GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimB in Sulfuritalea hydrogenivorans DSM 22779

Align 3-oxopimeloyl-CoA:CoA acetyltransferase (characterized)
to candidate WP_041097741.1 SUTH_RS05630 acetyl-CoA C-acyltransferase

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



>NCBI__GCF_000828635.1:WP_041097741.1
          Length = 392

 Score =  477 bits (1228), Expect = e-139
 Identities = 247/394 (62%), Positives = 300/394 (76%), Gaps = 2/394 (0%)

Query: 1   MTEAVIVSTARTPIGKAYRGALNATEGATLLGHAIEHAVKRAGIDPKEVEDVVMGAAMQQ 60
           MT+AVIVSTART + K+++GA N T GATL  H+++HAV RA IDP EVEDV+MG A  +
Sbjct: 1   MTDAVIVSTARTGLAKSWKGAFNMTHGATLGAHSVKHAVARAKIDPAEVEDVLMGCATPE 60

Query: 61  GATGGNIARKALLRAGLPVTTAGTTIDRQCASGLQAIALAARSVLFDGVEIAVGGGGESI 120
           GATG NIAR+  L AGLPVT  G T++R C+SGLQ IA+AA+ ++    +I V GG ESI
Sbjct: 61  GATGSNIARQIALAAGLPVTVPGATVNRFCSSGLQTIAMAAQRIIAGECDILVAGGVESI 120

Query: 121 SLVQNDKMNTFHAVDPALEAIKGDVYMAMLDTAETVAKRYGISRERQDEYSLESQRRTAA 180
           S VQ +  N     DPAL  IK +VY +ML TAE VAKRY I ++RQDEY + SQ R AA
Sbjct: 121 SCVQQEA-NRHMITDPALLKIKPEVYWSMLQTAEQVAKRYKIGKDRQDEYGVNSQLRAAA 179

Query: 181 AQQGGKFNDEIAPISTKMGVVDKATGAVSFKDITLSQDEGPRPETTAEGLAGLKAVRGEG 240
            Q  GKF DEI P++  MGV DKATGA+S K++T++ DEG RP+TT EG++ +++    G
Sbjct: 180 GQAAGKFADEIVPMTVTMGVADKATGALSTKEVTIAADEGIRPDTTLEGVSKIRSALPGG 239

Query: 241 FTITAGNASQLSDGASATVIMSDKTAAAKGLKPLGIFRGMVSYGCEPDEMGIGPVFAVPR 300
             ITAGNASQ SDG+SA+V+M+   A  KGL PLGIFRG    GCEPDEMGIGPVFAVP+
Sbjct: 240 -VITAGNASQFSDGSSASVVMNATVAERKGLTPLGIFRGFAVAGCEPDEMGIGPVFAVPK 298

Query: 301 LLKRHGLSVDDIGLWELNEAFAVQVLYCRDKLGIDPEKLNVNGGAISVGHPYGMSGARLA 360
           LLK+ GL+V DI LWELNEAFAVQVLY  D LGI  ++LNVNGGAI+VGHPYG+SGARL 
Sbjct: 299 LLKKAGLTVADIDLWELNEAFAVQVLYSADTLGIPLDRLNVNGGAIAVGHPYGVSGARLV 358

Query: 361 GHALIEGRRRKAKYAVVTMCVGGGMGSAGLFEIV 394
           GHALIEG+RR AK  VVTMC+GGG G+AGLFE+V
Sbjct: 359 GHALIEGKRRGAKLVVVTMCIGGGQGAAGLFEVV 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: 478
Number of extensions: 13
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: 392
Length adjustment: 31
Effective length of query: 364
Effective length of database: 361
Effective search space:   131404
Effective search space used:   131404
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 Apr 09 2024. 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