GapMind for catabolism of small carbon sources

 

Aligments for a candidate for gudD in Sinorhizobium meliloti 1021

Align Probable glucarate dehydratase; GDH; GlucD; EC 4.2.1.40 (uncharacterized)
to candidate SMa0056 SMa0056 dehydratase/enolase

Query= curated2:Q9RDE9
         (431 letters)



>FitnessBrowser__Smeli:SMa0056
          Length = 377

 Score =  155 bits (392), Expect = 2e-42
 Identities = 107/306 (34%), Positives = 152/306 (49%), Gaps = 34/306 (11%)

Query: 7   ITAVHLTPILVA-DPPLLNTQGVHQPYTPRLIVEVETADGVTGVGETYGDAKYLELA-RP 64
           IT +  T + V  + PL ++ G H     R IVEVET  G+ G+GE  G  +  E A R 
Sbjct: 6   ITDIRATTVTVPLEAPLRHSNGAHWGRFVRTIVEVETDVGIVGLGEMGGGGESAEAAFRA 65

Query: 65  FAAKLVGRQVSDLNGL-FTLADEVAVDSSRVFGQVDVGGLRGVQTADKLRLSVVSGFEVA 123
               L+G    +L  L F + +  A                   +    R  + +  E A
Sbjct: 66  LKPYLLGHDTFELENLRFMICNPTA-------------------SLYNNRTQMHAAIEFA 106

Query: 124 CLDALGKALGLPVHALLGGKVRDAVEYSAYLFYKWA--DHPEGVASEKDDWGAAVDPAGV 181
           CLD +GK LG+PV  LLGGK+RDAV +++Y+F++    D  EG     D          +
Sbjct: 107 CLDIMGKFLGVPVCDLLGGKMRDAVPFASYMFFRLPNKDTGEGETRTADQ---------L 157

Query: 182 VAQARAFTERYGFTSFKLKGGVFPPEEEIAAVKALAEAFPGHPLRLDPNGAWSVETSLKV 241
           + Q  A  ++ GFTS KLK GVFPP+ E+   +A A+A     +R DPN A+SVE +++ 
Sbjct: 158 IEQTLALKKKCGFTSHKLKSGVFPPDYELEVFRAWAKALGPDSVRYDPNAAFSVEEAIRF 217

Query: 242 AAELGDV-LEYLEDPALGTPAMAEVAAKTGVPLATNMCVTTFAEIQEAFTKGAVQVVLSD 300
           A  + D+  +Y EDP  G   M  V   T +PLATN  V  F ++       AV V+L D
Sbjct: 218 AKGIEDLNNDYYEDPTWGLNGMRRVRENTTMPLATNTVVVNFEQLATNILNPAVDVILLD 277

Query: 301 HHYWGG 306
             +WGG
Sbjct: 278 TTFWGG 283


Lambda     K      H
   0.319    0.135    0.410 

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: 362
Number of extensions: 16
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: 431
Length of database: 377
Length adjustment: 31
Effective length of query: 400
Effective length of database: 346
Effective search space:   138400
Effective search space used:   138400
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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