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1XBY

Structure of 3-keto-L-gulonate 6-phosphate decarboxylase E112D/T169A mutant with bound D-ribulose 5-phosphate

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0004590molecular_functionorotidine-5'-phosphate decarboxylase activity
A0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
A0016831molecular_functioncarboxy-lyase activity
A0019854biological_processL-ascorbic acid catabolic process
A0033982molecular_function3-dehydro-L-gulonate-6-phosphate decarboxylase activity
A0046872molecular_functionmetal ion binding
B0000287molecular_functionmagnesium ion binding
B0004590molecular_functionorotidine-5'-phosphate decarboxylase activity
B0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
B0016831molecular_functioncarboxy-lyase activity
B0019854biological_processL-ascorbic acid catabolic process
B0033982molecular_function3-dehydro-L-gulonate-6-phosphate decarboxylase activity
B0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues20
DetailsBINDING SITE FOR RESIDUE 5RP A 501
ChainResidue
AALA9
AGLY191
AARG192
AMG601
AHOH602
AHOH606
AHOH625
AHOH626
AHOH630
AHOH662
AHOH839
AASP11
AHOH850
AGLU33
AASP62
ALYS64
AHIS136
AGLY170
AGLY171
AILE189

site_idAC2
Number of Residues18
DetailsBINDING SITE FOR RESIDUE 5RP B 502
ChainResidue
BALA9
BASP11
BGLU33
BASP62
BLYS64
BHIS136
BGLY170
BGLY171
BGLY191
BARG192
BMG602
BHOH603
BHOH604
BHOH619
BHOH621
BHOH642
BHOH826
BHOH828

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG A 601
ChainResidue
AGLU33
AASP62
A5RP501
AHOH839
AHOH850

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG B 602
ChainResidue
BGLU33
BASP62
B5RP502
BHOH826
BHOH828

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsBINDING:
ChainResidueDetails
BASP11
BGLU33
BASP62
BARG192
AASP11
AGLU33
AASP62
AARG192

site_idSWS_FT_FI2
Number of Residues4
DetailsSITE: Transition state stabilizer
ChainResidueDetails
ALYS64
AASP67
BLYS64
BASP67

Catalytic Information from CSA
site_idMCSA1
Number of Residues9
DetailsM-CSA 236
ChainResidueDetails
ATHR36ground state destabiliser
AILE37ground state destabiliser
ALYS64attractive charge-charge interaction, electrostatic stabiliser, hydrogen bond donor
AASP67electrostatic stabiliser, hydrogen bond acceptor
AALA68ground state destabiliser
ALEU72ground state destabiliser
AASP112electrostatic stabiliser, hydrogen bond acceptor, increase acidity, increase basicity
AHIS136hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AARG139hydrogen bond donor, proton acceptor, proton donor

site_idMCSA2
Number of Residues9
DetailsM-CSA 236
ChainResidueDetails
BTHR36ground state destabiliser
BILE37ground state destabiliser
BLYS64attractive charge-charge interaction, electrostatic stabiliser, hydrogen bond donor
BASP67electrostatic stabiliser, hydrogen bond acceptor
BALA68ground state destabiliser
BLEU72ground state destabiliser
BASP112electrostatic stabiliser, hydrogen bond acceptor, increase acidity, increase basicity
BHIS136hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
BARG139hydrogen bond donor, proton acceptor, proton donor

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PDB entries from 2024-06-12

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