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4EFK

Pantothenate synthetase in complex with N,N-DIMETHYLTHIOPHENE-3-SULFONAMIDE

Functional Information from GO Data
ChainGOidnamespacecontents
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
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 Residues11
DetailsBINDING SITE FOR RESIDUE 0OC A 401
ChainResidue
APRO38
AGLN164
AHOH506
ATHR39
AMET40
APHE67
AASN69
AVAL142
AVAL143
ALEU146
APHE157

site_idAC2
Number of Residues2
DetailsBINDING SITE FOR RESIDUE 0OC A 402
ChainResidue
APRO70
AGLN72

site_idAC3
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL A 403
ChainResidue
AMET109
ATYR110
APRO111
AASP112
AGLY113
AARG115
ATHR116
ALYS145
BASP174

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE EOH A 404
ChainResidue
ALEU114
AARG115
ATHR117
BGLN119
BPRO120
BHOH675

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EOH A 405
ChainResidue
ATHR218
BHIS222
BTHR225

site_idAC6
Number of Residues2
DetailsBINDING SITE FOR RESIDUE IMD A 406
ChainResidue
APRO70
AGLN72

site_idAC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EOH A 407
ChainResidue
ASER24
AARG28
AVAL150
AARG151

site_idAC8
Number of Residues10
DetailsBINDING SITE FOR RESIDUE 0OC B 401
ChainResidue
BPRO38
BTHR39
BPHE67
BASN69
BVAL142
BVAL143
BLEU146
BGLN164
BEOH406
BHOH520

site_idAC9
Number of Residues3
DetailsBINDING SITE FOR RESIDUE GOL B 402
ChainResidue
BGLY244
BARG273
BGLY275

site_idBC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 B 403
ChainResidue
BHIS44
BHIS47
BASP161

site_idBC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL B 404
ChainResidue
AASP178
BALA21
BSER24
BARG25
BGLN148
BILE149
BVAL150
BARG151
BHOH597

site_idBC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE EOH B 406
ChainResidue
BTHR39
BMET40
BHIS47
B0OC401
BHOH687
BHOH705

site_idBC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EOH B 407
ChainResidue
BGLN206
BGLY275
BTHR276
BHOH566

site_idBC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EOH B 408
ChainResidue
BARG253
BLEU257
BGLY258
BPRO259

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 2024-09-04

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