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1KH1

Crystal Structure of Thermus thermophilus HB8 Argininosuccinate Synthetase

Functional Information from GO Data
ChainGOidnamespacecontents
A0000050biological_processurea cycle
A0000053biological_processargininosuccinate metabolic process
A0004055molecular_functionargininosuccinate synthase activity
A0005524molecular_functionATP binding
A0005737cellular_componentcytoplasm
A0006526biological_processarginine biosynthetic process
A0016874molecular_functionligase activity
B0000050biological_processurea cycle
B0000053biological_processargininosuccinate metabolic process
B0004055molecular_functionargininosuccinate synthase activity
B0005524molecular_functionATP binding
B0005737cellular_componentcytoplasm
B0006526biological_processarginine biosynthetic process
B0016874molecular_functionligase activity
C0000050biological_processurea cycle
C0000053biological_processargininosuccinate metabolic process
C0004055molecular_functionargininosuccinate synthase activity
C0005524molecular_functionATP binding
C0005737cellular_componentcytoplasm
C0006526biological_processarginine biosynthetic process
C0016874molecular_functionligase activity
D0000050biological_processurea cycle
D0000053biological_processargininosuccinate metabolic process
D0004055molecular_functionargininosuccinate synthase activity
D0005524molecular_functionATP binding
D0005737cellular_componentcytoplasm
D0006526biological_processarginine biosynthetic process
D0016874molecular_functionligase activity
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 510
ChainResidue
ASER8
AGLY10
AASP12
ATHR13
AHOH1457

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 B 1510
ChainResidue
BHOH1194
BHOH1226
BSER8
BGLY10
BASP12
BTHR13

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 C 2510
ChainResidue
CSER8
CGLY10
CASP12
CTHR13

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 D 3510
ChainResidue
DSER8
DGLY10
DASP12
DTHR13

Functional Information from PROSITE/UniProt
site_idPS00564
Number of Residues9
DetailsARGININOSUCCIN_SYN_1 Argininosuccinate synthase signature 1. AYSGGLDTS
ChainResidueDetails
AALA6-SER14

site_idPS00565
Number of Residues12
DetailsARGININOSUCCIN_SYN_2 Argininosuccinate synthase signature 2. GaTgKGNDqvRF
ChainResidueDetails
AGLY114-PHE125

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues12
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00005, ECO:0000269|PubMed:11844799, ECO:0000269|PubMed:12684518
ChainResidueDetails
AALA6
DALA6
DALA33
DGLY114
AALA33
AGLY114
BALA6
BALA33
BGLY114
CALA6
CALA33
CGLY114

site_idSWS_FT_FI2
Number of Residues40
DetailsBINDING:
ChainResidueDetails
ATYR84
ATYR270
BTYR84
BSER89
BTHR116
BASN120
BASP121
BARG124
BSER173
BSER182
BGLU258
ASER89
BTYR270
CTYR84
CSER89
CTHR116
CASN120
CASP121
CARG124
CSER173
CSER182
CGLU258
ATHR116
CTYR270
DTYR84
DSER89
DTHR116
DASN120
DASP121
DARG124
DSER173
DSER182
DGLU258
AASN120
DTYR270
AASP121
AARG124
ASER173
ASER182
AGLU258

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1kp2
ChainResidueDetails
AASP121
AARG92

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1kp2
ChainResidueDetails
BASP121
BARG92

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1kp2
ChainResidueDetails
CASP121
CARG92

site_idCSA4
Number of Residues2
DetailsAnnotated By Reference To The Literature 1kp2
ChainResidueDetails
DASP121
DARG92

site_idMCSA1
Number of Residues4
DetailsM-CSA 316
ChainResidueDetails
AASP12steric role
AARG92electrostatic stabiliser, hydrogen bond donor
AASP121proton acceptor, proton donor
ASER173hydrogen bond donor, steric role

site_idMCSA2
Number of Residues4
DetailsM-CSA 316
ChainResidueDetails
BASP12steric role
BARG92electrostatic stabiliser, hydrogen bond donor
BASP121proton acceptor, proton donor
BSER173hydrogen bond donor, steric role

site_idMCSA3
Number of Residues4
DetailsM-CSA 316
ChainResidueDetails
CASP12steric role
CARG92electrostatic stabiliser, hydrogen bond donor
CASP121proton acceptor, proton donor
CSER173hydrogen bond donor, steric role

site_idMCSA4
Number of Residues4
DetailsM-CSA 316
ChainResidueDetails
DASP12steric role
DARG92electrostatic stabiliser, hydrogen bond donor
DASP121proton acceptor, proton donor
DSER173hydrogen bond donor, steric role

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PDB entries from 2024-05-01

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