GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Pseudomonas litoralis 2SM5

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate WP_090275982.1 BLU11_RS18745 adenosylmethionine--8-amino-7-oxononanoate transaminase

Query= BRENDA::P42588
         (459 letters)



>NCBI__GCF_900105005.1:WP_090275982.1
          Length = 450

 Score =  174 bits (441), Expect = 5e-48
 Identities = 119/363 (32%), Positives = 185/363 (50%), Gaps = 42/363 (11%)

Query: 69  QAGSLNTLVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELL------ 122
           Q G    L D +G  ++D +  + +   GH NP +     NQ  KQ L + E +      
Sbjct: 34  QRGEGVWLHDFEGNRYLDAVSSWWVNAFGHANPYI-----NQRIKQQLDTLEHVILSGFS 88

Query: 123 DPLRAMLAKTLAALTPGKLKYSFFCNSGTESVEAALKLAKAYQSPRGK---FTFIATSGA 179
            P    L++ L A+TP  L   F+ ++G+  +E ALK++  Y    GK     FI  S +
Sbjct: 89  HPPVIELSERLVAITPEPLTRCFYADNGSSCIEVALKMSFHYWLNIGKPEKKRFITLSNS 148

Query: 180 FHGKSLGALSATAKSTFRKPFMPLLPGFRHVPFGN-----------------IEAMRTAL 222
           +HG++L  L+      +++ + PLL     VP  +                  E M  AL
Sbjct: 149 YHGETLATLAVGDVPLYKETYEPLLMEVITVPSPDCYDREPGSTWEEHSRLMFEHMERAL 208

Query: 223 NECKKTGDDVAAVILEP-IQGEGGVILPPPGYLTAVRKLCDEFGALMILDEVQTGMGRTG 281
            E     + VAAVI+EP IQ  GG+ +  P YL  +R+ CD +G  +I DE+  G GRTG
Sbjct: 209 AE---NHEQVAAVIVEPLIQCAGGMRMYHPVYLKLLREACDRYGVHLIHDEIAVGFGRTG 265

Query: 282 KMFACEHENVQPDILCLAKALGGGVMPIGATIATEEVFSVLFDN-----PFLHTTTFGGN 336
            MFACE  ++ PD LCL+KAL GG +P+   + T+ ++   +D+      FLH+ ++ GN
Sbjct: 266 SMFACEQADISPDFLCLSKALTGGYLPMSVCLTTDRIYEAFYDDYSSLRAFLHSHSYTGN 325

Query: 337 PLACAAALATINVLLEQNLPAQAEQKGDMLLDGFRQLAREYPDLVQEARGKGMLMAIEFV 396
           PLACAAALAT+++  + N+    +     +         ++P+ V E R  GM++AIE V
Sbjct: 326 PLACAAALATLDLFEQDNVIENNKTLAAHMAKATAHFT-DHPN-VAEVRQTGMVLAIEMV 383

Query: 397 DNE 399
            ++
Sbjct: 384 QDK 386


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: 482
Number of extensions: 28
Number of successful extensions: 6
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: 450
Length adjustment: 33
Effective length of query: 426
Effective length of database: 417
Effective search space:   177642
Effective search space used:   177642
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 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