GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argE in Pseudomonas putida KT2440

Align acetylornithine deacetylase (EC 3.5.1.16) (characterized)
to candidate PP_1525 PP_1525 Succinyl-diaminopimelate desuccinylase

Query= BRENDA::Q92Y75
         (374 letters)



>FitnessBrowser__Putida:PP_1525
          Length = 383

 Score =  101 bits (252), Expect = 3e-26
 Identities = 100/326 (30%), Positives = 145/326 (44%), Gaps = 25/326 (7%)

Query: 48  DRSNIFATIGPKEARGYIISGHMDVVPAAETG-WTSDPFRLRVEAD-RLYGRGTTDMKGF 105
           D  N +AT G ++      +GH DVVP      W  +PF   ++AD  L GRG  DMKG 
Sbjct: 52  DVDNFWATHGSQDGPVLCFAGHTDVVPTGPVQQWQHEPFEALIDADGMLCGRGAADMKGS 111

Query: 106 LAAVLAAVPKLAA-MPLRR-PLHLALSYDEEAGCR-GVPHMIARLPELCRQPLGAIIGEP 162
           LA+++ A  +     P  R  +   ++ DEE     G   ++ RL     +    I+GEP
Sbjct: 112 LASMVIASERFVQDYPNHRGKVAFLITSDEEGPAHHGTKAVVERLKARNERLDWCIVGEP 171

Query: 163 TGMRAI-----RAHKGKAAARLTVRGRSGHSSRPDQGLNAIHGVAGVLTQAVAEADRLVG 217
           +    +        +G   A+LT+RG+ GH + P    N IH  A  L +  AE      
Sbjct: 172 SSTTLLGDVVKNGRRGSLGAKLTIRGKQGHVAYPHLARNPIHLAAPALAELAAE-----H 226

Query: 218 GPFEHVFEPPYSSLQIGTVKGGQ-AVNIIPDSCEVEFEARAISGVDPAELLAPVRKTAEA 276
               + F PP +S QI  +  G  A N++P      F  R  +      L A V    + 
Sbjct: 227 WDEGNAFFPP-TSFQISNLNSGTGATNVVPGELTALFNFRFSTESTVEGLQARVSAILDK 285

Query: 277 LTTLGFEVEWQELSAYPALSLEPDAPL---AALLEELTGREALPAVSYGTEAGLF-QRAG 332
              L + V+W  LS  P L+ EP   L   AA ++ +TGR+  P+ S GT  G F    G
Sbjct: 286 -HELDWSVDW-ALSGLPFLT-EPGELLDAVAASIKGVTGRDTQPSTSGGTSDGRFIATMG 342

Query: 333 IDAIICGPGDIGRAHKPDEYILIDEL 358
              +  GP +    H+ DE IL  +L
Sbjct: 343 TQVVELGPVN-ATIHQVDERILASDL 367


Lambda     K      H
   0.319    0.137    0.410 

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: 333
Number of extensions: 16
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: 374
Length of database: 383
Length adjustment: 30
Effective length of query: 344
Effective length of database: 353
Effective search space:   121432
Effective search space used:   121432
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 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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