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5CBI

Crystal structure of Mycobacterium tuberculosis malate synthase in complex with 5-chloro-2-hydroxybenzonitrile

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 Residues6
Detailsbinding site for residue MG A 801
ChainResidue
AGLU434
AASP462
AHOH978
AHOH1001
AHOH1199
AHOH1223

site_idAC2
Number of Residues7
Detailsbinding site for residue 4ZC A 802
ChainResidue
AGLY324
AGLY325
AGLY326
APRO706
ALEU54
AASN55
AASP58

site_idAC3
Number of Residues11
Detailsbinding site for residue 4ZC A 803
ChainResidue
ALEU461
AMET515
ATHR517
ATRP541
AMET631
AGLU632
AASP633
AHOH1000
AHOH1062
AHOH1080
AHOH1187

site_idAC4
Number of Residues8
Detailsbinding site for residue 4ZC A 804
ChainResidue
AVAL118
APHE126
APRO543
APRO545
AALA619
AMET631
AHOH909
AHOH925

site_idAC5
Number of Residues6
Detailsbinding site for residue 4ZC A 805
ChainResidue
ATYR139
AASP140
ATYR143
AALA302
AASP304
AARG312

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
AVAL118
APRO543
AGLY618
AASP633
AARG125
ASER275
ALYS305
AARG312
AARG339
AGLU434
AGLY459
AASP462

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

219515

PDB entries from 2024-05-08

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