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3COW

Crystal Structure of Mycobacterium Tuberculosis Pantothenate Synthetase at 1.8 Ang resolution- in complex with sulphonamide inhibitor 2

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 Residues17
DetailsBINDING SITE FOR RESIDUE 52H A 401
ChainResidue
APRO38
APHE157
AGLY158
ALYS160
AASP161
AGLN164
APRO185
ATHR186
AMET195
ATHR39
AMET40
AHIS44
AGLY46
AHIS47
ALEU50
AGLN72
ATYR82

site_idAC2
Number of Residues16
DetailsBINDING SITE FOR RESIDUE 52H B 402
ChainResidue
BPRO38
BTHR39
BMET40
BHIS44
BGLY46
BHIS47
BLEU50
BGLN72
BPHE157
BGLY158
BLYS160
BASP161
BGLN164
BPRO185
BTHR186
BMET195

site_idAC3
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL A 707
ChainResidue
AMET109
ATYR110
APRO111
AASP112
AGLY113
AARG115
ATHR116
ALYS145
BASP174

site_idAC4
Number of Residues2
DetailsBINDING SITE FOR RESIDUE GOL A 708
ChainResidue
APRO111
AASP112

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EOH A 709
ChainResidue
ALEU114
AARG115
ATHR117
BGLN119
BPRO120

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EOH B 710
ChainResidue
BSER24
BARG25
BARG28
BARG151

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

220113

PDB entries from 2024-05-22

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