GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimB in Pseudomonas stutzeri RCH2

Align 3-oxopimeloyl-CoA:CoA acetyltransferase (characterized)
to candidate GFF3012 Psest_3070 3-oxoadipyl-CoA thiolase

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



>FitnessBrowser__psRCH2:GFF3012
          Length = 401

 Score =  251 bits (640), Expect = 3e-71
 Identities = 164/411 (39%), Positives = 225/411 (54%), Gaps = 32/411 (7%)

Query: 3   EAVIVSTARTPIGKAYRGALNATEGATLLGHAIEHAVKR-AGIDPKEVEDVVMGAAMQQG 61
           +  I    RTPIG+ + GAL A     L    +   ++R  G+DP  V++V MG+A Q G
Sbjct: 4   DVFICDAVRTPIGR-FGGALAAVRADDLAAIPLRALLERNPGLDPAAVDEVFMGSANQAG 62

Query: 62  ATGGNIARKALLRAGLPVTTAGTTIDRQCASGLQAIALAARSVLFDGVEIAVGGGGESIS 121
               N+AR ALL AGLP T  G T++R CASG+ A+  A R++    +E+A+ GG ES+S
Sbjct: 63  EDNRNVARMALLLAGLPETVPGVTLNRLCASGMDAVGTAFRAISSGELELAIAGGVESMS 122

Query: 122 LVQ----------------NDKMNTFHAVDPALEAIKGDVYMAMLDTAETVAKRYGISRE 165
                               D    +  ++P ++ + G    AM  TA+ VA  + + R 
Sbjct: 123 RAPYVMGKADTAFGRIQKIEDTTIGWRFINPKMKELYG--VDAMPQTADNVADEWQVGRA 180

Query: 166 RQDEYSLESQRRTAAAQQGGKFNDEIAPISTKMGVVDKATGAVSFKDITLSQDEGPRPET 225
            QD ++L SQ+R AAAQQ G F +EI P+     V+    G     +  +  DE PR +T
Sbjct: 181 DQDAFALRSQQRAAAAQQAGFFAEEIVPV-----VIRGKKG-----ETVVDTDEHPRADT 230

Query: 226 TAEGLAGLKAVRGEGFTITAGNASQLSDGASATVIMSDKTAAAKGLKPLGIFRGMVSYGC 285
           TAE LA LK V G   T+TAGNAS ++DGA+A ++ S +     GLKP     GM S G 
Sbjct: 231 TAEALAKLKPVNGPDKTVTAGNASGVNDGAAAMILASAEAVQKYGLKPRAKVLGMASAGV 290

Query: 286 EPDEMGIGPVFAVPRLLKRHGLSVDDIGLWELNEAFAVQVLYCRDKLGI--DPEKLNVNG 343
            P  MG GPV AV +L +R  ++V D  + ELNEAFA Q L     LG+  D  K+N NG
Sbjct: 291 APRIMGYGPVPAVRKLCERLNIAVSDFDVIELNEAFAAQGLAVTRDLGVPDDSPKVNPNG 350

Query: 344 GAISVGHPYGMSGARLAGHALIEGRRRKAKYAVVTMCVGGGMGSAGLFEIV 394
           GAI++GHP GMSGARL   A+ +  +   +  + TMCVG G G A + E V
Sbjct: 351 GAIALGHPLGMSGARLVLTAVHQLEKTGGRLGLATMCVGVGQGLALVVERV 401


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: 432
Number of extensions: 28
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: 395
Length of database: 401
Length adjustment: 31
Effective length of query: 364
Effective length of database: 370
Effective search space:   134680
Effective search space used:   134680
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 Sep 17 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