GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Acidimicrobium ferrooxidans DSM 10331

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; EC 2.3.1.9 (characterized)
to candidate WP_012784196.1 AFER_RS00545 acetyl-CoA C-acetyltransferase

Query= SwissProt::P45855
         (393 letters)



>NCBI__GCF_000023265.1:WP_012784196.1
          Length = 398

 Score =  372 bits (956), Expect = e-108
 Identities = 201/393 (51%), Positives = 258/393 (65%), Gaps = 1/393 (0%)

Query: 1   MRKTVIVSAARTPFGKFGGVLKEVKAAELGGIVMKEALQQAGVSGDDVEGNVMGMVVQAG 60
           M ++VIVS ARTP GK  G L  + A ELGG  +  AL++AGV+ D V+   MG V+QAG
Sbjct: 1   MSRSVIVSYARTPIGKLQGALASLSAMELGGRAIAGALERAGVAPDSVDYVFMGHVLQAG 60

Query: 61  SGQIPSRQAARLAGMPWSVPSETLNKVCASGLRAVTLCDQMIRAQDADILVAGGMESMSN 120
            GQI +RQAA  A +P +VP+ T+NKVC SGL AV L D ++      ++VAGGMESMS 
Sbjct: 61  QGQITARQAAVAANIPMTVPATTVNKVCLSGLNAVFLADLLLAQGRTSVVVAGGMESMSR 120

Query: 121 IPYAVPAGRWGARMGDGELRDLMVYDGLTCAFDEVHMAVHGNTAAK-EYAISRREQDEWA 179
            PY +P  R G RMGD  L D M+YDGL CAFD + M        + ++ +SR  QD +A
Sbjct: 121 APYVLPGARGGLRMGDAALIDSMLYDGLFCAFDRMAMGASTEHYCRVDHPVSRDRQDAFA 180

Query: 180 LRSHARAAKAADEGKFQDEIVPVNWIGRKGKPNVVDKDEAIRRDTSLDQLAKLAPIYASD 239
            RSH  AA+AA EG+  DEIVPV   GR+G+ +VV+ DE IR +T+++ LA+L P +A D
Sbjct: 181 ARSHELAARAAKEGRLADEIVPVTVAGRRGEVHVVEDDEGIRPETTVETLARLRPAFAED 240

Query: 240 GSITAGNAPGVNDGAGAFVLMSEEKAAELGKRPLATILGFSTTGMPAHELAAAPGFAINK 299
           G+ITAGNA  ++DGA A V+M  E+A   G  PL  ILG+     P   L   P  AI  
Sbjct: 241 GTITAGNASQISDGAAALVVMRAEEAERRGLTPLGEILGYGQVAGPDASLLHQPSNAIRA 300

Query: 300 LLKKNGLTVQDIDLFEVNEAFASVVLTCEKIVGFDLEKVNVNGGAIALGHPIGASGARIL 359
                GL    +DL E+NEAFA+V L     +G D  +VNVNGGAIALGHPIGASGARIL
Sbjct: 301 AASDAGLDPASLDLVEINEAFAAVALASMDDLGIDPARVNVNGGAIALGHPIGASGARIL 360

Query: 360 MTLVYELKRRGGGLGVAAICSGAAQGDAVLVQV 392
            +L+ EL+RRGGG+G AA+C G  QGDA++V+V
Sbjct: 361 GSLLLELRRRGGGVGAAALCGGGGQGDAMIVRV 393


Lambda     K      H
   0.317    0.134    0.387 

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: 453
Number of extensions: 17
Number of successful extensions: 2
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: 393
Length of database: 398
Length adjustment: 31
Effective length of query: 362
Effective length of database: 367
Effective search space:   132854
Effective search space used:   132854
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