GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dmeA in Rhizobium johnstonii 3841

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 WP_011653211.1 RL_RS19435 DMT family transporter

Query= TCDB::Q31PG5
         (330 letters)



>NCBI__GCF_000009265.1:WP_011653211.1
          Length = 305

 Score = 96.3 bits (238), Expect = 9e-25
 Identities = 82/307 (26%), Positives = 133/307 (43%), Gaps = 26/307 (8%)

Query: 24  LAIATALWGGTFTAGRIAVQQLSPLAVACGRYLLATTVLLLILWQ--REGWPPLNRRQQL 81
           L IAT  WGG   AG++A+  +SP+ +   R+ LA  ++ +I     R+ WP + +   L
Sbjct: 9   LVIATLCWGGNSVAGKLALGHISPMMLTFLRWFLAVAMIAVISVPQLRKDWPVVRKNLPL 68

Query: 82  LLFGLGVSGIALYNWLFFIGLSLIPASRAALIIALNPTAIALGAAIWTGDRLRSWQWAGV 141
           LLF  GV G  L+N + +  +    A   A+  A  P  I L   ++    +   Q  G 
Sbjct: 69  LLF-YGVIGYTLFNAMLYSAVQYTTAINVAIEQAGIPMLIFLLNFMFFRTGISLAQCLGF 127

Query: 142 GLSLIGAILLLGSRQAGALTLPGW--GDLALVGCVLCWTVYSLLAR----------QALR 189
           G++LIG  L         L       GD  ++  +  ++VY++  R           A+ 
Sbjct: 128 GMTLIGVALTAAHGDLATLLQLSLNRGDGLMLIAIAAYSVYTIFLRWKPPLDWRTLMAVP 187

Query: 190 SLSPLTVTTGACCWGSVLLIGLWLGQGAQLPVNVSFSTGSAIAFLGLGGTALAFCLYANG 249
           +L  +  +     W +      W  Q   +             +  +  + +A  LY  G
Sbjct: 188 ALGAMLTSLPLLLWEAGRGAARWPDQAGWV----------ITLYTAIFPSLVAQILYIKG 237

Query: 250 IERLGAARAGLFINLVPVFGSAIGALLLQEPLSGLTLLGGLLVLAGVGLGTLQRLQ-PVP 308
           +  +GA RAGLFINLVPVFG+ +   L+ E L    ++  +L L G+ +    R +   P
Sbjct: 238 VVAIGANRAGLFINLVPVFGTLLSVALIGERLQSFHVIALVLTLGGIAIAEKGRPKASSP 297

Query: 309 ISTTEPV 315
             T  PV
Sbjct: 298 TVTASPV 304


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: 283
Number of extensions: 16
Number of successful extensions: 2
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: 305
Length adjustment: 27
Effective length of query: 303
Effective length of database: 278
Effective search space:    84234
Effective search space used:    84234
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 Apr 09 2024. 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