GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Shewanella sp. ANA-3

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate 7023380 Shewana3_0610 bifunctional N-succinyldiaminopimelate-aminotransferase/acetylornithine transaminase protein (RefSeq)

Query= BRENDA::P42588
         (459 letters)



>FitnessBrowser__ANA3:7023380
          Length = 405

 Score =  189 bits (479), Expect = 2e-52
 Identities = 129/362 (35%), Positives = 193/362 (53%), Gaps = 21/362 (5%)

Query: 78  DTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLRAMLAKTLAALT 137
           D +G EFID  GG  +  +GH +P +V+A++ Q  K    S  + +     LA  L   T
Sbjct: 37  DQEGNEFIDFAGGIAVNCLGHCHPALVNALKTQGEKLWHLSNVMTNEPALELATKLVNST 96

Query: 138 PGKLKYSFFCNSGTESVEAALKLAKAYQSPR---GKFTFIATSGAFHGKSLGALSATAKS 194
             +  Y  F NSG E+ EAALKLA+ Y   +    K   IA   AFHG++   +S   ++
Sbjct: 97  FAERVY--FANSGAEANEAALKLARRYALEKFGVEKDEIIAFDKAFHGRTFFTVSVGGQA 154

Query: 195 TFRKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQGEGGVILPPPGYL 254
            +   F P      H+P+ ++ A+  A++      D   A++LEP+QGEGG+I   P +L
Sbjct: 155 AYSDGFGPKPQSITHLPYNDVAALEAAVS------DKTCAIMLEPLQGEGGIIDADPAFL 208

Query: 255 TAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGGGVMPIGATIA 314
            AVR+L ++  AL+I DEVQTG+GRTG+++A    ++ PDIL  AKALGGG  PI A + 
Sbjct: 209 KAVRELANKHNALVIFDEVQTGVGRTGELYAYMGTDIVPDILTTAKALGGG-FPIAAMLT 267

Query: 315 TEEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQKGDMLLDGFRQLA 374
           T E+   L      H +T+GGNPLACA   A ++V+    +    + +  +L DG  ++ 
Sbjct: 268 TAEIAEHL--KVGTHGSTYGGNPLACAIGNAVLDVVNTPEVLNGVKHREQLLRDGLNKIN 325

Query: 375 REYPDLVQEARGKGMLMAIEFVDNEIGYNFASEMFRQRVLVAGTLN---NAKTIRIEPPL 431
            +Y  +  E RGKG+L+    V NE  Y   S  F    +  G ++    A  +R  P L
Sbjct: 326 EKY-HVFSEIRGKGLLLGA--VLNE-QYQGRSRDFLVASVAEGLMSLMAGANVVRFAPSL 381

Query: 432 TL 433
            +
Sbjct: 382 VI 383


Lambda     K      H
   0.320    0.135    0.393 

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: 363
Number of extensions: 15
Number of successful extensions: 5
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: 459
Length of database: 405
Length adjustment: 32
Effective length of query: 427
Effective length of database: 373
Effective search space:   159271
Effective search space used:   159271
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 51 (24.3 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