GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapX in Pseudomonas fluorescens FW300-N2E3

Align Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized)
to candidate AO353_26890 AO353_26890 aspartate aminotransferase

Query= SwissProt::P16524
         (393 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_26890
          Length = 395

 Score =  186 bits (471), Expect = 1e-51
 Identities = 109/354 (30%), Positives = 188/354 (53%), Gaps = 5/354 (1%)

Query: 26  QHEDVISLTIGQPDFFTPHHVKAAAKKAIDENVTSYTPNAGYLELRQAVQLYMKKKADFN 85
           Q  DV+ L++G PDF TP  +  AA  ++    T Y+   G   LR ++     +++   
Sbjct: 30  QGVDVLLLSVGDPDFDTPKPIVQAAIDSLLAGDTHYSEVRGTRSLRTSIARRHTRRSGQV 89

Query: 86  YDAESEIIITTGASQAIDAAFRTILSPGDEVIMPGPIYPGYEPIINLCGAKPV-IVDTTS 144
            DA+  +++  GA  A+ +  + +L PGDEV++  P+Y  YE +   CGAK V I     
Sbjct: 90  VDAD-HVLVLPGAQCAVYSVVQCLLDPGDEVLVAEPMYVTYEGVFGACGAKVVPIAVRPE 148

Query: 145 HGFKLTARLIEDALTPNTKCVVLPYPSNPTGVTLSEEELKSIAALLKGRNVFVLSDEIYS 204
           +GF++    I   +TP T+ ++L  P+NP+G +LS    +++A L    +++++SDE+YS
Sbjct: 149 NGFRVDPTDIAARITPRTRAILLNSPNNPSGASLSLAIWQALARLCVKHDLWLISDEVYS 208

Query: 205 ELTYDRPHYSIATY--LRDQTIVINGLSKSHSMTGWRIGFLFAPKDIAKHILKVHQYNVS 262
           EL Y+  H S A+   + ++T  +N LSKSH+MTGWR+G++  PK + +H+  +    + 
Sbjct: 209 ELLYEGEHISPASLPGMAERTATVNSLSKSHAMTGWRVGWVIGPKRLTEHLENLSLCMLF 268

Query: 263 CASSISQKAALEAVTNGFDDALIMREQYKKRLDYVYDRLVSM-GLDVVKPSGAFYIFPSI 321
                 Q AA  A+     +  +MR +Y+ R D V  RL    G+  V P G  ++   +
Sbjct: 269 GIPDFVQNAARVALEADLPELALMRNEYRARRDLVCARLGDCPGISPVIPDGGMFVMVDV 328

Query: 322 KSFGMTSFDFSMALLEDAGVALVPGSSFSTYGEGYVRLSFACSMDTLREGLDRL 375
           +  G+ +  F+  LLE   V+++ G +F     G++R+        L E   R+
Sbjct: 329 RQTGVGAQAFAEKLLEGYAVSVLAGEAFGPSAAGHIRIGLVLDQQRLAEACRRI 382


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: 321
Number of extensions: 13
Number of successful extensions: 6
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: 395
Length adjustment: 31
Effective length of query: 362
Effective length of database: 364
Effective search space:   131768
Effective search space used:   131768
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