GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisH in Caulobacter crescentus NA1000

Align imidazole glycerol-phosphate synthase (EC 4.3.2.10) (characterized)
to candidate CCNA_03853 CCNA_03853 imidazole glycerol phosphate synthase, cyclase subunit

Query= BRENDA::Q9SZ30
         (592 letters)



>FitnessBrowser__Caulo:CCNA_03853
          Length = 260

 Score =  130 bits (327), Expect = 6e-35
 Identities = 101/313 (32%), Positives = 150/313 (47%), Gaps = 61/313 (19%)

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

Query: 340 FLNITGFRDFPLGDLPMIQVLRQTSKNVFVPLTVGGGIRDFTDASGRYYSSLEVAAEYFR 399
           FL+IT   +   G   ++ V+ +T++  F+P++VGGG+R  +D                 
Sbjct: 49  FLDITASSE---GRGLILDVISRTAEVCFMPVSVGGGVRQVSDMR-----------RLLL 94

Query: 400 SGADKISIGSDAVSAAEEFIKSGVKTGKSSLEQISRVYGNQAVVVSIDPRRVYVNHPDDV 459
           +GADK+S+ + AV   +  I  G              +G+Q VVV+ID +          
Sbjct: 95  AGADKVSVNTAAVENPD-LIAGGADA-----------FGSQCVVVAIDAKA--------- 133

Query: 460 PYKVIRVTNPGPNGEEYAWYQCTVSGGREGRPIGAFELAKAVEELGAGEILLNCIDCDGQ 519
                         E+ + +     GGR+   I   E A  V E GAGEILL  +D DG 
Sbjct: 134 -------------REDGSGWNVWTYGGRKDTGIDVVEWAAKVVERGAGEILLTSMDRDGA 180

Query: 520 GKGFDIDLVKLISDSVGIPVIASSGAGTPDHFSEVFEKTNASAALAAGIFHRKEVPIQSV 579
             G+DI L++ ++ +V +PVIAS GAG  +H  E   + +A+A LAA IFH  E+ I   
Sbjct: 181 KIGYDIPLLQAVTGAVNVPVIASGGAGKTEHLIEAAREGHAAAVLAASIFHFGEISIGEA 240

Query: 580 KEHLQEERIEVRI 592
           K+ + +  I VR+
Sbjct: 241 KQAMADAGIPVRL 253


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: 371
Number of extensions: 29
Number of successful extensions: 4
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: 260
Length adjustment: 30
Effective length of query: 562
Effective length of database: 230
Effective search space:   129260
Effective search space used:   129260
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 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