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4B6O

Structure of Mycobacterium tuberculosis Type II Dehydroquinase inhibited by (2S)-2-(4-methoxy)benzyl-3-dehydroquinic acid

Functional Information from GO Data
ChainGOidnamespacecontents
A0003855molecular_function3-dehydroquinate dehydratase activity
A0005829cellular_componentcytosol
A0008652biological_processamino acid biosynthetic process
A0009073biological_processaromatic amino acid family biosynthetic process
A0009423biological_processchorismate biosynthetic process
A0016829molecular_functionlyase activity
A0019631biological_processquinate catabolic process
Functional Information from PDB Data
site_idAC1
Number of Residues15
DetailsBINDING SITE FOR RESIDUE 3DQ A 1144
ChainResidue
AASN12
AHIS101
AILE102
ASER103
AARG112
AHOH2010
AHOH2085
AARG15
ATYR24
AASN75
AGLY77
AGLY78
AHIS81
AASP88
AGLU92

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 1145
ChainResidue
AARG50
ATRP61
AGLN64

site_idAC3
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SO4 A 1146
ChainResidue
ASER54
ASER54
ASER54
AHOH2054
AHOH2054
AHOH2054
AHOH2114
AHOH2114
AHOH2114

site_idAC4
Number of Residues8
DetailsBINDING SITE FOR RESIDUE SO4 A 1147
ChainResidue
AARG87
APHE111
AARG113
AHIS114
ASER115
ATYR116
APRO119
AHOH2075

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 1148
ChainResidue
AGLN57
AHOH2053
AHOH2115

Functional Information from PROSITE/UniProt
site_idPS01029
Number of Residues18
DetailsDEHYDROQUINASE_II Dehydroquinase class II signature. INGPNLgrLGrREpavYG
ChainResidueDetails
AILE8-GLY25

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton acceptor
ChainResidueDetails
ATYR24

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Proton donor
ChainResidueDetails
AHIS101

site_idSWS_FT_FI3
Number of Residues5
DetailsBINDING:
ChainResidueDetails
AARG112
AASN75
AHIS81
AASP88
AILE102

site_idSWS_FT_FI4
Number of Residues1
DetailsSITE: Transition state stabilizer
ChainResidueDetails
AARG19

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PDB entries from 2024-05-01

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