GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisF in Thauera aminoaromatica S2

Align Imidazole glycerol phosphate synthase subunit HisF; EC 4.3.2.10; IGP synthase cyclase subunit; IGP synthase subunit HisF; ImGP synthase subunit HisF; IGPS subunit HisF (uncharacterized)
to candidate WP_004307342.1 C665_RS09715 1-(5-phosphoribosyl)-5-[(5-phosphoribosylamino)methylideneamino]imidazole-4-carboxamide isomerase

Query= curated2:A4YI34
         (251 letters)



>NCBI__GCF_000310185.1:WP_004307342.1
          Length = 249

 Score =  104 bits (259), Expect = 2e-27
 Identities = 65/203 (32%), Positives = 104/203 (51%), Gaps = 10/203 (4%)

Query: 6   IIACLDVKDGKVVK---GVRFLDLKLKGDPAELASRYEEEGADEIVFLDISATVEGRKTL 62
           +I  +D+KDG+ V+   G          DP  +A  + E GA  +  +D++    G+   
Sbjct: 3   LIPAIDLKDGQCVRLKQGEMDDATVFSSDPGAMARHWLEAGARRLHLVDLNGAFAGKPKN 62

Query: 63  LEKVRETASVLS--IPLTVGGGVRTVEDVSNLLSNGADKVSLNTVAAENPSVVSMASREF 120
              +R    V+   IP+ +GGG+R ++ + + L NG   V + T A +NP  +  A   F
Sbjct: 63  GAAIRSITDVVGDDIPVQLGGGIRDLDTIEHYLDNGISYVIIGTAAVKNPGFLHDACSAF 122

Query: 121 GAQAVVVAIDAKRVGNGWRVFVRSGTKDTGLDAVDWAKRVEEMGAGEILLTSIDRDGTRD 180
               ++V +DAK      +V V   +K TG D VD A++ E+ G   ++ T I RDG   
Sbjct: 123 PGH-IIVGLDAK----DGKVAVDGWSKLTGHDVVDLARKFEDYGVESVIYTDIGRDGMLS 177

Query: 181 GYDLELTKAVVRATKVPVIASGG 203
           G ++E T  + RA ++PVIASGG
Sbjct: 178 GVNIEATVRLARALRIPVIASGG 200



 Score = 42.4 bits (98), Expect = 9e-09
 Identities = 34/94 (36%), Positives = 48/94 (51%), Gaps = 16/94 (17%)

Query: 6   IIACLDVKDGKV-VKGVRFLDLKLKG-DPAELASRYEEEGADEIVFLDISATVEGRKTLL 63
           II  LD KDGKV V G      KL G D  +LA ++E+ G + +++ DI     GR  +L
Sbjct: 126 IIVGLDAKDGKVAVDGWS----KLTGHDVVDLARKFEDYGVESVIYTDI-----GRDGML 176

Query: 64  EKVRETASV-----LSIPLTVGGGVRTVEDVSNL 92
             V   A+V     L IP+   GG+  + D+  L
Sbjct: 177 SGVNIEATVRLARALRIPVIASGGITDLRDIDAL 210


Lambda     K      H
   0.317    0.135    0.374 

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: 170
Number of extensions: 12
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 251
Length of database: 249
Length adjustment: 24
Effective length of query: 227
Effective length of database: 225
Effective search space:    51075
Effective search space used:    51075
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 46 (22.3 bits)

This GapMind analysis is from Apr 10 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