GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapX in Pseudomonas fluorescens GW456-L13

Align Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized)
to candidate PfGW456L13_3206 Aspartate aminotransferase (EC 2.6.1.1)

Query= SwissProt::P16524
         (393 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3206
          Length = 396

 Score =  196 bits (497), Expect = 1e-54
 Identities = 110/354 (31%), Positives = 194/354 (54%), Gaps = 5/354 (1%)

Query: 26  QHEDVISLTIGQPDFFTPHHVKAAAKKAIDENVTSYTPNAGYLELRQAVQLYMKKKADFN 85
           Q ED++ L++G PDF TP  +   A  ++    T Y    G   LR+A+    ++++  +
Sbjct: 30  QGEDILLLSVGDPDFDTPQPIVQGAIDSLLNGNTHYAEVRGKRALREAIARRHQQRSGQS 89

Query: 86  YDAESEIIITTGASQAIDAAFRTILSPGDEVIMPGPIYPGYEPIINLCGAKPVIVDTTS- 144
             A+ ++ +  GA  A+ +  + +L+PGDEVI+  P+Y  YE +   CGA  V V   S 
Sbjct: 90  VSAD-QVTVLAGAQCALFSVAQCVLNPGDEVIVAEPMYVTYEAVFGACGAVVVPVPVRSE 148

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

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

Query: 263 CASSISQKAALEAVTNGFDDALIMREQYKKRLDYVYDRLVSM-GLDVVKPSGAFYIFPSI 321
            +    Q AA+ A+ +   +   MRE Y++R D V D L    G+  +KP G  ++   I
Sbjct: 269 GSPDFIQDAAVVALESNLPELEAMREAYRQRRDLVCDSLADCPGVRALKPDGGMFVMLDI 328

Query: 322 KSFGMTSFDFSMALLEDAGVALVPGSSFSTYGEGYVRLSFACSMDTLREGLDRL 375
           +  G+++  F+  LL+  GV+++ G +F     G++RL      + LR+   R+
Sbjct: 329 RQTGLSAQAFADRLLDRHGVSVLAGEAFGPSAAGHIRLGLVVGAEPLRDACQRI 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: 324
Number of extensions: 17
Number of successful extensions: 5
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: 396
Length adjustment: 31
Effective length of query: 362
Effective length of database: 365
Effective search space:   132130
Effective search space used:   132130
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