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5EAR

Crystal structure of human WDR5 in complex with compound 9d

Functional Information from GO Data
ChainGOidnamespacecontents
A0000122biological_processnegative regulation of transcription by RNA polymerase II
A0000123cellular_componenthistone acetyltransferase complex
A0001501biological_processskeletal system development
A0005515molecular_functionprotein binding
A0005634cellular_componentnucleus
A0005654cellular_componentnucleoplasm
A0006094biological_processgluconeogenesis
A0006325biological_processchromatin organization
A0006355biological_processregulation of DNA-templated transcription
A0006357biological_processregulation of transcription by RNA polymerase II
A0035064molecular_functionmethylated histone binding
A0035097cellular_componenthistone methyltransferase complex
A0042393molecular_functionhistone binding
A0042800molecular_functionhistone H3K4 methyltransferase activity
A0044545cellular_componentNSL complex
A0044665cellular_componentMLL1/2 complex
A0044666cellular_componentMLL3/4 complex
A0045722biological_processpositive regulation of gluconeogenesis
A0045815biological_processtranscription initiation-coupled chromatin remodeling
A0045893biological_processpositive regulation of DNA-templated transcription
A0045995biological_processregulation of embryonic development
A0048188cellular_componentSet1C/COMPASS complex
A0051302biological_processregulation of cell division
A0051726biological_processregulation of cell cycle
A0071339cellular_componentMLL1 complex
A0072686cellular_componentmitotic spindle
A0090043biological_processregulation of tubulin deacetylation
A0140672cellular_componentATAC complex
B0000122biological_processnegative regulation of transcription by RNA polymerase II
B0000123cellular_componenthistone acetyltransferase complex
B0001501biological_processskeletal system development
B0005515molecular_functionprotein binding
B0005634cellular_componentnucleus
B0005654cellular_componentnucleoplasm
B0006094biological_processgluconeogenesis
B0006325biological_processchromatin organization
B0006355biological_processregulation of DNA-templated transcription
B0006357biological_processregulation of transcription by RNA polymerase II
B0035064molecular_functionmethylated histone binding
B0035097cellular_componenthistone methyltransferase complex
B0042393molecular_functionhistone binding
B0042800molecular_functionhistone H3K4 methyltransferase activity
B0044545cellular_componentNSL complex
B0044665cellular_componentMLL1/2 complex
B0044666cellular_componentMLL3/4 complex
B0045722biological_processpositive regulation of gluconeogenesis
B0045815biological_processtranscription initiation-coupled chromatin remodeling
B0045893biological_processpositive regulation of DNA-templated transcription
B0045995biological_processregulation of embryonic development
B0048188cellular_componentSet1C/COMPASS complex
B0051302biological_processregulation of cell division
B0051726biological_processregulation of cell cycle
B0071339cellular_componentMLL1 complex
B0072686cellular_componentmitotic spindle
B0090043biological_processregulation of tubulin deacetylation
B0140672cellular_componentATAC complex
Functional Information from PDB Data
site_idAC1
Number of Residues13
Detailsbinding site for residue 5MQ A 401
ChainResidue
ASER49
AILE305
AEDO406
AHOH575
AHOH578
ASER50
AALA65
AILE90
ASER91
APHE133
ASER175
ATYR191
ACYS261

site_idAC2
Number of Residues5
Detailsbinding site for residue EDO A 402
ChainResidue
ALYS123
AVAL158
ALYS159
AHOH560
AHOH705

site_idAC3
Number of Residues3
Detailsbinding site for residue EDO A 403
ChainResidue
ALYS165
ATHR200
AALA201

site_idAC4
Number of Residues3
Detailsbinding site for residue EDO A 404
ChainResidue
ALYS70
APHE79
AHOH501

site_idAC5
Number of Residues7
Detailsbinding site for residue EDO A 405
ChainResidue
ATHR40
ALEU206
AGLY299
ATHR301
AASP324
ATHR326
ALYS328

site_idAC6
Number of Residues4
Detailsbinding site for residue EDO A 406
ChainResidue
AASP107
APHE133
A5MQ401
AHOH514

site_idAC7
Number of Residues3
Detailsbinding site for residue EDO A 407
ChainResidue
APHE79
ALYS81
ATHR82

site_idAC8
Number of Residues4
Detailsbinding site for residue EDO A 408
ChainResidue
AASP98
AASN100
AHOH590
BLYS38

site_idAC9
Number of Residues4
Detailsbinding site for residue EDO A 409
ChainResidue
ATYR260
AASP302
AGLU322
AHOH542

site_idAD1
Number of Residues5
Detailsbinding site for residue EDO A 410
ChainResidue
ATYR228
ALYS250
AGLN289
AHOH507
AHOH535

site_idAD2
Number of Residues14
Detailsbinding site for residue 5MQ B 401
ChainResidue
BSER49
BSER50
BALA65
BILE90
BSER91
BPHE133
BSER175
BTYR191
BCYS261
BILE305
BEDO410
BHOH511
BHOH583
BHOH666

site_idAD3
Number of Residues5
Detailsbinding site for residue SO4 B 402
ChainResidue
BLYS123
BTHR124
BHOH501
BHOH516
BHOH647

site_idAD4
Number of Residues5
Detailsbinding site for residue EDO B 403
ChainResidue
BTYR228
BLEU240
BLYS250
BGLN289
BHOH519

site_idAD5
Number of Residues6
Detailsbinding site for residue EDO B 404
ChainResidue
ASER129
BTYR260
BASP302
BGLU322
BHOH669
BHOH721

site_idAD6
Number of Residues10
Detailsbinding site for residue EDO B 405
ChainResidue
BTHR40
BLEU206
BGLY299
BTHR301
BASP324
BTHR326
BLYS328
BHOH555
BHOH571
BHOH682

site_idAD7
Number of Residues6
Detailsbinding site for residue EDO B 406
ChainResidue
BALA42
BGLY43
BLYS70
BPHE79
BSER202
BHOH586

site_idAD8
Number of Residues4
Detailsbinding site for residue EDO B 407
ChainResidue
BTYR75
BHOH547
BPHE39
BALA74

site_idAD9
Number of Residues7
Detailsbinding site for residue EDO B 408
ChainResidue
BSER223
BPRO224
BASN225
BTYR228
BHOH519
BHOH534
BHOH695

site_idAE1
Number of Residues4
Detailsbinding site for residue EDO B 409
ChainResidue
BPHE79
BLYS81
BTHR82
BHOH707

site_idAE2
Number of Residues3
Detailsbinding site for residue EDO B 410
ChainResidue
BASP107
BPHE133
B5MQ401

site_idAE3
Number of Residues3
Detailsbinding site for residue EDO B 411
ChainResidue
BLYS123
BVAL158
BLYS159

site_idAE4
Number of Residues5
Detailsbinding site for residue EDO B 412
ChainResidue
BLEU143
BILE155
BLYS165
BTHR200
BALA201

Functional Information from PROSITE/UniProt
site_idPS00678
Number of Residues15
DetailsWD_REPEATS_1 Trp-Asp (WD) repeats signature. LVSAsdDkTLKIWDV
ChainResidueDetails
ALEU102-VAL116
AILE144-VAL158
AILE186-THR200
AILE274-LEU288

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsSITE: Important for interaction with histone H3
ChainResidueDetails
AASP107
APHE133
APHE263
AGLU322
BASP107
BPHE133
BPHE263
BGLU322

site_idSWS_FT_FI2
Number of Residues2
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
ALYS112
BLYS112

site_idSWS_FT_FI3
Number of Residues6
DetailsCROSSLNK: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2) => ECO:0007744|PubMed:28112733
ChainResidueDetails
BLYS46
ALYS27
ALYS46
BLYS27

221051

PDB entries from 2024-06-12

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