GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Alicycliphilus denitrificans K601

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate WP_013518270.1 ALIDE2_RS17550 aspartate aminotransferase family protein

Query= BRENDA::P42588
         (459 letters)



>NCBI__GCF_000204645.1:WP_013518270.1
          Length = 398

 Score =  217 bits (553), Expect = 5e-61
 Identities = 143/370 (38%), Positives = 203/370 (54%), Gaps = 22/370 (5%)

Query: 78  DTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLRAMLAKTLAALT 137
           D  G++++D LGG  +  +GH +P +V A+Q Q+AK    S     P +  LA+ L    
Sbjct: 33  DVNGKQYLDGLGGIAVNTLGHNHPRLVPALQEQIAKLIHTSNYYHVPGQEELARLLTGRA 92

Query: 138 PGKLKYSFFCNSGTESVEAALKLAKAYQSPRG--KFTFIATSGAFHGKSLGALSATAKST 195
             ++  +FFCN+G E+ E A+K+A+ Y   +G  K   +    AFHG+S+  ++AT    
Sbjct: 93  --RMTNAFFCNTGLEANECAIKIARKYGVDKGIEKPEIVVYDHAFHGRSIATMTATGNPK 150

Query: 196 FRKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQGEGGVILPPPGYLT 255
            R  F PLL GF  V   +IEA    L E  +   +V AV++EPIQGEGG+      YL 
Sbjct: 151 VRNGFGPLLEGFIRVAPNDIEA----LQEATEGNPNVVAVLMEPIQGEGGLHPMRVEYLQ 206

Query: 256 AVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGGGVMPIGATIAT 315
            VRKLCD  G L++LDEVQ GMGRTGK FA +   + PD++ LAK LG GV P+GA +A 
Sbjct: 207 QVRKLCDANGWLLMLDEVQAGMGRTGKWFAHQWAGIVPDVMTLAKGLGSGV-PVGAVLAH 265

Query: 316 EEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQKGDMLLDGFRQLAR 375
                VL   P  H +TFGGNPLA  A + TI ++ E+ L   A   G  L  G +Q   
Sbjct: 266 GAASEVL--KPGNHGSTFGGNPLAMRAGVETIRIMEEEGLLQNAADVGAHLKAGLQQALG 323

Query: 376 EYPDLVQEARGKGMLMAIEFVDNEIGYNFASEMFRQRVLVAGTLNNA---KTIRIEPPLT 432
             P  V E RG+G+++ +E +D   G      +   R   AG L +    + IR+ P LT
Sbjct: 324 SVPG-VNEVRGQGLIIGVE-LDRPCG------VLIDRAAQAGLLLSVTADRVIRLVPALT 375

Query: 433 LTIEQCELVI 442
           LT  + + ++
Sbjct: 376 LTRAEADEIV 385


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: 413
Number of extensions: 22
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: 398
Length adjustment: 32
Effective length of query: 427
Effective length of database: 366
Effective search space:   156282
Effective search space used:   156282
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 Apr 09 2024. 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