GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PRAI in Calditerrivibrio nitroreducens DSM 19672

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_013450396.1 CALNI_RS01310 imidazole glycerol phosphate synthase subunit HisF

Query= curated2:P9WMM4
         (244 letters)



>NCBI__GCF_000183405.1:WP_013450396.1
          Length = 253

 Score = 99.4 bits (246), Expect = 6e-26
 Identities = 67/213 (31%), Positives = 112/213 (52%), Gaps = 15/213 (7%)

Query: 5   LLPAVDVVEGRAVRLVQGKAGSQTEYGSAVDAALGWQRDGAEWIHLVDLDAAF-GRGSNH 63
           ++P +DV +GR V+  Q    +  + G  V  A  + R GA+ +  +D+ A+   RG   
Sbjct: 6   IIPCLDVKDGRVVKGTQFL--NLIDAGDPVQVAEEYDRQGADELTFLDITASHENRGIIL 63

Query: 64  ELLAEVVGKLDVQVELSGGIRDDESLAAALATGCARVNVGTAALENPQWCARVIGEHGDQ 123
           +++A+   K+ + + + GGIR  E +   L +G  +V++ TAA++NP +        G Q
Sbjct: 64  DVVAKTAEKVFMPLTVGGGIRTIEDIRKLLNSGADKVSINTAAVKNPDFVKDAALRFGSQ 123

Query: 124 VAVGLDVQIIDGEHRLRGRGWE--TDGG------DLWDVLERLDSEGCSRFVVTDITKDG 175
             V      ID + +  G GWE  T GG      D+ +   +++S G    ++T + KDG
Sbjct: 124 CIV----VAIDAKRKTNGSGWEVYTHGGRNPTGIDVLEWAVKMESFGAGEILLTSMDKDG 179

Query: 176 TLGGPNLDLLAGVADRTDAPVIASGGVSSLDDL 208
           T  G +L+L A V+D    PVIASGGV + +D+
Sbjct: 180 TKDGYDLELTAAVSDAIRIPVIASGGVGTKEDI 212



 Score = 40.8 bits (94), Expect = 3e-08
 Identities = 20/65 (30%), Positives = 32/65 (49%)

Query: 147 DGGDLWDVLERLDSEGCSRFVVTDITKDGTLGGPNLDLLAGVADRTDAPVIASGGVSSLD 206
           D GD   V E  D +G       DIT      G  LD++A  A++   P+   GG+ +++
Sbjct: 28  DAGDPVQVAEEYDRQGADELTFLDITASHENRGIILDVVAKTAEKVFMPLTVGGGIRTIE 87

Query: 207 DLRAI 211
           D+R +
Sbjct: 88  DIRKL 92


Lambda     K      H
   0.318    0.137    0.410 

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: 203
Number of extensions: 14
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: 244
Length of database: 253
Length adjustment: 24
Effective length of query: 220
Effective length of database: 229
Effective search space:    50380
Effective search space used:    50380
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 09 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