GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Acidovorax sp. GW101-3H11

Align low-specificity L-threonine aldolase (EC 4.1.2.48) (characterized)
to candidate Ac3H11_4475 Low-specificity L-threonine aldolase (EC 4.1.2.48)

Query= BRENDA::P75823
         (333 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_4475
          Length = 355

 Score =  325 bits (832), Expect = 1e-93
 Identities = 175/338 (51%), Positives = 229/338 (67%), Gaps = 22/338 (6%)

Query: 1   MIDLRSDTVTRPSRAMLEAMMAAPVGDDVYGDDPTVNALQDYAAELSGKEAAIFLPTGTQ 60
           M D RSDTVT+P+ AM EAM  AP+GDDV+ DDP+VNALQD+AAEL G EAA+F P+GTQ
Sbjct: 1   MPDFRSDTVTQPTPAMREAMFKAPLGDDVFADDPSVNALQDHAAELLGFEAALFAPSGTQ 60

Query: 61  ANLVALLSHCERGEEYIVGQAAHNYLFEAGGAAVLGSIQPQPIDAAADGTLPLDKVAMKI 120
            NL+AL  HC+RG+E IVGQ+ H Y +EAGG AVLGSIQPQP++   DGTL +  +A  I
Sbjct: 61  TNLIALWGHCQRGDEAIVGQSWHTYRWEAGGMAVLGSIQPQPVETQPDGTLRVADIAAAI 120

Query: 121 KPDDIHFARTKLLSLENTHNGKVLPREYLKEAWEFTRERNLALHVDGARIFNAVVAYG-- 178
           KPDD HFART+L+ LENT  G+VLP  Y+ +  +  R R LA+H+DGAR+FNA  A    
Sbjct: 121 KPDDPHFARTRLVVLENTTGGQVLPPAYIADVAQLARSRGLAMHLDGARMFNAATANAAR 180

Query: 179 ------CELKEITQYCDSFTICLSKGLGTPVGSLLVGNRDYIKRAIRWRKMTGGGMRQSG 232
                  E + +  + DS ++CLSKGLG PVGSL++G+RD+I++A R RK+ GGGMRQ+G
Sbjct: 181 NGTDVYAEARALCSHFDSASLCLSKGLGAPVGSLVLGSRDFIRQARRTRKILGGGMRQAG 240

Query: 233 ILAAAGIYALKNNVARLQEDHDNAAWMAEQLREAGAD---------VMRQDTNMLFVRVG 283
           +LAAAG YAL+++V RL +DH N   +A+ L EA            V+   TN+LF  + 
Sbjct: 241 VLAAAGSYALQHHVRRLADDHANLDRLAQGLAEANRSHPVLKDKITVLPWQTNILFTDLH 300

Query: 284 EENAAALGEYMKARNVLINAS-----PIVRLVTHLDVS 316
            E A A   ++    V + +S       +R VTHLDVS
Sbjct: 301 AEVAPAFTAWLAQHGVRVTSSLYGGATRLRWVTHLDVS 338


Lambda     K      H
   0.319    0.134    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: 388
Number of extensions: 14
Number of successful extensions: 2
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: 333
Length of database: 355
Length adjustment: 29
Effective length of query: 304
Effective length of database: 326
Effective search space:    99104
Effective search space used:    99104
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 (21.8 bits)
S2: 49 (23.5 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