GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Pseudomonas fluorescens FW300-N2E2

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate Pf6N2E2_4217 Glucosamine--fructose-6-phosphate aminotransferase [isomerizing] (EC 2.6.1.16)

Query= reanno::Caulo:CCNA_00453
         (363 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_4217
          Length = 610

 Score =  127 bits (318), Expect = 1e-33
 Identities = 101/311 (32%), Positives = 152/311 (48%), Gaps = 21/311 (6%)

Query: 66  VVTCARGSSDHAATFARYLIETKAGVLTSSAGPSVSSVYDASPNLEGALYLAISQSGKSP 125
           +V C  G+S HA   ARY +E  AG+       S    Y        +L++ ISQSG++ 
Sbjct: 298 IVAC--GTSYHAGMVARYWLEELAGIPCQVEVASEFR-YRKVVVQPDSLFVTISQSGETA 354

Query: 126 DLLAAVKAAKAAGAHA-VALVNVVDSPLAALADEVIPLHAGPELSVAATKSYIAALVAVT 184
           D LAA++ AK  G  A +A+ NV  S L   +D  +   AG E+ VA+TK++   LV + 
Sbjct: 355 DTLAALRNAKELGFLASLAICNVGISSLVRESDLTLLTQAGREIGVASTKAFTTQLVGLL 414

Query: 185 QLIAAWTE---------DAELTAALQDLPTALAAAWTLDWSLA--VERLKTASNLYVLGR 233
            L  +  +         +A L   L+ LP  L  A  +D ++    E     ++   LGR
Sbjct: 415 LLTLSLGQVRGTLGKGVEATLVEELRRLPARLGEALAMDSTVEKIAELFAEKNHTLFLGR 474

Query: 234 GVGFGVALEAALKFKETCGLHAEAFSAAEVLHGPMALVKDGFPALVFAQNDESRASVDEM 293
           G  F VA+E ALK KE   +HAEA+ A E+ HGP+ALV +  P +  A N+E    +   
Sbjct: 475 GAQFPVAMEGALKLKEISYIHAEAYPAGELKHGPLALVDNDMPVVTVAPNNELLEKLKSN 534

Query: 294 AAGLRARGASVLI-----AG-GGGDAPDALPTLASHPVLEPILMIQSFYRMANALSVARG 347
              +RARG  +++     AG   G+    +     H +L PIL       ++  ++V +G
Sbjct: 535 LQEVRARGGQLIVFADEKAGMTNGEGTHVVHMPHIHDILSPILYTIPLQLLSYYVAVLKG 594

Query: 348 YDPDSPPHLNK 358
            D D P +L K
Sbjct: 595 TDVDQPRNLAK 605


Lambda     K      H
   0.315    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: 371
Number of extensions: 15
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 363
Length of database: 610
Length adjustment: 33
Effective length of query: 330
Effective length of database: 577
Effective search space:   190410
Effective search space used:   190410
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 (21.6 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Sep 17 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