GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ2 in Dechlorosoma suillum PS

Align Beta-ketoadipyl CoA thiolase (EC 2.3.1.-) (characterized)
to candidate Dsui_0317 Dsui_0317 acetyl-CoA acetyltransferase

Query= reanno::Marino:GFF2751
         (415 letters)



>FitnessBrowser__PS:Dsui_0317
          Length = 399

 Score =  308 bits (789), Expect = 2e-88
 Identities = 188/415 (45%), Positives = 245/415 (59%), Gaps = 30/415 (7%)

Query: 7   LKDAYIVDAIRTPIGRYGGALSAVRADDLGAIPIKALAERYPDLDWSKIDDVLYGCANQA 66
           ++DAYIV A R P+ +  G     R DD+ A  +K++  + P LD + ++DV+ GCA   
Sbjct: 5   IQDAYIVAATRLPVAKRNGMFKTTRPDDMLAHALKSVMAQVPQLDPALVEDVIVGCAMPE 64

Query: 67  GEDNRDVARMSLLLAGLPVDVPGSTINRLCGSGMDAVGSAARAIRTGETQLMIAGGVESM 126
            E   +VAR+ LLLAGLP  VPG TINR C SG+ AV  AA  IR GE  +M+A G E+M
Sbjct: 65  AEQGMNVARIGLLLAGLPDTVPGLTINRFCSSGVQAVADAAARIRLGEADVMLAAGTETM 124

Query: 127 SRAPFVMGKADSAFSRKAEIFDTTIGWRFVNPVLKKQYGIDSMPETAENVAADFGISRED 186
           S    +MG   +  S    IF+        +  +   YG   M  TAE VA  +GISR+D
Sbjct: 125 SLMSQMMG---NKVSLNPAIFEK-------DENVAIAYG---MGLTAEKVAQKWGISRDD 171

Query: 187 QDAFALRSQQRTAAAQKEGRLAAEITPVTIPRRKQD---------PLVVDTDEHPR-ETS 236
           QDAFA+ S Q+  AA   G+   EI+P T+     D           V DTDE PR ++S
Sbjct: 172 QDAFAVASHQKAVAAIAAGKFKDEISPYTVRAHLPDLKSGTVRIVEKVCDTDEGPRPDSS 231

Query: 237 LEKLASLPTPFRENGTVTAGNASGVNDGACALLLAGADALKQYNLKPRARVVAMATAGVE 296
           L+ LA L   F   G+VTAGN+S ++DGA A+LL     LKQ+NL+P AR    + AGV 
Sbjct: 232 LQGLAKLKPVFNARGSVTAGNSSQMSDGAGAVLLVSEKILKQFNLQPLARFAGFSVAGVP 291

Query: 297 PRIMGFGPAPATRKVLATAGLELADMDVIELNEAFAAQALAVTRDLGLPDDAEHVNPNGG 356
           P IMG GP  A  KVLA AG++  D+D IELNEAFAAQALAVTR+LGL  D   +NP GG
Sbjct: 292 PEIMGIGPIAAIPKVLAQAGIKQDDLDWIELNEAFAAQALAVTRELGL--DPAKINPQGG 349

Query: 357 AIALGHPLGMSGARLVTTALNELERRHAAGQKARYALCTMCIGVGQGIALIIERM 411
           AIALGHPLG +GA    T ++ + R     +  ++ + TMCIG G G A + E +
Sbjct: 350 AIALGHPLGATGAIRTATLVHGMRR-----ENKKWGMVTMCIGTGMGAAGLFEAL 399


Lambda     K      H
   0.318    0.133    0.382 

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: 427
Number of extensions: 18
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: 415
Length of database: 399
Length adjustment: 31
Effective length of query: 384
Effective length of database: 368
Effective search space:   141312
Effective search space used:   141312
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 (21.7 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