GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimB in Pseudomonas fluorescens GW456-L13

Align 3-oxopimeloyl-CoA:CoA acetyltransferase (characterized)
to candidate PfGW456L13_4040 3-ketoacyl-CoA thiolase (EC 2.3.1.16) @ Acetyl-CoA acetyltransferase (EC 2.3.1.9)

Query= metacyc::MONOMER-20679
         (395 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4040
          Length = 391

 Score =  247 bits (630), Expect = 5e-70
 Identities = 158/401 (39%), Positives = 222/401 (55%), Gaps = 25/401 (6%)

Query: 3   EAVIVSTARTPIGKAYRGALNATEGATLLGHAIEHAVKR-AGIDPKEVEDVVMGAAMQQG 61
           + VIV   RTP+G++  G    T    +  H I   ++R   +DP EVEDV+ G   Q  
Sbjct: 7   DVVIVDFGRTPMGRSKGGMHRNTRAEDMSAHLISKLLERNVKVDPNEVEDVIWGCVNQTL 66

Query: 62  ATGGNIARKALLRAGLPVTTAGTTIDRQCASGLQAIALAARSVLFDGVEIAVGGGGESIS 121
             G NIAR A L   +P T+AG T+ R C S + A+  AA++++    ++ V GG E + 
Sbjct: 67  EQGWNIARMASLMTQIPHTSAGQTVSRLCGSSMSALHTAAQAIMTGNGDVFVVGGVEHMG 126

Query: 122 LVQNDKMNTFHAVDP----ALEAIKGDVYMAMLDTAETVAKRYGISRERQDEYSLESQRR 177
            V     +  H VDP    +L A K    M +  TAE + K +GI+RE+QD + + S + 
Sbjct: 127 HV-----SMMHGVDPNPHMSLYAAKASGMMGL--TAEMLGKMHGITREQQDAFGVRSHQL 179

Query: 178 TAAAQQGGKFNDEIAPISTKMGVVDKATGAVSFKDITLSQDEGPRPETTAEGLAGLK-AV 236
              A   GKF DEI P+           G +     T   DE  RPETT E LA LK A 
Sbjct: 180 AHKATVEGKFKDEIIPMQGY-----DENGFLK----TFDYDETIRPETTLESLAALKPAF 230

Query: 237 RGEGFTITAGNASQLSDGASATVIMSDKTAAAKGLKPLGIFRGMVSYGCEPDEMGIGPVF 296
             +G T+TAG +SQ++DGAS  ++MS + A   G++PL + R M   G +P  MG GPV 
Sbjct: 231 NPKGGTVTAGTSSQITDGASCMIVMSAQRAQDLGIQPLAVIRSMAVAGVDPAIMGYGPVP 290

Query: 297 AVPRLLKRHGLSVDDIGLWELNEAFAVQVL-YCRDKLGIDP--EKLNVNGGAISVGHPYG 353
           A  + LKR GL + DI  +ELNEAFA Q L   +D   +D   EK+N++GGAI++GHP+G
Sbjct: 291 ATQKALKRAGLGISDIDFFELNEAFAAQALPVLKDLKVLDKMNEKVNLHGGAIALGHPFG 350

Query: 354 MSGARLAGHALIEGRRRKAKYAVVTMCVGGGMGSAGLFEIV 394
            SGAR++G  L   ++    + V TMC+G G G + +FE V
Sbjct: 351 CSGARISGTLLNVMKQNGGTFGVATMCIGLGQGISTVFERV 391


Lambda     K      H
   0.316    0.134    0.378 

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: 398
Number of extensions: 23
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: 395
Length of database: 391
Length adjustment: 31
Effective length of query: 364
Effective length of database: 360
Effective search space:   131040
Effective search space used:   131040
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