GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Pseudovibrio axinellae Ad2

Align acetyl-CoA C-acetyltransferase (subunit 2/2) (EC 2.3.1.9) (characterized)
to candidate WP_068008846.1 PsAD2_RS17405 acetyl-CoA acetyltransferase

Query= BRENDA::I3R3D1
         (383 letters)



>NCBI__GCF_001623255.1:WP_068008846.1
          Length = 387

 Score =  189 bits (479), Expect = 1e-52
 Identities = 126/375 (33%), Positives = 199/375 (53%), Gaps = 13/375 (3%)

Query: 5   AIIGASMTQFGQ-RDAWIRELLAEAGQAALADADVSPDEIEHLYVSNMASGEFEGQTGVP 63
           AIIG + T FG+  D  +  L+ +  + A+ DA +S  +I+ + + +  +G  +      
Sbjct: 3   AIIGWAHTPFGKLADETVETLVTKVARQAIEDAGLSAQDIDEIVLGHFNAGFSKQDFTAS 62

Query: 64  NALAHDLAAMPAYTARIDQTSSSGGAGVYAAWQSVASGASDMTMLVGGEKMTHRSTAEAT 123
             L  D       T R++   ++G A V+   +S+ +G +   ++VG E+MT     E  
Sbjct: 63  LVLQADDKLRFKPTTRVENACATGSAAVHQGVKSIKAGDAKFVLVVGVEQMTTTPGPEIG 122

Query: 124 DVIASLTHPVEYKHGVTLPSFAGL---TARLYLDTYDAPRESLGKVAVKNHKNGLDNPHA 180
             +   ++  E   G T   FAG+    A +Y   Y    E+L  +A KNHKNG++NP+A
Sbjct: 123 ANLLKASYLPE--DGDTPAGFAGVFGKIAGMYFQKYGDQSEALAHIAAKNHKNGVENPYA 180

Query: 181 QFRKEVDLETVLD----SPVVADPLRLYDFCPITDGSAALVFCSESVAREYTDDYVVISG 236
           Q RK++ +E  L+    +P VA PL+  D   ++DG+AA+V    + A    D  V   G
Sbjct: 181 QMRKDLGVEFCLNESEKNPFVAGPLKRTDCSLVSDGAAAIVLTDTTTALS-ADKAVAFRG 239

Query: 237 IGGATDTHVVHERADPTTMGGVVNSSDIAYEMADLEPDDIDVAELHDMFTILEFLQSEDL 296
           +G A D   + +R D     G   +   A   A++  +D+   E HD FTI E ++ E +
Sbjct: 240 MGHAQDFLPMSKR-DILKFEGCTQAWKRALSQANITINDLSFVETHDCFTIAELIEYEAM 298

Query: 297 GFFEKGEGWKAVEEGVTDRDGELPINTSGGLKSKGHPLGASGVAQVYEIYKQLIGDAGDR 356
           G   +G+G KA+ EG T +DG+LP+N SGGLK+KGHP+GA+GV+       QL G AG  
Sbjct: 299 GLVPEGQGAKAILEGWTQKDGKLPVNPSGGLKAKGHPIGATGVSMHALTAMQLTGTAGGI 358

Query: 357 QVD-ADIGLACNVGG 370
           QV+ A++G   N+GG
Sbjct: 359 QVEGAELGGIFNMGG 373


Lambda     K      H
   0.315    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: 374
Number of extensions: 19
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: 383
Length of database: 387
Length adjustment: 30
Effective length of query: 353
Effective length of database: 357
Effective search space:   126021
Effective search space used:   126021
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: 42 (22.0 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