GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natC in Maridesulfovibrio zosterae DSM 11974

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_051249582.1 H589_RS0101625 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YY08
         (377 letters)



>NCBI__GCF_000425265.1:WP_051249582.1
          Length = 390

 Score = 80.1 bits (196), Expect = 1e-19
 Identities = 59/195 (30%), Positives = 95/195 (48%), Gaps = 17/195 (8%)

Query: 188 ILGLLATAIY----ISGVITLYNYIPKAGLMLVSLLVLA-FVFWRLEYLVRSPWGRVLKA 242
           I G+ A  IY     +G+   + ++ K  L+   +L L  F    +  L  S  GR  +A
Sbjct: 206 ITGIKAPGIYWPDFTNGMTFEHLWLKKLSLIYYVILALVVFTIIAVYRLNHSRIGRAWEA 265

Query: 243 IREDEEIPKAMGKNVFWYKLQSLMLGGAIAGIAGAFFAWQISAIYPDNFQPQLTFDSWIM 302
           IREDE   + MG   F+ KL +   G    G+AGAF+A ++  + P++F    +     M
Sbjct: 266 IREDETAAEVMGIPTFYMKLLAYCTGACFGGMAGAFYAARMRFVSPESFTFLESAMVLSM 325

Query: 303 VILGGAGNNIGSILGAVIYFAYDAITREVLPKIIPLDEARLGAFRIMCIGLILMVLMIWR 362
           V+LGG G+  G ILGA+   A   I R+               +R++  G ++ ++M++R
Sbjct: 326 VVLGGMGSIPGVILGALALIALPEIFRD------------FELYRMLVFGGVMTLMMLFR 373

Query: 363 PQGILGKKEELTLGK 377
           PQG+L  K  +   K
Sbjct: 374 PQGLLPPKRSMKADK 388



 Score = 78.6 bits (192), Expect = 3e-19
 Identities = 43/111 (38%), Positives = 67/111 (60%), Gaps = 2/111 (1%)

Query: 8   LAISTATFALFSLGLNLQWGFTGLINFGHIAFMTLGAYTTVLLSLK-GVPLFISAIVGAI 66
           +AI+   +    LGLN+  G  G+++ G+IAF  LGAYT  LLS+   +  ++   + A 
Sbjct: 98  VAINCMVYICLGLGLNIVVGLAGMLDLGYIAFYGLGAYTYALLSVTYKISFWLCLPLSAA 157

Query: 67  FAALLGLVIGFATLRLREDYLAIVTIGTGELIRLVVNN-QDLPVGDTWVSG 116
            A L   +IG+ ++R+R DYLAIVT+G  E++R+V NN   L  G   ++G
Sbjct: 158 VAGLGACIIGYCSMRMRGDYLAIVTLGFAEIVRMVFNNWMSLTNGPNGITG 208


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: 453
Number of extensions: 38
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 3
Number of HSP's successfully gapped: 2
Length of query: 377
Length of database: 390
Length adjustment: 30
Effective length of query: 347
Effective length of database: 360
Effective search space:   124920
Effective search space used:   124920
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: 50 (23.9 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