GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD in Sulfurivirga caldicuralii DSM 17737

Align Acetylornithine aminotransferase; ACOAT; EC 2.6.1.11 (uncharacterized)
to candidate WP_074200562.1 BUQ81_RS01125 adenosylmethionine--8-amino-7-oxononanoate transaminase

Query= curated2:P63566
         (403 letters)



>NCBI__GCF_900141795.1:WP_074200562.1
          Length = 428

 Score =  154 bits (390), Expect = 4e-42
 Identities = 116/339 (34%), Positives = 171/339 (50%), Gaps = 31/339 (9%)

Query: 25  EGIWLITEDGERYIDFAAGIAVNSLGHSHPHLVETLKTQAEKLWHL--SNVYEIPAQEKL 82
           EG  +I EDG R +D  +       G++HP LV  +  Q + + H+    +   PA + L
Sbjct: 31  EGRHIILEDGRRLVDGMSSWWAAIHGYNHPELVLAVARQLKTMPHIMFGGLTHEPAVD-L 89

Query: 83  GRRLVESTFAD--KVFFTNSGAEALECAIKTARRYQYVSGHPERFRIITFEGAFHGRTLA 140
             +LV  +     KVFF +SG+ A+E A+K A +Y      P++   +T    +HG T  
Sbjct: 90  AEKLVTLSPVPLKKVFFADSGSVAVEVALKIALQYWMARRKPQKHIFLTVRNGYHGDTFG 149

Query: 141 TIAA----GGQAKYLEGFGPKVE-------GFD---QVPFGDEAALRAAIT---PETAGI 183
            ++      G      G  PK         GFD     P  D AAL A +     E A I
Sbjct: 150 AMSVTDPDNGMHSLFAGVLPKHYFAPAPHMGFDLKLDEPADDIAALAAFLDHHHDEIAAI 209

Query: 184 LLEPI-QGEGGLRAFPEEFLRLVRQICDENGLLLLLDEVQTGVGRTGKLFAHEWAGIRPD 242
           +LEPI QG GG+R +   ++R +R I D+  +LL+ DE+ TG GRTGKLFA EWAGI PD
Sbjct: 210 ILEPIVQGAGGMRFYRPAYVRQLRAIADDYNVLLIFDEIATGFGRTGKLFACEWAGISPD 269

Query: 243 IMAIAKGIGGG-FPIGACLATAEAAKGM-----TAGMHGTTYGGNPLGMAVGNAVLDVVL 296
           IM + K + GG   + A L T E A  +      A MHG T+  NP   A  NA ++++L
Sbjct: 270 IMTVGKALTGGMMTLAATLTTEEVAYTLCNNPPRALMHGPTFMANPTACAAANASIELLL 329

Query: 297 ADGFMENVQATALVMKQGLASLVDRYPNVVSEIRGRGLL 335
              + + +Q     +++ L  L D +P  V+++R  G +
Sbjct: 330 KSAWQDRIQHIEAHLQEQLMPLSD-HPG-VADVRVLGAI 366


Lambda     K      H
   0.320    0.138    0.405 

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: 402
Number of extensions: 19
Number of successful extensions: 3
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: 403
Length of database: 428
Length adjustment: 31
Effective length of query: 372
Effective length of database: 397
Effective search space:   147684
Effective search space used:   147684
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