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1Q6L

Structure of 3-keto-L-gulonate 6-phosphate decarboxylase with bound L-threonohydroxamate 4-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 Residues5
DetailsBINDING SITE FOR RESIDUE MG A 5300
ChainResidue
AGLU33
AASP62
ATX45301
AHOH5372
AHOH5373

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG B 9300
ChainResidue
BHOH9408
BGLU33
BASP62
BTX49301
BHOH9407

site_idAC3
Number of Residues20
DetailsBINDING SITE FOR RESIDUE TX4 A 5301
ChainResidue
AALA9
AASP11
AGLU33
AASP62
ALYS64
AHIS136
ATHR169
AGLY171
AGLY191
AARG192
AMG5300
AHOH5303
AHOH5308
AHOH5312
AHOH5326
AHOH5372
AHOH5373
AHOH5376
AHOH5398
BASP67

site_idAC4
Number of Residues20
DetailsBINDING SITE FOR RESIDUE TX4 B 9301
ChainResidue
AASP67
BALA9
BASP11
BGLU33
BASP62
BLYS64
BHIS136
BTHR169
BGLY171
BGLY191
BARG192
BMG9300
BHOH9303
BHOH9314
BHOH9316
BHOH9407
BHOH9408
BHOH9409
BHOH9411
BHOH9413

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

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

Catalytic Information from CSA
site_idCSA1
Number of Residues9
Details
ChainResidueDetails
AHIS136
ALYS64
AGLU112
AARG139
AILE37
ATHR36
BALA68
BLEU72
BASP67

site_idCSA2
Number of Residues6
Details
ChainResidueDetails
BHIS136
BLYS64
BARG139
BGLU112
BILE37
BTHR36

site_idCSA3
Number of Residues9
Details
ChainResidueDetails
AHIS136
ALYS64
AGLU112
AARG139
AILE37
ATHR36
BALA68
BLEU72
BASP67

site_idCSA4
Number of Residues3
Details
ChainResidueDetails
AALA68
ALEU72
AASP67

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
AGLU112electrostatic 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
BGLU112electrostatic 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 2024-07-10

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