GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Skermanella stibiiresistens SB22

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate WP_037459887.1 N825_RS29855 glutamine--fructose-6-phosphate transaminase (isomerizing)

Query= reanno::Korea:Ga0059261_1644
         (347 letters)



>NCBI__GCF_000576635.1:WP_037459887.1
          Length = 609

 Score =  147 bits (371), Expect = 7e-40
 Identities = 100/321 (31%), Positives = 157/321 (48%), Gaps = 26/321 (8%)

Query: 43  LRASPPAVVVTCARGSSDHAATYAKYLIETLTGVPTASAALSVASLYDAPVAPGNGLCLA 102
           L A P   +V C  G++ +A   AKY +E +  VP      S     +AP+ P  GL L 
Sbjct: 289 LTAIPRVTIVAC--GTAFYAGMVAKYWLEQIARVPVELDIASEFRYREAPM-PAGGLALF 345

Query: 103 ISQSGKSPDLLATVEHQRKAGAFVVAMVNAEDSPLAALADIVIPLKAGPERSVAATKSYI 162
           ISQSG++ D L  + + ++ G  +++++N  +S ++  +D V+   AGPE  VA+TK++ 
Sbjct: 346 ISQSGETLDTLEALRYAKRQGQHILSVINVAESTISRESDAVLGTLAGPEIGVASTKAFT 405

Query: 163 CSLAAIAALVAAWA---------QDEALETAVADLPAQLERAFALDWSAAVTA--LTGAS 211
             L  +A    A A         Q+ A+ TA+ ++PA+       D    + A  +  A 
Sbjct: 406 TQLTVLACFALAMARARGAITAEQESAMSTALREVPARASDVLNHDERLRLLAHDVAEAR 465

Query: 212 GLFVLGRGYGYGIAQEAALKFKETCALHAESFSAAEVRHGPMAIVGEAFHVLAFASSDRA 271
               LGRG  Y IA E ALK KE   +HAE ++A E++HGP+A++ E   ++A A +D  
Sbjct: 466 DALYLGRGTSYPIALEGALKLKEISYIHAEGYAAGEMKHGPIALIDENVPIIALAPNDGL 525

Query: 272 GESVRETVAEFRSRGAEVLL----------ADPAARQAGLPAIAAHPAIEPILIVQSFYK 321
            +     + E  +RG +VLL           D       LP +  H  + PIL       
Sbjct: 526 FDKTASNIMEAAARGGQVLLLSDEAGVERMRDKVRWTVTLPTV--HAFVAPILYAIPMQL 583

Query: 322 MANALALARGCDPDSPPHLNK 342
           +A   A+ +G D D P +L K
Sbjct: 584 LAYHTAVIKGTDVDQPRNLAK 604


Lambda     K      H
   0.317    0.128    0.360 

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: 395
Number of extensions: 27
Number of successful extensions: 4
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: 347
Length of database: 609
Length adjustment: 33
Effective length of query: 314
Effective length of database: 576
Effective search space:   180864
Effective search space used:   180864
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Sep 24 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