GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cimH in Pseudomonas stutzeri RCH2

Align L-malate/citrate:H+ symporter (electroneutral) (characterized)
to candidate GFF3854 Psest_3924 Na+/citrate symporter

Query= TCDB::P94363
         (450 letters)



>FitnessBrowser__psRCH2:GFF3854
          Length = 437

 Score =  251 bits (642), Expect = 2e-71
 Identities = 142/421 (33%), Positives = 239/421 (56%), Gaps = 17/421 (4%)

Query: 36  IPLPVYALLFILITVFVMHHDVKSDILTSIAVMAFFGFTFAQIGKSIPIVRS-IGGPAIL 94
           +PLP++A+  +++   ++   + + ++ ++ VM   G      G  +PI+R+ +GG AI+
Sbjct: 27  LPLPLFAIALLVMAAAIVTDTLPTGMIGALLVMMLLGELLGFAGDRLPIIRTYLGGGAIM 86

Query: 95  ATFIPSAVVYYHLLPNDIVKSTTEFTENSNFLYLFIAGIVVGSILGMKRETLVKAFMKIF 154
           A F  +++VY+  LP  +      F +   FL  +IA ++ GSILGM  + LVK   +  
Sbjct: 87  ALFGAASMVYFGWLPAAVADDVASFMKGGGFLDFYIAALITGSILGMDAKVLVKVGSRYA 146

Query: 155 IPLIVGSVTAAIVGLAVGTLLGLGFQHTLLYIVIPIMAGGVGEGAIPLSIGYSDIMPISQ 214
           +PL+   + AA+  +AVG LLG   Q  ++ I +PIM GG+G GA+P+S  Y  ++    
Sbjct: 147 LPLLCSVLFAALFAMAVGALLGFSPQDAVVVIAMPIMGGGMGAGAVPMSQIYEQLLGQPA 206

Query: 215 GEAFALVLPSIMLGSLCAIILAGLLNRIGKKKPEWTGNGK----VDRSEEESPALEESQS 270
               ++++P++ LG++ AII+AGLLN +G + P  TGNG+    VD S++E P       
Sbjct: 207 SYYISILVPALALGNVFAIIIAGLLNGLGNRYPSLTGNGQMMPGVDVSDKEGP------- 259

Query: 271 GQQMFNLSLFASGGILAVSLYLVGMLAHDFFGFPAPVAMLLLAVLIKLFRLVPASIENGA 330
                 L     G + A+S ++ G +   F        M++L  L+K+  LVP SI + A
Sbjct: 260 ----ITLPALGIGLVAALSFFIAGQILGKFVPLHPYALMIVLVALLKVSNLVPESINDAA 315

Query: 331 FGVSRFFSTAVTYPLLFAIGVSMTPWDKLVAAFNLSNIITILSVVVTMMAVGFFTGKWLN 390
               RF +   T+ LLF IGV+ T   +++ A +L+ ++ + +VV          G+ + 
Sbjct: 316 SQWFRFVARNWTFALLFGIGVAFTDLGQVLDAISLTYVLIVFAVVAGAAFGAGLVGRLVG 375

Query: 391 MYPIETAI-INACHSGQGGTGDVAILSAAERLELMPFAQVSTRIGGAITVSLTLLLLHQF 449
            YPIE+AI    C +  GGTGDVA+LSAA R+ LMPFAQ+S+R+GGA+ + ++ +++  F
Sbjct: 376 FYPIESAITAGLCMANMGGTGDVAVLSAARRMSLMPFAQISSRLGGALILLISSVVVPLF 435

Query: 450 Y 450
           +
Sbjct: 436 F 436


Lambda     K      H
   0.326    0.141    0.412 

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: 623
Number of extensions: 37
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: 450
Length of database: 437
Length adjustment: 32
Effective length of query: 418
Effective length of database: 405
Effective search space:   169290
Effective search space used:   169290
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 (21.6 bits)
S2: 51 (24.3 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