GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natC in Frankia alni ACN14a

Align NatC, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized)
to candidate WP_041938756.1 FRAAL_RS03130 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YY08
         (377 letters)



>NCBI__GCF_000058485.1:WP_041938756.1
          Length = 515

 Score = 89.0 bits (219), Expect = 3e-22
 Identities = 59/152 (38%), Positives = 84/152 (55%), Gaps = 22/152 (14%)

Query: 15  FALFSLGLNLQWGFTGLINFGHIAFMTLGAYTTVLLSLKGV----------PLFISAIVG 64
           +AL +LGLN+  G+ GL++ G+IAF  +GAY T   + +            P F+  I  
Sbjct: 208 YALLALGLNVVVGYAGLLDLGYIAFFAIGAYATAYFTSQTAMPWHAPFVLNPFFVFPIA- 266

Query: 65  AIFAALLGLVIGFATLRLREDYLAIVTIGTGELIRLVVNNQDLPVGDT-WVSGAFGVQSY 123
            + AAL G+++G  TLRLR DYLAIVT+G GE+I LV NN D   G T    GAFGV   
Sbjct: 267 LVLAALAGVILGAPTLRLRGDYLAIVTLGFGEIIHLVANNAD---GITNGARGAFGVPHL 323

Query: 124 PIPL-------STEPNLFFRLLMIGILTLLFA 148
            I L         +P  ++ LL+  ++ ++ A
Sbjct: 324 SIDLLGIDYKWGIDPLPYYYLLLAIVIGVMIA 355



 Score = 74.3 bits (181), Expect = 7e-18
 Identities = 52/160 (32%), Positives = 83/160 (51%), Gaps = 14/160 (8%)

Query: 208 IPKAGLMLVSLLVLAFVFWRLEYLVRSPWGRVLKAIREDEEIPKAMGKNVFWYKLQSLML 267
           +P   L+L  ++ +   F RLE   RS  GR   AIREDE   +A G      KL +  +
Sbjct: 339 LPYYYLLLAIVIGVMIAFGRLE---RSRIGRSWAAIREDEIAAEATGVATLRMKLLAFAI 395

Query: 268 GGAIAGIAGAFFAWQISAIYPDNFQPQLTFDSWIMVILGGAGNNIGSILGAVIYFAYDAI 327
           G +++G AG  FA +     P +F  Q +F    +VI GG G+ +G ++GAV+       
Sbjct: 396 GASVSGFAGVLFASK-QFFNPQSFSLQASFFVVAVVIFGGMGSRLGVVVGAVVLQGLAFY 454

Query: 328 TREVLPKIIPLDEARLGAFRIMCIGLILMVLMIWRPQGIL 367
            R+   K+ P D       R +  G +++++MI+RPQG++
Sbjct: 455 LRD---KVQPAD-------RYIYFGAVIVIMMIFRPQGLV 484


Lambda     K      H
   0.328    0.145    0.441 

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: 542
Number of extensions: 27
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 377
Length of database: 515
Length adjustment: 32
Effective length of query: 345
Effective length of database: 483
Effective search space:   166635
Effective search space used:   166635
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: 51 (24.3 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