GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Halomonas desiderata SP1

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate WP_086509348.1 BZY95_RS07615 succinyldiaminopimelate transaminase

Query= BRENDA::Q9HUI9
         (393 letters)



>NCBI__GCF_002151265.1:WP_086509348.1
          Length = 408

 Score =  105 bits (262), Expect = 2e-27
 Identities = 114/373 (30%), Positives = 153/373 (41%), Gaps = 33/373 (8%)

Query: 37  LSVGDPDFDTPAPIVQAAIDSLLAGNTHYADVRGKRALRQRIAERHRRRSG-QAVDAE-Q 94
           L++G+P    P     A + +       Y    G   LR  IA   RRR     +D E Q
Sbjct: 34  LTIGEPQH-APFAGALATLHAHQLDFARYPATSGIPELRGAIAAWARRRFRLDGLDPERQ 92

Query: 95  VVVLAGAQCALYAVVQCLLNPGD--EVIVAEPMYVTYEAVFGACGARVVPVPVRSENGFR 152
           V+ + G + A++A VQ  L+      V V  P Y  YE      G +   +  R+E+GFR
Sbjct: 93  VLPVNGTREAIFAFVQAALDRSRPARVAVPNPFYQIYEGATLLAGGQPHYLDCRAESGFR 152

Query: 153 VQAEEVAALITPRTRAMALNSPHNPSGASLPRATWEALAELCMAHDLWMISDEVYSELLF 212
              + V A +    + + L SP NP+GA  PRA ++ L  L    D  + SDE YSEL  
Sbjct: 153 PDFDAVPAEVWREVQILFLCSPGNPTGAVTPRAEFQKLIALADEFDFIIASDECYSELYL 212

Query: 213 DGEHVSPASLPGMA-------DRTATLNSLSKSHAMTGWRVGWVVGPAALCAHLENLALC 265
           D +   P  L   A        R    +SLSK   + G R G+V G A L A  +     
Sbjct: 213 DEDAPPPGLLEACAAMGRHDYRRCLVFHSLSKRSNLPGLRSGFVAGDAELIAPFKRYRTY 272

Query: 266 MLYGSPEFIQDAACTALEAPLPELEAMREAYRRRRDLVIECLADSPGLRPLRPDGGMFVM 325
                   +Q A+ TA       + A R+AYR +   V E LA  P L    P+   ++ 
Sbjct: 273 HGCAMSLPLQHASITAWNDE-AHVRANRDAYREKFAAVTEILA--PVLEFPAPEASFYLW 329

Query: 326 VDIRPTGLSAQAFADRLLDRHGVSVLAGEAFG----------------PSAAGHIRLGLV 369
             +   G   +AF   L     VSVL G   G                   AG IRL LV
Sbjct: 330 PAV--PGGDDEAFTRELFAAEHVSVLPGSYMGRPTTGDGRGRADGRGDNPGAGRIRLALV 387

Query: 370 LGAEPLREACRRI 382
              EP  EA  RI
Sbjct: 388 AELEPTVEAAGRI 400


Lambda     K      H
   0.322    0.136    0.411 

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: 502
Number of extensions: 25
Number of successful extensions: 4
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: 393
Length of database: 408
Length adjustment: 31
Effective length of query: 362
Effective length of database: 377
Effective search space:   136474
Effective search space used:   136474
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 (21.9 bits)
S2: 50 (23.9 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