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4L9Y

Crystal Structure of Rhodobacter sphaeroides malyl-CoA lyase in complex with magnesium, glyoxylate, and propionyl-CoA

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0003824molecular_functioncatalytic activity
A0006107biological_processoxaloacetate metabolic process
A0016829molecular_functionlyase activity
A0043959molecular_functionL-erythro-3-methylmalyl-CoA lyase activity
A0046872molecular_functionmetal ion binding
A0047777molecular_function(S)-citramalyl-CoA lyase activity
A0050083molecular_functionmalyl-CoA lyase activity
B0000287molecular_functionmagnesium ion binding
B0003824molecular_functioncatalytic activity
B0006107biological_processoxaloacetate metabolic process
B0016829molecular_functionlyase activity
B0043959molecular_functionL-erythro-3-methylmalyl-CoA lyase activity
B0046872molecular_functionmetal ion binding
B0047777molecular_function(S)-citramalyl-CoA lyase activity
B0050083molecular_functionmalyl-CoA lyase activity
C0000287molecular_functionmagnesium ion binding
C0003824molecular_functioncatalytic activity
C0006107biological_processoxaloacetate metabolic process
C0016829molecular_functionlyase activity
C0043959molecular_functionL-erythro-3-methylmalyl-CoA lyase activity
C0046872molecular_functionmetal ion binding
C0047777molecular_function(S)-citramalyl-CoA lyase activity
C0050083molecular_functionmalyl-CoA lyase activity
D0000287molecular_functionmagnesium ion binding
D0003824molecular_functioncatalytic activity
D0006107biological_processoxaloacetate metabolic process
D0016829molecular_functionlyase activity
D0043959molecular_functionL-erythro-3-methylmalyl-CoA lyase activity
D0046872molecular_functionmetal ion binding
D0047777molecular_function(S)-citramalyl-CoA lyase activity
D0050083molecular_functionmalyl-CoA lyase activity
E0000287molecular_functionmagnesium ion binding
E0003824molecular_functioncatalytic activity
E0006107biological_processoxaloacetate metabolic process
E0016829molecular_functionlyase activity
E0043959molecular_functionL-erythro-3-methylmalyl-CoA lyase activity
E0046872molecular_functionmetal ion binding
E0047777molecular_function(S)-citramalyl-CoA lyase activity
E0050083molecular_functionmalyl-CoA lyase activity
F0000287molecular_functionmagnesium ion binding
F0003824molecular_functioncatalytic activity
F0006107biological_processoxaloacetate metabolic process
F0016829molecular_functionlyase activity
F0043959molecular_functionL-erythro-3-methylmalyl-CoA lyase activity
F0046872molecular_functionmetal ion binding
F0047777molecular_function(S)-citramalyl-CoA lyase activity
F0050083molecular_functionmalyl-CoA lyase activity
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG A 401
ChainResidue
AGLU141
AASP168
AHOH501
AHOH519
AHOH546
AHOH602

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CL A 402
ChainResidue
AASP168
AHOH501
AGLY165
AALA166
AALA167

site_idAC3
Number of Residues16
DetailsBINDING SITE FOR RESIDUE 1VU B 401
ChainResidue
AASP299
BPHE19
BGLY20
BARG24
BLYS30
BMET31
BARG76
BALA167
BILE180
BILE251
BHIS252
BPRO253
BGLV402
BHOH510
BHOH661
BHOH691

site_idAC4
Number of Residues10
DetailsBINDING SITE FOR RESIDUE GLV B 402
ChainResidue
BARG76
BGLU141
BGLY165
BALA166
BALA167
BASP168
BPRO223
B1VU401
BMG403
BHOH510

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG B 403
ChainResidue
BASP45
BGLU141
BASP168
BGLV402
BHOH510
BHOH724

site_idAC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG C 401
ChainResidue
CASP45
CGLU141
CASP168
CHOH502
CHOH503
CHOH507
CHOH763

site_idAC7
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CL C 402
ChainResidue
CGLY165
CALA166
CALA167
CASP168
CHOH502
CHOH627

site_idAC8
Number of Residues10
DetailsBINDING SITE FOR RESIDUE GLV D 401
ChainResidue
DARG76
DGLU141
DGLY165
DALA166
DALA167
DASP168
DPRO223
DTRP249
DMG402
DHOH501

site_idAC9
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG D 402
ChainResidue
DGLU141
DASP168
DGLV401
DHOH501
DHOH733

site_idBC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG E 401
ChainResidue
EASP45
EGLU141
EASP168
EHOH501
EHOH513
EHOH724
EHOH757

site_idBC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CL E 402
ChainResidue
EGLY165
EALA166
EALA167
EASP168
EPRO223
EHOH724

site_idBC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG F 401
ChainResidue
FASP45
FGLU141
FASP168
FHOH503
FHOH506
FHOH526
FHOH747

site_idBC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CL F 402
ChainResidue
FGLY165
FALA166
FALA167
FASP168
FPRO223
FHOH747

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:24206647, ECO:0007744|PDB:4L9Y
ChainResidueDetails
APHE19
EARG24
FPHE19
FARG24
AARG24
BPHE19
BARG24
CPHE19
CARG24
DPHE19
DARG24
EPHE19

site_idSWS_FT_FI2
Number of Residues18
DetailsBINDING: BINDING => ECO:0000269|PubMed:24206647, ECO:0007744|PDB:4L9Z
ChainResidueDetails
ALYS30
DLYS30
DALA167
DILE251
ELYS30
EALA167
EILE251
FLYS30
FALA167
FILE251
AALA167
AILE251
BLYS30
BALA167
BILE251
CLYS30
CALA167
CILE251

site_idSWS_FT_FI3
Number of Residues18
DetailsBINDING: BINDING => ECO:0000269|PubMed:24206647, ECO:0007744|PDB:4L9Y, ECO:0007744|PDB:4L9Z
ChainResidueDetails
AARG76
DARG76
DGLU141
DASP168
EARG76
EGLU141
EASP168
FARG76
FGLU141
FASP168
AGLU141
AASP168
BARG76
BGLU141
BASP168
CARG76
CGLU141
CASP168

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PDB entries from 2024-08-07

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