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1Q52

Crystal Structure of Mycobacterium tuberculosis MenB, a Key Enzyme in Vitamin K2 Biosynthesis

Functional Information from GO Data
ChainGOidnamespacecontents
A0005886cellular_componentplasma membrane
A0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
A0009234biological_processmenaquinone biosynthetic process
A0016829molecular_functionlyase activity
A0034214biological_processprotein hexamerization
B0005886cellular_componentplasma membrane
B0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
B0009234biological_processmenaquinone biosynthetic process
B0016829molecular_functionlyase activity
B0034214biological_processprotein hexamerization
C0005886cellular_componentplasma membrane
C0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
C0009234biological_processmenaquinone biosynthetic process
C0016829molecular_functionlyase activity
C0034214biological_processprotein hexamerization
D0005886cellular_componentplasma membrane
D0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
D0009234biological_processmenaquinone biosynthetic process
D0016829molecular_functionlyase activity
D0034214biological_processprotein hexamerization
E0005886cellular_componentplasma membrane
E0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
E0009234biological_processmenaquinone biosynthetic process
E0016829molecular_functionlyase activity
E0034214biological_processprotein hexamerization
F0005886cellular_componentplasma membrane
F0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
F0009234biological_processmenaquinone biosynthetic process
F0016829molecular_functionlyase activity
F0034214biological_processprotein hexamerization
G0005886cellular_componentplasma membrane
G0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
G0009234biological_processmenaquinone biosynthetic process
G0016829molecular_functionlyase activity
G0034214biological_processprotein hexamerization
H0005886cellular_componentplasma membrane
H0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
H0009234biological_processmenaquinone biosynthetic process
H0016829molecular_functionlyase activity
H0034214biological_processprotein hexamerization
I0005886cellular_componentplasma membrane
I0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
I0009234biological_processmenaquinone biosynthetic process
I0016829molecular_functionlyase activity
I0034214biological_processprotein hexamerization
J0005886cellular_componentplasma membrane
J0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
J0009234biological_processmenaquinone biosynthetic process
J0016829molecular_functionlyase activity
J0034214biological_processprotein hexamerization
K0005886cellular_componentplasma membrane
K0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
K0009234biological_processmenaquinone biosynthetic process
K0016829molecular_functionlyase activity
K0034214biological_processprotein hexamerization
L0005886cellular_componentplasma membrane
L0008935molecular_function1,4-dihydroxy-2-naphthoyl-CoA synthase activity
L0009234biological_processmenaquinone biosynthetic process
L0016829molecular_functionlyase activity
L0034214biological_processprotein hexamerization
Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues12
DetailsBinding site: {"description":"in other chain","evidences":[{"source":"HAMAP-Rule","id":"MF_01934","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"12909628","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"21830810","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues60
DetailsBinding site: {"description":"in other chain","evidences":[{"source":"HAMAP-Rule","id":"MF_01934","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"12909628","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues12
DetailsBinding site: {"description":"in other chain","evidences":[{"source":"HAMAP-Rule","id":"MF_01934","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"21830810","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues24
DetailsBinding site: {"evidences":[{"source":"UniProtKB","id":"P0ABU0","evidenceCode":"ECO:0000250"},{"source":"HAMAP-Rule","id":"MF_01934","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues12
DetailsSite: {"description":"Important for catalysis","evidences":[{"source":"HAMAP-Rule","id":"MF_01934","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"20643650","evidenceCode":"ECO:0000305"},{"source":"PubMed","id":"21830810","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues12
DetailsSite: {"description":"Important for catalysis","evidences":[{"source":"UniProtKB","id":"P0ABU0","evidenceCode":"ECO:0000250"},{"source":"HAMAP-Rule","id":"MF_01934","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"12909628","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues12
DetailsBinding site: {"description":"in other chain","evidences":[{"source":"PubMed","id":"12909628","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"21830810","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
AASP192
AASP185

site_idCSA10
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
JASP192
JASP185

site_idCSA11
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
KASP192
KASP185

site_idCSA12
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
LASP192
LASP185

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
BASP192
BASP185

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
CASP192
CASP185

site_idCSA4
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
DASP192
DASP185

site_idCSA5
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
EASP192
EASP185

site_idCSA6
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
FASP192
FASP185

site_idCSA7
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
GASP192
GASP185

site_idCSA8
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
HASP192
HASP185

site_idCSA9
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dci
ChainResidueDetails
IASP192
IASP185

site_idMCSA1
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
AGLY105electrostatic stabiliser, hydrogen bond donor
AGLY161electrostatic stabiliser, hydrogen bond donor
AASP185activator
ASER190activator
ATYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

site_idMCSA10
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
JGLY105electrostatic stabiliser, hydrogen bond donor
JGLY161electrostatic stabiliser, hydrogen bond donor
JASP185activator
JSER190activator
JTYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

site_idMCSA11
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
KGLY105electrostatic stabiliser, hydrogen bond donor
KGLY161electrostatic stabiliser, hydrogen bond donor
KASP185activator
KSER190activator
KTYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

site_idMCSA12
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
LGLY105electrostatic stabiliser, hydrogen bond donor
LGLY161electrostatic stabiliser, hydrogen bond donor
LASP185activator
LSER190activator
LTYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

site_idMCSA2
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
BGLY105electrostatic stabiliser, hydrogen bond donor
BGLY161electrostatic stabiliser, hydrogen bond donor
BASP185activator
BSER190activator
BTYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

site_idMCSA3
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
CGLY105electrostatic stabiliser, hydrogen bond donor
CGLY161electrostatic stabiliser, hydrogen bond donor
CASP185activator
CSER190activator
CTYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

site_idMCSA4
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
DGLY105electrostatic stabiliser, hydrogen bond donor
DGLY161electrostatic stabiliser, hydrogen bond donor
DASP185activator
DSER190activator
DTYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

site_idMCSA5
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
EGLY105electrostatic stabiliser, hydrogen bond donor
EGLY161electrostatic stabiliser, hydrogen bond donor
EASP185activator
ESER190activator
ETYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

site_idMCSA6
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
FGLY105electrostatic stabiliser, hydrogen bond donor
FGLY161electrostatic stabiliser, hydrogen bond donor
FASP185activator
FSER190activator
FTYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

site_idMCSA7
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
GGLY105electrostatic stabiliser, hydrogen bond donor
GGLY161electrostatic stabiliser, hydrogen bond donor
GASP185activator
GSER190activator
GTYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

site_idMCSA8
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
HGLY105electrostatic stabiliser, hydrogen bond donor
HGLY161electrostatic stabiliser, hydrogen bond donor
HASP185activator
HSER190activator
HTYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

site_idMCSA9
Number of Residues5
DetailsM-CSA 346
ChainResidueDetails
IGLY105electrostatic stabiliser, hydrogen bond donor
IGLY161electrostatic stabiliser, hydrogen bond donor
IASP185activator
ISER190activator
ITYR287electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar interaction, proton acceptor, proton donor, steric role

249697

PDB entries from 2026-02-25

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