GapMind for Amino acid biosynthesis

 

Alignments for a candidate for glnA in Pseudomonas putida KT2440

Align glutamine synthetase (EC 6.3.1.2) (characterized)
to candidate PP_4547 PP_4547 putative Glutamine synthetase

Query= BRENDA::O33342
         (457 letters)



>FitnessBrowser__Putida:PP_4547
          Length = 454

 Score =  176 bits (445), Expect = 2e-48
 Identities = 134/380 (35%), Positives = 181/380 (47%), Gaps = 17/380 (4%)

Query: 80  WDTGYGDMVMTPDLSTLRLIPW--LPGTALVIADLVWADGSEVAVS-PRSILRRQLDRLK 136
           WD G  D    P   +L  +PW  +P TA V   +  ++G   +++ PR +L R ++ LK
Sbjct: 74  WDVGDIDCRAYPLDGSLVRLPWRRVP-TAAVQVSMHPSEGLPASIADPRHVLLRTIEALK 132

Query: 137 ARGLVADVATELEFIVFDQPY----RQAWASGYRGLTPASDYNIDYAILASSRMEPLLRD 192
           A G    +A ELEF + DQ      R   A    G  P S     Y +    ++EP L D
Sbjct: 133 ADGYHPVMACELEFYLLDQQRDAQGRPQPALDNDGGRPRSTQV--YGLRELEQIEPFLAD 190

Query: 193 IRLGMAGAGLRFEAVKGECNMGQQEIGFRYDEALVTCDNHAIYKNGAKEIADQHGKSLTF 252
           +       G+       E   GQ EI   + +AL   D    YK   K +A  HG    F
Sbjct: 191 LYAACKAQGIPARTAISEYAPGQVEITLEHGDALQAMDQAVRYKRLVKGVAHAHGMQACF 250

Query: 253 MAK-YDEREGNSCHIHVSLRGTDGSAVFADSNGPHGMSSMFRSFVAGQLATLREFTLCYA 311
           MAK + +  G   H+H+SL  + G+ +FA  +     + + R  VAG L  LR+  L + 
Sbjct: 251 MAKPFAQLAGTGMHMHLSLADSAGNNLFASED--KAGTPLLRQAVAGMLRHLRDSLLLFC 308

Query: 312 PTINSYKRFADSSFAPTALAWGLDNRTCALRVVGHGQNIR-VECRVPGGDVNQYLAVAAL 370
           P  NS++RF  +S+AP A  WG+DNRT +LRV G   N R VE R+ G D N YLA AA+
Sbjct: 309 PNANSFRRFQANSYAPLAPTWGVDNRTVSLRVPGGPANSRHVEHRICGADANPYLAAAAI 368

Query: 371 IAGGLYGIERGLQLPEPCVGNAYQGADVERLPVTLADAAVLFEDSALVREAFGEDVVAHY 430
           +A   +GI   L    P  GN Y  A  E LP     A    + S   REA GED +  Y
Sbjct: 369 LAASHWGIREQLDPGAPVEGNGYAQA-TEHLPTDWLTALDALQHSDWAREALGEDFLGVY 427

Query: 431 LNNARVELAAFNAAVT--DW 448
           L   R E   F A V+  DW
Sbjct: 428 LKVKRAEYRQFMAEVSEQDW 447


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: 531
Number of extensions: 38
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: 454
Length adjustment: 33
Effective length of query: 424
Effective length of database: 421
Effective search space:   178504
Effective search space used:   178504
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