GapMind for catabolism of small carbon sources

 

Alignments for a candidate for alr in Synechococcus elongatus PCC 7942

Align lysine racemase (EC 5.1.1.5) (characterized)
to candidate Synpcc7942_2201 Synpcc7942_2201 alanine racemase

Query= BRENDA::Q04HB7
         (371 letters)



>FitnessBrowser__SynE:Synpcc7942_2201
          Length = 406

 Score =  164 bits (415), Expect = 4e-45
 Identities = 120/375 (32%), Positives = 194/375 (51%), Gaps = 25/375 (6%)

Query: 11  IEFSKSSLAYNVQYTKQ-VSGAKTLWLAVKSNAYGHGLLQVSKIARECGVDGLAVSVLDE 69
           +E  + ++A N +  +Q ++ +  L   VK++AYGHG + ++      G   L V+ + E
Sbjct: 29  VEVDQGAIAANTRQIRQFLAPSCELMAVVKADAYGHGAVAIASTVLGAGATALGVATIPE 88

Query: 70  GIAIRQAGIDDFILILGPI-DVKYAPIASKYHFLTTVSSLDWLKSADKILGK--EKLSVN 126
           G+ +R+AGI   IL+LG I         + +    ++S+        ++L +  + L V+
Sbjct: 89  GVRLREAGITAPILLLGSIHSPDEVQAIAHWQIQPSLSTPKQALICAEVLDRLGQSLPVH 148

Query: 127 LAVDTGMNRIGVRSKKDLKDEIEFLQ--EHSDHFSYDGIFTHFASSDNPDDHYFQRQKNR 184
           L +DTGM+R+G       +  +EFLQ            +++HFA++D+PD    Q+Q   
Sbjct: 149 LKLDTGMSRLGA----PWQTAVEFLQLVHGLPSLQLASLYSHFATADSPDRAPLQQQHAA 204

Query: 185 WYELI-----DGLIMPRYVHVMNSGAAMYHSKELPGCNSIARVGTVVYGVEPSEGVLGPI 239
           + + I     +GL +P+ +H+ NS A +  S          RVG  +YG+ P+   LG  
Sbjct: 205 FEQAIAQIQAEGLPVPK-LHIANSAATLLDSSLH---YDQVRVGLALYGLYPAPH-LGDR 259

Query: 240 DKLKPVFELKSALTFVKKIPAGEGISYGSKFVTSRDTWIGTLPIGYGDGW-LAEYQDFQL 298
             L P   +K+ +T V  +PAG+G+SYG ++VT R+T I  + IGY DG   A     ++
Sbjct: 260 LSLYPALSVKARVTHVTTLPAGQGVSYGHRYVTQRETPIAVVGIGYADGVPRALSNQMEV 319

Query: 299 LIDGQKCRQVGQIAMDQMMV---ALPHEYPIGTEVTLIGKSGKYENTLYDLHKHSGVPPW 355
           L  GQ+  Q+G I MDQMM+   A+P   P G  VTL+G+SG  + T  D    +    W
Sbjct: 320 LYRGQRLPQIGAITMDQMMIDISAMPQLAP-GDVVTLLGRSGSEQITADDWADRANTISW 378

Query: 356 KITVAFSDRLKRMVV 370
           +I   F DRL R  V
Sbjct: 379 EILCGFKDRLPRFAV 393


Lambda     K      H
   0.319    0.137    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: 374
Number of extensions: 23
Number of successful extensions: 6
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: 371
Length of database: 406
Length adjustment: 30
Effective length of query: 341
Effective length of database: 376
Effective search space:   128216
Effective search space used:   128216
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:

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