GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisF in Acidovorax sp. GW101-3H11

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 Ac3H11_4732 Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase (EC 5.3.1.16)

Query= curated2:A6TKT6
         (252 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_4732
          Length = 246

 Score =  106 bits (264), Expect = 5e-28
 Identities = 67/210 (31%), Positives = 110/210 (52%), Gaps = 11/210 (5%)

Query: 6   IIPCLDVRKGRVVK---GVNFVDIKDAGDPVALARAYNDQGADEIVFLDITASHEERYIL 62
           +IP +D++ G  V+   G          DP A+AR + D GA  +  +D+  +       
Sbjct: 3   LIPAIDLKDGHCVRLKQGDMDQSTTFGEDPAAMARKWVDAGARRLHLVDLNGAFAGVPKN 62

Query: 63  LDVVKKTSEEIF--IPLTVGGGIRTVEDMRQIIKSGADKVSINSSAVKNPSMITDCARQF 120
              +K   +E+   IP+ +GGGIR ++ + + I  G   V I ++AVKNP  + D    F
Sbjct: 63  YGAIKSILKEVGSDIPVQLGGGIRDLDTIEKYIDGGLRYVIIGTAAVKNPGFLKDACSAF 122

Query: 121 GSQAVVIAMDVKRGADGRYEVYVRGGREKTGLEAVDWARRVAQLGAGEILLTSMDRDGTK 180
           G   +++ +D K G     +V   G  + TG E VD A++    G   I+ T + RDG  
Sbjct: 123 GGH-IIVGLDAKDG-----KVATDGWSKLTGHEVVDLAKKFEDWGVESIIYTDIGRDGML 176

Query: 181 SGYDLEITKRISQAVNIPVIASGGAGSVQD 210
           SG +++ T +++QA++IPVIASGG  ++ D
Sbjct: 177 SGINIDATVKLAQALSIPVIASGGLSNMAD 206



 Score = 37.7 bits (86), Expect = 2e-07
 Identities = 23/87 (26%), Positives = 41/87 (47%), Gaps = 9/87 (10%)

Query: 15  GRVVKGVNFVDIKDAGDP---------VALARAYNDQGADEIVFLDITASHEERYILLDV 65
           G ++ G++  D K A D          V LA+ + D G + I++ DI        I +D 
Sbjct: 124 GHIIVGLDAKDGKVATDGWSKLTGHEVVDLAKKFEDWGVESIIYTDIGRDGMLSGINIDA 183

Query: 66  VKKTSEEIFIPLTVGGGIRTVEDMRQI 92
             K ++ + IP+   GG+  + D+ Q+
Sbjct: 184 TVKLAQALSIPVIASGGLSNMADIEQL 210


Lambda     K      H
   0.319    0.136    0.378 

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: 179
Number of extensions: 16
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: 252
Length of database: 246
Length adjustment: 24
Effective length of query: 228
Effective length of database: 222
Effective search space:    50616
Effective search space used:    50616
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 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