GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Azorhizobium caulinodans ORS 571

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate WP_012170514.1 AZC_RS10295 M20 aminoacylase family protein

Query= curated2:A8YUT2
         (384 letters)



>NCBI__GCF_000010525.1:WP_012170514.1
          Length = 386

 Score =  201 bits (511), Expect = 3e-56
 Identities = 119/369 (32%), Positives = 194/369 (52%), Gaps = 11/369 (2%)

Query: 8   ELIQIRRHLHEIPELALQEKETHDYLLKIIKGFNSEFLTIKVPEELPTAILVLIKGSNPQ 67
           E+   RR LH  PEL      T   + + +  F  + +   +     + ++ LI+G  P 
Sbjct: 13  EITAWRRDLHAHPELLYDLPRTSALVAERLTAFGCDEVVRGIGG---SGVVGLIRGKGPG 69

Query: 68  RTIGYRTDIDALPVEEKTNLPFSSTHPGIMHACGHDIHMSVALGLLSYFSENQP-KDNLL 126
           RTI  R D+DALP+ E T  P++ST PG MHACGHD H ++ LG     +E +     + 
Sbjct: 70  RTIALRADMDALPLTEITGAPYASTTPGKMHACGHDGHTAMLLGAAKILAETRNFSGTVA 129

Query: 127 FFFQPAEESESGGKKAYEDGIFEGKFRPDEFYGLHDNPELPAGAIGCREGTLFAGTTEVN 186
             FQPAEE  +G K   +DG+FE +F  +E YG+H+ P +  GA G   G + A    ++
Sbjct: 130 LVFQPAEEGGAGAKAMIDDGLFE-RFGIEEIYGMHNMPGIALGAFGMCHGPIMAAADVIH 188

Query: 187 IDLIGKGGHAAFPQNANDTVVAAASLIMQIQTVISRSIDPIQSGVITLGKVRAGTIRNVI 246
           ID+ G+G HAA P +  D V+  + +++  Q+++SR+IDP++S V+++ +  AGT  N+I
Sbjct: 189 IDIEGRGAHAAQPHDGVDPVLVGSHIVLAAQSLVSRTIDPLKSAVVSITQFNAGTTDNII 248

Query: 247 AGQTRIEGTIRGLTQKMILQIDQRLQDLCEGIARSYNMKVNLELNQGGYWPVENNPELTK 306
                + GT+R    ++   I+ RL  + E  A  +  K  L   +G  +P   N     
Sbjct: 249 PQTAHLCGTVRTYDPEVRDLIESRLAQIAETTAAVFGAKATLRYVRG--YPATRNHPAQT 306

Query: 307 NFISYMKNN---PEVDFVETKPKMTGEDFGFLLAKFPGTMFWLGVGDPDSQLHSANLNPD 363
           +F + + ++   P        P+M  EDF F L + PG   ++G GD  + LH+   + D
Sbjct: 307 DFAARVASDVAGPAAVDTAMPPRMGAEDFSFFLEQRPGAFVFIGNGD-TAGLHNPAYDFD 365

Query: 364 EKSIIRGVN 372
           +++I  G +
Sbjct: 366 DRAIANGTS 374


Lambda     K      H
   0.318    0.138    0.403 

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: 389
Number of extensions: 20
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: 384
Length of database: 386
Length adjustment: 30
Effective length of query: 354
Effective length of database: 356
Effective search space:   126024
Effective search space used:   126024
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 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