GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Acidovorax sp. GW101-3H11

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate Ac3H11_3135 Aspartate aminotransferase (EC 2.6.1.1)

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_3135
          Length = 394

 Score =  163 bits (412), Expect = 9e-45
 Identities = 107/343 (31%), Positives = 169/343 (49%), Gaps = 10/343 (2%)

Query: 23  RALARVEQG--EEILLLSVGDPDFDTPAPIVQAAIDSLLAGNTHYADVRGKRALRQRIAE 80
           +ALAR   G  E ++ L++G+PDF  P  + +AA  ++ +G T Y +  G  ALR+RI+ 
Sbjct: 23  QALAREVAGTREPMIFLNIGEPDFTAPPLVQEAAARAVHSGATQYTNALGLDALRERISS 82

Query: 81  RHRRRSGQAVDAEQVVVLAGAQCALYAVVQCLLNPGDEVIVAEPMYVTYEAVFGACGARV 140
            ++ R G  V A ++VV AGA  AL      L+  GDE+++ +P Y        A   + 
Sbjct: 83  WYQSRFGVNVPARRIVVTAGASAALQLACLALIESGDEILMPDPSYPCNRHFVSAAEGKA 142

Query: 141 VPVPVRSENGFRVQAEEVAALITPRTRAMALNSPHNPSGASLPRATWEALAELCMAHDLW 200
           V +P  +   +++ A++V A    +TR + L SP NP+G S+       + ++  +HD  
Sbjct: 143 VLLPTTAAERYQLSADKVRAAWNEKTRGVLLASPSNPTGTSIAPDELRRIHDVVRSHDGI 202

Query: 201 MISDEVYSELLFDGEHVSPASLPGMADRTATLNSLSKSHAMTGWRVGWVVGPAALCAHLE 260
            + DE+Y  L ++ E    A    + D   ++NS SK   MTGWR+GW+V P A+   +E
Sbjct: 203 TMIDEIYLGLSYEEEFGHTAL--AIDDNIISINSFSKYFNMTGWRLGWMVVPEAMVPVVE 260

Query: 261 NLALCMLYGSPEFIQDAACTALEA-PLPELEAMREAYRRRRDLVIECLADSPGLRPLRPD 319
            LA  +   +    Q AA    EA  + E E  R  ++ RRD  I  L       P++PD
Sbjct: 261 RLAQNLFICASTVSQYAALACFEAESIAEYERRRAEFKARRDFFIPALEKLGLAVPVKPD 320

Query: 320 GGMFVMVDIRPTG-----LSAQAFADRLLDRHGVSVLAGEAFG 357
           G  +   D            +  FA  L+ R  ++V  G  FG
Sbjct: 321 GAFYAWADCTQAAQRLGVTGSWDFAFELMRRAHIAVTPGRDFG 363


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: 380
Number of extensions: 24
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 393
Length of database: 394
Length adjustment: 31
Effective length of query: 362
Effective length of database: 363
Effective search space:   131406
Effective search space used:   131406
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 17 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