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5SW4

Crystal structure of native catalase-peroxidase KatG at pH8.0

Replaces:  2B2O
Functional Information from GO Data
ChainGOidnamespacecontents
A0004096molecular_functioncatalase activity
A0004601molecular_functionperoxidase activity
A0005829cellular_componentcytosol
A0006979biological_processresponse to oxidative stress
A0016491molecular_functionoxidoreductase activity
A0020037molecular_functionheme binding
A0042744biological_processhydrogen peroxide catabolic process
A0046872molecular_functionmetal ion binding
A0070301biological_processcellular response to hydrogen peroxide
A0098869biological_processcellular oxidant detoxification
B0004096molecular_functioncatalase activity
B0004601molecular_functionperoxidase activity
B0005829cellular_componentcytosol
B0006979biological_processresponse to oxidative stress
B0016491molecular_functionoxidoreductase activity
B0020037molecular_functionheme binding
B0042744biological_processhydrogen peroxide catabolic process
B0046872molecular_functionmetal ion binding
B0070301biological_processcellular response to hydrogen peroxide
B0098869biological_processcellular oxidant detoxification
Functional Information from PDB Data
site_idAC1
Number of Residues21
Detailsbinding site for residue HEM A 801
ChainResidue
AGLY104
AGLY282
ALYS283
ATHR284
AHIS285
ATHR323
ASER324
ATRP330
ATHR388
AOXY803
AHOH966
ALEU105
AHOH977
AHOH1015
AARG108
ATOX111
AVAL239
ALEU274
AILE275
AGLY278
AHIS279

site_idAC2
Number of Residues6
Detailsbinding site for residue NA A 802
ChainResidue
AGLY122
AARG123
AGLY124
ASER494
AHOH930
AHOH1032

site_idAC3
Number of Residues6
Detailsbinding site for residue OXY A 803
ChainResidue
AARG108
ATOX111
AHIS112
AHEM801
AHOH901
AHOH985

site_idAC4
Number of Residues2
Detailsbinding site for residue PO4 A 804
ChainResidue
AHOH1143
AHOH1186

site_idAC5
Number of Residues4
Detailsbinding site for residue MPD A 805
ChainResidue
ALEU209
ATHR323
ASER324
AHOH1524

site_idAC6
Number of Residues4
Detailsbinding site for residue MPD A 806
ChainResidue
AASP83
APRO154
AHOH1295
AHOH1476

site_idAC7
Number of Residues9
Detailsbinding site for residue TRS A 807
ChainResidue
AALA120
AARG492
AVAL593
AGLU595
ALYS620
AHOH922
AHOH1004
AHOH1076
AHOH1298

site_idAC8
Number of Residues19
Detailsbinding site for residue HEM B 801
ChainResidue
BGLY104
BLEU105
BTOX111
BVAL239
BLEU274
BGLY278
BHIS279
BGLY282
BLYS283
BTHR284
BHIS285
BTHR323
BSER324
BTRP330
BTHR388
BTRP420
BHOH929
BHOH1004
BHOH1005

site_idAC9
Number of Residues6
Detailsbinding site for residue NA B 802
ChainResidue
BGLY122
BARG123
BGLY124
BSER494
BHOH1054
BHOH1136

site_idAD1
Number of Residues1
Detailsbinding site for residue PO4 B 803
ChainResidue
BHOH1121

site_idAD2
Number of Residues2
Detailsbinding site for residue MPD B 804
ChainResidue
BTHR323
BSER324

site_idAD3
Number of Residues12
Detailsbinding site for residue TRS B 805
ChainResidue
BALA120
BASP121
BARG492
BVAL593
BGLU595
BLYS620
BLEU623
BHOH912
BHOH937
BHOH962
BHOH1309
BHOH1398

Functional Information from PROSITE/UniProt
site_idPS00435
Number of Residues11
DetailsPEROXIDASE_1 Peroxidases proximal heme-ligand signature. TVALIAGGHTF
ChainResidueDetails
ATHR271-PHE281

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000255|HAMAP-Rule:MF_01961
ChainResidueDetails
AHIS112
BHIS112

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: axial binding residue => ECO:0000255|HAMAP-Rule:MF_01961
ChainResidueDetails
AHIS279
BHIS279

site_idSWS_FT_FI3
Number of Residues2
DetailsSITE: Transition state stabilizer => ECO:0000255|HAMAP-Rule:MF_01961
ChainResidueDetails
AARG108
BARG108

site_idSWS_FT_FI4
Number of Residues2
DetailsCROSSLNK: Tryptophyl-tyrosyl-methioninium (Trp-Tyr) (with M-244) => ECO:0000255|HAMAP-Rule:MF_01961
ChainResidueDetails
ATOX111
BTOX111

site_idSWS_FT_FI5
Number of Residues4
DetailsCROSSLNK: Tryptophyl-tyrosyl-methioninium (Tyr-Met) (with W-91) => ECO:0000255|HAMAP-Rule:MF_01961
ChainResidueDetails
ATYR238
AMET264
BTYR238
BMET264

218853

PDB entries from 2024-04-24

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