GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ2 in Dinoroseobacter shibae DFL-12

Align Beta-ketoadipyl-CoA thiolase; 3-oxoadipyl-CoA thiolase; EC 2.3.1.174 (characterized)
to candidate 3606642 Dshi_0074 acetyl-CoA acetyltransferase (RefSeq)

Query= SwissProt::Q8VPF1
         (401 letters)



>FitnessBrowser__Dino:3606642
          Length = 392

 Score =  280 bits (716), Expect = 5e-80
 Identities = 171/403 (42%), Positives = 243/403 (60%), Gaps = 18/403 (4%)

Query: 3   REVYICDAVRTPIGRFGGSLAAVRADDLAAVPVKALVERNPQVDWSQLDEVYLGCANQAG 62
           R V IC A RTP+G F G  + V A  L    +   +  +  V  +Q++E+ +GC   AG
Sbjct: 2   RTVAICGAARTPMGGFQGVFSDVSAAQLGGAAIAGALA-DAGVAPAQVNELLMGCVLPAG 60

Query: 63  EDNRNVARMALLLAGLPDSVPGVTLNRLCASGMDAVGTAFRAIASGEAELVIAGGVESMS 122
           +  +  AR A   AGL D+VP  TLN++C SGM A   A   IA G+++LV+AGG+ESM+
Sbjct: 61  Q-GQAPARQAGYAAGLGDAVPATTLNKMCGSGMKAAMIACDQIALGQSDLVVAGGMESMT 119

Query: 123 RAPYVMGK--ADSAFGRGQKIEDTTIGWRFINPLMKAQYGVDAMPETADNVADDYKVSRA 180
            APY++ K    +  G GQ I+       F++ L  A      M   A++ A+ ++ +RA
Sbjct: 120 NAPYLLDKMRGGARIGHGQVIDHM-----FLDGLEDAYDKGRLMGTFAEDCAEAFQFTRA 174

Query: 181 DQDAFALRSQQLAGRAQAAGYFAEEIVPVVIKGKKGETVVDADEH---LRPDTTLEALAK 237
            QD +AL S + A  A+A+  FA E+VPV + G+KGETVV  DE     RP    E +  
Sbjct: 175 AQDTYALGSLENALAAEASEAFAMELVPVTVSGRKGETVVIRDEQPAAARP----EKIPH 230

Query: 238 LKPVNGPDKTVTAGNASGVNDGSVALILASAEAVKKHGLKARAKVLGMASAGVAPRVMGI 297
           LKP    D TVTA N+S ++DG+ AL+LA A   + HGL  RA+VLG AS    P +   
Sbjct: 231 LKPAFRKDGTVTAANSSSISDGAAALVLADAGQAEAHGLPVRARVLGHASHAQKPALFPT 290

Query: 298 GPVPAVRKLLERLNLSVADFDVIELNEAFAAQGLAVTRELGIADDDARVNPNGGAIALGH 357
            PVPA RKLL+RL   VAD D+ E+NEAFA   +A   E+G+  +  ++N NGGA ALGH
Sbjct: 291 APVPAARKLLDRLGWCVADVDLWEVNEAFAVVPMAFMHEMGVPRE--KMNVNGGACALGH 348

Query: 358 PLGASGARLVLTAVHQLEKSGGQRGLCTMCVGVGQGVALAVER 400
           P+GASGAR+++T ++ +E    +RG+  +C+G G+G A+A+ER
Sbjct: 349 PIGASGARILVTLLNAMEARDLKRGVAAICIGGGEGTAIALER 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: 433
Number of extensions: 24
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: 392
Length adjustment: 31
Effective length of query: 370
Effective length of database: 361
Effective search space:   133570
Effective search space used:   133570
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 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