GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Hydrogenophaga taeniospiralis NBRC 102512

Align low-specificity L-threonine aldolase (EC 4.1.2.48) (characterized)
to candidate WP_068174994.1 HTA01S_RS21310 low-specificity L-threonine aldolase

Query= BRENDA::P75823
         (333 letters)



>NCBI__GCF_001592305.1:WP_068174994.1
          Length = 357

 Score =  340 bits (873), Expect = 2e-98
 Identities = 179/340 (52%), Positives = 230/340 (67%), Gaps = 8/340 (2%)

Query: 1   MIDLRSDTVTRPSRAMLEAMMAAPVGDDVYGDDPTVNALQDYAAELSGKEAAIFLPTGTQ 60
           ++DLRSDTVT+P+ AM  AMMAAP+GDDV+GDDPTVNALQD  A ++GKEAA+F+P+GTQ
Sbjct: 3   IVDLRSDTVTQPTAAMRAAMMAAPLGDDVFGDDPTVNALQDRIAAITGKEAALFMPSGTQ 62

Query: 61  ANLVALLSHCERGEEYIVGQAAHNYLFEAGGAAVLGSIQPQPIDAAADGTLPLDKVAMKI 120
           +NL  +L+HC RG+EYIVGQ AH Y +E GGAAV GS+QPQP+   A G + L  +A  I
Sbjct: 63  SNLCGILAHCGRGDEYIVGQLAHTYRYEGGGAAVFGSVQPQPLVQDAAGCMALSDIAAAI 122

Query: 121 KPDDIHFARTKLLSLENTHNGKVLPREYLKEAWEFTRERNLALHVDGARIFNAVVAYGC- 179
           KPDD HFART+LL LENT NG V+P +YL++A E  R   LA H+DGAR+FNA VA    
Sbjct: 123 KPDDPHFARTRLLCLENTWNGHVMPDDYLRDATELARAHGLATHLDGARVFNAAVASAAM 182

Query: 180 ------ELKEITQYCDSFTICLSKGLGTPVGSLLVGNRDYIKRAIRWRKMTGGGMRQSGI 233
                  L+EI  + DS ++C SKGLG PVGS L G+R+ I+ A R RKM GGG+RQ+G+
Sbjct: 183 GQGATDRLREIADHFDSLSVCFSKGLGAPVGSALCGSRELIQSARRIRKMAGGGLRQAGL 242

Query: 234 LAAAGIYALKNNVARLQEDHDNAAWMAEQLRE-AGADVMRQDTNMLFVRVGEENAAALGE 292
           LAA  ++AL ++V RL +DH NA  +AE L    G  V    TN++FV V +     L +
Sbjct: 243 LAACALHALDHHVDRLADDHANARRLAEGLSGIEGLTVKSAQTNIVFVDVADGRGPGLLD 302

Query: 293 YMKARNVLINASPIVRLVTHLDVSREQLAEVAAHWRAFLA 332
           ++KA  VL      +R VTHLDV    +    A    F A
Sbjct: 303 FLKANGVLATGLIGLRFVTHLDVDAAGIDHALACVHRFFA 342


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: 371
Number of extensions: 10
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: 333
Length of database: 357
Length adjustment: 29
Effective length of query: 304
Effective length of database: 328
Effective search space:    99712
Effective search space used:    99712
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 10 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