GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gatY in Alicycliphilus denitrificans K601

Align D-tagatose-1,6-bisphosphate aldolase subunit GatY; TBPA; TagBP aldolase; D-tagatose-bisphosphate aldolase class II; Tagatose-bisphosphate aldolase; EC 4.1.2.40 (characterized)
to candidate WP_013723211.1 ALIDE2_RS22315 class II fructose-bisphosphate aldolase

Query= SwissProt::Q8VS16
         (284 letters)



>NCBI__GCF_000204645.1:WP_013723211.1
          Length = 354

 Score =  166 bits (421), Expect = 5e-46
 Identities = 109/328 (33%), Positives = 174/328 (53%), Gaps = 45/328 (13%)

Query: 1   MFIISSKNMLLKAQRLGYAVPAFNIHNLETMQVVVETAAELRSPLILAGTPGTYSYAGTG 60
           M ++S + +L  A   GY +PAFN++NLE +Q V+  A E+ +P+IL  + G   YAG  
Sbjct: 1   MPLVSMRELLDHAADSGYGIPAFNVNNLEQVQAVMAAADEVGAPVILQASAGARKYAGES 60

Query: 61  NVVAIARDLAKIWD-LPLAVHLDHHEDLADITRKVQAGIRSVMIDGS-------HSPFEE 112
            +  +    A+ +  +PL +H DH    A     ++ G  SVM+DGS        + F+ 
Sbjct: 61  FIKYLILAAAEAYSHIPLVMHQDHGTSPAVCEGALKLGFGSVMMDGSLKEDGKTPADFDY 120

Query: 113 NVALVKSVVELSHRYDASVEAELGRLG-------GVEDDLGVDAKDA---LYTNPEQGRE 162
           NV + + VVE++H+  A+VE ELG LG       G ED +G   K +   + T+PE+  +
Sbjct: 121 NVRVTRQVVEMAHKVGATVEGELGCLGSLETGEAGEEDGIGAAGKLSHAQMLTDPEEAAQ 180

Query: 163 FVARTGIDSLAVVIGTAHGLYA-AEPKLG----FAALPPISERV-DVPLVLHGASKLPDS 216
           FV  T +D+LA+ IGT+HG Y    P  G     + +  I  R+ +  LV+HG+S +P  
Sbjct: 181 FVKTTQLDALAIAIGTSHGAYKFTRPPTGDVLAISRVKEIHARIPNTHLVMHGSSSVPQD 240

Query: 217 ---------------------DIRRAISLGVCKVNVATELKIAFSDALKHYFEENPDANE 255
                                +I+ AI  GV K+N+ T++++A + A++ +  ENPD  +
Sbjct: 241 LLDIINQYGGKMKQTYGVPVKEIQEAIKHGVRKINIDTDIRMAMTGAVRKFQAENPDKFD 300

Query: 256 PRHYMKPAKAAMKDVVRKVIHVCGCEGQ 283
            R +MKPA+ A K + ++     GCEGQ
Sbjct: 301 MREWMKPAREAAKAICKQRYLEFGCEGQ 328


Lambda     K      H
   0.319    0.135    0.389 

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: 246
Number of extensions: 14
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: 284
Length of database: 354
Length adjustment: 27
Effective length of query: 257
Effective length of database: 327
Effective search space:    84039
Effective search space used:    84039
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: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. 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