELYS189
EARG190
EVAL191
ELYS192
ELEU198
ECYS199
EGLY200
ETHR201
EGLU203
EGLU230
ETYR235
EPRO236
EPHE239
EALA240
EASP241
EILE246

Functional Information from PROSITE/UniProt
site_idPS00107
Number of Residues24
DetailsPROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. LGTGSFGRVMlVkhkesgnh..........YAMK
ChainResidueDetails
ELEU49-LYS72

site_idPS00108
Number of Residues13
DetailsPROTEIN_KINASE_ST Serine/Threonine protein kinases active-site signature. LiYrDLKpeNLLI
ChainResidueDetails
ELEU162-ILE174

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues3
DetailsSITE: Important for inhibition => ECO:0000250
ChainResidueDetails
IARG15
IARG18
IARG19

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING:
ChainResidueDetails
ELEU49
ELYS72
EGLU121
ELYS168

site_idSWS_FT_FI3
Number of Residues1
DetailsMOD_RES: Deamidated asparagine; partial => ECO:0000269|PubMed:11141074
ChainResidueDetails
EASN2

site_idSWS_FT_FI4
Number of Residues1
DetailsMOD_RES: Phosphoserine; by autocatalysis => ECO:0000269|PubMed:11141074, ECO:0000269|PubMed:8395513
ChainResidueDetails
ESER10

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: Phosphothreonine => ECO:0000250|UniProtKB:P17612
ChainResidueDetails
ETHR48
ETHR195

site_idSWS_FT_FI6
Number of Residues1
DetailsMOD_RES: Phosphoserine => ECO:0000269|PubMed:22323819, ECO:0000305|PubMed:8395513
ChainResidueDetails
ESEP139

site_idSWS_FT_FI7
Number of Residues1
DetailsMOD_RES: Phosphothreonine; by PDPK1 => ECO:0000269|PubMed:22323819, ECO:0000269|PubMed:8395513, ECO:0000269|PubMed:9707564
ChainResidueDetails
ETPO197

site_idSWS_FT_FI8
Number of Residues1
DetailsMOD_RES: Phosphotyrosine => ECO:0000269|PubMed:21866565
ChainResidueDetails
ETYR330

site_idSWS_FT_FI9
Number of Residues1
DetailsMOD_RES: Phosphoserine => ECO:0000305|PubMed:8395513
ChainResidueDetails
ESEP338

site_idSWS_FT_FI10
Number of Residues1
DetailsLIPID: N-myristoyl glycine => ECO:0000269|PubMed:11141074
ChainResidueDetails
EGLY1

227111

PDB entries from 2024-11-06

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