GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Sphingomonas koreensis DSMZ 15582

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate Ga0059261_2226 Ga0059261_2226 Aspartate/tyrosine/aromatic aminotransferase

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__Korea:Ga0059261_2226
          Length = 399

 Score =  183 bits (465), Expect = 7e-51
 Identities = 121/372 (32%), Positives = 194/372 (52%), Gaps = 16/372 (4%)

Query: 30  QGEEILLLSVGDPDFDTPAPIVQAAIDSLLAGNTHYADVRGKRALRQRIAERHRRRSGQA 89
           QG +++ L  G+PDFDTP  + +AAI+++  G T Y +V G   L+  I  +  R +G  
Sbjct: 28  QGIDVIGLGAGEPDFDTPDFVKEAAIEAIRKGITKYTNVDGTPELKAAIVGKFARDNGLT 87

Query: 90  VDAEQVVVLAGAQCALYAVVQCLLNPGDEVIVAEPMYVTYEAVFGACGARVVPVPVRSEN 149
               Q+ V +G +  L+      ++ GDEV++  P +V+Y  V    G + V +   +E 
Sbjct: 88  YAENQISVNSGGKHTLFNAFCATIDAGDEVVIPAPYWVSYPDVVEFAGGKPVFIAAGAEA 147

Query: 150 GFRVQAEEVAALITPRTRAMALNSPHNPSGASLPRATWEALAELCMAH-DLWMISDEVYS 208
            ++++ E++ A IT RT+ + LNSP NP+GA+   A  +AL E+   H ++ + +D++Y 
Sbjct: 148 NYKIKPEQLEAAITARTKWVVLNSPSNPTGAAYSAAELKALGEVLERHPNVLIYADDMYE 207

Query: 209 ELLFDG-EHVSPASL-PGMADRTATLNSLSKSHAMTGWRVGWVVGPAALCAHLENLALCM 266
            +L+DG E  + A + P + +RT T N +SK++AMTGWR+G+  GP  L   +  L    
Sbjct: 208 HILYDGFEFATIAQVCPSLYERTLTANGVSKAYAMTGWRIGYAGGPQWLIKAMGKLQSQS 267

Query: 267 LYGSPEFIQDAACTALEAPLPELEAMREAYRRRRDLVIECLADSPGLRPLRPDGGMFVMV 326
                   Q A+  AL      L+    A+++RRDLV+  L    G+   RP+G  +V  
Sbjct: 268 TSNPCSVSQAASVAALNGDQSFLKDRAAAFQKRRDLVVSMLGQINGMNCPRPEGAFYVYP 327

Query: 327 DI-------RPTGL---SAQAFADRLLDRHGVSVLAGEAFGPSAAGHIRLGLVLGAEPLR 376
           +         P GL   + +     LLD   V+ + G AFG S A  +R+      + L 
Sbjct: 328 EFSQLIGKTTPKGLVIDTDETMVGYLLDDAKVAAVHGGAFGFSPA--LRISYATSEDVLA 385

Query: 377 EACRRI-ALCAA 387
           EAC RI   CAA
Sbjct: 386 EACGRIQEACAA 397


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: 392
Number of extensions: 22
Number of successful extensions: 3
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: 399
Length adjustment: 31
Effective length of query: 362
Effective length of database: 368
Effective search space:   133216
Effective search space used:   133216
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