GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctA in Pseudomonas simiae WCS417

Align Organic acid uptake porter, DctA of 444 aas and 8 - 10 putative TMSs (characterized)
to candidate GFF2281 PS417_11630 sodium:dicarboxylate symporter

Query= TCDB::Q848I3
         (444 letters)



>FitnessBrowser__WCS417:GFF2281
          Length = 434

 Score =  387 bits (994), Expect = e-112
 Identities = 203/418 (48%), Positives = 280/418 (66%), Gaps = 5/418 (1%)

Query: 2   TTRQPLYKSLYFQVIVAIAIGILLGHFYPQTGVALKPLGDGFIKLIKMVIAPIIFCTVVS 61
           T ++PLYK L FQVI A+ +GI  G   P+     K LGD F+KLIK  +AP++F TVV 
Sbjct: 5   TAKKPLYKDLTFQVIAAMFLGIAFGFLAPELAAGFKILGDIFLKLIKTAVAPLVFFTVVH 64

Query: 62  GIAGMQNMKSVGKTGGYALLYFEIVSTIALLIGLVVVNVVQPGNGMHIDVSTLDASKVAA 121
           GIA   ++K VGK G  AL+YFE+VSTIAL IGL+  N++Q G+GMH D     A+  AA
Sbjct: 65  GIASAGDIKRVGKVGLRALIYFEVVSTIALAIGLLWGNLLQIGSGMH-DAHPSSAAATAA 123

Query: 122 YVTAGKDQ---SIVGFILNVIPNTIVGAFANGDILQVLMFSVIFGFALHRLGAYGKPVL- 177
                K     S + FI  + P+  VGAFA G +LQVL+ SV+FGFAL  L    + V+ 
Sbjct: 124 SAAVAKGHAPASTLDFIYGIFPDNFVGAFAGGQLLQVLVISVLFGFALLALKPERREVIE 183

Query: 178 DFIDRFAHVMFNIINMIMKLAPIGALGAMAFTIGAYGVGSLVQLGQLMICFYITCVLFVL 237
           D ++R +   F  IN+IMK AP+GA G++A+ +G+ G   L+ L  L++ FY+    F+ 
Sbjct: 184 DGLNRISECFFEFINLIMKFAPLGAFGSVAYAVGSNGTAVLMSLANLVLMFYVGIAFFIC 243

Query: 238 VVLGAICRAHGFSVLKLIRYIREELLIVLGTSSSESALPRMLIKMERLGAKKSVVGLVIP 297
           VVLGA+CR  GFS+ + + YI++E+ IVLGT+SSESALPR+L K+E+ G  K  VGLV+P
Sbjct: 244 VVLGAVCRLSGFSLWRFLTYIKDEIFIVLGTASSESALPRLLQKLEKFGCSKQSVGLVLP 303

Query: 298 TGYSFNLDGTSIYLTMAAVFIAQATDTHMDITHQITLLLVLLLSSKGAAGVTGSGFIVLA 357
           TGY+FNLDGTSIY+++  +FIA A    +    Q+ ++ ++L++SKGAA V+G  F+V A
Sbjct: 304 TGYAFNLDGTSIYMSLCVLFIANAYGVPLSWEQQLGIIAIMLVTSKGAAAVSGGSFVVFA 363

Query: 358 ATLSAVGHLPVAGLALILGIDRFMSEARALTNLVGNAVATVVVAKWVKELDEDQLQAE 415
           AT++A+G LP  GLAL+ G+ RFMS A A  N +GN+VATVVV+KW  E  +   Q E
Sbjct: 364 ATVTAIGVLPAEGLALLFGVYRFMSMAIATCNTIGNSVATVVVSKWSGEFSQQTAQDE 421


Lambda     K      H
   0.326    0.142    0.402 

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: 527
Number of extensions: 23
Number of successful extensions: 3
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: 444
Length of database: 434
Length adjustment: 32
Effective length of query: 412
Effective length of database: 402
Effective search space:   165624
Effective search space used:   165624
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