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1WD9

Calcium bound form of human peptidylarginine deiminase type4 (PAD4)

Functional Information from GO Data
ChainGOidnamespacecontents
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 Residues5
DetailsBINDING SITE FOR RESIDUE CA A 900
ChainResidue
AGLN349
AGLU353
APHE407
ALEU410
AGLU411

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A 901
ChainResidue
AASP176
AASP179
AASN153
AASP155
AASP157
AASP165

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CA A 902
ChainResidue
AASP155
AASP157
AASP179
AASP388

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CA A 903
ChainResidue
AGLU351
AASP369
ASER370
AARG372
AASN373

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CA A 904
ChainResidue
AASP165
AASP168
AGLU170

site_idAC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 905
ChainResidue
ASER402
AGLY403
AARG441

site_idAC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 906
ChainResidue
AARG495
ASER496
ALYS499
ALYS615

site_idAC8
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 907
ChainResidue
AGLU511
ALYS525
AASN528

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: ACT_SITE => ECO:0000269|PubMed:15247907
ChainResidueDetails
AASP350
AHIS471
AASP473
AALA645

site_idSWS_FT_FI2
Number of Residues18
DetailsBINDING: BINDING => ECO:0000269|PubMed:15247907, ECO:0000269|PubMed:16567635, ECO:0000269|PubMed:17002273
ChainResidueDetails
AASN153
AGLU351
AGLU353
AASP369
ASER370
AASN373
AASP388
APHE407
ALEU410
AGLU411
AASP155
AASP157
AASP165
AASP168
AGLU170
AASP176
AASP179
AGLN349

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:21882827
ChainResidueDetails
AARG374
AARG639

site_idSWS_FT_FI4
Number of Residues6
DetailsMOD_RES: Citrulline => ECO:0000269|PubMed:20201080
ChainResidueDetails
AARG205
AARG212
AARG218
AARG372
AARG374
AARG383

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1wd8
ChainResidueDetails
AASP473
AASP350
AALA645
AHIS471

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 2024-10-30

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