GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gatD in Pseudomonas fluorescens FW300-N1B4

Align Glutamyl-tRNA(Gln) amidotransferase subunit D; Glu-ADT subunit D; EC 6.3.5.- (uncharacterized)
to candidate Pf1N1B4_2023 L-asparaginase (EC 3.5.1.1)

Query= curated2:Q8TV84
         (458 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_2023
          Length = 334

 Score =  139 bits (350), Expect = 1e-37
 Identities = 116/352 (32%), Positives = 169/352 (48%), Gaps = 31/352 (8%)

Query: 94  PKLPNVSVMSTGGTIACRVDYETGAVKPAFTAE--ELVGAVPELLDVINIVDARAVLDLL 151
           P   +V V+ TGGTI  +      A    F A   E + + PEL  V+     R +  L+
Sbjct: 7   PAAQHVMVLYTGGTIGMQASAHGLAPASGFEARMREYLHSQPEL--VVPQWRFREMAPLI 64

Query: 152 -SENMEPKHWMKIAEEVVDALSDPDVEGVVIGHGTDTMAFTAAALSFVIEGLNGPVVLVG 210
            S NM P +W ++ E VVDA+     + V+I HGTDT+A++AAA+SF + GL+  VV  G
Sbjct: 65  DSANMTPAYWQQLREAVVDAVDVQGCDSVLILHGTDTLAYSAAAMSFQLLGLHARVVFTG 124

Query: 211 AQRSSDRPSSDAASNLIAACAFAGDGEVGEVTVCMHGWTSDEVCLVHRGVRVRKMHTSRR 270
           +   +    SDA  NL  A    G G    V +  H    D         R  K+ +  R
Sbjct: 125 SMLPAGVTDSDAWENLSGALVALGQGLAPGVHLYFHSELLDP-------TRCAKVRSFGR 177

Query: 271 DAFRSVESIPIAKVDVKDLRNPKIEFLRSDYRRPEDGEPEISGGFEEKVALVKFAPGMDP 330
             F+ +E        VK    P     + +Y +P+            KVA +   PG+  
Sbjct: 178 HPFKRLER---QGGGVKATSVP----AQLNYNQPKQ---------LAKVAALPLFPGIGA 221

Query: 331 EVLDFYVDRGYRGIVLE--GTGLG-HVSEQWLESIERAVDDGIAVVMTSQCLYGRVNMNV 387
           E LD  ++ G +G+VLE  G+G G   +  +L S+ERA D G+ VV  +QC  G V ++V
Sbjct: 222 EQLDGLLNSGIQGLVLECYGSGTGPSDNPAFLASLERARDKGVVVVAVTQCHEGGVQLDV 281

Query: 388 YRTGRLLRAVGVIPGEDMLPEVAYVKLMYVLDRTDDIKEVERLMRTNIAGEI 439
           Y  G  LR  GV+ G  M  E A+ KL  +L    +  EV RL+  ++ GE+
Sbjct: 282 YEAGSRLRDAGVLSGGGMTREAAFGKLHALLGAGLETTEVRRLVELDLCGEL 333


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: 369
Number of extensions: 19
Number of successful extensions: 3
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: 334
Length adjustment: 31
Effective length of query: 427
Effective length of database: 303
Effective search space:   129381
Effective search space used:   129381
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