GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimB in Burkholderia phytofirmans PsJN

Align 3-oxopimeloyl-CoA:CoA acetyltransferase (characterized)
to candidate BPHYT_RS09180 BPHYT_RS09180 3-ketoacyl-CoA thiolase

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



>FitnessBrowser__BFirm:BPHYT_RS09180
          Length = 394

 Score =  237 bits (604), Expect = 5e-67
 Identities = 155/404 (38%), Positives = 211/404 (52%), Gaps = 29/404 (7%)

Query: 3   EAVIVSTARTPIGKAYRGALNATEGATLLGHAIEHAVKRAGIDPKEVEDVVMGAAMQQGA 62
           + V+VS  RT IG  + G+L       L    +   + RA +   EV  VV G  +    
Sbjct: 4   DVVVVSGVRTAIG-GFGGSLKDFSPTDLGARVVREVLARANVSGDEVGHVVFGNVVHTEP 62

Query: 63  TGGNIARKALLRAGLPVTTAGTTIDRQCASGLQAIALAARSVLFDGVEIAVGGGGESISL 122
               +AR A +  G+       T++R C SGLQAI  AA+SVL    +IA+GGG E++S 
Sbjct: 63  KDMYLARVAAINGGVAQHAPALTVNRLCGSGLQAIVSAAQSVLLGDADIAIGGGAENMSR 122

Query: 123 VQ--------NDKMNTFHAVDPALEAIKG---DVYMAMLDTAETVAKRYGISRERQDEYS 171
                       +M     VD  + A+      ++M +  TAE VA++Y ISRE QD  +
Sbjct: 123 APYSMPAARFGQRMGDARLVDMMVGALNDPFQSIHMGV--TAENVARKYDISREAQDALA 180

Query: 172 LESQRRTAAAQQGGKFNDEIAPIS--TKMGVVDKATGAVSFKDITLSQDEGPRPETTAEG 229
           LES RR A A   G F ++I PI+  +K G            D+    DE  R   + E 
Sbjct: 181 LESHRRAANAITSGYFKEQILPITIPSKKG------------DVVFDTDEHTRMSASPED 228

Query: 230 LAGLKAVRG-EGFTITAGNASQLSDGASATVIMSDKTAAAKGLKPLGIFRGMVSYGCEPD 288
            + LK V   E  T+TAGNAS ++D A+A V+M    A  +G+KPL         G +P 
Sbjct: 229 FSKLKPVFAKENGTVTAGNASGINDAAAAVVLMERSLAEQRGIKPLARLVSYAHAGVDPA 288

Query: 289 EMGIGPVFAVPRLLKRHGLSVDDIGLWELNEAFAVQVLYCRDKLGIDPEKLNVNGGAISV 348
            MGIGPV A  R L+R GL+V D+ + E NEAFA Q      +LG DP K+N NG  IS+
Sbjct: 289 YMGIGPVPATRRALERAGLTVADLDVIEANEAFAAQACAVSKELGFDPAKVNPNGSGISL 348

Query: 349 GHPYGMSGARLAGHALIEGRRRKAKYAVVTMCVGGGMGSAGLFE 392
           GHP G +GA +   AL E +R   +YA+VTMC+GGG G A +FE
Sbjct: 349 GHPIGATGALITVKALYELQRIGGRYALVTMCIGGGQGIAAIFE 392


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: 405
Number of extensions: 18
Number of successful extensions: 3
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: 394
Length adjustment: 31
Effective length of query: 364
Effective length of database: 363
Effective search space:   132132
Effective search space used:   132132
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