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1QQ6

STRUCTURE OF L-2-HALOACID DEHALOGENASE FROM XANTHOBACTER AUTOTROPHICUS WITH CHLOROACETIC ACID COVALENTLY BOUND

Functional Information from GO Data
ChainGOidnamespacecontents
A0016787molecular_functionhydrolase activity
A0018784molecular_function(S)-2-haloacid dehalogenase activity
A0019120molecular_functionhydrolase activity, acting on acid halide bonds, in C-halide compounds
B0016787molecular_functionhydrolase activity
B0018784molecular_function(S)-2-haloacid dehalogenase activity
B0019120molecular_functionhydrolase activity, acting on acid halide bonds, in C-halide compounds
Functional Information from PDB Data
site_idAC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 1001
ChainResidue
AASB8
AARG39
AASN115

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL B 1002
ChainResidue
BASB8
BARG39
BASN115

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Nucleophile => ECO:0000269|PubMed:10521454, ECO:0000269|PubMed:9407083
ChainResidueDetails
AASB8
BASB8

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:10521454, ECO:0000269|PubMed:9407083, ECO:0007744|PDB:1AQ6, ECO:0007744|PDB:1QQ5, ECO:0007744|PDB:1QQ6, ECO:0007744|PDB:1QQ7
ChainResidueDetails
AALA9
ASER114
BALA9
BSER114

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:10521454, ECO:0007744|PDB:1QQ6, ECO:0007744|PDB:1QQ7
ChainResidueDetails
AARG39
BARG39

site_idSWS_FT_FI4
Number of Residues6
DetailsSITE: Important for catalytic activity => ECO:0000305|PubMed:10521454, ECO:0000305|PubMed:9407083
ChainResidueDetails
ATHR12
ALYS147
ATYR153
BTHR12
BLYS147
BTYR153

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1lvh
ChainResidueDetails
AGLY116
ALYS147

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1lvh
ChainResidueDetails
BGLY116
BLYS147

site_idCSA3
Number of Residues3
DetailsAnnotated By Reference To The Literature 1lvh
ChainResidueDetails
ASER114
AARG39
AASP176

site_idCSA4
Number of Residues3
DetailsAnnotated By Reference To The Literature 1lvh
ChainResidueDetails
BSER114
BARG39
BASP176

site_idCSA5
Number of Residues8
DetailsAnnotated By Reference To The Literature 1lvh
ChainResidueDetails
AARG39
AASP176
ATHR12
APHE175
ALYS147
AASN173
ASER171
AASN115

site_idCSA6
Number of Residues8
DetailsAnnotated By Reference To The Literature 1lvh
ChainResidueDetails
BARG39
BASP176
BTHR12
BPHE175
BLYS147
BASN173
BSER171
BASN115

site_idMCSA1
Number of Residues10
DetailsM-CSA 36
ChainResidueDetails
AASB8hydrogen bond acceptor, nucleofuge, nucleophile
AASP176activator, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
ATHR12electrostatic stabiliser, hydrogen bond donor
AARG39electrostatic stabiliser, hydrogen bond donor
ASER114electrostatic stabiliser
AASN115electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor
ALYS147activator, hydrogen bond donor
ASER171electrostatic stabiliser, hydrogen bond donor
AASN173electrostatic stabiliser, hydrogen bond donor
APHE175electrostatic stabiliser, polar/non-polar interaction

site_idMCSA2
Number of Residues10
DetailsM-CSA 36
ChainResidueDetails
BASB8hydrogen bond acceptor, nucleofuge, nucleophile
BASP176activator, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
BTHR12electrostatic stabiliser, hydrogen bond donor
BARG39electrostatic stabiliser, hydrogen bond donor
BSER114electrostatic stabiliser
BASN115electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor
BLYS147activator, hydrogen bond donor
BSER171electrostatic stabiliser, hydrogen bond donor
BASN173electrostatic stabiliser, hydrogen bond donor
BPHE175electrostatic stabiliser, polar/non-polar interaction

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PDB entries from 2024-07-10

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