GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Paraburkholderia bryophila 376MFSha3.1

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate H281DRAFT_05564 H281DRAFT_05564 Aspartate/methionine/tyrosine aminotransferase

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__Burk376:H281DRAFT_05564
          Length = 392

 Score =  187 bits (476), Expect = 3e-52
 Identities = 127/370 (34%), Positives = 179/370 (48%), Gaps = 5/370 (1%)

Query: 17  AWDIHYRALARVEQGEEILLLSVGDPDFDTPAPIVQAAIDSLLAGNTHYADVRGKRALRQ 76
           A +   RA A   QG  I+ LS+G+PDF  P  +  AA +++   +  Y    G  ALR+
Sbjct: 15  AMEFGKRAAALEAQGHHIIKLSIGEPDFGAPPAVSLAAREAMDGRSLAYTSALGIPALRE 74

Query: 77  RIAERHRRRSGQAVDAEQVVVLAGAQCALYAVVQCLLNPGDEVIVAEPMYVTYEAVFGAC 136
            IA  +R      V + ++VV AGA  AL  V   L++PGDEVIV +P Y        + 
Sbjct: 75  AIAGFYREVHDVEVHSSRIVVTAGASAALLLVTAALVDPGDEVIVGDPSYPCNRQFLASF 134

Query: 137 GARVVPVPVRSENGFRVQAEEVAALITPRTRAMALNSPHNPSGASLPRATWEALAELCMA 196
           GA+V  VP  +   F++ A  V A  T +TR + + +P NP+G S+P    EA+      
Sbjct: 135 GAQVKLVPTDANTRFQLDAAAVRANWTEKTRGLMIATPSNPTGTSIPPHELEAICSWAHQ 194

Query: 197 HDLWMISDEVYSEL-LFDGEHVSPASLPGMADRTATLNSLSKSHAMTGWRVGWVVGPAAL 255
           H+ W I DE+Y  L   D    +P ++         +NS SK   MTGWR+GW V P AL
Sbjct: 195 HNAWRIVDEIYLNLGDHDAHGRAPQTVLSFDPDAIVINSFSKYFGMTGWRLGWCVVPDAL 254

Query: 256 CAHLENLALCMLYGSPEFIQDAACTA--LEAPLPELEAMREAYRRRRDLVIECLADSPGL 313
              +E LA    Y  P  I   A  A      L   EA R+ +  RR LV+  L      
Sbjct: 255 VPTMERLAQ-NYYICPSTISQHAALACFTRESLALCEARRQQFAERRALVLAGLERIGLP 313

Query: 314 RPLRPDGGMFVMVDIRPTGLSAQAFADRLLDRHGVSVLAGEAFGP-SAAGHIRLGLVLGA 372
            P+ PDG  +V  D+  TGL++  F +R L+   V++  G+ FG   A   +RL      
Sbjct: 314 VPVPPDGAFYVYFDVGHTGLTSWEFCERALEEAHVALTPGKDFGSCGAETFVRLSYAAST 373

Query: 373 EPLREACRRI 382
             L EA  R+
Sbjct: 374 SDLAEAIERL 383


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: 419
Number of extensions: 25
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: 392
Length adjustment: 31
Effective length of query: 362
Effective length of database: 361
Effective search space:   130682
Effective search space used:   130682
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