GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gatY in Paludibacter propionicigenes WB4

Align D-tagatose-1,6-bisphosphate aldolase subunit KbaY; TBPA; TagBP aldolase; D-tagatose-bisphosphate aldolase class II; Ketose 1,6-bisphosphate aldolase class II; Tagatose-bisphosphate aldolase; EC 4.1.2.40 (characterized)
to candidate WP_013445427.1 PALPR_RS09620 class II fructose-1,6-bisphosphate aldolase

Query= SwissProt::Q9KIP8
         (286 letters)



>NCBI__GCF_000183135.1:WP_013445427.1
          Length = 330

 Score =  179 bits (453), Expect = 1e-49
 Identities = 116/326 (35%), Positives = 170/326 (52%), Gaps = 46/326 (14%)

Query: 1   MSIISTKYLLQDAQANGYAVPAFNIHNAETIQAILEVCSEMRSPVILAGTPGTFKHIALE 60
           + +++T  L + A    YA+PAFN +N E +QAI+  C E +SPVIL  + G  K+ A +
Sbjct: 7   LGLVNTNDLFKKAIEGKYAIPAFNFNNMEQLQAIIAACVETKSPVILQVSSGARKY-ANQ 65

Query: 61  EIYALCSAYSTTY------NMPLALHLDHHESLDDIRRKVHAGVRSAMIDGSHFPFAENV 114
            +    +  +  Y      N+P+ LHLDH ++ +  +  + +G  S MIDGSH  + +N+
Sbjct: 66  TLLRYMAQGAVEYAKELGLNIPVVLHLDHGDTFELCKDCIDSGFSSVMIDGSHHSYEDNI 125

Query: 115 KLVKSVVDFCHSQDCSVEAELGRLGGVEDDMSVDAESAFLTDPQEAKRFVELTGVDSLAV 174
            L K VV++ H+   SVE ELG L GVEDD  V AE    T P+E   FV  TGVDSLA+
Sbjct: 126 ALTKKVVEYAHAHGVSVEGELGVLAGVEDD--VVAEHHTYTRPEEVVDFVTRTGVDSLAI 183

Query: 175 AIGTAHGLYSKT--------------PKIDFQRLAEI-REVVDVPLVLHGASDVPDEFV- 218
           +IGT+HG    T              P + F  L EI +++   P+VLHGAS VP E+V 
Sbjct: 184 SIGTSHGANKFTPAQCTRDENGILIPPPLRFDILEEIEKQIPGFPIVLHGASSVPQEYVA 243

Query: 219 --------------------RRTIELGVTKVNVATELKIAFAGAVKAWFAENPQGNDPRN 258
                               RR     V K+N+ ++ ++A   AV+   A  P   D R 
Sbjct: 244 TINKFGGALKDSIGIPEEQLRRAAASAVCKINIDSDGRLAMTAAVREVLATKPGEFDARK 303

Query: 259 YMRVGMDAMKEVVRNK-INVCGSANR 283
           Y+    D +K++  +K +NV GSA +
Sbjct: 304 YLGPARDELKKLYSHKTVNVLGSAGK 329


Lambda     K      H
   0.319    0.133    0.384 

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: 231
Number of extensions: 16
Number of successful extensions: 5
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: 286
Length of database: 330
Length adjustment: 27
Effective length of query: 259
Effective length of database: 303
Effective search space:    78477
Effective search space used:    78477
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 (21.8 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 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