GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Phaeobacter inhibens BS107

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate GFF2092 PGA1_c21250 aspartate aminotransferase AatA

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__Phaeo:GFF2092
          Length = 400

 Score =  202 bits (513), Expect = 2e-56
 Identities = 130/373 (34%), Positives = 191/373 (51%), Gaps = 20/373 (5%)

Query: 31  GEEILLLSVGDPDFDTPAPIVQAAIDSLLAGNTHYADVRGKRALRQRIAERHRRRSGQAV 90
           G +++ LS G+PDFDTP  I +AAI ++ AG T Y    G   L+Q + ++  R +G   
Sbjct: 30  GRDVIGLSAGEPDFDTPDNIKEAAIRAIQAGKTKYTAPDGIAELKQAVCDKFARDNGLEY 89

Query: 91  DAEQVVVLAGAQCALYAVVQCLLNPGDEVIVAEPMYVTYEAVFGACGARVVPVPVRSENG 150
              QV V  G +  LY  +   LNPGDEV++  P +V+Y  +    G   + V    E G
Sbjct: 90  TPAQVSVGTGGKQILYNALMATLNPGDEVVIPAPYWVSYPDMVRLAGGTPICVESSLETG 149

Query: 151 FRVQAEEVAALITPRTRAMALNSPHNPSGASLPRATWEALAELCMAH-DLWMISDEVYSE 209
           F++  +++ A ITP+T+    NSP NP+GA       +AL ++ + H  +W+++D++Y  
Sbjct: 150 FKITPDQLEAAITPKTKWFVFNSPSNPTGAGYHPNELKALTDVLLRHPHVWVMTDDMYEH 209

Query: 210 LLFDG-EHVSPASL-PGMADRTATLNSLSKSHAMTGWRVGWVVGPAALCAHLENLALCML 267
           L+FD     +PA + P + DRT T N +SK++AMTGWR+G+  GP  L   +  +     
Sbjct: 210 LVFDDFTFCTPAQIEPKLYDRTLTCNGVSKAYAMTGWRIGYAAGPKPLIDAMRKIQSQST 269

Query: 268 YGSPEFIQDAACTALEAPLPELEAMREAYRRRRDLVIECLADSPGLRPLRPDGGMFVMVD 327
                  Q AA  AL      +      +RRRRDLVI  L+   G+    PDG  +V   
Sbjct: 270 SNPCTISQWAAVEALNGTQDYILPNTAVFRRRRDLVISMLSQIEGVACPVPDGAFYVYPS 329

Query: 328 IRPTGL------------SAQAFADRLLDRHGVSVLAGEAFGPSAAGHIRLGLVLGAEPL 375
           I   GL              +AFA  LL+   V+V+ G A+G S   + R+      E L
Sbjct: 330 I--AGLIGRTSAGGVAITDDEAFAKALLEEADVAVVHGAAYGLSP--NFRISYAAADETL 385

Query: 376 REACRRI-ALCAA 387
            EACRRI   CAA
Sbjct: 386 TEACRRIQVFCAA 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: 415
Number of extensions: 23
Number of successful extensions: 7
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: 400
Length adjustment: 31
Effective length of query: 362
Effective length of database: 369
Effective search space:   133578
Effective search space used:   133578
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