GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ2 in Rhizobium leguminosarum WSM1325

Align Beta-ketoadipyl-CoA thiolase; 3-oxoadipyl-CoA thiolase; EC 2.3.1.174 (characterized)
to candidate WP_012759437.1 RLEG_RS20540 acetyl-CoA C-acetyltransferase

Query= SwissProt::Q8VPF1
         (401 letters)



>NCBI__GCF_000023185.1:WP_012759437.1
          Length = 393

 Score =  318 bits (815), Expect = 2e-91
 Identities = 182/396 (45%), Positives = 258/396 (65%), Gaps = 11/396 (2%)

Query: 5   VYICDAVRTPIGRFGGSLAAVRADDLAAVPVKALVERNPQVDWSQLDEVYLGCANQAGED 64
           + I  A RT +G F G+ A V A +L A  +K  +ER   VD  ++DEV LG    AGE 
Sbjct: 6   IVIASAGRTAVGAFNGAFATVLAHELGAAVIKGALER-AGVDAGEVDEVILGQVLAAGE- 63

Query: 65  NRNVARMALLLAGLPDSVPGVTLNRLCASGMDAVGTAFRAIASGEAELVIAGGVESMSRA 124
            +N AR A + AG+P       +N+LC SG+ AV    + IA+G+A++++AGG ESMS A
Sbjct: 64  GQNPARQAAMKAGIPQEATAWGVNQLCGSGLRAVALGMQQIATGDAKIIVAGGQESMSMA 123

Query: 125 PYVMGKADSAFGRGQKIEDTTIGWRFINPLMKAQYGVDAMPETADNVADDYKVSRADQDA 184
           P+             K+ DT I     + L  A +G   M  TA+NVA  +++SR DQD 
Sbjct: 124 PHAAHLRGGVKMGDMKMIDTMIK----DGLTDAFHGYH-MGITAENVARQWQLSRDDQDQ 178

Query: 185 FALRSQQLAGRAQAAGYFAEEIVPVVIKGKKGETVVDADEHLRPDTTLEALAKLKPVNGP 244
           FA+ SQ  A  AQ AG F +EI+P VIK +KG+  VDADE++R   T+EA+ KL+P    
Sbjct: 179 FAVSSQNKAEAAQKAGRFVDEIIPYVIKTRKGDVTVDADEYIRHGATIEAMGKLRPAFDK 238

Query: 245 DKTVTAGNASGVNDG-SVALILASAEAVKKHGLKARAKVLGMASAGVAPRVMGIGPVPAV 303
           D TVTA NASG+NDG +VA++++ AEAV++ G++  A+++  A+AGV P++MG GP+PA 
Sbjct: 239 DGTVTAANASGLNDGAAVAVLMSEAEAVRR-GVQPLARIVSWATAGVDPQIMGTGPIPAS 297

Query: 304 RKLLERLNLSVADFDVIELNEAFAAQGLAVTRELGIADDDARVNPNGGAIALGHPLGASG 363
           RK LE+   SV D D++E NEAFAAQ  AVT++LG   D + VN NGGAIA+GHP+GASG
Sbjct: 298 RKALEKAGWSVNDLDLVEANEAFAAQACAVTKDLGW--DPSIVNVNGGAIAIGHPIGASG 355

Query: 364 ARLVLTAVHQLEKSGGQRGLCTMCVGVGQGVALAVE 399
           AR++ T + ++++ G ++GL T+C+G G GVA+  E
Sbjct: 356 ARVLNTLLFEMKRRGAKKGLATLCIGGGMGVAMCFE 391


Lambda     K      H
   0.317    0.134    0.379 

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: 448
Number of extensions: 20
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: 401
Length of database: 393
Length adjustment: 31
Effective length of query: 370
Effective length of database: 362
Effective search space:   133940
Effective search space used:   133940
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 (21.6 bits)
S2: 50 (23.9 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