GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Cereibacter sphaeroides ATCC 17029

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate WP_002719654.1 RSPH17029_RS05915 glutamine--fructose-6-phosphate transaminase (isomerizing)

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



>NCBI__GCF_000015985.1:WP_002719654.1
          Length = 603

 Score =  136 bits (342), Expect = 2e-36
 Identities = 101/313 (32%), Positives = 149/313 (47%), Gaps = 24/313 (7%)

Query: 51  VVTCARGSSDHAATYAKYLIETLTGVPTASAALSVASLYDAPVAPGNGLCLAISQSGKSP 110
           V   A G++ +A   AKY  E + G+P A   ++    Y  PV       + +SQSG++ 
Sbjct: 289 VTLVACGTASYACHVAKYWFEQIAGLP-ADVDIASEFRYREPVLSPTSWAVFVSQSGETA 347

Query: 111 DLLATVEHQRKAGAFVVAMVNAEDSPLAALADIVIPLKAGPERSVAATKSYICSLAAIAA 170
           D LA + H   A A  +A+VN   S +A  A++ +P+ AG E  VA+TK++ C L  +A 
Sbjct: 348 DTLAALRHAGDAVARTLAVVNVPTSSIAREANLALPILAGIEVGVASTKAFTCQLTVLAL 407

Query: 171 LVAAWAQD----EALE-----TAVADLPAQLERAFAL--DWSAAVTALTGASGLFVLGRG 219
           L    AQD    +A E      A+A LP  +  A  L  D       L  A  +  LGRG
Sbjct: 408 LALKAAQDRGRIDAAELGRRLDALATLPGLMNHALRLADDIRDLAGELAEAQDILFLGRG 467

Query: 220 YGYGIAQEAALKFKETCALHAESFSAAEVRHGPMAIVGEAFHVLAFASSDRAGESVRETV 279
             Y +A E ALK KE   +HAE +++ E++HGP+A++     V+  A  D   +     +
Sbjct: 468 PMYPLALEGALKLKEISYIHAEGYASGELKHGPIALIDNRVPVIVMAPRDALFDKTVSNM 527

Query: 280 AEFRSRGAEVLLADPAA----------RQAGLPAIAAHPAIEPILIVQSFYKMANALALA 329
            E  +R  +VLL   A           R   LP +A    + PIL       +A   A+A
Sbjct: 528 QEVMARHGKVLLISDARGIEEAGAGCWRTLALPQVA--DFLAPILYAVPAQLLAYHTAIA 585

Query: 330 RGCDPDSPPHLNK 342
           +G D D P +L K
Sbjct: 586 KGTDVDQPRNLAK 598


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: 455
Number of extensions: 25
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: 603
Length adjustment: 33
Effective length of query: 314
Effective length of database: 570
Effective search space:   178980
Effective search space used:   178980
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 Apr 10 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