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1N2J

Crystal Structure of a Pantothenate Synthetase from M. tuberculosis in complex with pantoate

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 Residues1
DetailsBINDING SITE FOR RESIDUE SO4 B 601
ChainResidue
BARG154

site_idAC2
Number of Residues2
DetailsBINDING SITE FOR RESIDUE SO4 A 602
ChainResidue
APRO58
AARG154

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 603
ChainResidue
AHIS44
AHIS47
ALYS160
ASER196
ASER197

site_idAC4
Number of Residues8
DetailsBINDING SITE FOR RESIDUE PAF A 1001
ChainResidue
ATHR39
AMET40
AGLN72
AVAL142
AGLN164
AHOH1003
AHOH1084
APRO38

site_idAC5
Number of Residues8
DetailsBINDING SITE FOR RESIDUE PAF B 1002
ChainResidue
BPRO38
BTHR39
BGLN72
BVAL142
BGLN164
BHOH1037
BHOH1092
BHOH1118

site_idAC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE BAL B 801
ChainResidue
BGLU128
BARG132
BASP161
BARG198
BLEU280
BHOH1013
BHOH1049

site_idAC7
Number of Residues3
DetailsBINDING SITE FOR RESIDUE BAL A 802
ChainResidue
AALA108
APRO111
AHOH1088

site_idAC8
Number of Residues11
DetailsBINDING SITE FOR RESIDUE GOL B 501
ChainResidue
BHIS44
BGLY46
BGLY158
BGLU159
BLYS160
BVAL184
BPRO185
BTHR186
BVAL187
BHOH1117
BHOH1123

site_idAC9
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL A 502
ChainResidue
AMET109
ATYR110
APRO111
AASP112
AGLY113
AARG115
ATHR116
ALYS145
BASP174

site_idBC1
Number of Residues2
DetailsBINDING SITE FOR RESIDUE GOL A 503
ChainResidue
ALEU11
AVAL13

site_idBC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EOH B 701
ChainResidue
AGLN148
AARG151
BASN176

site_idBC3
Number of Residues2
DetailsBINDING SITE FOR RESIDUE EOH B 702
ChainResidue
BTHR105
BTHR106

site_idBC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EOH B 703
ChainResidue
AASN176
BGLN148
BARG151

site_idBC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EOH B 704
ChainResidue
BGLN206
BGLY244
BLEU274
BGLY275

site_idBC6
Number of Residues2
DetailsBINDING SITE FOR RESIDUE EOH B 705
ChainResidue
BALA284
BHOH1104

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 2024-10-30

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