GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1747 in Desulfovibrio vulgaris Miyazaki F

Align TM1747, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate 8500162 DvMF_0920 binding-protein-dependent transport systems inner membrane component (RefSeq)

Query= TCDB::Q9X269
         (341 letters)



>FitnessBrowser__Miya:8500162
          Length = 343

 Score =  196 bits (499), Expect = 6e-55
 Identities = 117/332 (35%), Positives = 190/332 (57%), Gaps = 26/332 (7%)

Query: 25  LKFLLKRLLTIAISMVVVIVITYVLMWLAPGNFFELQRVRDAIARVTTPDDPAYQATLKG 84
           L+ + ++L  +      + +I++ ++ LAPG+  ++Q         TT +  A   T K 
Sbjct: 5   LRRMARKLAWMLFVFWGITIISFWVIHLAPGSPTDMQ---------TTMNPLAGAETRKR 55

Query: 85  FEERYGLNNPLWKQILMYLKGAVVFKFGPSFSDPARNIEDLIKEKFPITFTLALSSILFA 144
            E  YGL+ PL  Q + +L       FG S S   R + D IKE+ P+T  + ++S++  
Sbjct: 56  LEALYGLDKPLHVQYVQWLGRLSRLDFGNSMSSDPRPVWDKIKERLPLTVGMNVASLVLT 115

Query: 145 LVVGVPLGILAALKKNTWIDYTAMTVSV-IGVAIPSYVVAVFLILIFSIYLGWLPTSG-- 201
           ++  +P+G+ +A  +    D  AMTV V IG A+P + +A+ L+L+F I+L WLP SG  
Sbjct: 116 MLCAIPIGVASAHWQGRLFD-RAMTVLVFIGFAMPGFWLALLLMLLFGIHLQWLPLSGLT 174

Query: 202 -------------WEGIRTKILPTIALALGPLASVARFTRVSLLDTLNQDFIRTAYAKGG 248
                        W+ +    +P      G LA ++RF R S+L+ L QD+I TA AKG 
Sbjct: 175 SLDHAAMSPMGKAWDIMAHLAMPIFIYTFGSLAGLSRFMRASMLEVLRQDYILTARAKGL 234

Query: 249 DDRTVIMKHALRPSMIPLVTIVGPQMAYLMVGTVWVENIFRIPGLGQLFANAAVTRDYPL 308
             RTVI +HALR +++P++TI+G  +  L+ G+V +E+IF +PGLGQLF  A + RDYPL
Sbjct: 235 PVRTVIFRHALRNALLPVITILGLSLPGLIGGSVIIESIFALPGLGQLFYQAVMARDYPL 294

Query: 309 LVTSTFILALTVMIMNLIVDVLYAILDPRIKL 340
           ++ +  + A+  ++ NL+ D+ Y + DPRI+L
Sbjct: 295 IMGNLVLGAVLTLVGNLLADLCYGLADPRIRL 326


Lambda     K      H
   0.328    0.143    0.429 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 309
Number of extensions: 16
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 341
Length of database: 343
Length adjustment: 29
Effective length of query: 312
Effective length of database: 314
Effective search space:    97968
Effective search space used:    97968
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory