GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Williamsia sterculiae CPCC 203464

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate WP_076482969.1 BW971_RS20655 acetylornithine transaminase

Query= BRENDA::P42588
         (459 letters)



>NCBI__GCF_900156495.1:WP_076482969.1
          Length = 395

 Score =  246 bits (629), Expect = 7e-70
 Identities = 156/372 (41%), Positives = 207/372 (55%), Gaps = 30/372 (8%)

Query: 78  DTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLRAMLAKTLAAL- 136
           D  G+E+ID L G  +  +GH NP VV+AV  QL      S   L      LA+ L A  
Sbjct: 34  DADGKEYIDLLAGIAVNVLGHANPAVVAAVTTQLGTLGHTSNLYLSEPVVRLAEELVARF 93

Query: 137 -TPGKLKYSFFCNSGTESVEAALKLAKAYQSPRGKFTFIATSGAFHGKSLGALSATAKST 195
             PG++   FFCNSG E+ EAA K+A+    P      IA   AFHG+++GAL+ T +  
Sbjct: 94  GQPGRV---FFCNSGAEANEAAFKIARRTGRPE----IIAAEKAFHGRTMGALALTGQPA 146

Query: 196 FRKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQGEGGVILPPPGYLT 255
            R PF P+ PG RHVPFG+I+A+R A++E        AA++LEPI GE GV++PP GYLT
Sbjct: 147 KRTPFEPMPPGVRHVPFGDIDALRAAVSE------QTAAIVLEPILGEAGVVVPPDGYLT 200

Query: 256 AVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGGGVMPIGATIAT 315
           A R++    GAL++LDEVQTG+GRTG  FA +   V PD++ LAK LGGG +PIGA +AT
Sbjct: 201 AAREIATANGALLVLDEVQTGVGRTGNFFAHQAVGVVPDVVTLAKGLGGG-LPIGACLAT 259

Query: 316 EEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQKGDMLLDGFRQLAR 375
                +L   P  H TTFGGNP+  AAALA +  L +++L A+    G        +L  
Sbjct: 260 GPAAGLL--EPGQHGTTFGGNPVCAAAALAVLRELDDRDLVARTALLGKKFATDIEELGH 317

Query: 376 EYPDLVQEARGKGMLMAIEFVDNEIGYNFASEMFRQRVLVAGTLNN---AKTIRIEPPLT 432
               LV   RG G+L+ +            +         AG L N   A  IR+ PPL 
Sbjct: 318 ---PLVSHVRGAGLLLGVVLTAQR------AAAVEAAARDAGFLINAPAADVIRLAPPLV 368

Query: 433 LTIEQCELVIKA 444
           LT EQ +  + A
Sbjct: 369 LTDEQADAFVGA 380


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: 463
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: 395
Length adjustment: 32
Effective length of query: 427
Effective length of database: 363
Effective search space:   155001
Effective search space used:   155001
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