GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PRAI in Phaeobacter inhibens BS107

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 GFF1767 PGA1_c17910 1-(5-phosphoribosyl)-5-[(5- phosphoribosylamino)methylideneamino] imidazole-4-carboxamide isomerase-like protein

Query= curated2:P9WMM4
         (244 letters)



>FitnessBrowser__Phaeo:GFF1767
          Length = 247

 Score =  113 bits (283), Expect = 3e-30
 Identities = 76/240 (31%), Positives = 125/240 (52%), Gaps = 10/240 (4%)

Query: 3   LILLPAVDVVEGRAVRLVQGKAGSQTEYG-SAVDAALGWQRDGAEWIHLVDLDAAFGRGS 61
           +++ P +++ +GR V L +G+  +   +    V  A  +  DGAEW+HL D DA  G   
Sbjct: 1   MMIYPTMELKDGRCVTLDKGRLDTAMVWHVDPVATACSFAADGAEWMHLTDFDAIEGDNR 60

Query: 62  NHELLAEVVGKLDVQVELSGGIRDDESLAAALATGCARVNVGTAALENPQWCARVIGEHG 121
           N  L+ E++    + V+L GG+R  E +   +  G  RV VGT A ++P+    +   + 
Sbjct: 61  NAGLVEEIIRTAGIPVQLGGGMRSREHVEHWIDKGAGRVVVGTLAAQDPEMVRMLTRLYP 120

Query: 122 DQVAVGLDVQIIDGEHRLRGRGWETDGGDLWDV-LERLDSEGCSRFVVTDITKDGTLGGP 180
           DQ+ + +DV     E ++   GW   G    +  +E       +  ++TDI  D +    
Sbjct: 121 DQIVLAVDV----WEGQVMTDGWRQAGSFTPEAFIEAFADCPFAGIIITDIESDMSDVEA 176

Query: 181 NLDLLAGVADRTDAPVIASGGVSSLDDLRAIATLTHRG-VEGAIVGKALYARRFTLPQAL 239
            L L+AG+A++   PVIASG V + DD   +A L + G V G +VG+AL+ +  TL +AL
Sbjct: 177 QLGLIAGLAEKARTPVIASGVVRTADD---VARLKYIGSVSGTLVGRALFRKTLTLAEAL 233


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: 157
Number of extensions: 10
Number of successful extensions: 3
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: 244
Length of database: 247
Length adjustment: 24
Effective length of query: 220
Effective length of database: 223
Effective search space:    49060
Effective search space used:    49060
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