5EAR
Crystal structure of human WDR5 in complex with compound 9d
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0000122 | biological_process | negative regulation of transcription by RNA polymerase II |
A | 0000123 | cellular_component | histone acetyltransferase complex |
A | 0001501 | biological_process | skeletal system development |
A | 0005515 | molecular_function | protein binding |
A | 0005634 | cellular_component | nucleus |
A | 0005654 | cellular_component | nucleoplasm |
A | 0006094 | biological_process | gluconeogenesis |
A | 0006325 | biological_process | chromatin organization |
A | 0006355 | biological_process | regulation of DNA-templated transcription |
A | 0006357 | biological_process | regulation of transcription by RNA polymerase II |
A | 0035097 | cellular_component | histone methyltransferase complex |
A | 0042393 | molecular_function | histone binding |
A | 0042800 | molecular_function | histone H3K4 methyltransferase activity |
A | 0044545 | cellular_component | NSL complex |
A | 0044665 | cellular_component | MLL1/2 complex |
A | 0044666 | cellular_component | MLL3/4 complex |
A | 0045722 | biological_process | positive regulation of gluconeogenesis |
A | 0045815 | biological_process | transcription initiation-coupled chromatin remodeling |
A | 0045893 | biological_process | positive regulation of DNA-templated transcription |
A | 0045995 | biological_process | regulation of embryonic development |
A | 0048188 | cellular_component | Set1C/COMPASS complex |
A | 0051302 | biological_process | regulation of cell division |
A | 0051726 | biological_process | regulation of cell cycle |
A | 0071339 | cellular_component | MLL1 complex |
A | 0072686 | cellular_component | mitotic spindle |
A | 0140004 | molecular_function | histone H3Q5ser reader activity |
A | 0140109 | molecular_function | histone H3K4me1 reader activity |
A | 0140672 | cellular_component | ATAC complex |
B | 0000122 | biological_process | negative regulation of transcription by RNA polymerase II |
B | 0000123 | cellular_component | histone acetyltransferase complex |
B | 0001501 | biological_process | skeletal system development |
B | 0005515 | molecular_function | protein binding |
B | 0005634 | cellular_component | nucleus |
B | 0005654 | cellular_component | nucleoplasm |
B | 0006094 | biological_process | gluconeogenesis |
B | 0006325 | biological_process | chromatin organization |
B | 0006355 | biological_process | regulation of DNA-templated transcription |
B | 0006357 | biological_process | regulation of transcription by RNA polymerase II |
B | 0035097 | cellular_component | histone methyltransferase complex |
B | 0042393 | molecular_function | histone binding |
B | 0042800 | molecular_function | histone H3K4 methyltransferase activity |
B | 0044545 | cellular_component | NSL complex |
B | 0044665 | cellular_component | MLL1/2 complex |
B | 0044666 | cellular_component | MLL3/4 complex |
B | 0045722 | biological_process | positive regulation of gluconeogenesis |
B | 0045815 | biological_process | transcription initiation-coupled chromatin remodeling |
B | 0045893 | biological_process | positive regulation of DNA-templated transcription |
B | 0045995 | biological_process | regulation of embryonic development |
B | 0048188 | cellular_component | Set1C/COMPASS complex |
B | 0051302 | biological_process | regulation of cell division |
B | 0051726 | biological_process | regulation of cell cycle |
B | 0071339 | cellular_component | MLL1 complex |
B | 0072686 | cellular_component | mitotic spindle |
B | 0140004 | molecular_function | histone H3Q5ser reader activity |
B | 0140109 | molecular_function | histone H3K4me1 reader activity |
B | 0140672 | cellular_component | ATAC complex |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 13 |
Details | binding site for residue 5MQ A 401 |
Chain | Residue |
A | SER49 |
A | ILE305 |
A | EDO406 |
A | HOH575 |
A | HOH578 |
A | SER50 |
A | ALA65 |
A | ILE90 |
A | SER91 |
A | PHE133 |
A | SER175 |
A | TYR191 |
A | CYS261 |
site_id | AC2 |
Number of Residues | 5 |
Details | binding site for residue EDO A 402 |
Chain | Residue |
A | LYS123 |
A | VAL158 |
A | LYS159 |
A | HOH560 |
A | HOH705 |
site_id | AC3 |
Number of Residues | 3 |
Details | binding site for residue EDO A 403 |
Chain | Residue |
A | LYS165 |
A | THR200 |
A | ALA201 |
site_id | AC4 |
Number of Residues | 3 |
Details | binding site for residue EDO A 404 |
Chain | Residue |
A | LYS70 |
A | PHE79 |
A | HOH501 |
site_id | AC5 |
Number of Residues | 7 |
Details | binding site for residue EDO A 405 |
Chain | Residue |
A | THR40 |
A | LEU206 |
A | GLY299 |
A | THR301 |
A | ASP324 |
A | THR326 |
A | LYS328 |
site_id | AC6 |
Number of Residues | 4 |
Details | binding site for residue EDO A 406 |
Chain | Residue |
A | ASP107 |
A | PHE133 |
A | 5MQ401 |
A | HOH514 |
site_id | AC7 |
Number of Residues | 3 |
Details | binding site for residue EDO A 407 |
Chain | Residue |
A | PHE79 |
A | LYS81 |
A | THR82 |
site_id | AC8 |
Number of Residues | 4 |
Details | binding site for residue EDO A 408 |
Chain | Residue |
A | ASP98 |
A | ASN100 |
A | HOH590 |
B | LYS38 |
site_id | AC9 |
Number of Residues | 4 |
Details | binding site for residue EDO A 409 |
Chain | Residue |
A | TYR260 |
A | ASP302 |
A | GLU322 |
A | HOH542 |
site_id | AD1 |
Number of Residues | 5 |
Details | binding site for residue EDO A 410 |
Chain | Residue |
A | TYR228 |
A | LYS250 |
A | GLN289 |
A | HOH507 |
A | HOH535 |
site_id | AD2 |
Number of Residues | 14 |
Details | binding site for residue 5MQ B 401 |
Chain | Residue |
B | SER49 |
B | SER50 |
B | ALA65 |
B | ILE90 |
B | SER91 |
B | PHE133 |
B | SER175 |
B | TYR191 |
B | CYS261 |
B | ILE305 |
B | EDO410 |
B | HOH511 |
B | HOH583 |
B | HOH666 |
site_id | AD3 |
Number of Residues | 5 |
Details | binding site for residue SO4 B 402 |
Chain | Residue |
B | LYS123 |
B | THR124 |
B | HOH501 |
B | HOH516 |
B | HOH647 |
site_id | AD4 |
Number of Residues | 5 |
Details | binding site for residue EDO B 403 |
Chain | Residue |
B | TYR228 |
B | LEU240 |
B | LYS250 |
B | GLN289 |
B | HOH519 |
site_id | AD5 |
Number of Residues | 6 |
Details | binding site for residue EDO B 404 |
Chain | Residue |
A | SER129 |
B | TYR260 |
B | ASP302 |
B | GLU322 |
B | HOH669 |
B | HOH721 |
site_id | AD6 |
Number of Residues | 10 |
Details | binding site for residue EDO B 405 |
Chain | Residue |
B | THR40 |
B | LEU206 |
B | GLY299 |
B | THR301 |
B | ASP324 |
B | THR326 |
B | LYS328 |
B | HOH555 |
B | HOH571 |
B | HOH682 |
site_id | AD7 |
Number of Residues | 6 |
Details | binding site for residue EDO B 406 |
Chain | Residue |
B | ALA42 |
B | GLY43 |
B | LYS70 |
B | PHE79 |
B | SER202 |
B | HOH586 |
site_id | AD8 |
Number of Residues | 4 |
Details | binding site for residue EDO B 407 |
Chain | Residue |
B | TYR75 |
B | HOH547 |
B | PHE39 |
B | ALA74 |
site_id | AD9 |
Number of Residues | 7 |
Details | binding site for residue EDO B 408 |
Chain | Residue |
B | SER223 |
B | PRO224 |
B | ASN225 |
B | TYR228 |
B | HOH519 |
B | HOH534 |
B | HOH695 |
site_id | AE1 |
Number of Residues | 4 |
Details | binding site for residue EDO B 409 |
Chain | Residue |
B | PHE79 |
B | LYS81 |
B | THR82 |
B | HOH707 |
site_id | AE2 |
Number of Residues | 3 |
Details | binding site for residue EDO B 410 |
Chain | Residue |
B | ASP107 |
B | PHE133 |
B | 5MQ401 |
site_id | AE3 |
Number of Residues | 3 |
Details | binding site for residue EDO B 411 |
Chain | Residue |
B | LYS123 |
B | VAL158 |
B | LYS159 |
site_id | AE4 |
Number of Residues | 5 |
Details | binding site for residue EDO B 412 |
Chain | Residue |
B | LEU143 |
B | ILE155 |
B | LYS165 |
B | THR200 |
B | ALA201 |
Functional Information from PROSITE/UniProt
site_id | PS00678 |
Number of Residues | 15 |
Details | WD_REPEATS_1 Trp-Asp (WD) repeats signature. LVSAsdDkTLKIWDV |
Chain | Residue | Details |
A | LEU102-VAL116 | |
A | ILE144-VAL158 | |
A | ILE186-THR200 | |
A | ILE274-LEU288 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 8 |
Details | SITE: Important for interaction with histone H3 |
Chain | Residue | Details |
A | ASP107 | |
A | PHE133 | |
A | PHE263 | |
A | GLU322 | |
B | ASP107 | |
B | PHE133 | |
B | PHE263 | |
B | GLU322 |
site_id | SWS_FT_FI2 |
Number of Residues | 2 |
Details | MOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861 |
Chain | Residue | Details |
A | LYS112 | |
B | LYS112 |
site_id | SWS_FT_FI3 |
Number of Residues | 6 |
Details | CROSSLNK: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2) => ECO:0007744|PubMed:28112733 |
Chain | Residue | Details |
A | LYS27 | |
A | LYS46 | |
B | LYS27 | |
B | LYS46 |