Rv3116 (moeB2)
Current annotations:
TBCAP: (community-based annotations - see table at bottom of page )
TBDB: molybdopterin biosynthesis protein MoeB
REFSEQ: molybdenum cofactor biosynthesis protein MoeB
PATRIC: Sulfur carrier protein adenylyltransferase ThiF
TUBERCULIST: Probable molybdenum cofactor biosynthesis protein MoeB2 (MPT-synthase sulfurylase) (molybdopterin synthase sulphurylase)
NCBI: Probable molybdenum cofactor biosynthesis protein MoeB2 (MPT-synthase sulfurylase) (molybdopterin synthase sulphurylase)
updated information (H37Rv4):
gene name: moeB2
function: aka 'moeBR'
reference: Voss (2011); PMID: 22140533
Coordinates in H37Rv: 3482776 - 3483945
Gene length: 1170 bp (with stop codon), 389 aa (without stop codon)
Operon:
Trans-membrane region:
Role: I.G.4 - Molybdopterin
GO terms:
GO:0016779 - nucleotidyltransferase activity (Uniprot)
GO:0008641 - ubiquitin-like modifier activating enzyme activity (Uniprot)
Reaction(s) (based on iSM810 metabolic model):
Gene Expression Profile (Transcriptional Responses to Drugs; Boshoff et al, 2004)
Gene Modules extracted from cluster analysis of 249 transcriptomic datasets using ICA
Orthologs among selected mycobacteria
Protein structure:
Search for Latest Homologs in PDB
Top 10 Homologs in PDB (as of Apr 2026): PDB aa ident species PDB title 6YUB 46% Chaetomium thermophilum Crystal structure of Uba4 from Chaetomium thermophilum 6Z6S 45% Chaetomium thermophilum var. thermophilum DSM 1495 Crystal structure of Uba4-Urm1 from Chaetomium thermophilum 6YUC 45% Chaetomium thermophilum Crystal structure of Uba4-Urm1 from Chaetomium thermophilum 5VE3 44% Paraburkholderia phytofirmans (strain DSM 17436 / LMG 22146 / PsJN) Crystal structure of wild-type persulfide dioxygenase-rhodanese fusion protein from Burkholderia phytofirmans 5VE5 43% Paraburkholderia phytofirmans (strain DSM 17436 / LMG 22146 / PsJN) Crystal structure of persulfide dioxygenase rhodanese fusion protein with rhodanese domain inactivating mutation (C314S) from Burkholderia phytofirmans in complex with glutathione 5VE4 43% Paraburkholderia phytofirmans (strain DSM 17436 / LMG 22146 / PsJN) Crystal structure of persulfide dioxygenase-rhodanese fusion protein with rhodanese domain inactivating mutation (C314S) from Burkholderia phytofirmans 3ICT 41% Bacillus anthracis Crystal structure of reduced Bacillus anthracis CoADR-RHD 3ICS 41% Bacillus anthracis Crystal structure of partially reduced Bacillus anthracis CoADR-RHD 3ICR 41% Bacillus anthracis Crystal structure of oxidized Bacillus anthracis CoADR-RHD 1JWB 40% Escherichia coli Structure of the Covalent Acyl-Adenylate Form of the MoeB-MoaD Protein Complex
Links to additional information on moeB2:
Amino Acid Sequence
MTEALIPAPSQISLTRDEVRRYSRHLIIPDIGVNGQQRLKDARVLCIGAGGLGSPALLYLAAAGVGTIGIIDGDHVDESNLQRQIIHGTSDVGRPKVESA
AEAVAEINPHVRVTQYREMLTHDNALEIFGDHDLIVDGTDNFTTRYLINDAAVLAGKPYVWGSIYRFNGQTSVFWPGRGPCYRCLHPAPPPPGLVPSCAE
GGVLGAICATIASIQVTEVLKLLTGVGTPLVGRLLMYEALDATYHQIRIAKNPDCAICGDAPTITELVDDSVSCASTQSVDPELVISCDELRTKQQSDQN
FLLVDVREPAEFDIAHIPGSILIPKGEIGSAAGLAQLPLDKEIVLYCKSGIRSAQALTTLKAAGLHNVKHLDGGIAEWTRTIDSSLLVY
(
Nucleotide sequence available on
KEGG )
Additional Information
MtbTnDB - interactive tool for exploring a database of published TnSeq datasets for Mtb
TnSeqCorr - genes with correlated TnSeq profiles across ~100 conditions
Rv3116/moeB2,
gene len: 1169 bp, num TA sites: 29
condition dataset call medium method notes
in-vitro DeJesus 2017 mBio non-essential 7H9 HMM fully saturated, 14 TnSeq libraries combined
in-vitro Sassetti 2003 Mol Micro non-essential 7H9 TRASH essential if hybridization ratio<0.2
in-vivo (mice) Sassetti 2003 PNAS non-essential BL6 mice TRASH essential if hybridization ratio<0.4, min over 4 timepoints (1-8 weeks)
in-vitro (glycerol) Griffin 2011 PPath non-essential M9 minimal+glycerol Gumbel 2 replicates; Padj<0.05
in-vitro (cholesterol) Griffin 2011 PPath non-essential M9 minimal+cholesterol Gumbel 3 replicates; Padj<0.05
differentially essential in cholesterol Griffin 2011 PPath NO (LFC=0.03) cholesterol vs glycerol resampling-SR YES if Padj<0.05, else not significant; LFC<0 means less insertions/more essential in cholesterol
in-vitro Smith 2022 eLife non-essential 7H9 HMM 6 replicates (raw data in Subramaniam 2017, PMID 31752678)
in-vivo (mice) Smith 2022 eLife non-essential BL6 mice HMM 6 replicates (raw data in Subramaniam 2017, PMID 31752678)
differentially essential in mice Smith 2022 eLife NO (LFC=0.288) in-vivo vs in-vitro ZINB YES if Padj<0.05, else not significant; LFC<0 means less insertions/more essential in mice
in-vitro (minimal) Minato 2019 mSys non-essential minimal medium HMM
in-vitro (YM rich medium) Minato 2019 mSys non-essential YM rich medium HMM 7H9 supplemented with ~20 metabolites (amino acids, cofactors)
differentially essential in YM rich medium Minato 2019 mSys NO (LFC=0.36) YM rich vs minimal medium resampling
Analysis of Positive Selection in Clinical Isolates
*new*
data from Culviner et al (2025) (55,259 Mtb clinical isolates)
overall pN/pS for Rv3116: 0.765036223
lineage-specific pN/pS in L1: 0.715792989
lineage-specific pN/pS in L2: 0.992656316
lineage-specific pN/pS in L3: 1.050429964
lineage-specific pN/pS in L4: 0.656209777
Analysis of dN/dS (omega) in a global collection of 10k Mtb clinical isolates using GenomegaMap (Window model)
clinical isolates collection: global set of 10,626 Mtb genomes
In the omega plots, the black line shows the mean estimate of omega (dN/dS) at each codon, and the blue lines are the bounds for the 95% credible interval (95%CI, from MCMC sampling).
A gene is under significant positive selection if the lower-bound of the 95%CI of omega (lower blue line) exceeds 1.0 at any codon.
global set of 10,626 Mtb clinical isolates
under significant positive selection? NO
omega peak height (95%CI lower bound) 1.6 (0.85)
codons under selection
omega plots
genetic variants* link
* example format for variants: "D27 (GAC): D27H (CAC,11)" means "Asp27 (native codon GAC) mutated to His (codon CAC) in 11 isolates"
TnSeq Data No data currently available.
No TnSeq data currently available for this Target.
RNASeq Data No data currently available.
No RNA-Seq data currently available for this Target.
Metabolomic Profiles No data currently available.
No Metabolomic data currently available for this Target.
Proteomic Data No data currently available.
No Proteomic data currently available for this Target.
Regulatory Relationships from Systems Biology
BioCyc
Gene interactions based on ChIPSeq and Transcription Factor Over-Expression (TFOE) (Systems Biology )
NOTE:
see table of TFOE interactions below
Interactions based on ChIPSeq data
RNA processing and modification
Energy production and conversion
Chromatin structure and dynamics
Amino acid transport and metabolism
Cell cycle control, cell division, chromosome partitioning
Carbohydrate transport and metabolism
Nucleotide transport and metabolism
Lipid transport and metabolism
Coenzyme transport and metabolism
Translation, ribosomal structure and biogenesis
Cell wall/membrane/envelope biogenesis
Replication, recombination and repair
Posttranslational modification, protein turnover, chaperones
Secondary metabolites biosynthesis, transport and catabolism
Inorganic ion transport and metabolism
General function prediction only
Intracellular trafficking, secretion, and vesicular transport
Signal transduction mechanisms
Differentially expressed as result of RNASeq in glycerol environment (Only top 20 genes shown sorted by log fold change with p_adj 0.05).
Conditionally essential as result of TNSeq (Only top 20 genes shown sorted by log fold change with p_adj 0.05).
Binds To:
No bindings to other targets were found.
Bound By:
No bindings from other targets were found.
Binds To:
No bindings to other targets were found.
Bound By:
TFOE = Transcription Factor Over-Expression study
significance criteria used in paper: greater than 2-fold change (|LFC|>=1.0) and Padj<0.01
no significant interactions found
Upregulates:
Does not upregulate other genes.
Upregulated by:
Not upregulated by other genes.
Downregulates:
Does not downregulate other genes.
Downregulated by:
Not downregulated by other genes.
Property Value Creator Evidence PMID Comment
Citation Crystal structure of a sulfur carrier protein complex found in the cysteine biosynthetic pathway of Mycobacterium tuberculosis. CT. Jurgenson, KE. Burns et al. Biochemistry 2008 kaveri.verma ISS 18771296 Structural Analysis
Interaction PhysicalInteraction Rv0868c kaveri.verma ISS Structural AnalysisCT. Jurgenson, KE. Burns et al. Crystal structure of a sulfur carrier protein complex found in the cysteine biosynthetic pathway of Mycobacterium tuberculosis. Biochemistry 2008
Symbol moeBR mwilliams thiosulfate:sulfurtransferase activityauthors,M. Voss,M. Nimtz,S. Leimkhler Elucidation of the dual role of mycobacterial MoeZR in molybdenum cofactor biosynthesis and cysteine biosynthesis. PLoS ONE 2011
Citation Elucidation of the dual role of mycobacterial MoeZR in molybdenum cofactor biosynthesis and cysteine biosynthesis. authors,M. Voss,M. Nimtz,S. Leimkhler PLoS ONE 2011 mwilliams 22140533 thiosulfate:sulfurtransferase activity
Citation Elucidation of the dual role of mycobacterial MoeZR in molybdenum cofactor biosynthesis and cysteine biosynthesis. authors,M. Voss,M. Nimtz,S. Leimkhler PLoS ONE 2011 mwilliams 22140533 Co-expression with either M. tuberculosis MoaD1 or MoaD2 in E. coli resulted in sulfurated MoaD homologues
Citation The temporal expression profile of Mycobacterium tuberculosis infection in mice. authors,AM. Talaat,R. Lyons,ST. Howard,SA. Johnston Proc. Natl. Acad. Sci. U.S.A. 2004 mwilliams 15070764 Highly expressed in mice lungs and not in vitro
Citation Insights from the complete genome sequence of Mycobacterium marinum on the evolution of Mycobacterium tuberculosis. authors,TP. Stinear,T. Seemann,PF. Harrison,GA. Jenkin,JK. Davies,PD. Johnson,Z. Abdellah,C. Arrowsmith,T. Chillingworth,C. Churcher,K. Clarke,A. Cronin,P. Davis,I. Goodhead,N. Holroyd,K. Jagels,A. Lord,S. Moule,K. Mungall,H. Norbertczak,MA. Quail,E. Rabbinowitsch,D. Walker,B. White,S. Whitehead,PL. Small,R. Brosch,L. Ramakrishnan,MA. Fischbach,J. Parkhill,ST. Cole Genome Res. 2008 mwilliams 18403782 Acquired by horizontal gene transfer
Citation In silico reconstruction of the metabolic pathways of Lactobacillus plantarum: comparing predictions of nutrient requirements with those from growth experiments. authors,B. Teusink,FH. van Enckevort,C. Francke,A. Wiersma,A. Wegkamp,EJ. Smid,RJ. Siezen Appl. Environ. Microbiol. 2005 jjmcfadden 16269766 Inferred from direct assay
Other EC: jjmcfadden Inferred from direct assayauthors,B. Teusink,FH. van Enckevort,C. Francke,A. Wiersma,A. Wegkamp,EJ. Smid,RJ. Siezen In silico reconstruction of the metabolic pathways of Lactobacillus plantarum: comparing predictions of nutrient requirements with those from growth experiments. Appl. Environ. Microbiol. 2005