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ADENYLOSUCCINATE SYNTHETASE INHIBITED BY HYDANTOCIDIN 5'-MONOPHOSPHATE

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0000287molecular_functionmagnesium ion binding
A0004019molecular_functionadenylosuccinate synthase activity
A0005515molecular_functionprotein binding
A0005525molecular_functionGTP binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006164biological_processpurine nucleotide biosynthetic process
A0006974biological_processDNA damage response
A0015949biological_processnucleobase-containing small molecule interconversion
A0016020cellular_componentmembrane
A0016874molecular_functionligase activity
A0044208biological_process'de novo' AMP biosynthetic process
A0046040biological_processIMP metabolic process
A0046086biological_processadenosine biosynthetic process
A0046872molecular_functionmetal ion binding
A0097216molecular_functionguanosine tetraphosphate binding
Functional Information from PDB Data
site_idAC1
Number of Residues10
DetailsBINDING SITE FOR RESIDUE SO4 A 442
ChainResidue
AASP13
ANA547
AGLU14
AGLY15
ALYS16
AGLY17
AGLY40
AHIS41
ASO4443
AHOH535

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 444
ChainResidue
AARG131
AGLY298
AALA299
AARG303
AARG305

site_idAC3
Number of Residues12
DetailsBINDING SITE FOR RESIDUE SO4 A 443
ChainResidue
AGLY12
AASP13
ALYS16
AALA39
AGLY40
AHIS41
AALA223
AGLN224
ASO4442
AH5P453
ANA547
AHOH594

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE NA A 547
ChainResidue
AASP13
AGLY40
ASO4442
ASO4443
AHOH594

site_idAC5
Number of Residues19
DetailsBINDING SITE FOR RESIDUE H5P A 453
ChainResidue
AASN38
AGLY127
ATHR128
ATHR129
AARG143
AGLN224
ALEU228
AVAL238
ATHR239
AVAL273
AARG303
ASO4443
AHOH521
AHOH575
AHOH577
AHOH590
AHOH591
AHOH592
AHOH595

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE BME A 459
ChainResidue
ACYS291
ALYS292
APHE297
AARG304
AGLU404
AGLY407

Functional Information from PROSITE/UniProt
site_idPS00513
Number of Residues12
DetailsADENYLOSUCCIN_SYN_2 Adenylosuccinate synthetase active site. GIGPaYedKvaR
ChainResidueDetails
AGLY132-ARG143

site_idPS01266
Number of Residues8
DetailsADENYLOSUCCIN_SYN_1 Adenylosuccinate synthetase GTP-binding site. QWGDEGKG
ChainResidueDetails
AGLN10-GLY17

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton acceptor
ChainResidueDetails
AGLU14

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Proton donor
ChainResidueDetails
ATHR42

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00011, ECO:0000269|PubMed:10346917
ChainResidueDetails
AARG306
ALEU332
ATHR415
AASP13

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00011, ECO:0000269|PubMed:10346917, ECO:0000269|PubMed:8961938, ECO:0000269|PubMed:9000627
ChainResidueDetails
AGLU14
AHIS41

site_idSWS_FT_FI5
Number of Residues1
DetailsBINDING: in other chain
ChainResidueDetails
AALA39

site_idSWS_FT_FI6
Number of Residues4
DetailsBINDING: in other chain => ECO:0000255|HAMAP-Rule:MF_00011, ECO:0000269|PubMed:10346917, ECO:0000269|PubMed:9000627
ChainResidueDetails
AGLY130
AGLY225
ASER240
AARG304

site_idSWS_FT_FI7
Number of Residues1
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00011, ECO:0000269|PubMed:10346917, ECO:0000269|PubMed:9000627
ChainResidueDetails
AARG144

site_idSWS_FT_FI8
Number of Residues1
DetailsBINDING:
ChainResidueDetails
ATHR300

Catalytic Information from CSA
site_idMCSA1
Number of Residues5
DetailsM-CSA 65
ChainResidueDetails
ATHR42electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AGLU14electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, metal ligand, proton acceptor, proton donor
AGLY17electrostatic stabiliser, hydrogen bond donor
AHIS41metal ligand
AGLY225electrostatic stabiliser, hydrogen bond donor

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PDB entries from 2024-06-12

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