GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dmeA in Pseudomonas simiae WCS417

Align Possible transporter of polar amino acids including glutamate, glutamine and aspartate, DmeA. It complements a sepJ mutation in Anabaena (TC# 2.A.7.23.2), and SepJ complements a dmeA mutation. Alternatively, and less likely, it could be an activator of an ABC transporter catalyzing uptake of these amino acids (characterized)
to candidate GFF2747 PS417_14010 multidrug transporter

Query= TCDB::Q31PG5
         (330 letters)



>FitnessBrowser__WCS417:GFF2747
          Length = 307

 Score =  170 bits (430), Expect = 5e-47
 Identities = 117/286 (40%), Positives = 159/286 (55%), Gaps = 11/286 (3%)

Query: 22  LQLAIATALWGGTFTAGRIAVQQLSPLAVACGRYLLATTVLLLILWQREGWPPLNR---R 78
           ++LA  T +WGGTF AGR     + PL  A  R+ LA+  LL  L       PL R   R
Sbjct: 11  MKLAAVTMIWGGTFVAGRYLSGTVDPLLAASLRFALASLALLGFLGLAR--IPLARPSPR 68

Query: 79  QQLLLFGLGVSGIALYNWLFFIGLSLIPASRAALIIALNPTAIALGAAIWTGDRLRSWQW 138
           Q L L  LG  GI  YN  FF GL  I ASRA+LI+ALNP  I L +     +RL +   
Sbjct: 69  QLLQLGMLGFFGIFFYNLCFFYGLQSINASRASLIVALNPAVIGLASRWLFKERLGASNV 128

Query: 139 AGVGLSLIGAILLLGSRQAGALT--LPGW-GDLALVGCVLCWTVYSLLARQALRSLSPLT 195
           AG+ L L GA +++ SR    L      W GDL + GCV+ W +YSL +R   +SL PL 
Sbjct: 129 AGILLCLTGAAVVIVSRNPHVLNEATSSWRGDLLIFGCVVGWGIYSLFSRGLNQSLGPLQ 188

Query: 196 VTTGACCWGSVLLIGLWLGQGA---QLPVNVSFSTGSAIAFLGLGGTALAFCLYANGIER 252
             T +   G+++L    L  G    +    +  + G ++A+LG+ G+ALA+  Y +GI R
Sbjct: 189 TVTWSILLGTLMLTLTTLIMGRFTLEAMGRLQTAQGLSLAYLGVLGSALAYIGYYDGIRR 248

Query: 253 LGAARAGLFINLVPVFGSAIGALLLQEPLSGLTLLGGLLVLAGVGL 298
           +GA R+G+FI L P+     GALLL EPLS   L+GG ++L G+ L
Sbjct: 249 IGATRSGVFIALNPLTAVICGALLLDEPLSLPMLIGGAVILLGIYL 294


Lambda     K      H
   0.325    0.142    0.454 

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: 296
Number of extensions: 22
Number of successful extensions: 6
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: 330
Length of database: 307
Length adjustment: 27
Effective length of query: 303
Effective length of database: 280
Effective search space:    84840
Effective search space used:    84840
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 48 (23.1 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