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 3609950 Dshi_3331 acetyl-CoA acetyltransferase (RefSeq)

Query= SwissProt::Q8VPF1
         (401 letters)



>FitnessBrowser__Dino:3609950
          Length = 394

 Score =  353 bits (907), Expect = e-102
 Identities = 201/399 (50%), Positives = 264/399 (66%), Gaps = 9/399 (2%)

Query: 1   MSREVYICDAVRTPIGRFGGSLAAVRADDLAAVPVKALVERNPQVDWSQLDEVYLGCANQ 60
           + +++ I D  RT IG FGGSLA      L A   KA +ER+  V+ +Q+  V  G    
Sbjct: 3   LDQDIVILDGARTAIGTFGGSLAGTAPITLGATVAKAALERSG-VEGAQIGHVVFGHVIN 61

Query: 61  AGEDNRNVARMALLLAGLPDSVPGVTLNRLCASGMDAVGTAFRAIASGEAELVIAGGVES 120
               +  ++R+A + AG+PD+ P + +NRLC SG  A+ +  +++  G+A+  +AGG ES
Sbjct: 62  TEPRDMYLSRVAAMEAGIPDTTPAMNVNRLCGSGAQALVSVIQSLMLGDAQFGLAGGAES 121

Query: 121 MSRAPYVMGKADSAFGRGQKIEDTTIGWRFINPLMKAQYGVDAMPETADNVADDYKVSRA 180
           MSR+PY M  A      GQK+ D T     +  L    +G   M  TA+NVA ++ + RA
Sbjct: 122 MSRSPYAMPVARW----GQKMGDATAMDMMLGAL-NCPFGTGHMGVTAENVAAEHGIGRA 176

Query: 181 DQDAFALRSQQLAGRAQAAGYFAEEIVPVVIKGKKGETVVDADEHLRPDTTLEALAKLKP 240
           DQDAFAL SQ  A RAQ AG+F  +IVPV +K K+       DEH +P TT EALA L+ 
Sbjct: 177 DQDAFALESQARAARAQEAGHFNSQIVPVPVKVKRDMVDFVRDEHPKP-TTAEALAGLRT 235

Query: 241 VNGPDKTVTAGNASGVNDGSVALILASAEAVKKHGLKARAKVLGMASAGVAPRVMGIGPV 300
           V   D TVTAGNASG+NDG+ AL+LA A A +  GLK RA++LG A AGV P VMGIGPV
Sbjct: 236 VFQKDGTVTAGNASGINDGAAALVLARASAAESAGLKPRARILGYAHAGVRPEVMGIGPV 295

Query: 301 PAVRKLLERLNLSVADFDVIELNEAFAAQGLAVTRELGIADDDARVNPNGGAIALGHPLG 360
           PAV+ LL + +LSV+DFDVIE NEAFAAQ LAV + LG+  D A+VNPNGGAIALGHP+G
Sbjct: 296 PAVQALLAKTDLSVSDFDVIESNEAFAAQALAVNKGLGL--DPAKVNPNGGAIALGHPVG 353

Query: 361 ASGARLVLTAVHQLEKSGGQRGLCTMCVGVGQGVALAVE 399
           A+GA + L A+++LE+ GG+R L TMC+G GQG+ALA E
Sbjct: 354 ATGAIIALKALYELERIGGKRALVTMCIGGGQGIALAFE 392


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: 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: 394
Length adjustment: 31
Effective length of query: 370
Effective length of database: 363
Effective search space:   134310
Effective search space used:   134310
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.

Links

Downloads

Related tools

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