GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Herbaspirillum seropedicae SmR1

Align Aspartate/prephenate aminotransferase; AspAT / PAT; EC 2.6.1.1; EC 2.6.1.79 (characterized)
to candidate HSERO_RS15115 HSERO_RS15115 aminotransferase

Query= SwissProt::A3PMF8
         (400 letters)



>FitnessBrowser__HerbieS:HSERO_RS15115
          Length = 385

 Score =  167 bits (422), Expect = 6e-46
 Identities = 110/371 (29%), Positives = 187/371 (50%), Gaps = 19/371 (5%)

Query: 28  AAGRDVIGLGAGEPDFDTPDNIKAAAKRAIDAGRTKYTAVDGIPELKRAICEKFERENGL 87
           A+ +  + LG G PDF     + AA  +A+  G  +Y  + G+P L+ AI EK E+  G 
Sbjct: 25  ASEKGAVNLGQGFPDFHCDPALVAAVTQAMQEGLNQYPPMAGVPVLREAIAEKVEKLYGH 84

Query: 88  KYTP-AQVTVGTGGKQILYNALVATLNPGDEVIIPAPYWVSYPDMVLLAGGTPVSVAAGM 146
           +Y P +++TV  G  Q +  +++  ++PGDEVI+  P +  Y   + LAGG PV V   +
Sbjct: 85  RYDPVSEITVTAGATQGILTSVLCAVHPGDEVIVIEPVYDCYVPAIELAGGVPVFVQMEV 144

Query: 147 -ETGFKLTPEQLEAAITPRTKWFIFNSPSNPTGAAYTRAELAALCEVLMRHPQVWIMSDD 205
              G+ +  ++++AA+TP+T+  + N+P NPTG+    A++AAL ++ +R   + I+SD+
Sbjct: 145 GAQGYSIPWDKVKAAVTPKTRMIMVNTPHNPTGSVMRAADVAALADI-VRGTDILILSDE 203

Query: 206 MYEHLVFDDFDFTTPAQIEPGLYDRTLTCNGVSKAYCMTGWRIGYAAGPVELIRAMGTIQ 265
           +YEH+V+D     + A+  P L +R+   +   K Y +TGW++GY A P  L      + 
Sbjct: 204 VYEHMVYDGQPHESLAR-HPELAERSFINSSFGKTYHVTGWKVGYVAAPAALTAEFRKVH 262

Query: 266 SQSTSNPCSIAQYAALEALSGPQEFLATNREAFQRRRDLVVSMLNEAKGVTCPNPEGAFY 325
             +     +  QY     +  P  +L      +Q +RDL  + L   +    P+ +G ++
Sbjct: 263 QFNVFTVNTPVQYGLAAYMKDPAPYLDL-PAFYQHKRDLFRTGLANTRFELLPS-QGTYF 320

Query: 326 VYPDISGCIGKTSAGGAKITDDEAFASALLEETGVAVVFGAAFGLSPN----FRISYATA 381
                  C+     G      +  F   L  E GVA +  +AF  +P      R  +A  
Sbjct: 321 ------QCV---KYGAISALPEAEFCKWLTSEIGVAAIPVSAFYNTPRESGIVRFCFAKK 371

Query: 382 DEVLREACARI 392
           DE L+ A  R+
Sbjct: 372 DETLQLALERL 382


Lambda     K      H
   0.318    0.134    0.399 

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: 384
Number of extensions: 19
Number of successful extensions: 5
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: 400
Length of database: 385
Length adjustment: 31
Effective length of query: 369
Effective length of database: 354
Effective search space:   130626
Effective search space used:   130626
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 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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