GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1747 in Rhodopseudomonas pseudopalustris DSM 123

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 WP_011501573.1 BMY71_RS04155 ABC transporter permease

Query= TCDB::Q9X269
         (341 letters)



>NCBI__GCF_900110435.1:WP_011501573.1
          Length = 325

 Score =  185 bits (469), Expect = 2e-51
 Identities = 118/331 (35%), Positives = 180/331 (54%), Gaps = 24/331 (7%)

Query: 22  MRFLKFLLKRLLTIAISMVVVIVITYVLMWLAPGNFFELQRVRDAIARVTTPDDPAYQAT 81
           MR L    +RL     ++ ++++  +VL+  APG+        DA+       D A    
Sbjct: 1   MRILSLAGRRLAASIPTLFLILIGIFVLLQFAPGDTV------DAMMAQMGGGDAATARE 54

Query: 82  LKGFEERYGLNNPLWKQILMYLKGAVVFKFGPSFSDPARNIEDLIKEKFPITFTLALSSI 141
           L+ F   YGL+  +  Q+  YL   V F  G S S   + +  +I E+ P T  L  +S+
Sbjct: 55  LRQF---YGLDLSVPMQLGNYLWRLVRFDLGFS-SIYGKPVATVILERLPPTLLLMTASL 110

Query: 142 LFALVVGVPLGILAALKKNTWIDYTAMTVSVIGVAIPSYVVAVFLILIFSIYLGWLPTSG 201
            FA   G+ LG++AA   N W D    T+ +I  A PS+   +  I++FS+YL WLP  G
Sbjct: 111 SFAFFAGLVLGVIAARGVNKWPDTLISTLGLIFYATPSFWFGLMAIVVFSVYLQWLPAGG 170

Query: 202 WEGIRTK--------------ILPTIALALGPLASVARFTRVSLLDTLNQDFIRTAYAKG 247
           +E I                 +LPT+ L L  LA   R  R S+L+ LN DF+RTA AKG
Sbjct: 171 FEDIGAASTGLARTLDIASHLVLPTLTLGLIFLAIYLRIMRASMLEVLNLDFVRTARAKG 230

Query: 248 GDDRTVIMKHALRPSMIPLVTIVGPQMAYLMVGTVWVENIFRIPGLGQLFANAAVTRDYP 307
            D+  ++++H LR +++P+VT++G Q   ++ G+V VE++F +PGLG+L   + V RD  
Sbjct: 231 LDETRIVVRHVLRNALLPMVTLIGLQAGTMLGGSVVVESVFSLPGLGRLAYESVVQRDLN 290

Query: 308 LLVTSTFILALTVMIMNLIVDVLYAILDPRI 338
            L+   F+ AL V+ +N +VD+LYA LDPRI
Sbjct: 291 TLLGIVFVSALLVIAVNFLVDLLYARLDPRI 321


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: 251
Number of extensions: 14
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: 325
Length adjustment: 28
Effective length of query: 313
Effective length of database: 297
Effective search space:    92961
Effective search space used:    92961
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 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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