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3IVG

Crystal structure of pantothenate synthetase in complex with 2-(2-((benzofuran-2-sulfonamido)methyl)-5-methoxy-1H-indol-1-yl)acetic acid

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0000287molecular_functionmagnesium ion binding
A0004592molecular_functionpantoate-beta-alanine ligase activity
A0005515molecular_functionprotein binding
A0005524molecular_functionATP binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0015940biological_processpantothenate biosynthetic process
A0016874molecular_functionligase activity
A0019482biological_processbeta-alanine metabolic process
A0030145molecular_functionmanganese ion binding
A0046872molecular_functionmetal ion binding
B0000166molecular_functionnucleotide binding
B0000287molecular_functionmagnesium ion binding
B0004592molecular_functionpantoate-beta-alanine ligase activity
B0005515molecular_functionprotein binding
B0005524molecular_functionATP binding
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0015940biological_processpantothenate biosynthetic process
B0016874molecular_functionligase activity
B0019482biological_processbeta-alanine metabolic process
B0030145molecular_functionmanganese ion binding
B0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL A 302
ChainResidue
AMET40
AGLN72
AVAL139
AVAL142
AGLN164
AHOH440

site_idAC2
Number of Residues2
DetailsBINDING SITE FOR RESIDUE GOL A 303
ChainResidue
APRO111
AASP112

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EOH A 304
ChainResidue
ATHR117
AHOH530
BGLN119
BPRO120
AARG115

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EOH A 305
ChainResidue
ATHR218
BHIS222
BTHR225

site_idAC5
Number of Residues2
DetailsBINDING SITE FOR RESIDUE EOH A 306
ChainResidue
AASN176
BGLY18

site_idAC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EDO A 307
ChainResidue
APRO70
AMET71
ALEU114

site_idAC7
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO A 308
ChainResidue
AMET109
ATYR110
AGLY113
AARG115
ATHR116
ALYS145
BASP174

site_idAC8
Number of Residues10
DetailsBINDING SITE FOR RESIDUE GOL A 309
ChainResidue
AGLY46
ALEU50
AGLY158
AGLU159
ALYS160
AVAL184
APRO185
ATHR186
AVAL187
AHOH318

site_idAC9
Number of Residues3
DetailsBINDING SITE FOR RESIDUE GOL A 310
ChainResidue
AMET71
ALEU114
ATHR134

site_idBC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL B 302
ChainResidue
AGLN148
AARG151
BLEU147
BGLN148
BARG151
BLEU177
BASP178
BHOH324

site_idBC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EOH B 303
ChainResidue
BLYS160
BTHR186
BALA194
BLEU280
BASP281
BASN282
BHOH370

site_idBC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EOH B 304
ChainResidue
BGLU251
BLEU252
BARG253
BHOH328
BHOH336

site_idBC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EOH B 422
ChainResidue
BSER24
BARG28
BVAL150
BARG151

site_idBC5
Number of Residues16
DetailsBINDING SITE FOR RESIDUE FG5 B 305
ChainResidue
BPRO38
BTHR39
BMET40
BHIS44
BGLY46
BHIS47
BGLN72
BVAL142
BLYS160
BASP161
BPRO185
BVAL187
BMET195
BSER196
BHOH387
BHOH433

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton donor
ChainResidueDetails
AHIS47
BHIS47

site_idSWS_FT_FI2
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:16460002
ChainResidueDetails
AMET40
AGLY158
AVAL187
AMET195
BMET40
BGLY158
BVAL187
BMET195

site_idSWS_FT_FI3
Number of Residues10
DetailsBINDING:
ChainResidueDetails
AGLN72
BGLN164
AASP88
AASP89
AGLN92
AGLN164
BGLN72
BASP88
BASP89
BGLN92

site_idSWS_FT_FI4
Number of Residues2
DetailsMOD_RES: N-acetylthreonine => ECO:0007744|PubMed:21969609
ChainResidueDetails
AALA2
BALA2

Catalytic Information from CSA
site_idMCSA1
Number of Residues10
DetailsM-CSA 229
ChainResidueDetails
AMET40electrostatic stabiliser
AARG198electrostatic stabiliser, hydrogen bond donor
AHIS44electrostatic stabiliser, hydrogen bond donor, van der waals interaction
AHIS47electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor, van der waals interaction
AASP88metal ligand
AASP89metal ligand
AGLN92metal ligand
ALYS160electrostatic stabiliser
ASER196electrostatic stabiliser, hydrogen bond donor
ASER197electrostatic stabiliser, hydrogen bond donor

site_idMCSA2
Number of Residues10
DetailsM-CSA 229
ChainResidueDetails
BMET40electrostatic stabiliser
BARG198electrostatic stabiliser, hydrogen bond donor
BHIS44electrostatic stabiliser, hydrogen bond donor, van der waals interaction
BHIS47electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor, van der waals interaction
BASP88metal ligand
BASP89metal ligand
BGLN92metal ligand
BLYS160electrostatic stabiliser
BSER196electrostatic stabiliser, hydrogen bond donor
BSER197electrostatic stabiliser, hydrogen bond donor

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PDB entries from 2025-06-11

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