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1SWW

Crystal structure of the phosphonoacetaldehyde hydrolase D12A mutant complexed with magnesium and substrate phosphonoacetaldehyde

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0003824molecular_functioncatalytic activity
A0016787molecular_functionhydrolase activity
A0019700biological_processorganic phosphonate catabolic process
A0046872molecular_functionmetal ion binding
A0050194molecular_functionphosphonoacetaldehyde hydrolase activity
B0000287molecular_functionmagnesium ion binding
B0003824molecular_functioncatalytic activity
B0016787molecular_functionhydrolase activity
B0019700biological_processorganic phosphonate catabolic process
B0046872molecular_functionmetal ion binding
B0050194molecular_functionphosphonoacetaldehyde hydrolase activity
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG A 501
ChainResidue
AALA12
AALA14
AASP186
AASP190
APOA600
AHOH656

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG B 502
ChainResidue
BTHR187
BASP190
BPOA700
BHOH717
BALA12
BALA14
BASP186

site_idAC3
Number of Residues11
DetailsBINDING SITE FOR RESIDUE POA A 600
ChainResidue
AALA12
ATRP13
AALA14
ALYS53
ATHR125
ATHR126
AGLY127
ATYR128
AARG160
AMG501
AHOH656

site_idAC4
Number of Residues14
DetailsBINDING SITE FOR RESIDUE POA B 700
ChainResidue
BALA12
BTRP13
BALA14
BGLY50
BTHR125
BTHR126
BGLY127
BTYR128
BARG160
BASP186
BASP190
BMG502
BHOH717
BHOH759

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Nucleophile
ChainResidueDetails
AALA12
BALA12

site_idSWS_FT_FI2
Number of Residues2
DetailsACT_SITE: Schiff-base intermediate with substrate
ChainResidueDetails
ALYS53
BLYS53

site_idSWS_FT_FI3
Number of Residues6
DetailsBINDING:
ChainResidueDetails
AALA12
AALA14
AASP186
BALA12
BALA14
BASP186

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1lvh
ChainResidueDetails
ATHR126
AARG160

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1lvh
ChainResidueDetails
BTHR126
BARG160

site_idCSA3
Number of Residues5
DetailsAnnotated By Reference To The Literature 1lvh
ChainResidueDetails
AMET49
AHIS56
ALYS53
AALA45
AALA12

site_idCSA4
Number of Residues5
DetailsAnnotated By Reference To The Literature 1lvh
ChainResidueDetails
BMET49
BHIS56
BLYS53
BALA45
BALA12

site_idMCSA1
Number of Residues8
DetailsM-CSA 181
ChainResidueDetails
AALA12hydrogen bond acceptor, metal ligand, nucleofuge, nucleophile
AALA14metal ligand
AALA45electrostatic stabiliser, hydrogen bond acceptor
AMET49activator, electrostatic stabiliser, hydrogen bond acceptor
ALYS53covalently attached, electron pair acceptor, electron pair donor, hydrogen bond acceptor, hydrogen bond donor, nucleofuge, nucleophile, polar interaction, proton acceptor, proton donor
AHIS56hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AARG160electrostatic stabiliser, hydrogen bond donor
AASP186metal ligand

site_idMCSA2
Number of Residues8
DetailsM-CSA 181
ChainResidueDetails
BALA12hydrogen bond acceptor, metal ligand, nucleofuge, nucleophile
BALA14metal ligand
BALA45electrostatic stabiliser, hydrogen bond acceptor
BMET49activator, electrostatic stabiliser, hydrogen bond acceptor
BLYS53covalently attached, electron pair acceptor, electron pair donor, hydrogen bond acceptor, hydrogen bond donor, nucleofuge, nucleophile, polar interaction, proton acceptor, proton donor
BHIS56hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
BARG160electrostatic stabiliser, hydrogen bond donor
BASP186metal ligand

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PDB entries from 2024-08-28

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