GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Desulfotalea psychrophila LSv54

Align low-specificity L-threonine aldolase (EC 4.1.2.48) (characterized)
to candidate WP_041278382.1 DP_RS05040 low-specificity L-threonine aldolase

Query= BRENDA::P75823
         (333 letters)



>NCBI__GCF_000025945.1:WP_041278382.1
          Length = 337

 Score =  369 bits (947), Expect = e-107
 Identities = 191/325 (58%), Positives = 240/325 (73%), Gaps = 11/325 (3%)

Query: 2   IDLRSDTVTRPSRAMLEAMMAAPVGDDVYGDDPTVNALQDYAAELSGKEAAIFLPTGTQA 61
           IDLRSDTVT+P+  M EAM  A VGDDVYGDDP++N L+DYAAE  G EAA+F P+GT A
Sbjct: 4   IDLRSDTVTKPTPKMQEAMFRAEVGDDVYGDDPSINMLEDYAAERFGFEAALFTPSGTAA 63

Query: 62  NLVALLSHCERGEEYIVGQAAHNYLFEAGGAAVLGSIQPQPIDAAADGTLPLDKVAMKIK 121
           NL+AL+SHC RG+EY+VGQ AH Y +E GGAA+LGSIQPQPI+ A DG+L LD++  +IK
Sbjct: 64  NLIALMSHCGRGDEYLVGQDAHTYRYEGGGAAILGSIQPQPIEFAKDGSLDLDRIEEEIK 123

Query: 122 PDDIHFARTKLLSLENTHNGKVLPREYLKEAWEFTRERNLALHVDGARIFNAVVAYGCEL 181
           PDD H+ART+LL LENT  GKVLP EYL+ A  F+ ++ LALH+DGAR FNA VA   ++
Sbjct: 124 PDDFHYARTRLLCLENTQGGKVLPMEYLERARYFSLQKGLALHLDGARAFNAAVALDIDI 183

Query: 182 KEITQYCDSFTICLSKGLGTPVGSLLVGNRDYIKRAIRWRKMTGGGMRQSGILAAAGIYA 241
           K+IT   DS +ICLSKGLG PVGSLL G+   I +A RWRK+TGG MRQ+G LAAAG+YA
Sbjct: 184 KKITGLFDSASICLSKGLGAPVGSLLCGSVPLINQARRWRKVTGGAMRQAGSLAAAGLYA 243

Query: 242 LKNNVARLQEDHDNAAWMAEQLR------EAGADVMRQDTNMLFVRVGEENAAALGEYMK 295
           L+N+V RL  DHDNA  + E L+      +   DV    TNM+FV+  E  +  L E++K
Sbjct: 244 LENHVERLSLDHDNAKRLQEGLKKYPTFCQISEDV---QTNMVFVQFQE--SRRLAEFLK 298

Query: 296 ARNVLINASPIVRLVTHLDVSREQL 320
            +N+LI+     RLVTHLD+S E +
Sbjct: 299 TKNILISEDKTTRLVTHLDISGEDI 323


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: 359
Number of extensions: 7
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: 337
Length adjustment: 28
Effective length of query: 305
Effective length of database: 309
Effective search space:    94245
Effective search space used:    94245
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 Jul 25 2024. The underlying query database was built on Jul 25 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