GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Pseudomonas benzenivorans DSM 8628

Align acetyl-CoA C-acetyltransferase (EC 2.3.1.9) (characterized)
to candidate WP_090442262.1 BLS63_RS07895 acetyl-CoA C-acyltransferase FadA

Query= BRENDA::Q0KAI3
         (392 letters)



>NCBI__GCF_900100495.1:WP_090442262.1
          Length = 391

 Score =  249 bits (636), Expect = 1e-70
 Identities = 160/400 (40%), Positives = 222/400 (55%), Gaps = 23/400 (5%)

Query: 2   QQAVIVDAIRSPMGRSKPGSAFTELHATELLAQVIKGLVERN-KLDPGLVDDVITGCVTQ 60
           + AVIVD  R+PMGRSK G       A  L A +I G++ RN KLDP  V+DVI GCV Q
Sbjct: 6   RDAVIVDFGRTPMGRSK-GGMHRNTRAENLSASLITGVLARNAKLDPAEVEDVIWGCVNQ 64

Query: 61  AGEQSAGPGRVAWLAAGFPDHVPATTIDRKCGSSQQAVHFAAQGIMAGAYDIVIACGIES 120
             EQ     R+A L    P    A T+ R CGSS  A+H A Q I  G  D+ +  G+E 
Sbjct: 65  TLEQGWNIARMASLMTPIPHTSAAQTVSRLCGSSMSALHTAVQAIQTGNGDVFVIGGVEH 124

Query: 121 MSRVPMGSARIGQNPYGPSMEARYAPGLVSQGVAAELVAAKYELSRHDMDSYSARSHELA 180
           M  V M    +  NP+  S+ A  A G++  G+ AE++   + +SR   D++  RSH LA
Sbjct: 125 MGHVSMMHG-VDPNPH-MSLYAAKASGMM--GLTAEMLGKMHGISREKQDAFGERSHRLA 180

Query: 181 ATARESGAFRREILGIS--TPNGLV---EQDETIRPGTSVEKLGTLQASFRNDELSARFP 235
             A   G F+ EI+ +     NG +   + DETIRP T++E L  L+ +F          
Sbjct: 181 HKATVEGKFKDEIIPMQGYDENGFLKVFDYDETIRPETTLESLAALKPAFNPK------- 233

Query: 236 QIGWNVTAGNASQISDGASAMLLMSESMAQRLGLKPRARFVAFDVCGDDPVMMLTAPIPA 295
             G  VTAG +SQI+DGAS M++MS   AQ LG++P A   A  V G DP +M   P+P+
Sbjct: 234 --GGTVTAGTSSQITDGASCMIVMSAQRAQDLGIQPMAVVRAMAVAGVDPAIMGYGPVPS 291

Query: 296 SQRAIKKSGLKLDQIDHYEINEAFACVPLAW---QRALGADPARLNPRGGAIALGHPLGA 352
           +Q+A+K++GL +  ID  E+NEAFA   L      + L     ++N  GGAIALGHP G 
Sbjct: 292 TQKALKRAGLTIADIDFVELNEAFAAQALPVLKDLKLLDVMEQKVNLHGGAIALGHPFGC 351

Query: 353 SGVRLMTTMLHALEDSGQRYGLQSMCEAGGMANATIIERL 392
           SG R+  T+L+ ++ +G   G+ +MC   G    T+ ER+
Sbjct: 352 SGARISGTLLNVMKQNGGTLGVSTMCIGLGQGITTVFERI 391


Lambda     K      H
   0.318    0.132    0.384 

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: 351
Number of extensions: 23
Number of successful extensions: 6
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: 392
Length of database: 391
Length adjustment: 31
Effective length of query: 361
Effective length of database: 360
Effective search space:   129960
Effective search space used:   129960
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 24 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