GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Pseudomonas stutzeri RCH2

Align low-specificity L-threonine aldolase (EC 4.1.2.48) (characterized)
to candidate GFF2934 Psest_2990 Threonine aldolase

Query= BRENDA::P75823
         (333 letters)



>FitnessBrowser__psRCH2:GFF2934
          Length = 341

 Score =  360 bits (924), Expect = e-104
 Identities = 182/329 (55%), Positives = 239/329 (72%), Gaps = 1/329 (0%)

Query: 2   IDLRSDTVTRPSRAMLEAMMAAPVGDDVYGDDPTVNALQDYAAELSGKEAAIFLPTGTQA 61
           IDLRSDTVT+P+  M EAM  A  GDDVYG+DPTV+ L+   A   G  AA+F+P+GT +
Sbjct: 4   IDLRSDTVTQPTADMREAMFRAETGDDVYGEDPTVSRLERQLAGDLGFSAAMFVPSGTMS 63

Query: 62  NLVALLSHCERGEEYIVGQAAHNYLFEAGGAAVLGSIQPQPIDAAADGTLPLDKVAMKIK 121
           NL+AL++HCERG+EYIVGQ AH Y +E GGAAVLGSIQPQPI+  ADGTL L ++   IK
Sbjct: 64  NLLALMAHCERGDEYIVGQQAHTYKYEGGGAAVLGSIQPQPIEMEADGTLDLRRIEAAIK 123

Query: 122 PDDIHFARTKLLSLENTHNGKVLPREYLKEAWEFTRERNLALHVDGARIFNAVVAYGCEL 181
           PD+ HFAR++LL LENT +GKVLP +YL  A +FTR+R+LALH+DGAR+FNA V  GC+ 
Sbjct: 124 PDNFHFARSRLLVLENTMHGKVLPLDYLAAARDFTRQRDLALHLDGARLFNAAVKLGCDA 183

Query: 182 KEITQYCDSFTICLSKGLGTPVGSLLVGNRDYIKRAIRWRKMTGGGMRQSGILAAAGIYA 241
           +EIT++ D+ ++CLSKGLG PVGS+L G+  +I +A R RKM GGGMRQ+GILAAAG+YA
Sbjct: 184 REITRHFDTVSVCLSKGLGAPVGSVLCGDDAFIAKARRLRKMVGGGMRQAGILAAAGLYA 243

Query: 242 LKNNVARLQEDHDNAAWMAEQLREAGADVMRQDTNMLFVRVGEENAAALGEYMKARNVLI 301
           L++N+ RL +DH  A W+  +L   G  V    TNM++V +G + A AL  +   R + +
Sbjct: 244 LEHNIDRLADDHRRAEWLGNELAALGFAVEPVQTNMVYVEMGAQ-ATALTAFCAQRGIRL 302

Query: 302 NASPIVRLVTHLDVSREQLAEVAAHWRAF 330
             +  +RLVTHLDV  E +  V   +  F
Sbjct: 303 TPAARLRLVTHLDVHDEHVPRVVGAFAEF 331


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: 364
Number of extensions: 8
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: 341
Length adjustment: 28
Effective length of query: 305
Effective length of database: 313
Effective search space:    95465
Effective search space used:    95465
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