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4M6U

P. putida mandelate racemase co-crystallized with tartronic acid

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0009063biological_processamino acid catabolic process
A0016052biological_processcarbohydrate catabolic process
A0016836molecular_functionhydro-lyase activity
A0016853molecular_functionisomerase activity
A0018838molecular_functionmandelate racemase activity
A0018924biological_processmandelate metabolic process
A0019596biological_processmandelate catabolic process
A0046872molecular_functionmetal ion binding
B0000287molecular_functionmagnesium ion binding
B0009063biological_processamino acid catabolic process
B0016052biological_processcarbohydrate catabolic process
B0016836molecular_functionhydro-lyase activity
B0016853molecular_functionisomerase activity
B0018838molecular_functionmandelate racemase activity
B0018924biological_processmandelate metabolic process
B0019596biological_processmandelate catabolic process
B0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG A 401
ChainResidue
AASP195
AGLU221
AGLU247
ATTN402
AHOH839

site_idAC2
Number of Residues10
DetailsBINDING SITE FOR RESIDUE TTN A 402
ChainResidue
AGLU221
AGLU247
AHIS297
AGLU317
ALEU319
AMG401
ALYS164
ALYS166
AASP195
AASN197

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG B 401
ChainResidue
BASP195
BGLU221
BGLU247
BTTN402
BHOH787

site_idAC4
Number of Residues10
DetailsBINDING SITE FOR RESIDUE TTN B 402
ChainResidue
BLYS164
BLYS166
BASP195
BASN197
BGLU221
BGLU247
BHIS297
BGLU317
BMG401
BHOH787

Functional Information from PROSITE/UniProt
site_idPS00908
Number of Residues26
DetailsMR_MLE_1 Mandelate racemase / muconate lactonizing enzyme family signature 1. AaAGIDmAAwDAlGKvhetPLvkLLG
ChainResidueDetails
AALA103-GLY128

site_idPS00909
Number of Residues32
DetailsMR_MLE_2 Mandelate racemase / muconate lactonizing enzyme family signature 2. ImvDyNqsldvpaAikrsqaLqqegvtwIEEP
ChainResidueDetails
AILE192-PRO223

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton acceptor; specific for S-mandelate
ChainResidueDetails
ALYS166
BLYS166

site_idSWS_FT_FI2
Number of Residues2
DetailsACT_SITE: Proton acceptor; specific for R-mandelate
ChainResidueDetails
AHIS297
BHIS297

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:7893689, ECO:0000269|PubMed:7893690, ECO:0000305|PubMed:1892834
ChainResidueDetails
BGLU247
BGLU317
AGLU317
BASP195
BGLU221
AASP195
AGLU221
AGLU247

Catalytic Information from CSA
site_idMCSA1
Number of Residues9
DetailsM-CSA 187
ChainResidueDetails
ALYS164electrostatic stabiliser, hydrogen bond donor
ALYS166electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AASP195metal ligand
AASN197electrostatic stabiliser
AGLU221metal ligand
AGLU247metal ligand
AASP270electrostatic stabiliser, hydrogen bond acceptor, increase basicity
AHIS297electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AGLU317electrostatic stabiliser, hydrogen bond donor, proton acceptor, proton donor

site_idMCSA2
Number of Residues9
DetailsM-CSA 187
ChainResidueDetails
BLYS164electrostatic stabiliser, hydrogen bond donor
BLYS166electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
BASP195metal ligand
BASN197electrostatic stabiliser
BGLU221metal ligand
BGLU247metal ligand
BASP270electrostatic stabiliser, hydrogen bond acceptor, increase basicity
BHIS297electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
BGLU317electrostatic stabiliser, hydrogen bond donor, proton acceptor, proton donor

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PDB entries from 2024-06-12

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