GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PRAI in Pelobacter propionicus DSM 2379

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_011736886.1 PPRO_RS15170 imidazole glycerol phosphate synthase subunit HisF

Query= curated2:P60583
         (243 letters)



>NCBI__GCF_000015045.1:WP_011736886.1
          Length = 253

 Score = 83.6 bits (205), Expect = 3e-21
 Identities = 66/217 (30%), Positives = 105/217 (48%), Gaps = 23/217 (10%)

Query: 4   LLPAVDVVDGRAVRLVQGKAGSETEYGSALDAALGWQRDGAEWIHLVDLDAAFGRGSNRE 63
           ++P +DV  GR V+ VQ     +   G  ++ A  + R GA+ +  +D+ A+      R+
Sbjct: 6   IIPCLDVKGGRVVKGVQFLELRDA--GDPVEIAEIYDRQGADELTFLDITAS---SDERD 60

Query: 64  LLAEVVGKLDVRV----ELSGGIRDDDSLAAALATGCARVNLGTAALENPQWCARAIGEH 119
           ++ +VV +   RV     + GGIR    +   L  G  + ++ TAA+  P++   A    
Sbjct: 61  IIIDVVRRTAERVFMPLTVGGGIRTVQDIRRLLNAGADKTSINTAAVHRPEFVREAAERF 120

Query: 120 GDK-VAVGLDVQIIDGQHRLRGRGWE--TDGG------DLWEVLERLERQGCSRYVVTDV 170
           G +   V +D + + G+ R     WE  T GG      D  E   R+E  G    ++T +
Sbjct: 121 GSQCTVVAIDARRVPGEKR-----WEVYTHGGRNPTGIDAVEWAVRMEEFGSGEILLTSM 175

Query: 171 TKDGTLGGPNLDLLGAVADRTDAPVIASGGVSSLDDL 207
             DGT  G +L+L  AV D    PVIASGGV +L+ L
Sbjct: 176 DCDGTKDGYDLELTRAVVDAVSIPVIASGGVGNLEHL 212



 Score = 37.7 bits (86), Expect = 2e-07
 Identities = 18/65 (27%), Positives = 31/65 (47%)

Query: 146 DGGDLWEVLERLERQGCSRYVVTDVTKDGTLGGPNLDLLGAVADRTDAPVIASGGVSSLD 205
           D GD  E+ E  +RQG       D+T         +D++   A+R   P+   GG+ ++ 
Sbjct: 28  DAGDPVEIAEIYDRQGADELTFLDITASSDERDIIIDVVRRTAERVFMPLTVGGGIRTVQ 87

Query: 206 DLRAI 210
           D+R +
Sbjct: 88  DIRRL 92


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: 195
Number of extensions: 11
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: 243
Length of database: 253
Length adjustment: 24
Effective length of query: 219
Effective length of database: 229
Effective search space:    50151
Effective search space used:    50151
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