GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gltS in Pseudomonas stutzeri A1501

Align Glutamate:Na+ symporter (characterized)
to candidate WP_041755326.1 PST_RS03540 sodium/glutamate symporter

Query= TCDB::P73275
         (402 letters)



>NCBI__GCF_000013785.1:WP_041755326.1
          Length = 406

 Score =  312 bits (799), Expect = 1e-89
 Identities = 169/386 (43%), Positives = 249/386 (64%), Gaps = 6/386 (1%)

Query: 14  VAILVLYIGKYLTKKIKFLQSFNIPDAVSGGVLASLFFGLIYGIFRTEVAFNFPIRDAFL 73
           +AI++L+ GK L +  + L+ ++IP++V GG L +    +++ +   EV F+  +RD  L
Sbjct: 16  LAIMLLFAGKSLVQHYEPLRRYSIPESVLGGFLCTSVTAVLFFMLDIEVVFDLEVRDVML 75

Query: 74  IIFFTCIGLSSKLKVLLQGGKPLLILLATAVSFLVIQNFVGVGMASLLGQALPVGLLSGS 133
           + FF  IGL S ++ L++GG+PLLILL  A  F+V+QN + +G+AS  G     GL+ GS
Sbjct: 76  LYFFAGIGLKSDIRNLVKGGRPLLILLVLASLFIVLQNLLSMGVASGFGLDPRAGLMLGS 135

Query: 134 ISLSGGHGTAIAWSPVFYDNHGIRNASEIAIACATFGLVFGGIVGGPIAKFLIIRNKLEP 193
           ISLSGG GT +AW+P+F +  GI NA E+ IA  T GL+    +GGPIA +LI R+ L P
Sbjct: 136 ISLSGGVGTTLAWAPLFTEQLGIGNAMELGIASNTVGLIAACCIGGPIANYLIRRHALTP 195

Query: 194 DCDTKDLTIGIRRDQDNVQ--IDYNTMLHTILVIGVTIGLGYEINDLVAKLGLMLPAFVS 251
             D+ DL +G+     ++   I +  +L   + + +T+ LG+  N L+   G+ LP+FVS
Sbjct: 196 SRDS-DLEVGVPATSADISAPISHYDILWAWMWLNMTLMLGHGFNLLLLNSGITLPSFVS 254

Query: 252 CLLAGIVLTNTIPLAF---KKFPWPAETPSLALISDVSLGLFLAISLMSLQLWTLADIGG 308
           CLLAGIV+ N +  A    +   W      LALISD+ LG+FL ++LM LQLW L  +  
Sbjct: 255 CLLAGIVIRNLLQAAIGGQRIKHWSGAGQGLALISDICLGMFLVMALMGLQLWQLGGVLV 314

Query: 309 VIALILLVQFMATVLYSIAVVFPLMGRDYNAAVVCSGYSGLTLGATPTAIANMTAVTEKF 368
            +   L +Q   T+LY++ +VF  MGR+Y A+V+ +G+ G+ LG+T TAI NMTAVT+++
Sbjct: 315 FVVTALTLQITLTILYTVLLVFRCMGRNYEASVIAAGFGGIALGSTATAIVNMTAVTQRY 374

Query: 369 GAAPQAFIVVPLVGAFFIDIANAFVI 394
           GAA QAFI+VPLV  FFIDI NA +I
Sbjct: 375 GAAHQAFIIVPLVCGFFIDIVNALII 400


Lambda     K      H
   0.329    0.145    0.427 

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: 487
Number of extensions: 27
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: 402
Length of database: 406
Length adjustment: 31
Effective length of query: 371
Effective length of database: 375
Effective search space:   139125
Effective search space used:   139125
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