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4ENP

Structure of E530A variant E. coli KatE

Functional Information from GO Data
ChainGOidnamespacecontents
A0004096molecular_functioncatalase activity
A0004601molecular_functionperoxidase activity
A0005506molecular_functioniron ion binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006972biological_processhyperosmotic response
A0006974biological_processDNA damage response
A0006979biological_processresponse to oxidative stress
A0020037molecular_functionheme binding
A0042744biological_processhydrogen peroxide catabolic process
A0042802molecular_functionidentical protein binding
A0046872molecular_functionmetal ion binding
A0098869biological_processcellular oxidant detoxification
B0004096molecular_functioncatalase activity
B0004601molecular_functionperoxidase activity
B0005506molecular_functioniron ion binding
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006972biological_processhyperosmotic response
B0006974biological_processDNA damage response
B0006979biological_processresponse to oxidative stress
B0020037molecular_functionheme binding
B0042744biological_processhydrogen peroxide catabolic process
B0042802molecular_functionidentical protein binding
B0046872molecular_functionmetal ion binding
B0098869biological_processcellular oxidant detoxification
C0004096molecular_functioncatalase activity
C0004601molecular_functionperoxidase activity
C0005506molecular_functioniron ion binding
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0006972biological_processhyperosmotic response
C0006974biological_processDNA damage response
C0006979biological_processresponse to oxidative stress
C0020037molecular_functionheme binding
C0042744biological_processhydrogen peroxide catabolic process
C0042802molecular_functionidentical protein binding
C0046872molecular_functionmetal ion binding
C0098869biological_processcellular oxidant detoxification
D0004096molecular_functioncatalase activity
D0004601molecular_functionperoxidase activity
D0005506molecular_functioniron ion binding
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0006972biological_processhyperosmotic response
D0006974biological_processDNA damage response
D0006979biological_processresponse to oxidative stress
D0020037molecular_functionheme binding
D0042744biological_processhydrogen peroxide catabolic process
D0042802molecular_functionidentical protein binding
D0046872molecular_functionmetal ion binding
D0098869biological_processcellular oxidant detoxification
Functional Information from PDB Data
site_idAC1
Number of Residues23
DetailsBINDING SITE FOR RESIDUE HEM A 801
ChainResidue
AARG125
APHE214
AHIS275
APHE391
ALEU407
AARG411
ASER414
ATYR415
ATHR418
AGLN419
AARG422
AILE126
AHOH922
AHOH966
AHOH994
DASP118
AVAL127
AHIS128
AARG165
AGLY184
AVAL199
AGLY200
AASN201

site_idAC2
Number of Residues25
DetailsBINDING SITE FOR RESIDUE HEM B 801
ChainResidue
BARG125
BILE126
BVAL127
BHIS128
BARG165
BGLY184
BVAL199
BGLY200
BASN201
BPHE206
BPHE214
BILE274
BHIS275
BPHE391
BLEU407
BARG411
BSER414
BTYR415
BTHR418
BGLN419
BARG422
BHOH969
BHOH1014
BHOH1042
CASP118

site_idAC3
Number of Residues25
DetailsBINDING SITE FOR RESIDUE HEM C 801
ChainResidue
BASP118
CARG125
CILE126
CVAL127
CHIS128
CARG165
CGLY184
CVAL199
CGLY200
CASN201
CPHE206
CPHE214
CILE274
CHIS275
CPHE391
CLEU407
CARG411
CSER414
CTYR415
CTHR418
CGLN419
CARG422
CHOH1015
CHOH1058
CHOH1087

site_idAC4
Number of Residues23
DetailsBINDING SITE FOR RESIDUE HEM D 801
ChainResidue
DARG125
DILE126
DVAL127
DHIS128
DARG165
DGLY184
DVAL199
DGLY200
DASN201
DPHE206
DPHE214
DHIS275
DPHE391
DLEU407
DARG411
DSER414
DTYR415
DTHR418
DGLN419
DARG422
DHOH1069
DHOH1112
DHOH1139

Functional Information from PROSITE/UniProt
site_idPS00437
Number of Residues9
DetailsCATALASE_1 Catalase proximal heme-ligand signature. RLFSYtDTQ
ChainResidueDetails
AARG411-GLN419

site_idPS00438
Number of Residues17
DetailsCATALASE_2 Catalase proximal active site signature. FdHeripERivHarGSA
ChainResidueDetails
APHE117-ALA133

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsACT_SITE: ACT_SITE => ECO:0000255|PROSITE-ProRule:PRU10013
ChainResidueDetails
AHIS128
AASN201
BHIS128
BASN201
CHIS128
CASN201
DHIS128
DASN201

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: axial binding residue
ChainResidueDetails
ATYR415
BTYR415
CTYR415
DTYR415

site_idSWS_FT_FI3
Number of Residues8
DetailsCROSSLNK: 3'-histidyl-3-tyrosine (His-Tyr)
ChainResidueDetails
AHIS392
ATYR415
BHIS392
BTYR415
CHIS392
CTYR415
DHIS392
DTYR415

Catalytic Information from CSA
site_idMCSA1
Number of Residues3
DetailsM-CSA 573
ChainResidueDetails
AHIS128proton shuttle (general acid/base)
AASN201electrostatic stabiliser
AHIS392proton shuttle (general acid/base)

site_idMCSA2
Number of Residues3
DetailsM-CSA 573
ChainResidueDetails
BHIS128proton shuttle (general acid/base)
BASN201electrostatic stabiliser
BHIS392proton shuttle (general acid/base)

site_idMCSA3
Number of Residues3
DetailsM-CSA 573
ChainResidueDetails
CHIS128proton shuttle (general acid/base)
CASN201electrostatic stabiliser
CHIS392proton shuttle (general acid/base)

site_idMCSA4
Number of Residues3
DetailsM-CSA 573
ChainResidueDetails
DHIS128proton shuttle (general acid/base)
DASN201electrostatic stabiliser
DHIS392proton shuttle (general acid/base)

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PDB entries from 2024-05-01

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