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_033100343.1 JG50_RS0106665 acetylornithine transaminase

Query= BRENDA::P42588
         (459 letters)



>NCBI__GCF_000763315.1:WP_033100343.1
          Length = 393

 Score =  205 bits (522), Expect = 2e-57
 Identities = 139/376 (36%), Positives = 203/376 (53%), Gaps = 21/376 (5%)

Query: 66  VEWQAGSLNTLVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLD-P 124
           V +  G+   L D QG+ ++D   G G+ N+GH +P +  A+ +Q A+   H+  L   P
Sbjct: 12  VRFVKGNGAVLEDDQGKTYLDFASGIGVTNLGHNHPRIKQALLDQ-AEAVWHTSNLFQVP 70

Query: 125 LRAMLAKTLAALTPGKLKYSFFCNSGTESVEAALKLAKAYQSPRGKFT---FIATSGAFH 181
            +   A+ L  LT   L   FFCNSG E+ EAA+KLA+ +       +    I   G+FH
Sbjct: 71  AQEKAAQRLTRLTG--LGAVFFCNSGAEANEAAIKLARKWAQEAKVISEPEIITFQGSFH 128

Query: 182 GKSLGALSATAKSTFRKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQ 241
           G++L  L+AT +   +  F PL  GFR VPFG++EA++ A      TG   AAV+LE +Q
Sbjct: 129 GRTLATLTATGQDKVKHGFSPLPRGFRTVPFGDLEAVKQA------TGATTAAVLLELVQ 182

Query: 242 GEGGVILPPPGYLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKA 301
           GEGGV    P ++  +   C E   L+++DEVQTG+GRTG  FA +   ++PD++  AK 
Sbjct: 183 GEGGVRPANPDFIEGLSAWCKEKEILLMVDEVQTGIGRTGAAFAFQTYGLKPDVITAAKG 242

Query: 302 LGGGVMPIGATIATEEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQ 361
           LG G  PIGA IA EE+  VL   P  H TTFGGNPLA A A A +  L E  +  + + 
Sbjct: 243 LGNG-FPIGAMIAREELKPVL--GPGTHGTTFGGNPLATAVAAAVLAELEETPILEETKA 299

Query: 362 KGDMLLDGFRQLAREYPDLVQEARGKGMLMAIEFVDNEIGYNFASEMFRQRVLVAGTLNN 421
           KG++            P +V   R KG++  +EF D  +     + + +  V +      
Sbjct: 300 KGELFARLLTDELSGLPGMV-SVRVKGLMAGVEF-DQPVAPIITALLGKGLVTLPA---G 354

Query: 422 AKTIRIEPPLTLTIEQ 437
            K +R+ PPL +T +Q
Sbjct: 355 EKVLRLLPPLIVTEDQ 370


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: 409
Number of extensions: 20
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: 393
Length adjustment: 32
Effective length of query: 427
Effective length of database: 361
Effective search space:   154147
Effective search space used:   154147
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