GapMind for Amino acid biosynthesis

 

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

Align glutamine synthetase (EC 6.3.1.2) (characterized)
to candidate Pf1N1B4_3464 glutamine synthetase family protein

Query= BRENDA::O33342
         (457 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3464
          Length = 447

 Score =  184 bits (466), Expect = 7e-51
 Identities = 128/377 (33%), Positives = 188/377 (49%), Gaps = 19/377 (5%)

Query: 85  GDMVMTPDLSTLRLIPWLPGT-ALVIADLVWADGSEVAVSPRSILRRQLDRLKARGLVAD 143
           GD+ + PD + +  +PW     AL I D     G    +S R  L+  + R  A GL   
Sbjct: 72  GDLALVPDPAQIHRLPWSQQPRALAICDADELTGESSPLSTRGQLKAVIARYAALGLAPV 131

Query: 144 VATELEFIVF------DQPYRQAWASGYRGLTPASDYNIDYAILASSRMEPLLRDIRLGM 197
           VATELEF VF       QP++       R      D +  +++ +++ + P   ++   M
Sbjct: 132 VATELEFFVFAPNPDPTQPFQPPLGLDGR----REDGHSAFSVSSNNGLRPFFNEVYECM 187

Query: 198 AGAGLRFEAVKGECNMGQQEIGFRYDEALVTCDNHAIYKNGAKEIADQHGKSLTFMAK-Y 256
           A  GL  +    E  + Q EI   + + L+  D   ++K+  KE+A +HG ++  MAK  
Sbjct: 188 AALGLPRDTFMHEMGVSQFEINLLHGDPLLLADQTLLFKHLLKEVALKHGLTVVCMAKPL 247

Query: 257 DEREGNSCHIHVSLR--GTDGSAVFADSNGPHGMSSMFRSFVAGQLATLREFTLCYAPTI 314
               G+S HIH S+   GT G  VF+D  G    ++ FR F+ GQ A + +FT  +AP +
Sbjct: 248 AHTPGSSMHIHQSIVEIGT-GRNVFSDKAGEP--TATFRHFIGGQQAGMADFTALFAPNV 304

Query: 315 NSYKRFADSSFAPTALAWGLDNRTCALRVVGHGQNI-RVECRVPGGDVNQYLAVAALIAG 373
           NSY+R      +P    W  DNR   LR+        RVE R+PG D N YLA+AA +A 
Sbjct: 305 NSYQRLCHPFASPNNACWSHDNRAAGLRIPASSPVARRVENRLPGADANPYLAIAASLAS 364

Query: 374 GLYGIERGLQLPEPCVGNAYQGADVERLPVTLADAAVLFEDSALVREAFGEDVVAHYLNN 433
           GLYGIE  L+  EP  G  +   D   LP TL  A    + S L +E FG++ +  Y+ +
Sbjct: 365 GLYGIENKLEPSEPIQGE-FVVPDNLSLPCTLHAALERLKRSQLAKELFGKEFIEGYIAS 423

Query: 434 ARVELAAFNAAVTDWER 450
             +EL +F   +T WER
Sbjct: 424 KTMELTSFFDEITPWER 440


Lambda     K      H
   0.321    0.137    0.417 

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: 537
Number of extensions: 32
Number of successful extensions: 6
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: 457
Length of database: 447
Length adjustment: 33
Effective length of query: 424
Effective length of database: 414
Effective search space:   175536
Effective search space used:   175536
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: 51 (24.3 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