GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Rhizobium leguminosarum bv. trifolii WSM1325

Align LL-diaminopimelate aminotransferase; DAP-AT; DAP-aminotransferase; LL-DAP-aminotransferase; EC 2.6.1.83 (uncharacterized)
to candidate WP_012755978.1 RLEG_RS01285 pyridoxal phosphate-dependent aminotransferase

Query= curated2:B1I544
         (392 letters)



>NCBI__GCF_000023185.1:WP_012755978.1
          Length = 388

 Score =  152 bits (383), Expect = 2e-41
 Identities = 109/352 (30%), Positives = 165/352 (46%), Gaps = 4/352 (1%)

Query: 34  VISLGIGDPDVPTPDHIIEAAEKELKIPANHQYPSSAGMPAYRRAVADWYARRFGVELDP 93
           ++ L +G+ D+PTPD I  AA   L       Y    G+P  R+A++D+Y R FG+ L  
Sbjct: 32  LLPLWVGEGDLPTPDFISRAAMDALASGETF-YTWQRGIPELRQALSDYYDRHFGIRLPV 90

Query: 94  QREVVSLIGSKEGIAHLPWCFVDPGDVVLVPDPGYPVYAGGTILAGGIPHPVPLT-AGNG 152
           +   V+  G  + I         PGD ++   P +P  A    +AG     V L   G  
Sbjct: 91  EHFYVTGSGM-QAIQIAVQALTSPGDELVYLSPSWPNIAAALEIAGARSLSVELQFEGGK 149

Query: 153 FLPDLAAIPAETARRAKVMFINYPNNPTGAVASKEFFARVVDFAREYGILVCHDAAYSEI 212
           +  DL  I      + K +FIN P+NPTG  A+K+    ++  AR++ + +  D  Y+  
Sbjct: 150 WAVDLDRIETAITPKTKGIFINTPSNPTGWTATKQDLGDLLALARKHDLWIMADEIYARY 209

Query: 213 AFDGYRPPSFLEVAGAREVGIEFHSVSKTYNMTGWRAGWAAGNAGAVEALGRLKSNLDSG 272
            F G R PSFL+V    +  I  +S SK ++MTGWR GW        + L  L     SG
Sbjct: 210 YFAGGRAPSFLDVMEPDDKIIFVNSFSKNWSMTGWRVGWIVAPPEMGQVLENLIQYSTSG 269

Query: 273 VFQVVQYAAIAALNGPQDGVQSLCEMYRERRDLVVDTLNDLGWRLT-RPRATFYIWAPVP 331
           V Q +Q  A+AAL+   D V +        RD + D L       T +P    Y +  + 
Sbjct: 270 VAQFMQKGAVAALDQGDDFVAANIAKAARSRDTLCDALVATNRVETLKPDGAIYAFLKID 329

Query: 332 AGHDASSFAEMVLEKAGVVITPGTGYGTYGEGYFRISLTLPTPRLVEAMERL 383
              D+ + A  +++K GV + PGT +G+ GE + R        ++  A ERL
Sbjct: 330 GVADSRTAALDIVDKTGVGLAPGTAFGSGGELFLRACFLRDPTQVAIAAERL 381


Lambda     K      H
   0.321    0.139    0.430 

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: 288
Number of extensions: 14
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: 392
Length of database: 388
Length adjustment: 31
Effective length of query: 361
Effective length of database: 357
Effective search space:   128877
Effective search space used:   128877
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 Jul 25 2024. The underlying query database was built on Jul 25 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