Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

5K7G

IRAK4 in complex with AZ3862

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 Residues3
Detailsbinding site for residue SO4 A 501
ChainResidue
AGLY195
AGLY196
ALYS313

site_idAC2
Number of Residues3
Detailsbinding site for residue SO4 A 502
ChainResidue
ATHR365
ALYS367
ALYS441

site_idAC3
Number of Residues11
Detailsbinding site for residue 6R0 A 503
ChainResidue
ATYR262
AVAL263
ATYR264
AMET265
AASP272
ALEU318
AHOH627
AHOH646
AMET192
AALA211
ALYS213

site_idAC4
Number of Residues4
Detailsbinding site for residue SO4 B 501
ChainResidue
AHIS166
ASER167
BHIS166
BSER167

site_idAC5
Number of Residues3
Detailsbinding site for residue SO4 B 502
ChainResidue
BTHR365
BLYS367
BLYS441

site_idAC6
Number of Residues9
Detailsbinding site for residue 6R0 B 503
ChainResidue
BMET192
BALA211
BLYS213
BTYR262
BVAL263
BMET265
BASP272
BLEU318
BHOH641

site_idAC7
Number of Residues14
Detailsbinding site for residue 6R0 C 501
ChainResidue
CMET192
CVAL200
CALA211
CLYS213
CTYR262
CVAL263
CTYR264
CMET265
CASP272
CLEU277
CLEU318
CSER328
CHOH651
CHOH652

site_idAC8
Number of Residues3
Detailsbinding site for residue SO4 D 501
ChainResidue
DPHE165
DHIS166
DSER167

site_idAC9
Number of Residues11
Detailsbinding site for residue 6R0 D 502
ChainResidue
DMET192
DVAL200
DALA211
DLYS213
DTYR262
DVAL263
DTYR264
DMET265
DASP272
DLEU318
DHOH645

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

222926

PDB entries from 2024-07-24

PDB statisticsPDBj update infoContact PDBjnumon