GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Burkholderia phytofirmans PsJN

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate BPHYT_RS15405 BPHYT_RS15405 aminotransferase

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__BFirm:BPHYT_RS15405
          Length = 398

 Score =  179 bits (453), Expect = 2e-49
 Identities = 123/369 (33%), Positives = 175/369 (47%), Gaps = 13/369 (3%)

Query: 31  GEEILLLSVGDPDFDTPAPIVQAAIDSLLAGNTHYADVRGKRALRQRIAERHRRRSGQAV 90
           G +I+ + +G+PDF  P P+++AA  +L  G T Y    G  ALR+ I+  +    G  V
Sbjct: 37  GRDIIHMGIGEPDFTAPEPVIEAAASALRRGVTQYTSALGLHALREAISAHYADFYGVDV 96

Query: 91  DAEQVVVLAGAQCALYAVVQCLLNPGDEVIVAEPMYVTYEAVFGACGARVVPVPVRSENG 150
           D  ++VV AGA  AL      L++  DEV++ +P Y        A   R V VP      
Sbjct: 97  DPARIVVTAGASAALLLACAALVDRDDEVLMPDPCYPCNRHFVIAAEGRPVMVPSGPAER 156

Query: 151 FRVQAEEVAALITPRTRAMALNSPHNPSGASLPRATWEALAELCMAHDLWMISDEVYSEL 210
           F++ A +V  L    TR + L SP NP+G S+  A  E + +   A   + I DE+Y  L
Sbjct: 157 FQLTAADVERLWNEHTRGVLLASPSNPTGTSIEPAELERIVKAVRARGGFTIVDEIYQGL 216

Query: 211 LFDGEHVSPASLPGMADRTATLNSLSKSHAMTGWRVGWVVGPAALCAHLENLALCMLYGS 270
            +D + VS  S     D   T+NS SK   MTGWR+GW+V P  + +  E LA  +   +
Sbjct: 217 SYDAKPVSALS---FGDDVITVNSFSKYFNMTGWRLGWLVVPPGMVSAFEKLAQNLFICA 273

Query: 271 PEFIQDAACTALE-APLPELEAMREAYRRRRDLVIECLADSPGLRPLRPDGGMFVMVDIR 329
               Q AA    E   +   EA R+ ++RRRD +   L       P+ PDG  +V  D R
Sbjct: 274 SALAQHAALACFEPETIAIYEARRQEFKRRRDFIAPALESLGFSVPVMPDGAFYVYADCR 333

Query: 330 PTGLSA----QAFADRLLDRHGVSVLAGEAFGPSA-AGHIRLGLVLGAEPLREACRRIAL 384
               SA     A    +L   GV ++ G  FG  A   +IRL        L EA  R+  
Sbjct: 334 TVAHSAAGDSAALTKAMLHDAGVVLVPGMDFGTHAPKDYIRLSYATAYPKLEEAVDRL-- 391

Query: 385 CAAELLGQA 393
             A+L G+A
Sbjct: 392 --AKLFGKA 398


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: 430
Number of extensions: 28
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: 398
Length adjustment: 31
Effective length of query: 362
Effective length of database: 367
Effective search space:   132854
Effective search space used:   132854
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