GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Cupriavidus basilensis 4G11

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate RR42_RS18215 RR42_RS18215 amidohydrolase

Query= curated2:B1MZM9
         (387 letters)



>FitnessBrowser__Cup4G11:RR42_RS18215
          Length = 397

 Score =  214 bits (545), Expect = 3e-60
 Identities = 123/344 (35%), Positives = 192/344 (55%), Gaps = 13/344 (3%)

Query: 9   LQTFRRELHQIPETALEEFKTHDYLLTKLKSWQQDYMTIKTVEALPTAILV-YFQGTNPV 67
           +++ RR++H  PE   +E +T D +   L +W      I+    L T  LV   +  +  
Sbjct: 14  IRSIRRDIHAHPELCFKEERTSDVVAQNLAAWG-----IEVHRGLGTTGLVGVIRNGSSK 68

Query: 68  RTIGYRTDIDALPIQEATGLDFASQHPGKMHACGHDVHMTMALGLAQYFSQHQPKDNLI- 126
           R+IG R D+DALP+QEA      SQH G+MHACGHD H  M LG A+Y ++H+  D  I 
Sbjct: 69  RSIGLRADMDALPLQEANTFGHRSQHDGRMHACGHDGHTAMLLGAARYLAEHRNFDGTIN 128

Query: 127 IFFQPAEEAESGGKVAYDMGLFEGKWRPDEFYGIHDQPNLPAGTLSTLAGTLFAGTAELK 186
           + FQPAEE   G +     GLFE ++  D  +G+H+ P +PAG+  T AG L A + E +
Sbjct: 129 LIFQPAEEGGGGAREMIKDGLFE-RFPCDAVFGMHNWPGMPAGSFGTTAGPLMASSNEFR 187

Query: 187 VDVIGTGGHAAYPHLAKDPIVIAAELIIQLQTVVSRSVDPIAGGVVSVGVINGGFANNVI 246
           + V G G HAA PH   DP+   A+++  LQ +++R+  PI   V+SV   +GG A N++
Sbjct: 188 IVVRGKGAHAALPHNGNDPVFTGAQIVSALQGIITRNKRPIDAAVISVTQFHGGDATNIV 247

Query: 247 PDQVHFEGTVRSMTRTGLETMLTRIRKIAEGLAIANEVTINVSLESGSYLPVEN---DPI 303
           PDQV   GTVR+ T   L+ +  R+ ++++ +A A + T+       +Y P  N   +  
Sbjct: 248 PDQVWIGGTVRTFTLPVLDLIERRMEEVSKAVASAFDCTVEFEFHR-NYPPTVNSATETA 306

Query: 304 LATQVINFMQKQSDINFELAQPAMTGEDFGYLLQHIPGVMLWLG 347
            A +V + +    +++  + +P M  EDF ++L   PG  L++G
Sbjct: 307 FAVEVASELVGAGNVDGNI-EPTMGAEDFSFMLLEKPGCYLFIG 349


Lambda     K      H
   0.319    0.135    0.398 

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: 408
Number of extensions: 26
Number of successful extensions: 5
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: 387
Length of database: 397
Length adjustment: 31
Effective length of query: 356
Effective length of database: 366
Effective search space:   130296
Effective search space used:   130296
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 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