GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Methylobacterium nodulans ORS 2060

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate WP_015929551.1 MNOD_RS13935 M20 aminoacylase family protein

Query= curated2:A8YUT2
         (384 letters)



>NCBI__GCF_000022085.1:WP_015929551.1
          Length = 388

 Score =  218 bits (556), Expect = 2e-61
 Identities = 134/368 (36%), Positives = 197/368 (53%), Gaps = 13/368 (3%)

Query: 8   ELIQIRRHLHEIPELALQEKETHDYLLKIIKGFNSEFLTIKVPEELP-TAILVLIKGSNP 66
           EL+ IRR LH  PE+  +E  T   + + ++ +      I+V   +  T I+ ++ G   
Sbjct: 13  ELVAIRRDLHAHPEIGFEETRTSAIVAQRLEAWG-----IEVHRGIGRTGIVGILTGRGT 67

Query: 67  Q-RTIGYRTDIDALPVEEKTNLPFSSTHPGIMHACGHDIHMSVALGLLSYFSENQPKD-N 124
             R IG R D+DALP+EE TNLP+ ST PG MHACGHD H ++ LG   Y S+ +  D  
Sbjct: 68  SARRIGLRADMDALPIEEATNLPYRSTKPGTMHACGHDGHTTMLLGAARYLSQTRDFDGT 127

Query: 125 LLFFFQPAEESESGGKKAYEDGIFEGKFRPDEFYGLHDNPELPAGAIGCREGTLFAGTTE 184
            +F FQPAEE   G +    D +FE +F  DE YGLH+ P    G +  R G   A    
Sbjct: 128 AVFIFQPAEEGLGGARAMLADRLFE-RFPCDEVYGLHNQPNGQHGRLSIRRGPAMAAADF 186

Query: 185 VNIDLIGKGGHAAFPQNANDTVVAAASLIMQIQTVISRSIDPIQSGVITLGKVRAGTIRN 244
            +I + G+G HAA P    D VV  A+L+  +Q V+SR+ DPI S V+++ +V+AG   N
Sbjct: 187 FDIRITGRGAHAAQPNRGIDPVVIQAALVQALQAVVSRNTDPIHSAVLSITRVQAGAAYN 246

Query: 245 VIAGQTRIEGTIRGLTQKMILQIDQRLQDLCEGIARSYNMKVNLELNQGGYWPVENNPEL 304
           VI  + ++ GTIR     +   + QRL++ C GIA ++  ++ +E+ Q  +  + N+   
Sbjct: 247 VIPEEAQLAGTIRTFDDGVRAMVSQRLRETCAGIAAAFGAEITVEI-QDVFSVLRNSDVQ 305

Query: 305 TKNFISYMKN--NPEVDFVETKPKMTGEDFGFLLAKFPGTMFWLGVGDPDSQLHSANLNP 362
           T   +        PE    + +PKM  EDF  +L   PG   WLG G   + LH+A  + 
Sbjct: 306 TAAALEVATELFGPEKVDADPEPKMGSEDFADMLLAVPGAYAWLG-GKAGAALHNAAYDF 364

Query: 363 DEKSIIRG 370
           D+  I  G
Sbjct: 365 DDSIIPLG 372


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: 333
Number of extensions: 17
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: 384
Length of database: 388
Length adjustment: 30
Effective length of query: 354
Effective length of database: 358
Effective search space:   126732
Effective search space used:   126732
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.

Links

Downloads

Related tools

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