GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisH in Methyloferula stellata AR4 AR4T

Align imidazole glycerol-phosphate synthase (EC 4.3.2.10) (characterized)
to candidate WP_026595512.1 A3OQ_RS0105060 imidazole glycerol phosphate synthase subunit HisF

Query= BRENDA::Q9SZ30
         (592 letters)



>NCBI__GCF_000385335.1:WP_026595512.1
          Length = 261

 Score =  142 bits (358), Expect = 2e-38
 Identities = 106/313 (33%), Positives = 153/313 (48%), Gaps = 62/313 (19%)

Query: 280 LAKRVIACLDVRTNDKGDLVVTKGDQYDVREQSNENEVRNLGKPVDLAGQYYKDGADEIS 339
           L  R+I CLDV+     D  V KG         N  ++R+ G PV+ A  Y   GADE+ 
Sbjct: 2   LKSRIIPCLDVK-----DGRVVKG--------INFLDLRDAGDPVECAIAYDAAGADELC 48

Query: 340 FLNITGFRDFPLGDLPMIQVLRQTSKNVFVPLTVGGGIRDFTDASGRYYSSLEVAAEYFR 399
           FL+IT   +       M+ V+R+T++  F+PLTVGGG+R   D             +   
Sbjct: 49  FLDITASHE---DRGIMLDVVRRTAEACFMPLTVGGGVRVLDDIR-----------KLLL 94

Query: 400 SGADKISIGSDAVSAAEEFIKSGVKTGKSSLEQISRVYGNQAVVVSIDPRRVYVNHPDDV 459
           +GADK+SI + AVS    F+K+  +            +GNQ +VV+ID +          
Sbjct: 95  AGADKVSINTAAVSD-RAFVKAAAEK-----------FGNQCIVVAIDAK---------- 132

Query: 460 PYKVIRVTNPGPNGEEYAWYQCTVSGGREGRPIGAFELAKAVEELGAGEILLNCIDCDGQ 519
                  T PG        ++    GGR+   I A + A+ V  LGAGE+LL  +D DG 
Sbjct: 133 ------ATAPGK-------WEIFTHGGRKPTGIDAIQYAREVVALGAGELLLTSMDRDGT 179

Query: 520 GKGFDIDLVKLISDSVGIPVIASSGAGTPDHFSEVFEKTNASAALAAGIFHRKEVPIQSV 579
             GFD+ L + ++D+V +PVIAS G GT  H  E   +  A+A LAA IFH     I   
Sbjct: 180 KSGFDLALTRAVTDAVSVPVIASGGVGTLAHLVEGIREGGATAVLAASIFHFGTFSIGEA 239

Query: 580 KEHLQEERIEVRI 592
           K ++ E  + +R+
Sbjct: 240 KHYMAEHGVAIRL 252


Lambda     K      H
   0.317    0.135    0.391 

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: 365
Number of extensions: 21
Number of successful extensions: 5
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: 592
Length of database: 261
Length adjustment: 31
Effective length of query: 561
Effective length of database: 230
Effective search space:   129030
Effective search space used:   129030
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: 50 (23.9 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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