GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PRAI in Sphingomonas wittichii RW1

Align Phosphoribosyl isomerase A; 1-(5-phosphoribosyl)-5-[(5-phosphoribosylamino)methylideneamino] imidazole-4-carboxamide isomerase; EC 5.3.1.16; N-(5'-phosphoribosyl)anthranilate isomerase; PRAI; EC 5.3.1.24; Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase (uncharacterized)
to candidate WP_012048927.1 SWIT_RS13765 1-(5-phosphoribosyl)-5-((5-phosphoribosylamino)methylideneamino)imidazole-4-carboxamide isomerase

Query= curated2:P60583
         (243 letters)



>NCBI__GCF_000016765.1:WP_012048927.1
          Length = 243

 Score =  156 bits (394), Expect = 4e-43
 Identities = 96/240 (40%), Positives = 134/240 (55%), Gaps = 7/240 (2%)

Query: 2   LILLPAVDVVDGRAVRLVQGKAGSETEYGS-ALDAALGWQRDGAEWIHLVDLDAAF-GRG 59
           +I+ PA+D+  G+ VRL +G     T YG    D A  +   GAEW+H+VDLD AF GR 
Sbjct: 3   IIVFPAIDLKGGQVVRLAEGDMDRATVYGDDPADQARRFAEAGAEWLHVVDLDGAFAGRA 62

Query: 60  SNRELLAEVVGKLDVRVELSGGIRDDDSLAAALATGCARVNLGTAALENPQWCARAIGEH 119
            N E +  ++     +VEL GGIRD   +   LA G  RV +GTAAL+NP     A  E 
Sbjct: 63  VNAEAVEAIIKAFPGKVELGGGIRDRAGIDRWLALGVERVIIGTAALQNPDLVREAAKEL 122

Query: 120 GDKVAVGLDVQIIDGQHRLRGRGW-ETDGGDLWEVLERLERQGCSRYVVTDVTKDGTLGG 178
             ++ VG+D +  DG   +   GW E     + ++ +R    G +  + TDV +DG L G
Sbjct: 123 PGRIVVGVDAR--DGF--VATHGWAEVSTVGITDLADRFADAGVASLLFTDVGRDGLLKG 178

Query: 179 PNLDLLGAVADRTDAPVIASGGVSSLDDLRAIATLTGRGVEGAIVGKALYAGRFTLPQAL 238
            N++   A+A     PVIASGGV+S+ D+ A+    G G+EG I G+ALY GR  L +AL
Sbjct: 179 CNVEATVALARHASIPVIASGGVASIADIAALVPHAGDGIEGVITGRALYDGRLDLAEAL 238


Lambda     K      H
   0.318    0.138    0.407 

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: 239
Number of extensions: 20
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: 243
Length of database: 243
Length adjustment: 23
Effective length of query: 220
Effective length of database: 220
Effective search space:    48400
Effective search space used:    48400
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