GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Pseudomonas fluorescens FW300-N1B4

Align acetyl-CoA C-acetyltransferase (EC 2.3.1.9) (characterized)
to candidate Pf1N1B4_3904 3-ketoacyl-CoA thiolase (EC 2.3.1.16) @ Acetyl-CoA acetyltransferase (EC 2.3.1.9)

Query= BRENDA::Q0K368
         (391 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3904
          Length = 383

 Score =  261 bits (666), Expect = 3e-74
 Identities = 162/394 (41%), Positives = 233/394 (59%), Gaps = 20/394 (5%)

Query: 6   IVAAVRTAGGR-KGGKLSGWHPADLAAQVLDALVERT-GADPALVEDVIMGCVSQVGEQA 63
           IV   RT  GR KGG        D++A ++  L+ER    DP+ VEDVI GCV+Q  EQ 
Sbjct: 2   IVDFGRTPMGRSKGGMHRNTRAEDMSAHLISKLLERNVKVDPSEVEDVIWGCVNQTLEQG 61

Query: 64  GNVARNAILASRLPESVPGTSVDRQCGSSQQALHFAAQAVMSGAMDIVIAAGVESMTRVP 123
            N+AR A L +++P +  G +V R CGSS  ALH AAQA+M+G  D+ +  GVE M  V 
Sbjct: 62  WNIARMASLMTQIPHTAAGQTVSRLCGSSMSALHTAAQAIMTGNGDVFVVGGVEHMGHVS 121

Query: 124 MGLSSQLPAKNGFGVPKSPGIEARYPGVQFSQFTGAEMIARKYDLSREQLDAYALQSHQR 183
           M            GV  +P +              AEM+ + + ++REQ DA+ ++SHQ 
Sbjct: 122 MM----------HGVDPNPHMSLYAAKASGMMGLTAEMLGKMHGITREQQDAFGVRSHQL 171

Query: 184 AIAATKSGRFTAEILPVEVRTADGANGEMHTTDEGVRYDATLESIGSVK--LIAEGGRVT 241
           A  AT  G+F  EI+P++    +G   ++   DE +R + TLES+ ++K     +GG VT
Sbjct: 172 AHKATLEGKFKDEIIPMQGYDENGFL-KLFDYDETIRPETTLESLAALKPAFNPKGGTVT 230

Query: 242 AASASQICDGAAGLMVVNEAGLKKLGVKPLARVHAMTVIGHDPVVMLEAPLPATEVALKK 301
           A ++SQI DGA+ ++V++    + LG++P+A + +M V G DP +M   P+PAT+ ALK+
Sbjct: 231 AGTSSQITDGASCMIVMSAQRAQDLGIQPMAVIRSMAVAGVDPAIMGYGPVPATQKALKR 290

Query: 302 AGLRIGDIDLFEVNEAFA----PVPLAWLKATGADPARLNVHGGAIALGHPLGGSGAKLM 357
           AGL I DID FE+NEAFA    PV L  LK       ++N+HGGAIALGHP G SGA++ 
Sbjct: 291 AGLGINDIDFFELNEAFAAQALPV-LKDLKVLDKMNEKVNLHGGAIALGHPFGCSGARIS 349

Query: 358 TTLVHALHTHGKRYGLQTMCEGGGLANVTIVERL 391
            TL++ +  +G  +G+ TMC G G    T+ ER+
Sbjct: 350 GTLLNVMKQNGGTFGVATMCIGLGQGISTVFERV 383


Lambda     K      H
   0.317    0.132    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: 412
Number of extensions: 21
Number of successful extensions: 4
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: 391
Length of database: 383
Length adjustment: 30
Effective length of query: 361
Effective length of database: 353
Effective search space:   127433
Effective search space used:   127433
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.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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