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3FJ4

Crystal structure of muconate lactonizing enzyme from Pseudomonas Fluorescens complexed with muconolactone

Functional Information from GO Data
ChainGOidnamespacecontents
A0006518biological_processpeptide metabolic process
A0009063biological_processamino acid catabolic process
A0016853molecular_functionisomerase activity
A0016854molecular_functionracemase and epimerase activity
A0018849molecular_functionmuconate cycloisomerase activity
A0018850molecular_functionchloromuconate cycloisomerase activity
A0030145molecular_functionmanganese ion binding
A0046872molecular_functionmetal ion binding
B0006518biological_processpeptide metabolic process
B0009063biological_processamino acid catabolic process
B0016853molecular_functionisomerase activity
B0016854molecular_functionracemase and epimerase activity
B0018849molecular_functionmuconate cycloisomerase activity
B0018850molecular_functionchloromuconate cycloisomerase activity
B0030145molecular_functionmanganese ion binding
B0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues13
DetailsBINDING SITE FOR RESIDUE MUC A 383
ChainResidue
AHIS24
ALYS275
ATHR303
AGLU329
AMG1001
AILE56
ATYR61
ATHR143
ALYS169
ALYS171
AASP200
AASN202
AASP251

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG A1001
ChainResidue
AASP200
AASN202
AGLU226
AASP251
AMUC383
AHOH503

site_idAC3
Number of Residues15
DetailsBINDING SITE FOR RESIDUE MUC B 383
ChainResidue
BHIS24
BILE56
BTYR61
BTHR143
BLYS169
BLYS171
BASP200
BASN202
BASP251
BLYS275
BTHR303
BGLU329
BPHE331
BHOH502
BMG1002

site_idAC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG B1002
ChainResidue
BASP200
BASN202
BGLU226
BASP251
BMUC383
BHOH501
BHOH502

Functional Information from PROSITE/UniProt
site_idPS00908
Number of Residues26
DetailsMR_MLE_1 Mandelate racemase / muconate lactonizing enzyme family signature 1. AkSGIEsALlDAqGKrlglPVseLLG
ChainResidueDetails
AALA106-GLY131

site_idPS00909
Number of Residues32
DetailsMR_MLE_2 Mandelate racemase / muconate lactonizing enzyme family signature 2. VrvDvNqawdeavAlracriLggngidlIEQP
ChainResidueDetails
AVAL197-PRO228

Catalytic Information from CSA
site_idCSA1
Number of Residues3
DetailsAnnotated By Reference To The Literature 1muc
ChainResidueDetails
AGLU329
ALYS169
ALYS171

site_idCSA2
Number of Residues3
DetailsAnnotated By Reference To The Literature 1muc
ChainResidueDetails
BGLU329
BLYS169
BLYS171

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1muc
ChainResidueDetails
ALYS275
ALYS171

site_idCSA4
Number of Residues2
DetailsAnnotated By Reference To The Literature 1muc
ChainResidueDetails
BLYS275
BLYS171

site_idMCSA1
Number of Residues8
DetailsM-CSA 269
ChainResidueDetails
AHIS24steric role
ALYS169electrostatic stabiliser
ALYS171electrostatic stabiliser, proton donor
AASP200metal ligand
AGLU226metal ligand
AASP251metal ligand
ALYS275electrostatic stabiliser
AGLU329proton acceptor, proton donor

site_idMCSA2
Number of Residues8
DetailsM-CSA 269
ChainResidueDetails
BHIS24steric role
BLYS169electrostatic stabiliser
BLYS171electrostatic stabiliser, proton donor
BASP200metal ligand
BGLU226metal ligand
BASP251metal ligand
BLYS275electrostatic stabiliser
BGLU329proton acceptor, proton donor

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PDB entries from 2025-06-18

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