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 GFF3829 PGA1_262p02330 putative aspartate aminotransferase

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__Phaeo:GFF3829
          Length = 395

 Score =  307 bits (787), Expect = 3e-88
 Identities = 161/383 (42%), Positives = 231/383 (60%), Gaps = 1/383 (0%)

Query: 1   MRYSDFTQRIAGDGAAAWDIHYRALARVEQGEEILLLSVGDPDFDTPAPIVQAAIDSLLA 60
           MR +D T+R+AG G A W++H  A   +  G +I+ +++G+PD  TP  ++Q A  +++A
Sbjct: 1   MRMTDVTRRLAGLGGAKWEVHLTAREMIAAGADIIEMTIGEPDVPTPEALMQTAGAAMMA 60

Query: 61  GNTHYADVRGKRALRQRIAERHRRRSGQAVDAEQVVVLAGAQCALYAVVQCLLNPGDEVI 120
           G T Y+D RG+  LRQ +AER+   +G+A+  + V+   G Q ALYAV+  +   GDEV+
Sbjct: 61  GRTGYSDGRGEANLRQTLAERYSASTGRAIGPDNVLCFPGTQTALYAVLMGVAEHGDEVL 120

Query: 121 VAEPMYVTYEAVFGACGARVVPVPVRSENGFRVQAEEVAALITPRTRAMALNSPHNPSGA 180
           V +PMY TYE V  A GA +VPVP+R E+GFR+QA ++A  ITPR+RA+ L +PHNP+G+
Sbjct: 121 VGDPMYATYEGVIRASGADMVPVPLRPEHGFRMQANDIAEKITPRSRAILLTTPHNPTGS 180

Query: 181 SLPRATWEALAELCMAHDLWMISDEVYSELLFD-GEHVSPASLPGMADRTATLNSLSKSH 239
            L     +A+  L   HDLW+ISDEVY +L+FD  E VSP +    ADR   ++S+SKSH
Sbjct: 181 ILTVEDLDAIGRLADVHDLWIISDEVYEQLVFDAAEFVSPLARAAFADRVIVVSSISKSH 240

Query: 240 AMTGWRVGWVVGPAALCAHLENLALCMLYGSPEFIQDAACTALEAPLPELEAMREAYRRR 299
           A  G+R GW +   A C  L  L+  ML+G+  FI D    A+    P  E MR  +  R
Sbjct: 241 AAPGFRSGWCIASKAFCDGLLPLSETMLFGNQPFIADMTEQAVREGSPVAEGMRARFAAR 300

Query: 300 RDLVIECLADSPGLRPLRPDGGMFVMVDIRPTGLSAQAFADRLLDRHGVSVLAGEAFGPS 359
              + E L     LR   P+ GMF M+++  TGL   A+A  LL   GV+V+ G +FG S
Sbjct: 301 AAKLAERLHRDTALRVHSPEAGMFAMINVAATGLDGDAYAQDLLHSAGVAVMPGSSFGES 360

Query: 360 AAGHIRLGLVLGAEPLREACRRI 382
             G +R+ L +  +    A  RI
Sbjct: 361 LRGWVRVALTIEDDAFDRALTRI 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: 443
Number of extensions: 21
Number of successful extensions: 2
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: 395
Length adjustment: 31
Effective length of query: 362
Effective length of database: 364
Effective search space:   131768
Effective search space used:   131768
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