GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisH in Desulfovibrio vulgaris Hildenborough

Align imidazole glycerol-phosphate synthase (EC 4.3.2.10) (characterized)
to candidate 209220 DVU0286 imidazoleglycerol phosphate synthase, cyclase subunit

Query= BRENDA::Q9SZ30
         (592 letters)



>MicrobesOnline__882:209220
          Length = 259

 Score =  144 bits (364), Expect = 3e-39
 Identities = 102/314 (32%), Positives = 158/314 (50%), Gaps = 59/314 (18%)

Query: 280 LAKRVIACLDVRTNDKGDLVVTKGDQYDVREQSNENEVRNLGKPVDLAGQYYKDGADEIS 339
           L+KR+I CLDVR        +TKG ++       E  V ++G PV  A +YY++GADEI 
Sbjct: 2   LSKRIIPCLDVRAGR-----LTKGVKF-------EGNV-DIGDPVATARRYYEEGADEIV 48

Query: 340 FLNITGFRDFPLGDLPM-IQVLRQTSKNVFVPLTVGGGIRDFTDASGRYYSSLEVAAEYF 398
           F +IT   +    D  + + V+ + +  +F+P +VGGGI    D                
Sbjct: 49  FYDITASHE----DRGIFLDVVERVASEIFIPFSVGGGINTVDDMRA-----------VL 93

Query: 399 RSGADKISIGSDAVSAAEEFIKSGVKTGKSSLEQISRVYGNQAVVVSIDPRRVYVNHPDD 458
            +GA+K+S+ S AV   +             + Q +  +G+QA+VV +D ++V       
Sbjct: 94  MAGAEKVSVNSGAVKTPD------------IISQGAAAFGSQAIVVGMDVKQV------- 134

Query: 459 VPYKVIRVTNPGPNGEEYAWYQCTVSGGREGRPIGAFELAKAVEELGAGEILLNCIDCDG 518
                   +   P+G     Y+  + GGR+   + A E AK  E LGAGE+ +N ID DG
Sbjct: 135 ------EKSATIPSG-----YEIVIHGGRKYMGMDAIEWAKTCESLGAGELCVNSIDADG 183

Query: 519 QGKGFDIDLVKLISDSVGIPVIASSGAGTPDHFSEVFEKTNASAALAAGIFHRKEVPIQS 578
              G+++ L ++ISD+V IPVIAS GAG+P+H  +   +  ASAAL A I H     I  
Sbjct: 184 TKDGYELTLTRMISDAVTIPVIASGGAGSPEHMYDALTRGGASAALIASIVHYGTYTIPD 243

Query: 579 VKEHLQEERIEVRI 592
           +K  +     ++R+
Sbjct: 244 LKRRISGMGAKMRM 257


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: 373
Number of extensions: 22
Number of successful extensions: 6
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: 259
Length adjustment: 30
Effective length of query: 562
Effective length of database: 229
Effective search space:   128698
Effective search space used:   128698
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.

Links

Downloads

Related tools

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