GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Sulfurivirga caldicuralii DSM 17737

Align Acetylornithine/succinyldiaminopimelate aminotransferase; ACOAT; DapATase; Succinyldiaminopimelate transferase; EC 2.6.1.11; EC 2.6.1.17 (uncharacterized)
to candidate WP_074200562.1 BUQ81_RS01125 adenosylmethionine--8-amino-7-oxononanoate transaminase

Query= curated2:P59317
         (406 letters)



>NCBI__GCF_900141795.1:WP_074200562.1
          Length = 428

 Score =  150 bits (378), Expect = 9e-41
 Identities = 114/345 (33%), Positives = 171/345 (49%), Gaps = 32/345 (9%)

Query: 32  QGSRIWDQQGKEYVDFAGGIAVTALGHCHPALVNALKTQGETLWHIS-NVFTNEPALRLG 90
           +G  I  + G+  VD          G+ HP LV A+  Q +T+ HI     T+EPA+ L 
Sbjct: 31  EGRHIILEDGRRLVDGMSSWWAAIHGYNHPELVLAVARQLKTMPHIMFGGLTHEPAVDLA 90

Query: 91  RKLIEATFA--ERVVFMNSGTEANETAFKLARHYACVRHSPFKTKIIAFHNAFHGRSLFT 148
            KL+  +    ++V F +SG+ A E A K+A  Y   R  P K   +   N +HG +   
Sbjct: 91  EKLVTLSPVPLKKVFFADSGSVAVEVALKIALQYWMARRKPQKHIFLTVRNGYHGDTFGA 150

Query: 149 VSV------------GGQPKYSDGFGPKPA---DI-IHVPFNDLHAVKAVMDDH---TCA 189
           +SV            G  PK+   F P P    D+ +  P +D+ A+ A +D H     A
Sbjct: 151 MSVTDPDNGMHSLFAGVLPKHY--FAPAPHMGFDLKLDEPADDIAALAAFLDHHHDEIAA 208

Query: 190 VVVEPI-QGEGGVTAATPEFLQGLRELCDQHQALLVFDEVQCGMGRTGDLFAYMHYGVTP 248
           +++EPI QG GG+    P +++ LR + D +  LL+FDE+  G GRTG LFA    G++P
Sbjct: 209 IILEPIVQGAGGMRFYRPAYVRQLRAIADDYNVLLIFDEIATGFGRTGKLFACEWAGISP 268

Query: 249 DILTSAKALGGG-FPVSAMLTTAEIASAF-----HPGSHGSTYGGNPLACAVAGAAFDII 302
           DI+T  KAL GG   ++A LTT E+A            HG T+  NP ACA A A+ +++
Sbjct: 269 DIMTVGKALTGGMMTLAATLTTEEVAYTLCNNPPRALMHGPTFMANPTACAAANASIELL 328

Query: 303 NTPEVLEGIQAKRQHFVDHLQKIDQQYDVFSDIRGMGLLIGAELK 347
                 + IQ    H  + L  +     V +D+R +G +   EL+
Sbjct: 329 LKSAWQDRIQHIEAHLQEQLMPLSDHPGV-ADVRVLGAIGVIELE 372


Lambda     K      H
   0.322    0.138    0.416 

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: 432
Number of extensions: 26
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: 406
Length of database: 428
Length adjustment: 31
Effective length of query: 375
Effective length of database: 397
Effective search space:   148875
Effective search space used:   148875
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 (21.9 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