GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SfMCT in Calditerrivibrio nitroreducens DSM 19672

Align L-lactate transporter; SfMCT (characterized)
to candidate WP_013450393.1 CALNI_RS01295 MFS transporter

Query= SwissProt::A0LNN5
         (412 letters)



>NCBI__GCF_000183405.1:WP_013450393.1
          Length = 380

 Score =  168 bits (425), Expect = 3e-46
 Identities = 117/382 (30%), Positives = 180/382 (47%), Gaps = 36/382 (9%)

Query: 29  YAWSVFIKPLNAEFGWSRAEIAMAFAICCLIFGLMTFPAGRLSDKMGPRKVVMTGGVLLA 88
           Y+WSV++K + A    S+A+  + F++   IF      +G++  K+GP+   + GG L  
Sbjct: 20  YSWSVYVKDIKAILNISQAQAQLPFSVFYFIFPATMIISGKILKKLGPQISTIVGGTLFG 79

Query: 89  IGFILSGFIQSKYQLYIT-YGVIAGFGGGMIYLPPIATAPKWWPDRRALATGFAVVGLGL 147
            G+I+S F  S +   I   G+IAG G G+ Y+ PI+T  KW+PD++ L TG AV G G 
Sbjct: 80  AGWIISSFGGSNFIFTILGNGLIAGLGAGIAYIVPISTCIKWFPDKKGLITGIAVAGFGG 139

Query: 148 GSFLMGPLATYIIEKPGMGWR--YVFWYCGVAMGIMALIAGAFLEPPPAGWKPAGYTPPA 205
           G+ L+  L   +I     GW    VF   G    I+ ++AG F++ PP+      Y P  
Sbjct: 140 GAALVSFLGGTLIAN---GWTPFQVFRALGSIFLILIILAGFFMKNPPSNNTHDTYLP-- 194

Query: 206 PPAGAAAPKVTRDWTYEEAKGDTKFWLLYLAYFCGSFAGLMVIGHLAGFGRDAGLTAMAA 265
                          Y E   D KF  LY A F G  AG  V  ++    R A +T  A 
Sbjct: 195 -------------LKYRELLVDKKFLFLYFAMFVGLAAGFAVNANIKELSRTASMT--AG 239

Query: 266 AGAVSSLAFSNAATRILSGWFVDK------IGIRVYFAALFALQTAAMIAIFQLGGSVVG 319
             AV+  A  NA  R+  G   D+      + + + F A+    +  M+       S  G
Sbjct: 240 VSAVAFFAIFNALGRVSWGALFDRFDYIKSLQLNLLFQAIILFLSPIML------NSATG 293

Query: 320 LSIVAIVIGWNYGAMFTLFPATCLQFYGPTAQGSNYGLLFTACGLAGFAGPWVGGWLKDT 379
           L I A++ G NYG +  ++  +  + +G    G  YGLLF++  + G   P   G++ D 
Sbjct: 294 LQIFAVLTGLNYGGVLVMYAGSVAKIWGAENVGMVYGLLFSS-NIPGALAPIFAGYIYDK 352

Query: 380 TGTYYLPFLCAAALCALGTAIV 401
           TG++ +     A L  LG  I+
Sbjct: 353 TGSFTIALYTIAILLILGIIIL 374


Lambda     K      H
   0.327    0.142    0.475 

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: 509
Number of extensions: 31
Number of successful extensions: 5
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: 412
Length of database: 380
Length adjustment: 31
Effective length of query: 381
Effective length of database: 349
Effective search space:   132969
Effective search space used:   132969
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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