GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ2 in Sinorhizobium medicae WSM419

Align Beta-ketoadipyl-CoA thiolase; 3-oxoadipyl-CoA thiolase; EC 2.3.1.174 (characterized)
to candidate YP_001328778.1 Smed_3117 acetyl-CoA acetyltransferase

Query= SwissProt::Q8VPF1
         (401 letters)



>NCBI__GCF_000017145.1:YP_001328778.1
          Length = 393

 Score =  313 bits (801), Expect = 7e-90
 Identities = 176/397 (44%), Positives = 254/397 (63%), Gaps = 9/397 (2%)

Query: 5   VYICDAVRTPIGRFGGSLAAVRADDLAAVPVKALVERNPQVDWSQLDEVYLGCANQAGED 64
           + I  A RT +G F G+     A +L A  VKA++ER   V+  ++DEV LG    AGE 
Sbjct: 6   IVIASAARTAVGSFNGAFGNTPAHELGAAAVKAVLER-AGVEAGEVDEVILGQVLPAGE- 63

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

Query: 125 PYVMGKADSAFGRGQKIEDTTIGWRFINPLMKAQYGVDAMPETADNVADDYKVSRADQDA 184
           P+             K+ DT I     + L  A YG   M  TA+NVA  ++++R +QD 
Sbjct: 124 PHCAHLRGGVKMGDYKMIDTMIK----DGLTDAFYGYH-MGTTAENVARKWQLTREEQDE 178

Query: 185 FALRSQQLAGRAQAAGYFAEEIVPVVIKGKKGETVVDADEHLRPDTTLEALAKLKPVNGP 244
           FAL SQ  A  AQ AG FA+EIVP V+K +KG+  VD DE++R   TLE++AKL+P    
Sbjct: 179 FALASQNKAEAAQKAGRFADEIVPFVVKTRKGDVTVDQDEYIRHGATLESIAKLRPAFDK 238

Query: 245 DKTVTAGNASGVNDGSVALILASAEAVKKHGLKARAKVLGMASAGVAPRVMGIGPVPAVR 304
           + TVTA NASG+NDG+ A +L +     + G++  A+++  A+AGV P++MG GP+PA R
Sbjct: 239 EGTVTAANASGLNDGAAAALLMTEAEAGRRGIQPLARIVSWATAGVDPQIMGTGPIPASR 298

Query: 305 KLLERLNLSVADFDVIELNEAFAAQGLAVTRELGIADDDARVNPNGGAIALGHPLGASGA 364
           K LE+   SVA+ +++E NEAFAAQ  AV ++LG   D + VN NGGAIA+GHP+GASGA
Sbjct: 299 KALEKAGWSVAEIELVEANEAFAAQACAVNKDLGW--DPSIVNVNGGAIAIGHPIGASGA 356

Query: 365 RLVLTAVHQLEKSGGQRGLCTMCVGVGQGVALAVERV 401
           R++ T + ++++    +GL T+C+G G GVA+ VER+
Sbjct: 357 RVLNTLLFEMKRRNVSKGLATLCIGGGMGVAMCVERL 393


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: 441
Number of extensions: 15
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: 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