GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimB in Derxia gummosa DSM 723

Align 3-oxopimeloyl-CoA:CoA acetyltransferase (characterized)
to candidate WP_028311694.1 H566_RS0112420 acetyl-CoA C-acyltransferase

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



>NCBI__GCF_000482785.1:WP_028311694.1
          Length = 398

 Score =  265 bits (676), Expect = 2e-75
 Identities = 160/399 (40%), Positives = 226/399 (56%), Gaps = 10/399 (2%)

Query: 1   MTEAVIVSTARTPIGKAYRGALNATEGATLLGHAIEHAVKRA-GIDPKEVEDVVMGAAMQ 59
           + +A +V+  RTP+ +   GA        LL HA+   V RA G+DP E+ DV++G AM 
Sbjct: 5   LQDAYLVAAVRTPVARR-NGAFRHARPDDLLAHALRELVARAPGLDPAEIADVIVGCAMP 63

Query: 60  QGATGGNIARKALLRAGLPVTTAGTTIDRQCASGLQAIALAARSVLFDGVEIAVGGGGES 119
           +   G N+AR  LL AGLP +  G T++R CASGLQA+A AA  +     E+ +  G ES
Sbjct: 64  EAEQGMNVARIGLLLAGLPASVPGFTVNRFCASGLQAVADAAARIRSGEAEVMIAAGVES 123

Query: 120 ISLVQNDKMNTFHAVDPALEAIKGDVYMA----MLDTAETVAKRYGISRERQDEYSLESQ 175
           ++++     N    V P     + D + A    M  TAE VA+R+ +SR  QD +++ES 
Sbjct: 124 MTVMTKMMGNR---VRPNPAFFEHDEHRAIAWGMGLTAEEVARRWNVSRAEQDAFAVESH 180

Query: 176 RRTAAAQQGGKFNDEIAPISTKMGVVDKATGAVSFKDITLSQDEGPRPETTAEGLAGLKA 235
           +R  AA   G+F DEIAP  T       + G        ++ DEGPR + + E +  L+ 
Sbjct: 181 KRAIAAIDAGRFADEIAPYITT-SARPGSDGQPLRTTSVVTHDEGPRRDASPERIGALRP 239

Query: 236 VRGEGFTITAGNASQLSDGASATVIMSDKTAAAKGLKPLGIFRGMVSYGCEPDEMGIGPV 295
           V     ++TAGNASQ+SDGA+A ++MS+      GL+P+  F      G  P+ MGIGPV
Sbjct: 240 VFAADGSVTAGNASQMSDGAAAVLLMSEVALKRSGLQPIARFVAHAVAGVPPEVMGIGPV 299

Query: 296 FAVPRLLKRHGLSVDDIGLWELNEAFAVQVLYCRDKLGIDPEKLNVNGGAISVGHPYGMS 355
            A+PR L R G   D +   ELNEAFA Q +  R  LG+DP ++N  GGAI++GHP G +
Sbjct: 300 EAIPRALARAGWRQDSLDWIELNEAFAAQAIAVRRTLGLDPAQINPLGGAIALGHPLGAT 359

Query: 356 GARLAGHALIEGRRRKAKYAVVTMCVGGGMGSAGLFEIV 394
           GA      L   +R  A+  +VTMC+G GMG+AG+ E V
Sbjct: 360 GAIRTATLLAAMKRGDARRGMVTMCIGTGMGAAGVIERV 398


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: 425
Number of extensions: 20
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: 398
Length adjustment: 31
Effective length of query: 364
Effective length of database: 367
Effective search space:   133588
Effective search space used:   133588
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