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4X8C

Crystal structure of human peptidylarginine deiminase type4 (PAD4) in complex with GSK147

Functional Information from GO Data
ChainGOidnamespacecontents
A0002376biological_processimmune system process
A0004668molecular_functionprotein-arginine deiminase activity
A0005509molecular_functioncalcium ion binding
A0005515molecular_functionprotein binding
A0005634cellular_componentnucleus
A0005654cellular_componentnucleoplasm
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006325biological_processchromatin organization
A0006334biological_processnucleosome assembly
A0006338biological_processchromatin remodeling
A0016787molecular_functionhydrolase activity
A0019827biological_processstem cell population maintenance
A0032991cellular_componentprotein-containing complex
A0036211biological_processprotein modification process
A0042802molecular_functionidentical protein binding
A0043687biological_processpost-translational protein modification
A0045087biological_processinnate immune response
A0046872molecular_functionmetal ion binding
A0140794molecular_functionhistone arginine deiminase activity
A0140795molecular_functionhistone H3R2 arginine deiminase activity
A0140796molecular_functionhistone H3R8 arginine deiminase activity
A0140797molecular_functionhistone H3R17 arginine deiminase activity
A0140798molecular_functionhistone H3R26 arginine deiminase activity
Functional Information from PDB Data
site_idAC1
Number of Residues4
Detailsbinding site for residue CA A 701
ChainResidue
AGLU353
APHE407
ALEU410
AGLU411

site_idAC2
Number of Residues3
Detailsbinding site for residue CA A 702
ChainResidue
AASN153
AASP176
AASP179

site_idAC3
Number of Residues11
Detailsbinding site for residue 3YZ A 703
ChainResidue
AASP473
APHE515
AALA581
APHE582
APRO584
AASN585
AASN588
APHE634
AVAL643
AVAL469
AHIS471

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsActive site: {"evidences":[{"source":"PubMed","id":"15247907","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues10
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"15247907","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"16567635","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17002273","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues3
DetailsModified residue: {"description":"Citrulline","evidences":[{"source":"PubMed","id":"20201080","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idMCSA1
Number of Residues4
DetailsM-CSA 594
ChainResidueDetails
AASP350electrostatic stabiliser
AHIS471proton acceptor, proton donor
AASP473electrostatic stabiliser
AALA645nucleofuge, nucleophile, proton acceptor, proton donor

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PDB entries from 2025-07-30

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