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4CXK

G9 mutant of PAS, arylsulfatase from Pseudomonas Aeruginosa

Functional Information from GO Data
ChainGOidnamespacecontents
A0004065molecular_functionarylsulfatase activity
A0005737cellular_componentcytoplasm
A0008081molecular_functionphosphoric diester hydrolase activity
A0016787molecular_functionhydrolase activity
A0046872molecular_functionmetal ion binding
B0004065molecular_functionarylsulfatase activity
B0005737cellular_componentcytoplasm
B0008081molecular_functionphosphoric diester hydrolase activity
B0016787molecular_functionhydrolase activity
B0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CA B 1528
ChainResidue
BASP13
BASP14
BDDZ51
BASP317
BASN318

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CA A 1528
ChainResidue
AASN318
AASP13
AASP14
ADDZ51
AASP317

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 A 1529
ChainResidue
ADDZ51
ALYS113
AHIS115
AHIS211
ALYS375
AHOH2060

site_idAC4
Number of Residues10
DetailsBINDING SITE FOR RESIDUE PEG B 1529
ChainResidue
BALA216
BARG218
BILE350
BGLY351
BSER352
BHOH2149
BHOH2210
BHOH2212
BHOH2345
BHOH2468

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 B 1530
ChainResidue
BDDZ51
BLYS113
BHIS115
BHIS211
BLYS375
BHOH2080

Functional Information from PROSITE/UniProt
site_idPS00149
Number of Residues11
DetailsSULFATASE_2 Sulfatases signature 2. GYqTlmAGK.WH
ChainResidueDetails
AGLY105-HIS115

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Nucleophile => ECO:0000269|PubMed:11435113, ECO:0000269|PubMed:9748219
ChainResidueDetails
ADDZ51
BDDZ51

site_idSWS_FT_FI2
Number of Residues2
DetailsACT_SITE: ACT_SITE => ECO:0000250|UniProtKB:P15289
ChainResidueDetails
AHIS115
BHIS115

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:11435113
ChainResidueDetails
AASP13
AASP14
AASP317
AASN318
BASP13
BASP14
BASP317
BASN318

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: via 3-oxoalanine => ECO:0000269|PubMed:11435113
ChainResidueDetails
ADDZ51
BDDZ51

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: 3-oxoalanine (Cys) => ECO:0000269|PubMed:11435113, ECO:0000269|PubMed:9748219
ChainResidueDetails
ADDZ51
BDDZ51

Catalytic Information from CSA
site_idMCSA1
Number of Residues10
DetailsM-CSA 661
ChainResidueDetails
AASP13metal ligand
ATHR379electrostatic stabiliser
AASP14metal ligand
ADDZ51covalently attached, increase electrophilicity, metal ligand, nucleophile, proton donor
ALEU59electrostatic stabiliser
AGLY117electrostatic stabiliser, increase electrophilicity
ALYS119electrostatic stabiliser, proton acceptor
AGLN215electrostatic stabiliser, proton donor
AGLU321activator, increase nucleophilicity, metal ligand, proton acceptor
AGLY322metal ligand

site_idMCSA2
Number of Residues10
DetailsM-CSA 661
ChainResidueDetails
BASP13metal ligand
BTHR379electrostatic stabiliser
BASP14metal ligand
BDDZ51covalently attached, increase electrophilicity, metal ligand, nucleophile, proton donor
BLEU59electrostatic stabiliser
BGLY117electrostatic stabiliser, increase electrophilicity
BLYS119electrostatic stabiliser, proton acceptor
BGLN215electrostatic stabiliser, proton donor
BGLU321activator, increase nucleophilicity, metal ligand, proton acceptor
BGLY322metal ligand

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PDB entries from 2025-06-18

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