Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

6ZA4

M. tuberculosis salicylate synthase MbtI in complex with 5-(3-cyanophenyl)furan-2-carboxylate

Functional Information from GO Data
ChainGOidnamespacecontents
A0000162biological_processtryptophan biosynthetic process
A0000287molecular_functionmagnesium ion binding
A0004106molecular_functionchorismate mutase activity
A0005886cellular_componentplasma membrane
A0008909molecular_functionisochorismate synthase activity
A0009058biological_processbiosynthetic process
A0009697biological_processsalicylic acid biosynthetic process
A0010106biological_processcellular response to iron ion starvation
A0016829molecular_functionlyase activity
A0016833molecular_functionoxo-acid-lyase activity
A0016853molecular_functionisomerase activity
A0019540biological_processcatechol-containing siderophore biosynthetic process
A0043904molecular_functionisochorismate pyruvate lyase activity
A0046872molecular_functionmetal ion binding
A0052572biological_processresponse to host immune response
B0000162biological_processtryptophan biosynthetic process
B0000287molecular_functionmagnesium ion binding
B0004106molecular_functionchorismate mutase activity
B0005886cellular_componentplasma membrane
B0008909molecular_functionisochorismate synthase activity
B0009058biological_processbiosynthetic process
B0009697biological_processsalicylic acid biosynthetic process
B0010106biological_processcellular response to iron ion starvation
B0016829molecular_functionlyase activity
B0016833molecular_functionoxo-acid-lyase activity
B0016853molecular_functionisomerase activity
B0019540biological_processcatechol-containing siderophore biosynthetic process
B0043904molecular_functionisochorismate pyruvate lyase activity
B0046872molecular_functionmetal ion binding
B0052572biological_processresponse to host immune response
C0000162biological_processtryptophan biosynthetic process
C0000287molecular_functionmagnesium ion binding
C0004106molecular_functionchorismate mutase activity
C0005886cellular_componentplasma membrane
C0008909molecular_functionisochorismate synthase activity
C0009058biological_processbiosynthetic process
C0009697biological_processsalicylic acid biosynthetic process
C0010106biological_processcellular response to iron ion starvation
C0016829molecular_functionlyase activity
C0016833molecular_functionoxo-acid-lyase activity
C0016853molecular_functionisomerase activity
C0019540biological_processcatechol-containing siderophore biosynthetic process
C0043904molecular_functionisochorismate pyruvate lyase activity
C0046872molecular_functionmetal ion binding
C0052572biological_processresponse to host immune response
D0000162biological_processtryptophan biosynthetic process
D0000287molecular_functionmagnesium ion binding
D0004106molecular_functionchorismate mutase activity
D0005886cellular_componentplasma membrane
D0008909molecular_functionisochorismate synthase activity
D0009058biological_processbiosynthetic process
D0009697biological_processsalicylic acid biosynthetic process
D0010106biological_processcellular response to iron ion starvation
D0016829molecular_functionlyase activity
D0016833molecular_functionoxo-acid-lyase activity
D0016853molecular_functionisomerase activity
D0019540biological_processcatechol-containing siderophore biosynthetic process
D0043904molecular_functionisochorismate pyruvate lyase activity
D0046872molecular_functionmetal ion binding
D0052572biological_processresponse to host immune response
Functional Information from PDB Data
site_idAC1
Number of Residues10
Detailsbinding site for residue M83 A 501
ChainResidue
ALYS205
AHOH700
AILE207
ATHR361
ATYR385
ALEU404
AALA418
AGLY419
ALYS438
AHOH654

site_idAC2
Number of Residues10
Detailsbinding site for residue M83 B 501
ChainResidue
BLYS205
BILE207
BTHR361
BTYR385
BARG405
BALA418
BGLY419
BLYS438
BHOH631
BHOH763

site_idAC3
Number of Residues1
Detailsbinding site for residue CL B 502
ChainResidue
BARG189

site_idAC4
Number of Residues10
Detailsbinding site for residue M83 C 501
ChainResidue
CLYS205
CILE207
CTHR361
CTYR385
CLEU404
CARG405
CALA418
CGLY419
CLYS438
CHOH647

site_idAC5
Number of Residues9
Detailsbinding site for residue M83 D 501
ChainResidue
DLYS205
DILE207
DTHR361
DTYR385
DARG405
DALA418
DGLY419
DLYS438
DHOH627

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton donor => ECO:0000250|UniProtKB:Q9X9I8
ChainResidueDetails
AGLU252
BGLU252
CGLU252
DGLU252

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:20512795, ECO:0000269|PubMed:22607697
ChainResidueDetails
AGLY270
BGLY270
CGLY270
DGLY270

site_idSWS_FT_FI3
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:20512795
ChainResidueDetails
AGLU297
DGLU297
DGLU431
DGLU434
AGLU431
AGLU434
BGLU297
BGLU431
BGLU434
CGLU297
CGLU431
CGLU434

site_idSWS_FT_FI4
Number of Residues16
DetailsBINDING: BINDING => ECO:0000269|PubMed:16923875, ECO:0000269|PubMed:20512795, ECO:0000269|PubMed:22607697
ChainResidueDetails
ATYR385
CARG405
CGLY419
CLYS438
DTYR385
DARG405
DGLY419
DLYS438
AARG405
AGLY419
ALYS438
BTYR385
BARG405
BGLY419
BLYS438
CTYR385

site_idSWS_FT_FI5
Number of Residues4
DetailsSITE: Could activate a water molecule for attack at the C2 of chorismate and involved in recognition/elimination of the C4 hydroxyl => ECO:0000269|PubMed:17240979
ChainResidueDetails
ALEU268
BLEU268
CLEU268
DLEU268

222624

PDB entries from 2024-07-17

PDB statisticsPDBj update infoContact PDBjnumon