GapMind for catabolism of small carbon sources

 

Alignments for a candidate for astA in Marinobacter adhaerens HP15

Align Arginine N-succinyltransferase (EC 2.3.1.109) (characterized)
to candidate GFF2696 HP15_2640 arginine/ornithine succinyltransferase

Query= reanno::SB2B:6938907
         (339 letters)



>FitnessBrowser__Marino:GFF2696
          Length = 379

 Score =  276 bits (705), Expect = 8e-79
 Identities = 146/334 (43%), Positives = 201/334 (60%), Gaps = 8/334 (2%)

Query: 2   LIIRPIRASDFDALYRIAVESGHGFTSLPVNEDLLRRKIARSEASFQKVVETPYDEGYLM 61
           +IIRPI   D DAL +IAVESG GFTSL  + D L RKI  S  SF + V TP DE YL 
Sbjct: 7   MIIRPITPKDLDALMQIAVESGPGFTSLMPDRDALSRKIDHSVESFARTVTTPGDEHYLF 66

Query: 62  VLEDTQTQEVVGTCALEAAVGMEDAFYHYRLGTEVYHSQQINVRNEVETLTLCHDYTGAA 121
           VLED+ T +++GT  +EAA G+     H+R    ++H +    R+  E+LT C  YTG  
Sbjct: 67  VLEDSATGQIMGTTGIEAAAGLSRPLVHFRRNAVIHHEEDPRKRHAEESLTRCQHYTGCT 126

Query: 122 ELCTLFLRGAYRKDNNGRMLSRSRFLFLAQHANRFGETVIAEMRGVSDENGNSPFYGWLQ 181
           E+C+L+LR  +R+ N G++LSR RFLF+A H  RF +TVIAEMRGVSD  G SPF+ WL+
Sbjct: 127 EVCSLYLRPGFRRANAGKLLSRVRFLFMALHPERFADTVIAEMRGVSDHAGRSPFWDWLK 186

Query: 182 KHFLGIDFVEADYLSGLGRKAFMAEMMPRNPVYVCLLPEEAQKVIGEVHTNTRPALSLLR 241
            H   +DF+ A  L+  G+  F+   +P  P++   + + A+ VIG+VH +TRPA  +L 
Sbjct: 187 HHVADLDFMSATQLACCGQSGFVERFIPATPLFTRQMTDAARAVIGQVHEDTRPARHMLE 246

Query: 242 AEGFRCRGYVDIFDGGPTVECNLQDIRGVRESRLLTVRIGEMPASD--------DSFILS 293
            EGFR RG+VD+ DGGPT+EC   DI  VR++ L   R+ +   S          S I++
Sbjct: 247 REGFRHRGFVDLLDGGPTLECARSDIASVRDTLLTRARLQKGNRSSWNIAGNTVGSAIVA 306

Query: 294 NTQLVDYRATSVELMVSSDSDEVILSPELAAGLL 327
           N     +RAT  E ++ +     +  PE  A  L
Sbjct: 307 NAGCSGFRATVTEQVLPNPDANSLSVPEQLANEL 340


Lambda     K      H
   0.321    0.137    0.397 

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: 301
Number of extensions: 10
Number of successful extensions: 1
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: 339
Length of database: 379
Length adjustment: 29
Effective length of query: 310
Effective length of database: 350
Effective search space:   108500
Effective search space used:   108500
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: 49 (23.5 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