GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisF in Desulfurobacterium atlanticum DSM 15668

Align imidazole glycerol-phosphate synthase (subunit 2/2) (EC 4.3.2.10) (characterized)
to candidate WP_089323241.1 CHB58_RS06180 1-(5-phosphoribosyl)-5-[(5-phosphoribosylamino)methylideneamino]imidazole-4-carboxamide isomerase

Query= BRENDA::A4WHB6
         (251 letters)



>NCBI__GCF_900188395.1:WP_089323241.1
          Length = 242

 Score =  116 bits (291), Expect = 4e-31
 Identities = 81/213 (38%), Positives = 116/213 (54%), Gaps = 8/213 (3%)

Query: 5   VIPCLDM-DGKAGVVVKGVNFEGVREVGD-PVEMAVRYEEEGADEIAILDITATPEGRST 62
           +IP +D+ DGK   + KG   + V+E  D PVE A+ ++ +GA  + ++D+    EG   
Sbjct: 4   LIPAVDIKDGKCVRLYKG-RADAVKEYFDNPVEAALLWQNKGATRLHVVDLDGAFEGVPK 62

Query: 63  FVESVRRVAEAVSIPVLVGGGVRGIEDAAALFKAGADKVSVNTAAVKNPRLVSEIAREFG 122
            ++ V  + + +SIPV  GGGVR +E   AL  AG D++ V T AV+NP L  E+   F 
Sbjct: 63  NIKIVEEIVKRLSIPVQFGGGVRTVEAVKALKDAGVDRIIVGTVAVENPELFEEMIDVF- 121

Query: 123 SQSTVVAIDAKLVGGRYEVFVRGGKEPTGLDAVEWAKKVEELGAGEILLTSIDKDGTRLG 182
               V+ +DAK       +  RG  E T L AVE+AKK E+      + T I +DGT  G
Sbjct: 122 PDGMVLGVDAK----DGYMTTRGWVEKTELKAVEFAKKYEDEPIWGFVYTDISRDGTLEG 177

Query: 183 YDVELIRRVAEAVKIPVIASGGAGALEHFYEAA 215
            + E + R A +VK PVIASGG    E  +  A
Sbjct: 178 PNFEEVERFAGSVKKPVIASGGIAREEDVFRLA 210



 Score = 27.3 bits (59), Expect = 3e-04
 Identities = 15/63 (23%), Positives = 29/63 (46%), Gaps = 2/63 (3%)

Query: 167 GEILLTSIDKDGTRLGY--DVELIRRVAEAVKIPVIASGGAGALEHFYEAAAAGADAVLA 224
           G   L  +D DG   G   +++++  + + + IPV   GG   +E       AG D ++ 
Sbjct: 44  GATRLHVVDLDGAFEGVPKNIKIVEEIVKRLSIPVQFGGGVRTVEAVKALKDAGVDRIIV 103

Query: 225 ASL 227
            ++
Sbjct: 104 GTV 106


Lambda     K      H
   0.318    0.136    0.375 

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: 180
Number of extensions: 13
Number of successful extensions: 4
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: 242
Length adjustment: 24
Effective length of query: 227
Effective length of database: 218
Effective search space:    49486
Effective search space used:    49486
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 (21.7 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