GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Pseudarthrobacter sulfonivorans Ar51

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; Beta-ketothiolase; EC 2.3.1.9 (characterized)
to candidate WP_058929217.1 AU252_RS01510 acetyl-CoA C-acyltransferase

Query= SwissProt::P07097
         (392 letters)



>NCBI__GCF_001484605.1:WP_058929217.1
          Length = 389

 Score =  299 bits (765), Expect = 1e-85
 Identities = 177/389 (45%), Positives = 230/389 (59%), Gaps = 3/389 (0%)

Query: 5   SIVIASARTAVGSFNGAFANTPAHELGATVISAVLERAGVAAGEVNEVILGQVLPAGEGQ 64
           +++   ART    FNG FA+ PA  LGA  I+A L RAGV   +V  VI G VL AG GQ
Sbjct: 3   ALIAGYARTPFSRFNGRFASIPATALGAHAITAALRRAGVTPTDVQYVIAGHVLQAGTGQ 62

Query: 65  NPARQAAMKAGVPQEATAWGMNQLCGSGLRAVALGMQQIATGDASIIVAGGMESMSMAPH 124
           NPARQ+A+ A +P    A  +N +C SG+ AV    + I+ G+A I+VA G ESMS+APH
Sbjct: 63  NPARQSAVGADIPLTIPALTLNAVCLSGMEAVVAAERMISGGEADIVVAVGQESMSLAPH 122

Query: 125 CAHLAGGVKMGDFKMIDTMIKDGLTDAFYGYHMGTTAENVAKQWQLSRDEQDAFAVASQN 184
             H   G K G  +++DT+  DGLTDAF    MG + E+    + L R  QDA+A AS  
Sbjct: 123 VFHARAGQKYGALEVMDTLELDGLTDAFERRSMGISTEDGNTAYGLDRTCQDAWAAASHQ 182

Query: 185 KAEAAQKDGRFKDEIVPFIVKGRKGDITVDADEYIRHGATLDSMAKLRPAFDKEGTVTAG 244
           +A+A         EI P+ V   +G+  V  D+ +R G T +S+A LR AF KEGT+TAG
Sbjct: 183 RADA--HTAFLAGEIEPYTVVSSRGNTVVADDDGVRTGTTTESLASLRTAFGKEGTITAG 240

Query: 245 NASGLNDGAAAALLMSEAEASRRGIQPLGRIVSWATVGVDPKVMGTGPIPASRKALERAG 304
           N+S + DGAAA +L+SE+ A + G+ PL R+ S A V      +   P  A   AL   G
Sbjct: 241 NSSQITDGAAALVLVSESAADQLGLSPLARVESHALVAGPDVRLHDQPANAILAALRSIG 300

Query: 305 WKIGDLDLVEANEAFAAQACAVNKDLGWDPSIVNVNGGAIAIGHPIGASGARILNTLLFE 364
               DL  VE NEAFAA +    + LG  P IVN  GGAIA+GHPIGASGARI+ TL  +
Sbjct: 301 AGTEDLTAVEINEAFAAVSVQSVRTLGVSPDIVNTRGGAIALGHPIGASGARIVGTLARQ 360

Query: 365 MKRRG-ARKGLATLCIGGGMGVAMCIESL 392
           +   G  R G A +C GGG G A+ + SL
Sbjct: 361 LVELGPGRLGAAAICGGGGQGSAIVLRSL 389


Lambda     K      H
   0.317    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: 365
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: 392
Length of database: 389
Length adjustment: 31
Effective length of query: 361
Effective length of database: 358
Effective search space:   129238
Effective search space used:   129238
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 Apr 09 2024. 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