GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisF in Bacteroides thetaiotaomicron VPI-5482

Align Imidazole glycerol phosphate synthase subunit HisF; EC 4.3.2.10; IGP synthase cyclase subunit; IGP synthase subunit HisF; ImGP synthase subunit HisF; IGPS subunit HisF (uncharacterized)
to candidate 350907 BT1379 phosphoribosylformimino-5-aminoimidazole carboxamide ribonucleotide (ProFAR) isomerase (NCBI ptt file)

Query= curated2:Q12UY6
         (273 letters)



>FitnessBrowser__Btheta:350907
          Length = 239

 Score = 70.5 bits (171), Expect = 3e-17
 Identities = 60/263 (22%), Positives = 116/263 (44%), Gaps = 37/263 (14%)

Query: 6   IIPCLDVTLDASGGTVVKGVEFVDLKKA--GDPVDLAKRYNEQGADELVFLDITASHEGR 63
           IIP +D+     G  V       D KK    +PV++AK +   G   L  +D+  +    
Sbjct: 4   IIPAIDII---DGKCVRLSQGDYDSKKVYNENPVEVAKEFEANGVRRLHVVDLDGAASHH 60

Query: 64  STMIDVIERTANEVFIPLTVGGGINSVEDVRQILRAGADKVSVNTAAVKNPEFIREASNI 123
                V+E+ A    + +  GGG+ S ED++    +GA  V+  + AVK+PE       +
Sbjct: 61  VVNHRVLEQIATRTSLIVDFGGGVKSDEDLKIAFESGAQMVTGGSVAVKDPELFCHWLEV 120

Query: 124 FGSQCIVTAIDCKRNLDVENNQDKTILELEDGTLAWYEVVIYGGREPTGLDTVQWAKKVE 183
           +GS+ I+   D K                       +++ + G ++ +  +   + +   
Sbjct: 121 YGSEKIILGADVKE----------------------HKIAVNGWKDESACELFPFLEDYI 158

Query: 184 ELGSGEILLTSMNRDGTYDGFDIPITKKLSEEL-DIPIIASGGVGNPEHMYKGFVDGKAD 242
             G  +++ T ++ DG   G  I + K++ E+  ++ ++ASGGV N +      +    +
Sbjct: 159 NKGIQKVICTDISCDGMLKGPSIDLYKEMLEKFPNLYLMASGGVSNVDD-----IIALNE 213

Query: 243 AGLAASIF----HFGEYTVRDVK 261
           AG+   IF    + G  T++D++
Sbjct: 214 AGVPGVIFGKALYEGHITLKDLR 236


Lambda     K      H
   0.317    0.137    0.392 

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: 192
Number of extensions: 6
Number of successful extensions: 2
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: 273
Length of database: 239
Length adjustment: 24
Effective length of query: 249
Effective length of database: 215
Effective search space:    53535
Effective search space used:    53535
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 (21.6 bits)
S2: 47 (22.7 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