GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapE in Klebsiella michiganensis M5al

Align Succinyl-diaminopimelate desuccinylase; SDAP desuccinylase; EC 3.5.1.18; N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase (uncharacterized)
to candidate BWI76_RS10270 BWI76_RS10270 acetylornithine deacetylase

Query= curated2:B2FIC0
         (375 letters)



>FitnessBrowser__Koxy:BWI76_RS10270
          Length = 391

 Score =  111 bits (277), Expect = 4e-29
 Identities = 99/313 (31%), Positives = 141/313 (45%), Gaps = 24/313 (7%)

Query: 66  HTDVVPTGPRESWTSDPFTPHIRDGVLYGRGAADMKGSVAAFVVAAEQFVADHPDHPGTL 125
           H D VP G    WTSDPFT   R G LYGRGA D KG + A V A     A      GTL
Sbjct: 77  HIDTVPAG--SGWTSDPFTLAERGGRLYGRGACDAKGPLVAMVEALRLLAATRQRWSGTL 134

Query: 126 AVLLTSDEEGDAIDGVRHVARLFAARGQRIDWCITGEPSSTATLGDLLRVGRRGSLSAKL 185
             + T+DEE  A +G +   R        ID+ + GEP+S AT         +GSL  ++
Sbjct: 135 MGVFTADEE-VASEGAKFYVR---DNPPAIDFAVIGEPTSNATFS-----AHKGSLRPRV 185

Query: 186 RVQGVQGHVAYPEKARNPIHQAAPALAELCARRWDD----GYESFPPTSLQISNIHAGTG 241
           RV+GV  H   PE   N I+Q+A  L  +            ++     SL ++ IH G  
Sbjct: 186 RVKGVTAHSGTPELGVNAIYQSARLLGLIEEAHHQQVRCRCHDLVGNASLTVTRIHGG-H 244

Query: 242 ANNVIPGELDVDFNIRYNPHWDAPKLEAEITALLE----RHGLQYTLKWHRSGEPFYTPE 297
           A+NV+P   ++  + R  P  D   ++AE+  LL+      G++  +   +      T  
Sbjct: 245 ADNVVPDSCELLLDRRMVPGEDEAVVKAELQQLLDHAHAHAGVEAEIIAWQPTTGGATQT 304

Query: 298 GTLRAIARAVLA---EHIGRAPEESTGGGTSDARFIAPLGAQCIEVGPVNASI-HQVDEN 353
            +  AI    LA    H    P      G  D      LGA+ + +GP + ++ H+ DE 
Sbjct: 305 DSSEAIVEQSLAACRRHGQSEPGPFGFQGGCDLVHFRSLGAKGVVIGPGSLAVAHKPDEF 364

Query: 354 VRVDDLEALPGLY 366
           V VD+  A   +Y
Sbjct: 365 VPVDEFIAAAYIY 377


Lambda     K      H
   0.319    0.137    0.421 

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: 428
Number of extensions: 28
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: 375
Length of database: 391
Length adjustment: 30
Effective length of query: 345
Effective length of database: 361
Effective search space:   124545
Effective search space used:   124545
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