GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapE in Azorhizobium caulinodans ORS 571

Align Predicted dapE by GapMind curators (no experimental data)
to candidate WP_012170602.1 AZC_RS10745 M20 aminoacylase family protein

Query= predicted:L0FXC2
         (397 letters)



>NCBI__GCF_000010525.1:WP_012170602.1
          Length = 387

 Score =  247 bits (631), Expect = 4e-70
 Identities = 150/377 (39%), Positives = 208/377 (55%), Gaps = 8/377 (2%)

Query: 18  IAIRRHIHAHPELSFEEHQTCAFVEKHLQEIGITNIQRKANTGLVALIEGKNPSKKVIAL 77
           +AIRR IHAHPE+ FEE +T A V + L   G+   +    TG+V ++ G     + I L
Sbjct: 15  VAIRRDIHAHPEIGFEEVRTSALVAEKLASWGVEVHRGIGKTGVVGVLHGAKGPGRRIGL 74

Query: 78  RADMDALPIVEQNDVPYKSNKEGVMHACGHDVHTSSLLGAASILHAVKDQFEGTVKLIFQ 137
           RADMDALP+ E  ++P+ S   G  H CGHD HT+ LLGAA  L A  + F GTV  IFQ
Sbjct: 75  RADMDALPMDEATNLPFSSKYPGKFHGCGHDGHTTMLLGAARYL-ASNNDFAGTVHFIFQ 133

Query: 138 PGEEKIPGGASLMIKDKALENPRPSGIVGQHVMPLIDAGKVGFRKGMYMASADELYLKVI 197
           P EE + GGA  M+ DK  E      + G H  P I+AGKV    G   A AD   +K+ 
Sbjct: 134 PAEEGL-GGARAMLADKLFERFPCDEVYGLHNAPNIEAGKVRIFAGPAQAGADFFDIKIT 192

Query: 198 GKGGHGAMPETLVDPVLIASHIIVALQQVISRNASPKVPSVLSFGRIEALGATNVIPNEV 257
           G+G HGA PE   DPV+ A+ ++ ALQ ++SRNA P+  +VLS  +I +  A NVIP E 
Sbjct: 193 GRGSHGARPEVSRDPVIAATALVQALQSIVSRNADPQHAAVLSVTKIHSGSAYNVIPQEA 252

Query: 258 NIQGTFRTLDETWRAEAHQKMVKIAEGIAEGMGGSVDFEVRKGYPFLQNAPELTDRAYKA 317
            + GT R  D        Q+M  +A GIA      +D E+R  +  L N    +D A K+
Sbjct: 253 TLGGTTRFFDAATGELMRQRMRTVAAGIAATFEMEIDVEIRSIFDVLVNHEAQSDAAAKS 312

Query: 318 AQAYLGEEN-VEDLDIWMAAEDFSYYTQEMDGCFYRLGIRNEEKGITSGVHTPTFDIDES 376
               +G EN + D+   M +EDF+   + + G ++ +G      G    VH P F +DE+
Sbjct: 313 IAKIVGAENLLTDVAPIMGSEDFADMLRAVPGAYFWVG-----HGGDVPVHNPGFVLDEA 367

Query: 377 ALEVGAGLMAWIAINEL 393
            L +G+ L+A +A + L
Sbjct: 368 ILPIGSSLLATVATDRL 384


Lambda     K      H
   0.317    0.134    0.387 

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: 395
Number of extensions: 15
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: 397
Length of database: 387
Length adjustment: 31
Effective length of query: 366
Effective length of database: 356
Effective search space:   130296
Effective search space used:   130296
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 (21.6 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