GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1747 in Marinobacter adhaerens HP15

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 GFF1851 HP15_1808 peptide ABC transporter, permease protein

Query= TCDB::Q9X269
         (341 letters)



>FitnessBrowser__Marino:GFF1851
          Length = 361

 Score =  145 bits (367), Expect = 1e-39
 Identities = 104/360 (28%), Positives = 174/360 (48%), Gaps = 52/360 (14%)

Query: 27  FLLKRLLTIAISMVVVIVITYVLMWLAPGNFFELQRVRD-------AIARVT-------- 71
           ++L+RL  I  +++ ++++ +V++  APG   E Q + +       A+AR +        
Sbjct: 4   YILRRLALIIPTLIGIMLLNFVIVQAAPGGPVE-QLIAEMEGHGGSALARASGGGTGGEV 62

Query: 72  ------------TPDDPAYQATLKGFEERYGLNNPLWKQILMYLKGAVVFKFGPSFSDPA 119
                        PD+      LK  E  YG + P  ++    L     F FG SF    
Sbjct: 63  ADSSGDTRGSRGIPDE-----LLKEIEVMYGFDKPAHERFFKMLGDYATFNFGDSFFRE- 116

Query: 120 RNIEDLIKEKFPITFTLALSSILFALVVGVPLGILAALKKNTWIDYTAMTVSVIGVAIPS 179
           +++ DLI +K P++ +L L S L    + +PLGI  A+   +  D    +  V+G AIP 
Sbjct: 117 KSVIDLIIDKMPVSISLGLWSTLIIYFISIPLGIRKAVTDGSRFDVWTSSAIVVGYAIPG 176

Query: 180 YVVAVFLILIFS--IYLGWLPTSGWEGIR-------TKI--------LPTIALALGPLAS 222
           ++ A+ LI++F+   Y  W P  G             KI        LP  A  +G  A+
Sbjct: 177 FLFAILLIVLFAGGSYFDWFPLRGLTSSNFDELTWYQKIGDYFWHLALPVTANVIGGFAT 236

Query: 223 VARFTRVSLLDTLNQDFIRTAYAKGGDDRTVIMKHALRPSM-IPLVTIVGPQMAYLMVGT 281
           +   T+ S LD + + ++ TA AKG D + V+  H  R +M I + ++ G  +A    G+
Sbjct: 237 LTLLTKNSFLDEIGKQYVVTARAKGLDQKEVLYGHVFRNAMLIVIASLPGVLVALFFTGS 296

Query: 282 VWVENIFRIPGLGQLFANAAVTRDYPLLVTSTFILALTVMIMNLIVDVLYAILDPRIKLD 341
           + +E IF + GLG L   AA+ RDYP++  + +I  L  +I+ LI D+ Y ++DPRI  +
Sbjct: 297 LLIEVIFSLDGLGLLGFEAALNRDYPVIFGTLYIFTLMGLILKLISDITYVLVDPRIDFE 356


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: 306
Number of extensions: 18
Number of successful extensions: 4
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: 361
Length adjustment: 29
Effective length of query: 312
Effective length of database: 332
Effective search space:   103584
Effective search space used:   103584
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