GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Acidovorax sp. GW101-3H11

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate Ac3H11_3072 Glucosamine--fructose-6-phosphate aminotransferase [isomerizing] (EC 2.6.1.16)

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



>FitnessBrowser__acidovorax_3H11:Ac3H11_3072
          Length = 641

 Score =  122 bits (305), Expect = 3e-32
 Identities = 101/316 (31%), Positives = 151/316 (47%), Gaps = 30/316 (9%)

Query: 51  VVTCARGSSDHAATYAKYLIETLTGVPTASAALSVASLYDAPVAPGNG--LCLAISQSGK 108
           V+  A G+S ++   AKY +E + G+PT    + VAS Y    +  N   L + I+QSG+
Sbjct: 327 VLILACGTSYYSGCAAKYWLEEIAGIPTQ---VEVASEYRYRTSVPNPRTLVVTITQSGE 383

Query: 109 SPDLLATVEHQRKAGA-FVVAMVNAEDSPLAALADIVIPLKAGPERSVAATKSYICSLAA 167
           + D LA + H +  G    + + N   S +     +    +AG E  VA+TK++   LA 
Sbjct: 384 TADTLAALRHAQSLGMQHTLTICNVVTSAMVRECKLAYITRAGVEIGVASTKAFTTQLAG 443

Query: 168 IAALVAAWAQDE---------ALETAVADLPAQLERAFALD-----WSAAVTALTGASGL 213
           +  L  A AQ +         A   A+  LP  L+   AL+     W+     +  A   
Sbjct: 444 LFLLTLALAQSKGRLSEEQEAAHLKAMRHLPVALQAVLALEPQLISWAEDFARMENA--- 500

Query: 214 FVLGRGYGYGIAQEAALKFKETCALHAESFSAAEVRHGPMAIVGEAFHVLAFASSDRAGE 273
             LGRG  Y IA E ALK KE   +HAE++ A E++HGP+A+V  A  V+  A +D   E
Sbjct: 501 LFLGRGLHYPIALEGALKLKEISYIHAEAYPAGELKHGPLALVTSAMPVVTVAPNDALLE 560

Query: 274 SVRETVAEFRSR-GAEVLLADPAAR---QAGLPAIAA---HPAIEPILIVQSFYKMANAL 326
            ++  + E R+R G   +LAD         G+  I     + A+ P+L V     +A   
Sbjct: 561 KLKSNMQEVRARAGVLYVLADGDTHIESSEGIHVIRMPEHYGALSPLLHVVPLQLLAYHT 620

Query: 327 ALARGCDPDSPPHLNK 342
           A ARG D D P +L K
Sbjct: 621 ACARGTDVDKPRNLAK 636


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: 431
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: 641
Length adjustment: 33
Effective length of query: 314
Effective length of database: 608
Effective search space:   190912
Effective search space used:   190912
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 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