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6C8P

Crystal structure of Mycobacterium tuberculosis malate synthase in complex with 2-F-phenyldiketoacid

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0001968molecular_functionfibronectin binding
A0003824molecular_functioncatalytic activity
A0004474molecular_functionmalate synthase activity
A0005515molecular_functionprotein binding
A0005518molecular_functioncollagen binding
A0005576cellular_componentextracellular region
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0005886cellular_componentplasma membrane
A0006097biological_processglyoxylate cycle
A0006099biological_processtricarboxylic acid cycle
A0009274cellular_componentpeptidoglycan-based cell wall
A0009436biological_processglyoxylate catabolic process
A0009986cellular_componentcell surface
A0015936biological_processcoenzyme A metabolic process
A0016740molecular_functiontransferase activity
A0042603cellular_componentcapsule
A0042803molecular_functionprotein homodimerization activity
A0043236molecular_functionlaminin binding
A0044406biological_processadhesion of symbiont to host
A0046810molecular_functionhost cell extracellular matrix binding
A0046872molecular_functionmetal ion binding
A0120225molecular_functioncoenzyme A binding
Functional Information from PDB Data
site_idAC1
Number of Residues5
Detailsbinding site for residue MG A 801
ChainResidue
AGLU434
AASP462
AEQA804
AHOH957
AHOH974

site_idAC2
Number of Residues6
Detailsbinding site for residue MG A 802
ChainResidue
AHOH1301
AHOH1404
AHIS235
AHOH976
AHOH1192
AHOH1197

site_idAC3
Number of Residues6
Detailsbinding site for residue MG A 803
ChainResidue
AHOH987
AHOH1014
AHOH1073
AHOH1095
AHOH1389
AHOH1399

site_idAC4
Number of Residues14
Detailsbinding site for residue EQA A 804
ChainResidue
AVAL118
AARG339
AGLU434
AGLY459
APHE460
ALEU461
AASP462
AMET515
ATRP541
AMET631
AASP633
AMG801
AHOH974
AHOH1101

site_idAC5
Number of Residues4
Detailsbinding site for residue PEG A 805
ChainResidue
AGLU59
AGLY89
AHOH1223
AHOH1323

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton acceptor
ChainResidueDetails
AARG339

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Proton donor
ChainResidueDetails
AASP633

site_idSWS_FT_FI3
Number of Residues12
DetailsBINDING:
ChainResidueDetails
ASER275
AARG312
AARG339
AGLU434
AGLY459
AASP462
APRO543
ALYS305
AGLY618
AASP633
AVAL118
AARG125

site_idSWS_FT_FI4
Number of Residues1
DetailsMOD_RES: Cysteine sulfenic acid (-SOH) => ECO:0000255|HAMAP-Rule:MF_00641
ChainResidueDetails
AALA619

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PDB entries from 2024-06-12

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