GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Synechococcus elongatus PCC 7942

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate Synpcc7942_0256 Synpcc7942_0256 Peptidase M20D, amidohydrolase

Query= curated2:B7GIC0
         (378 letters)



>FitnessBrowser__SynE:Synpcc7942_0256
          Length = 408

 Score =  243 bits (619), Expect = 9e-69
 Identities = 143/368 (38%), Positives = 204/368 (55%), Gaps = 9/368 (2%)

Query: 6   RRDLHQIPELGFQEFKTQQYILDYLATLPSERLQIKTWRTGILVRVHGTAPTKTIGYRAD 65
           R+ LH+ PELGFQE +T  +I   L  L     Q     TGI+  + G     T+  RAD
Sbjct: 37  RQQLHRRPELGFQEQETAAFIAARLTEL-GVSFQAGVAGTGIVAEIAGQRSGPTLAIRAD 95

Query: 66  MDGLPIDEQTDVPFRSTHEGRMHACGHDMHMAIALGVLTHV-VHHPIRDDMLFIFQPAEE 124
           MD LPI E  ++P+RS  +GRMHACGHD H+AIALG    +  +      +  IFQPAEE
Sbjct: 96  MDALPILEANEIPYRSEIDGRMHACGHDGHVAIALGTAACLQANSDFAGRVKIIFQPAEE 155

Query: 125 GPGGALPMLESDEMKQWMPDMILALHIAPAYPVGTIATKEGLLFANTSELFIDLIGKGGH 184
           GPGGA PM+    ++    D I+ LH+    P+G +  + G L A      + + G+GGH
Sbjct: 156 GPGGAAPMIAEGVLENPAVDAIIGLHLWNYLPLGKVGVRSGPLMAAVELFDLTIQGRGGH 215

Query: 185 AAFPHETKDMVVAASSLIMQLQTIVSRNVNPLDSAVITIGKLTSGTVQNVIAERARLEGT 244
           AA P    D V+ AS ++  LQ+IVSRNV+PL SAV+TIG L +GT  NVIA+RA+L+GT
Sbjct: 216 AAIPQNCIDAVLVASQIVTLLQSIVSRNVDPLHSAVVTIGSLHAGTTYNVIADRAQLKGT 275

Query: 245 IRTLSPEAMEKVKGRIEAIVRGIEVAYDCQAHIDYGSMYYQVYNDETLTNEFMQFVEK-- 302
           +R         ++ RIE IV G+  ++     ++Y  +Y  V ND  + +      E+  
Sbjct: 276 VRYFDDRYQGFLQERIEQIVAGVCNSHGATYELNYRKLYPAVINDSAIADLVRSVAEEVL 335

Query: 303 ETDVHLVRCQEAMTGEDFGYMLARIPGFMFWLGVQS-----PFGLHHAKLNPNEEAIDVA 357
           E  + +V   + M  ED  Y L ++PG  F+LG  +      F  HH + N +E A+ + 
Sbjct: 336 EPPLGVVPDCQTMGAEDMSYFLQKVPGCYFFLGSANLDRGLNFPHHHPRFNFDETALALG 395

Query: 358 IQLLTRYV 365
           ++L  R V
Sbjct: 396 VELFLRCV 403


Lambda     K      H
   0.322    0.137    0.411 

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: 381
Number of extensions: 13
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: 378
Length of database: 408
Length adjustment: 31
Effective length of query: 347
Effective length of database: 377
Effective search space:   130819
Effective search space used:   130819
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.

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