GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysT in Hydrogenovibrio marinus DSM 11271

Align Probable methanogen homoaconitase large subunit; HACN; EC 4.2.1.114; Homoaconitate hydratase (uncharacterized)
to candidate WP_029908844.1 P166_RS0103590 bifunctional aconitate hydratase 2/2-methylisocitrate dehydratase

Query= curated2:Q8PZT3
         (391 letters)



>NCBI__GCF_000711315.1:WP_029908844.1
          Length = 857

 Score = 95.9 bits (237), Expect = 4e-24
 Identities = 96/356 (26%), Positives = 140/356 (39%), Gaps = 55/356 (15%)

Query: 74  GEGICHQVLPENGFALPGKLLVGADSHSCTYGAFGAFATGVGATDMAEIFATGKLWFKVP 133
           G+G+ H  L  N   LP  +  G DSH+  +    +F  G G          G +   +P
Sbjct: 465 GDGVIHSWL--NRLLLPDTVGTGGDSHT-RFPIGISFPAGSGLVAFGATL--GVMPLNMP 519

Query: 134 ESFRMTVEGSLDKHVYAKDL--------------TLYLIGKTGIAGATYKAVEFYGQAIS 179
           ES  +  +G +   +  +DL              T+   GK  I       +E     + 
Sbjct: 520 ESVLVRFKGEMQPGITLRDLVNAIPYQAIQDGLLTVEKKGKKNIFNGRVLEIE----GLD 575

Query: 180 ELSVAGRMTLCNMAIEMGAKTGIVP-PDEKTFDFLK-NRAVAPY---------------- 221
            L V     L + + E  A   +V   +E   ++LK N A+  +                
Sbjct: 576 HLKVEQAFELSDASAERSANGCVVKLAEEPIIEYLKSNMALIDWMVENGYQDARTLLRRR 635

Query: 222 ----------EPVYSDPDASYLKEFVYDAGDI-EPQVACPHQVDNVKPVGEVEGTHVDQV 270
                     E + +D DA Y      D   I EP VACP+  D+VK +  V G  +D+V
Sbjct: 636 DEMQAWIDAPELLEADADADYAAVIEIDLNTIKEPIVACPNDPDDVKLLSAVSGDKIDEV 695

Query: 271 FIGTCTNGRLEDLEVAASVLKG-KKVTVRTIIIPASRSTLLAAIKNGTMEILLKAGVTLA 329
           FIG+C    +     A  VL+  K V  R  I P ++      I+ G   I  K G    
Sbjct: 696 FIGSCMT-NIGHYRAAGKVLENMKNVPTRLWIAPPTKMDERQLIEEGYYSIYGKVGARTE 754

Query: 330 TPGCGPCLGAHQGVLGEGEVCVSTANRNFKGRMGKDGFIYLASPATAAASALTGEI 385
            PGC  C+G +Q  + +G    ST+ RNF  R+G    +YL S   AA  A  G I
Sbjct: 755 MPGCSLCMG-NQARVADGATVFSTSTRNFPNRLGNGANVYLGSAELAAVCAAVGRI 809


Lambda     K      H
   0.318    0.135    0.401 

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: 699
Number of extensions: 37
Number of successful extensions: 3
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: 391
Length of database: 857
Length adjustment: 36
Effective length of query: 355
Effective length of database: 821
Effective search space:   291455
Effective search space used:   291455
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 (21.7 bits)
S2: 53 (25.0 bits)

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