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

4YO6

Irak4-inhibitor co-structure

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 Residues9
Detailsbinding site for residue 4GD A 501
ChainResidue
AMET192
AGLY193
AVAL200
AALA211
ATYR262
AVAL263
ATYR264
AMET265
AGLY268

site_idAC2
Number of Residues11
Detailsbinding site for residue 4GD B 501
ChainResidue
BMET192
BGLY193
BVAL200
BALA211
BTYR262
BVAL263
BTYR264
BMET265
BGLY268
BLEU318
BASP329

site_idAC3
Number of Residues10
Detailsbinding site for residue 4GD C 501
ChainResidue
CMET192
CALA211
CLYS213
CVAL246
CTYR262
CVAL263
CTYR264
CMET265
CGLY268
CLEU318

site_idAC4
Number of Residues11
Detailsbinding site for residue 4GD D 501
ChainResidue
DMET192
DGLY193
DVAL200
DALA211
DTYR262
DVAL263
DTYR264
DMET265
DGLY268
DLEU318
DHOH654

site_idAC5
Number of Residues15
Detailsbinding site for residue 4GD D 502
ChainResidue
BCYS289
BASP422
BSER425
BMET457
BTHR458
BALA459
CTYR171
CHOH602
CHOH604
DHIS166
DPHE168
DVAL205
DASN206
DTHR208
DVAL210

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
ATPO342
BTPO342
CTPO342
DTPO342

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

222036

PDB entries from 2024-07-03

PDB statisticsPDBj update infoContact PDBjnumon