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3GP0

Crystal Structure of Human Mitogen Activated Protein Kinase 11 (p38 beta) in complex with Nilotinib

Functional Information from GO Data
ChainGOidnamespacecontents
A0000165biological_processMAPK cascade
A0000166molecular_functionnucleotide binding
A0001649biological_processosteoblast differentiation
A0004672molecular_functionprotein kinase activity
A0004674molecular_functionprotein serine/threonine kinase activity
A0004707molecular_functionMAP kinase activity
A0005515molecular_functionprotein binding
A0005524molecular_functionATP binding
A0005634cellular_componentnucleus
A0005654cellular_componentnucleoplasm
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006468biological_processprotein phosphorylation
A0010628biological_processpositive regulation of gene expression
A0016301molecular_functionkinase activity
A0016740molecular_functiontransferase activity
A0031098biological_processstress-activated protein kinase signaling cascade
A0032735biological_processpositive regulation of interleukin-12 production
A0035556biological_processintracellular signal transduction
A0038066biological_processp38MAPK cascade
A0045648biological_processpositive regulation of erythrocyte differentiation
A0051149biological_processpositive regulation of muscle cell differentiation
A0051403biological_processstress-activated MAPK cascade
A0051604biological_processprotein maturation
A0060038biological_processcardiac muscle cell proliferation
A0060043biological_processregulation of cardiac muscle cell proliferation
A0060044biological_processnegative regulation of cardiac muscle cell proliferation
A0060348biological_processbone development
A0070269biological_processpyroptotic inflammatory response
A0071347biological_processcellular response to interleukin-1
A0071493biological_processcellular response to UV-B
A0090398biological_processcellular senescence
A0098586biological_processcellular response to virus
A0106310molecular_functionprotein serine kinase activity
A1904784biological_processNLRP1 inflammasome complex assembly
Functional Information from PDB Data
site_idAC1
Number of Residues13
DetailsBINDING SITE FOR RESIDUE NIL A 1
ChainResidue
AALA51
ALEU167
AASP168
APHE169
AHOH441
ALYS53
AARG67
AGLU71
AVAL83
AILE84
ATHR106
AMET109
AHIS148

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE EDO A 351
ChainResidue
AGLN22
AGLN25
AARG73
AASP324
AHOH390
AHOH518

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CL A 352
ChainResidue
AARG23
AARG45
AASP88
AHOH542

Functional Information from PROSITE/UniProt
site_idPS00107
Number of Residues25
DetailsPROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. VGSGAYGSVCsAydarlrqkv.........AVKK
ChainResidueDetails
AVAL30-LYS54

site_idPS01351
Number of Residues104
DetailsMAPK MAP kinase signature. FqsliharrtyRElrllkhlkhenviglldvftpatsiedfsevylvttlmgadlnnivkcqalsdehvqflvyqllrglkyihsagiih.........RDlKpsnvavnedC
ChainResidueDetails
APHE59-CYS162

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues20
DetailsRegion: {"description":"Disordered","evidences":[{"source":"SAM","id":"MobiDB-lite","evidenceCode":"ECO:0000256"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues12
DetailsCompositional bias: {"description":"Acidic residues","evidences":[{"source":"SAM","id":"MobiDB-lite","evidenceCode":"ECO:0000256"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues1
DetailsActive site: {"description":"Proton acceptor","evidences":[{"source":"PROSITE-ProRule","id":"PRU00159","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues1
DetailsBinding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU00159","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues1
DetailsBinding site: {}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues1
DetailsModified residue: {"description":"Phosphotyrosine; by MAP2K3, MAP2K4 and MAP2K6","evidences":[{"source":"PubMed","id":"38270553","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"15356147","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues1
DetailsModified residue: {"description":"Phosphotyrosine; by ZAP70","evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
ASER154
AASP150

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
ALYS152
AASP150

site_idCSA3
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
ALYS152
ATHR185
AASP150

site_idCSA4
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
AASN155
ALYS152
AASP150

239149

PDB entries from 2025-07-23

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