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3ORN

Mitogen-activated protein kinase kinase 1 (MEK1) in complex with CH4987655 and MgAMP-PNP

Functional Information from GO Data
ChainGOidnamespacecontents
A0004672molecular_functionprotein kinase activity
A0005524molecular_functionATP binding
A0006468biological_processprotein phosphorylation
Functional Information from PDB Data
site_idAC1
Number of Residues20
DetailsBINDING SITE FOR RESIDUE ANP A 1
ChainResidue
AMG2
AGLU144
AMET146
ASER150
AGLN153
ALYS192
ASER194
AASN195
ALEU197
AASP208
A3OR400
AGLY75
AHOH435
AGLY77
AASN78
AGLY79
AVAL82
AALA95
ALYS97
AMET143

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE MG A 2
ChainResidue
AANP1
AASN195
AASP208

site_idAC3
Number of Residues18
DetailsBINDING SITE FOR RESIDUE 3OR A 400
ChainResidue
AANP1
AGLY80
ALYS97
ALEU115
ALEU118
AVAL127
AILE141
AMET143
AHIS188
AARG189
AASP208
APHE209
AGLY210
AVAL211
ASER212
ALEU215
AILE216
AASN221

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PGE A 401
ChainResidue
AILE186
AVAL211
AGLY213
AHOH423

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 402
ChainResidue
ATHR226
AARG227
AHOH416

site_idAC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 403
ChainResidue
ALEU101
AGLU102
AHIS239

site_idAC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 404
ChainResidue
ALYS104
AARG181
ASER241
AVAL242

site_idAC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 405
ChainResidue
AGLY202
AVAL369
AASP370
APHE371
AALA372

site_idAC9
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 406
ChainResidue
ASER331
ALEU332
AGLU333
AARG363

site_idBC1
Number of Residues1
DetailsBINDING SITE FOR RESIDUE SO4 A 407
ChainResidue
ALYS70

Functional Information from PROSITE/UniProt
site_idPS00107
Number of Residues24
DetailsPROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. LGAGNGGVVFkVshkpsglv..........MARK
ChainResidueDetails
ALEU74-LYS97

site_idPS00108
Number of Residues13
DetailsPROTEIN_KINASE_ST Serine/Threonine protein kinases active-site signature. ImHrDVKpsNILV
ChainResidueDetails
AILE186-VAL198

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton acceptor => ECO:0000255|PROSITE-ProRule:PRU00159, ECO:0000255|PROSITE-ProRule:PRU10027
ChainResidueDetails
AASP190

site_idSWS_FT_FI2
Number of Residues5
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00159, ECO:0000269|PubMed:15543157, ECO:0000269|PubMed:17880056, ECO:0000269|PubMed:18951019, ECO:0000269|PubMed:19019675, ECO:0000269|PubMed:19706763, ECO:0000269|PubMed:21310613
ChainResidueDetails
AMET143
ASER150
ALYS192
AASP208
ALEU74

site_idSWS_FT_FI3
Number of Residues1
DetailsBINDING: BINDING => ECO:0000269|PubMed:19161339, ECO:0007744|PDB:3EQH
ChainResidueDetails
ALYS97

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:19161339, ECO:0007744|PDB:3EQF
ChainResidueDetails
ASER194
AGLU144

site_idSWS_FT_FI5
Number of Residues1
DetailsMOD_RES: Phosphoserine; by BRAF and RAF1 => ECO:0000269|PubMed:10409742, ECO:0000269|PubMed:20956560, ECO:0000269|PubMed:29433126, ECO:0000269|PubMed:8131746
ChainResidueDetails
ASER218

site_idSWS_FT_FI6
Number of Residues1
DetailsMOD_RES: Phosphoserine; by BRAF and RAF1 => ECO:0000269|PubMed:20956560, ECO:0000269|PubMed:29433126, ECO:0000269|PubMed:8131746
ChainResidueDetails
ASER222

site_idSWS_FT_FI7
Number of Residues1
DetailsMOD_RES: Phosphothreonine => ECO:0007744|PubMed:18691976
ChainResidueDetails
AVAL318

site_idSWS_FT_FI8
Number of Residues1
DetailsMOD_RES: Phosphothreonine; by MAPK1 => ECO:0000250|UniProtKB:Q01986
ChainResidueDetails
ALYS324

site_idSWS_FT_FI9
Number of Residues1
DetailsMOD_RES: Phosphoserine; by PAK => ECO:0000269|PubMed:16129686
ChainResidueDetails
APHE330

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PDB entries from 2024-06-12

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