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4YHZ

Crystal structure of 304M3-B Fab in complex with H3K4me3 peptide

Functional Information from PDB Data
site_idAC1
Number of Residues11
Detailsbinding site for residue GOL H 301
ChainResidue
HASP31
HHOH412
HHOH465
HTYR32
HGLN53
HPHE100
HPHE100
HVAL101
HVAL101
HARG102
HTRP106

site_idAC2
Number of Residues6
Detailsbinding site for residue GOL H 302
ChainResidue
HPHE104
HTRP106
HTRP106
HHOH454
PM3L4
PTHR6

site_idAC3
Number of Residues5
Detailsbinding site for residue GOL H 303
ChainResidue
HARG30
HASP73
HASN74
HALA75
HHOH457

site_idAC4
Number of Residues3
Detailsbinding site for residue GOL H 304
ChainResidue
HPHE27
HARG98
HHOH401

site_idAC5
Number of Residues2
Detailsbinding site for residue GOL H 305
ChainResidue
HARG16
HSER17

site_idAC6
Number of Residues7
Detailsbinding site for residue GOL L 301
ChainResidue
LGLN36
LARG38
LILE57
LPRO58
LPHE61
LGLY80
LASP81

site_idAC7
Number of Residues4
Detailsbinding site for residue GOL L 302
ChainResidue
LPRO58
LGLU59
LARG60
LARG76

site_idAC8
Number of Residues3
Detailsbinding site for residue SO4 L 303
ChainResidue
LGLY67
LASN68
LTHR69

site_idAC9
Number of Residues15
Detailsbinding site for Ligand residues M3L P 4 through GLN P 5 bound to THR P 3
ChainResidue
HTRP33
HASP50
HGLY103
HTRP106
HGOL302
HHOH427
LASP29
LTRP90
LTYR97
LHOH404
PTHR3
PTHR6
PTHR6
PALA7
PHOH102

Functional Information from PROSITE/UniProt
site_idPS00178
Number of Residues12
DetailsAA_TRNA_LIGASE_I Aminoacyl-transfer RNA synthetases class-I signature. PgqTArITCGGT
ChainResidueDetails
LPRO14-THR25

site_idPS00290
Number of Residues7
DetailsIG_MHC Immunoglobulins and major histocompatibility complex proteins signature. YICNVNH
ChainResidueDetails
HTYR202-HIS208
LTYR193-HIS199

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsMOD_RES: Citrulline; alternate => ECO:0000269|PubMed:16567635
ChainResidueDetails
PARG2

site_idSWS_FT_FI2
Number of Residues1
DetailsMOD_RES: Phosphothreonine; by HASPIN => ECO:0000269|PubMed:15681610, ECO:0000269|PubMed:16185088
ChainResidueDetails
PTHR3

site_idSWS_FT_FI3
Number of Residues1
DetailsMOD_RES: N6-methyllysine; alternate => ECO:0000269|PubMed:16267050, ECO:0000269|PubMed:16457588, ECO:0000269|PubMed:17194708
ChainResidueDetails
PM3L4

site_idSWS_FT_FI4
Number of Residues1
DetailsMOD_RES: 5-glutamyl serotonin; alternate => ECO:0000269|PubMed:30867594
ChainResidueDetails
PGLN5

site_idSWS_FT_FI5
Number of Residues1
DetailsMOD_RES: Phosphothreonine; by PKC => ECO:0000269|PubMed:20228790
ChainResidueDetails
PTHR6

site_idSWS_FT_FI6
Number of Residues1
DetailsMOD_RES: Symmetric dimethylarginine; by PRMT5; alternate => ECO:0000250|UniProtKB:P68433
ChainResidueDetails
PARG8

site_idSWS_FT_FI7
Number of Residues1
DetailsMOD_RES: N6-methyllysine; alternate => ECO:0000269|PubMed:11242053, ECO:0000269|PubMed:16185088, ECO:0000269|PubMed:16267050, ECO:0000269|PubMed:16457588, ECO:0000269|PubMed:17194708
ChainResidueDetails
PLYS9

site_idSWS_FT_FI8
Number of Residues1
DetailsMOD_RES: Phosphoserine; alternate; by AURKB, AURKC, RPS6KA3, RPS6KA4 and RPS6KA5 => ECO:0000269|PubMed:10464286, ECO:0000269|PubMed:11856369, ECO:0000269|PubMed:12560483, ECO:0000269|PubMed:15681610, ECO:0000269|PubMed:16185088, ECO:0000269|PubMed:16457588
ChainResidueDetails
PSER10

site_idSWS_FT_FI9
Number of Residues1
DetailsMOD_RES: Phosphothreonine; by PKC and CHEK1 => ECO:0000269|PubMed:12560483, ECO:0000269|PubMed:18066052, ECO:0000269|PubMed:18243098, ECO:0000269|PubMed:22901803
ChainResidueDetails
PTHR11

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PDB entries from 2024-05-01

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