GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapX in Acidovorax sp. GW101-3H11

Align Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized)
to candidate Ac3H11_3135 Aspartate aminotransferase (EC 2.6.1.1)

Query= SwissProt::P16524
         (393 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_3135
          Length = 394

 Score =  191 bits (484), Expect = 4e-53
 Identities = 121/357 (33%), Positives = 191/357 (53%), Gaps = 10/357 (2%)

Query: 28  EDVISLTIGQPDFFTPHHVKAAAKKAIDENVTSYTPNAGYLELRQAVQLYMKKKADFNYD 87
           E +I L IG+PDF  P  V+ AA +A+    T YT   G   LR+ +  + + +   N  
Sbjct: 34  EPMIFLNIGEPDFTAPPLVQEAAARAVHSGATQYTNALGLDALRERISSWYQSRFGVNVP 93

Query: 88  AESEIIITTGASQAIDAAFRTILSPGDEVIMPGPIYPGYEPIINLCGAKPVIVDTTS-HG 146
           A   I++T GAS A+  A   ++  GDE++MP P YP     ++    K V++ TT+   
Sbjct: 94  AR-RIVVTAGASAALQLACLALIESGDEILMPDPSYPCNRHFVSAAEGKAVLLPTTAAER 152

Query: 147 FKLTARLIEDALTPNTKCVVLPYPSNPTGVTLSEEELKSIAALLKGRNVFVLSDEIYSEL 206
           ++L+A  +  A    T+ V+L  PSNPTG +++ +EL+ I  +++  +   + DEIY  L
Sbjct: 153 YQLSADKVRAAWNEKTRGVLLASPSNPTGTSIAPDELRRIHDVVRSHDGITMIDEIYLGL 212

Query: 207 TYDRPHYSIATYLRDQTIVINGLSKSHSMTGWRIGFLFAPKDIAKHILKVHQYNVSCASS 266
           +Y+      A  + D  I IN  SK  +MTGWR+G++  P+ +   + ++ Q    CAS+
Sbjct: 213 SYEEEFGHTALAIDDNIISINSFSKYFNMTGWRLGWMVVPEAMVPVVERLAQNLFICAST 272

Query: 267 ISQKAALEAV-TNGFDDALIMREQYKKRLDYVYDRLVSMGLDV-VKPSGAFYIF----PS 320
           +SQ AAL         +    R ++K R D+    L  +GL V VKP GAFY +     +
Sbjct: 273 VSQYAALACFEAESIAEYERRRAEFKARRDFFIPALEKLGLAVPVKPDGAFYAWADCTQA 332

Query: 321 IKSFGMT-SFDFSMALLEDAGVALVPGSSFSTYG-EGYVRLSFACSMDTLREGLDRL 375
            +  G+T S+DF+  L+  A +A+ PG  F T+  E ++R S A SM  L E + RL
Sbjct: 333 AQRLGVTGSWDFAFELMRRAHIAVTPGRDFGTFDPERFIRFSTANSMAQLEESVARL 389


Lambda     K      H
   0.319    0.135    0.388 

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: 276
Number of extensions: 14
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: 393
Length of database: 394
Length adjustment: 31
Effective length of query: 362
Effective length of database: 363
Effective search space:   131406
Effective search space used:   131406
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 (21.8 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