GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Desulfovibrio vulgaris Hildenborough

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate 208065 DVU2568 peptidase, M20/M25/M40 family

Query= curated2:Q5WF94
         (374 letters)



>MicrobesOnline__882:208065
          Length = 412

 Score =  231 bits (590), Expect = 2e-65
 Identities = 138/374 (36%), Positives = 191/374 (51%), Gaps = 21/374 (5%)

Query: 6   LIHIRRAFHQIPELGFNEFKTQKLLLDTISNME-QTRLQIKTWKTAVFVRVEGRQDYTIA 64
           +I  RRA H IPE GF E  T   + +T+S +    R  I T      +   G +   + 
Sbjct: 30  IIAHRRALHAIPETGFEERCTAAYVAETLSGLGLPVRTGIATTGVTALLDT-GLEGPVVM 88

Query: 65  YRADMDGLPITEETGYSFASKHEGAMHACGHDFHMTIALG---LLDHFASHEP---ECHL 118
            RADMD LP+TE TG  FAS+HEG MHACGHD HM + LG   +L      EP      +
Sbjct: 89  LRADMDALPVTEATGLPFASRHEGRMHACGHDAHMAMLLGAAEMLSAIVREEPGRLRGKV 148

Query: 119 LFIFQPAEEGPGGAKPIIEADVLGAWQPDEIYALHIDPNLPVGSIATKPGLLFANTSELF 178
           LF+FQPAEEGPGGA P+I   VL   + D     H+ P+LPVG++  KPG L A      
Sbjct: 149 LFLFQPAEEGPGGAAPMIAEGVLDEPKVDVCLGAHVWPSLPVGTVGVKPGPLMAAMDRFE 208

Query: 179 IDFQGKGGHAAYPHTANDMVVACAHFVTQVQTVVARNIDPLDSAVVTLGVIAGGTKQNVI 238
           +   G+GGHAA PH   D +      V  +Q VV+R  DPL+  ++T+G +  GT  NVI
Sbjct: 209 LAVHGRGGHAATPHLCVDALETATQVVGALQRVVSRMTDPLEPVILTIGELHAGTAYNVI 268

Query: 239 AATARLEGTIRTLSMASMEVVKSRLEAIAAGIEASFACKIAIDYGSNYCEVYNDPELAEA 298
              AR+ GT+RT S       + R+  +A G+ A+      +D+   +  V N P +AE 
Sbjct: 269 PGEARMAGTVRTFSPDVRAAWEDRIRTVADGVCAAMGATATLDFHYCHGPVINTPRVAEV 328

Query: 299 FAAFSKTRKGITFVEAEEAMT-------GEDFGYFLKQYPGVMFWLGVDSPYGLHDSRLQ 351
                  R+ +     E+A+T       GEDF  FL++ PG  F++G      +H+ R  
Sbjct: 329 ------VRRAVVEARGEQAVTTPTPTLGGEDFSCFLERIPGCFFFVGCGGDVPIHNPRFD 382

Query: 352 PSEEAIGIAIEHMV 365
             E  + +  E  V
Sbjct: 383 LDERCLALGAETFV 396


Lambda     K      H
   0.321    0.136    0.406 

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: 409
Number of extensions: 11
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: 412
Length adjustment: 31
Effective length of query: 343
Effective length of database: 381
Effective search space:   130683
Effective search space used:   130683
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 (21.9 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