GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gatD in Shewanella loihica PV-4

Align Glutamyl-tRNA(Gln) amidotransferase subunit D; Glu-ADT subunit D; EC 6.3.5.- (uncharacterized)
to candidate 5209470 Shew_1940 cytoplasmic asparaginase I (RefSeq)

Query= curated2:A5UK11
         (436 letters)



>FitnessBrowser__PV4:5209470
          Length = 337

 Score =  156 bits (395), Expect = 8e-43
 Identities = 113/348 (32%), Positives = 179/348 (51%), Gaps = 24/348 (6%)

Query: 90  KQNISIISTGGTVSSIIDYRTGAVHPKFTAADLIKANPELL--DYANYNVKALYNIL-SE 146
           K +I +  TGGT+         A  P F   D +KA PE    +  ++ +     ++ S 
Sbjct: 3   KPSIYVAYTGGTIGMQKTDNGFAPVPGFLT-DCVKAMPEFFHQEMPDFVISEYCPLIDSS 61

Query: 147 NMQPKYWVEAAESIANDIS---DGSDGIVIAHGTDTLHYTAAALSFMLK-TPVPIVITGA 202
           NM P  W    + IA+DI    D  DG VI HGTDT+ +TA+ALSFML+    P+++TG+
Sbjct: 62  NMAPTDW----QMIADDIKANYDKYDGFVILHGTDTMAFTASALSFMLQGLTKPVIVTGS 117

Query: 203 QRSSDRPSSDANMNLIDSV-VAAKSDIAEVSVCMHGSLNDSYTYLHKGTKVRKMHTSRRD 261
           Q    +  SD   NL++++ +AA   +AEV +  +  L        +G +  K H    D
Sbjct: 118 QIPLAQLRSDGQTNLLNALYIAANYPVAEVCLFFNNKL-------FRGNRTTKAHADGFD 170

Query: 262 TFRSINYEPIAKIENHSVDINPNYRYTKRNENELEVNSAVEEKVGLIKSFPGICEELIEY 321
            F S N+ PI       + +    R ++   N L VN    + +G++  +PGI  E+I+ 
Sbjct: 171 AFASPNF-PILLEAGIKIRLKAG-RISESKANTLTVNKISPQPIGVVTLYPGITTEIIDN 228

Query: 322 HIDKGYKGLVIEGTGLGHVPD--KLITPLARAHDENIPVVMTSQCLYGRVNMNVYSTGRE 379
            + +  K L++   G+G+ P   +L+  L +A++  I +V  +QCL G+VNM  Y+TG  
Sbjct: 229 ILQQPVKALILLTYGVGNAPQNPELLECLRKANERGIILVNLTQCLQGKVNMGGYATGNA 288

Query: 380 ILNAGVISGRDMTPETAYVKLSWVLGQTNDIGEVAKLMNKNIAGEFNE 427
           +  AGVISG DMT E A  KL ++L       ++   M +++ GE  E
Sbjct: 289 LAKAGVISGFDMTTEAALTKLHYLLSTELSPSDIRVQMQQDLCGELTE 336


Lambda     K      H
   0.313    0.132    0.373 

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: 338
Number of extensions: 19
Number of successful extensions: 4
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: 436
Length of database: 337
Length adjustment: 30
Effective length of query: 406
Effective length of database: 307
Effective search space:   124642
Effective search space used:   124642
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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