GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Thermoactinomyces daqus H-18

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate WP_033101768.1 JG50_RS0114245 ornithine--oxo-acid transaminase

Query= BRENDA::P42588
         (459 letters)



>NCBI__GCF_000763315.1:WP_033101768.1
          Length = 397

 Score =  246 bits (629), Expect = 7e-70
 Identities = 135/377 (35%), Positives = 216/377 (57%), Gaps = 22/377 (5%)

Query: 78  DTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLRAMLAKTLAALT 137
           D  G  ++D L  +   N GHR+P ++ A++ Q  K  L S+   +    +  + +A LT
Sbjct: 36  DADGNRYMDMLSAYSALNHGHRHPRLIQALKEQADKVTLTSRAFHNDQLGLFYEKVAKLT 95

Query: 138 PGKLKYSFFCNSGTESVEAALKLAKAY-----QSPRGKFTFIATSGAFHGKSLGALSATA 192
             ++      N+G E+VE A+K  + +     + P  +   I  +  FHG+++ A+S ++
Sbjct: 96  DKEMVLPM--NTGAEAVETAIKAVRRWAYDVKKVPDNQAEIIVCADNFHGRTVTAVSLSS 153

Query: 193 KSTFRKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQGEGGVILPPPG 252
              +++ F PL PGF+ +P+G++EA+R A+        + AA + EPIQGE GVI+PP G
Sbjct: 154 NDEYKRGFGPLTPGFKVIPYGDLEALRQAITP------NTAAFLFEPIQGEAGVIVPPEG 207

Query: 253 YLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGGGVMPIGAT 312
           +L    +LC E   L + DE+QTG GRTG++FAC+ E+V+PD+  + KALGGGVMPI A 
Sbjct: 208 FLKQAYELCKEHHVLFVADEIQTGFGRTGQLFACDWEDVKPDLYIMGKALGGGVMPISAV 267

Query: 313 IATEEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQKGDMLLDGFRQ 372
            A  EV  V    P  H +TFGGNPLACA A+A ++VL+E+ LP ++ + G   ++  R+
Sbjct: 268 AADREVLGVF--EPGSHGSTFGGNPLACAVAIAALDVLIEEELPKRSRELGAYFIEELRK 325

Query: 373 LAREYPDLVQEARGKGMLMAIEFVDNEIGYNFASEMFRQRVLVAGTLNNAKTIRIEPPLT 432
           +       ++E RGKG+ + +E    E    +   + ++ +L   T  N  TIR  PPL 
Sbjct: 326 INN---PKIKEVRGKGLFIGMEL--TEAARPYCESLMQEGLLCKETHEN--TIRFAPPLI 378

Query: 433 LTIEQCELVIKAARKAL 449
           +T E+ +L +   RK +
Sbjct: 379 ITREELDLALDKVRKVM 395


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: 443
Number of extensions: 24
Number of successful extensions: 7
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: 397
Length adjustment: 32
Effective length of query: 427
Effective length of database: 365
Effective search space:   155855
Effective search space used:   155855
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