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6O8U

Crystal structure of IRAK4 in complex with compound 23

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0004672molecular_functionprotein kinase activity
A0004674molecular_functionprotein serine/threonine kinase activity
A0005524molecular_functionATP binding
A0006468biological_processprotein phosphorylation
A0007165biological_processsignal transduction
B0000287molecular_functionmagnesium ion binding
B0004672molecular_functionprotein kinase activity
B0004674molecular_functionprotein serine/threonine kinase activity
B0005524molecular_functionATP binding
B0006468biological_processprotein phosphorylation
B0007165biological_processsignal transduction
C0000287molecular_functionmagnesium ion binding
C0004672molecular_functionprotein kinase activity
C0004674molecular_functionprotein serine/threonine kinase activity
C0005524molecular_functionATP binding
C0006468biological_processprotein phosphorylation
C0007165biological_processsignal transduction
D0000287molecular_functionmagnesium ion binding
D0004672molecular_functionprotein kinase activity
D0004674molecular_functionprotein serine/threonine kinase activity
D0005524molecular_functionATP binding
D0006468biological_processprotein phosphorylation
D0007165biological_processsignal transduction
Functional Information from PDB Data
site_idAC1
Number of Residues13
Detailsbinding site for residue LS7 A 501
ChainResidue
AILE185
APRO266
AGLY268
ALEU318
AHOH636
AMET192
AGLY193
AVAL200
AALA211
ATYR262
AVAL263
ATYR264
AMET265

site_idAC2
Number of Residues4
Detailsbinding site for residue SO4 A 502
ChainResidue
ALYS448
DTYR204
DTHR208
DTHR209

site_idAC3
Number of Residues7
Detailsbinding site for residue GOL A 503
ChainResidue
ALEU271
ATYR354
AGLU379
APRO385
AALA386
AVAL387
AHOH650

site_idAC4
Number of Residues14
Detailsbinding site for residue LS7 B 501
ChainResidue
BMET192
BGLY193
BVAL200
BALA211
BTYR262
BVAL263
BTYR264
BMET265
BPRO266
BGLY268
BALA315
BLEU318
BASP329
BHOH660

site_idAC5
Number of Residues5
Detailsbinding site for residue SO4 B 502
ChainResidue
ALYS174
AASN179
BASP422
BSER423
CASN207

site_idAC6
Number of Residues13
Detailsbinding site for residue LS7 C 501
ChainResidue
CMET192
CGLY193
CVAL200
CALA211
CTYR262
CVAL263
CTYR264
CMET265
CPRO266
CGLY268
CALA315
CLEU318
CHOH639

site_idAC7
Number of Residues4
Detailsbinding site for residue SO4 C 502
ChainResidue
CTRP285
CCYS289
CASP422
CSER425

site_idAC8
Number of Residues12
Detailsbinding site for residue LS7 D 501
ChainResidue
DMET192
DGLY193
DVAL200
DALA211
DTYR262
DVAL263
DMET265
DPRO266
DGLY268
DALA315
DLEU318
DHOH648

site_idAC9
Number of Residues3
Detailsbinding site for residue SO4 D 502
ChainResidue
DTHR365
DLYS367
DLYS441

site_idAD1
Number of Residues4
Detailsbinding site for residue SO4 D 503
ChainResidue
AASN207
DASP422
DSER423
DHOH632

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton acceptor => ECO:0000255|PROSITE-ProRule:PRU00159
ChainResidueDetails
AASP311
BASP311
CASP311
DASP311

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00159
ChainResidueDetails
AMET192
BMET192
CMET192
DMET192

site_idSWS_FT_FI3
Number of Residues12
DetailsBINDING:
ChainResidueDetails
ALYS213
DLYS213
DLYS313
DASP329
ALYS313
AASP329
BLYS213
BLYS313
BASP329
CLYS213
CLYS313
CASP329

site_idSWS_FT_FI4
Number of Residues4
DetailsMOD_RES: Phosphothreonine => ECO:0000269|PubMed:17312103, ECO:0000269|Ref.32
ChainResidueDetails
ATHR342
BTHR342
CTHR342
DTHR342

site_idSWS_FT_FI5
Number of Residues4
DetailsMOD_RES: Phosphothreonine => ECO:0000269|PubMed:17161373, ECO:0000269|PubMed:17312103, ECO:0000269|Ref.32
ChainResidueDetails
ATPO345
BTPO345
CTPO345
DTPO345

site_idSWS_FT_FI6
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0000269|PubMed:17161373, ECO:0000269|PubMed:17312103
ChainResidueDetails
ASEP346
BSEP346
CSEP346
DSEP346

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PDB entries from 2024-10-16

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