GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gatD in Pseudomonas simiae WCS417

Align Glutamyl-tRNA(Gln) amidotransferase subunit D; Glu-ADT subunit D; EC 6.3.5.- (uncharacterized)
to candidate GFF5498 PS417_28140 asparaginase

Query= curated2:Q8TV84
         (458 letters)



>FitnessBrowser__WCS417:GFF5498
          Length = 325

 Score =  137 bits (344), Expect = 7e-37
 Identities = 111/356 (31%), Positives = 167/356 (46%), Gaps = 51/356 (14%)

Query: 98  NVSVMSTGGTIACRVDYETGAVKPAFTAE--ELVGAVPELLDVINIVDARAVLDLLSENM 155
           NV V+ TGGTI  +      A    F A   E +  +P         +   ++D  S NM
Sbjct: 6   NVMVLYTGGTIGMQASTHGLAPASGFEARMREQLAHLPA--PAWRFQEMAPLID--SANM 61

Query: 156 EPKHWMKIAEEVVDALSDPDVEGVVIGHGTDTMAFTAAALSFVIEGLNGPVVLVGAQRSS 215
            P +W ++   VV+A+ D   + V+I HGTDT+A++AAA+SF + GL  PVV  G+   +
Sbjct: 62  TPAYWQRLRTAVVEAVDD-GCDAVLILHGTDTLAYSAAAMSFQLLGLPAPVVFTGSMLPA 120

Query: 216 DRPSSDAASNLIAACAFAGDGEVGEVTVCMHGWTSDEVCLVHRGVRVRKMHTSRRDAFRS 275
             P SDA  N+  A A  G G    V +  HG        +    R  K+ +  R+ F +
Sbjct: 121 GVPDSDAWENVSGALAALGKGIAPGVHLYFHG-------ALMAPTRCAKIRSFGRNPFAA 173

Query: 276 V---------ESIPIAKVDVKDLRNPKIEFLRSDYRRPEDGEPEISGGFEEKVALVKFAP 326
           +         ESIP A                 DYR+P+             V ++   P
Sbjct: 174 LNRQGGAARAESIPQAL----------------DYRQPKA---------LASVGVLPLVP 208

Query: 327 GMDPEVLDFYVDRGYRGIVLE--GTGLGHVSE-QWLESIERAVDDGIAVVMTSQCLYGRV 383
           G+    LD  +  G + ++LE  G+G G     ++L S++RA D G+ VV  +QC  G V
Sbjct: 209 GIGAAQLDAVIGSGIQALILECFGSGTGPSDNPEFLASLQRAQDQGVVVVAITQCHEGGV 268

Query: 384 NMNVYRTGRLLRAVGVIPGEDMLPEVAYVKLMYVLDRTDDIKEVERLMRTNIAGEI 439
            ++VY  G  LR VGV+ G  M  E A+ KL  ++    D +EV RL+  ++ GE+
Sbjct: 269 ELDVYEAGSRLRGVGVLSGGGMTREAAFGKLNALIGAGLDTQEVRRLVELDLCGEL 324


Lambda     K      H
   0.318    0.139    0.404 

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: 343
Number of extensions: 26
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: 458
Length of database: 325
Length adjustment: 30
Effective length of query: 428
Effective length of database: 295
Effective search space:   126260
Effective search space used:   126260
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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