GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CBS in Trichodesmium erythraeum IMS101 Annotated Metagenome-Assembled Genome

Align cystathionine β-synthase (EC 4.2.1.22) (characterized)
to candidate 2629601377 Ga0074568_113444 cysteine synthase A

Query= metacyc::MONOMER-22007
         (524 letters)



>IMG__TrieryIMS101_FD:2629601377
          Length = 326

 Score =  249 bits (636), Expect = 1e-70
 Identities = 132/329 (40%), Positives = 198/329 (60%), Gaps = 8/329 (2%)

Query: 81  NILPNILNKVGNTPLVRINKIGKYFGLKCELLAKCEYFNAGGSVKDRISLRMVEDAERAG 140
           +I P  +  VGNTPL+R+N   +  G  CE+L K E+ N GGSVKDR +L +++DAE  G
Sbjct: 2   DIKPGFIGTVGNTPLIRLNSFSEETG--CEILGKAEFLNPGGSVKDRAALYIIKDAEEKG 59

Query: 141 ILKPGDTIIEPTSGNTGIGLALAAAVKGYRCIIVMPEKMSMEKVDVLRALGAEIVRTPTT 200
           +LKPG T++E T+GNTGIGLA     KGY+C+IV+PE  S+EK+D LR LGAE+   P  
Sbjct: 60  LLKPGGTVVEGTAGNTGIGLAHICNAKGYKCLIVIPETQSVEKMDALRTLGAEVKPVPAV 119

Query: 201 ARFDSPESHVGVAWRLKNEIPNAHILDQYRNASNPLTHYDTTAEEILQQCEGKIDMLVAT 260
             + +P ++V ++ +L + I NA   +Q+ N +N + HY+TT  EI +Q +GK+D  VA 
Sbjct: 120 P-YKNPNNYVKMSGKLASTIENAIWANQFDNLANRIAHYETTGPEIWEQTDGKVDAWVAA 178

Query: 261 AGTGGTITGISRKLKEKCPGCKIIGVDPEGSIL---AQPDELNKTDKTMYEVEGIGYDFV 317
            GTGGT  G+S  LKEK P  K +  DP GS L    +  E++    ++   EGIG   +
Sbjct: 179 TGTGGTFAGVSLFLKEKNPQIKTVLADPMGSGLYSYVKTGEISSEGNSI--TEGIGNSRI 236

Query: 318 PTVLDRSLVDQWYKSNDEESFALARMLIREEGLLCGGSSGSAMSVAVKAAKELKEGQRCV 377
              ++  ++D   + +D+E+  +   L+R++GL  GGS G  +  AV  AK++  G   V
Sbjct: 237 TKNMENVMIDDAIRVDDKEAVRVVYQLLRKDGLFMGGSVGINVGAAVALAKQMGPGHTIV 296

Query: 378 VIFPDSIRNYMSKFLSDKWMIQKGFMTEE 406
            +  DS   Y SK  + +W+  K  + +E
Sbjct: 297 TVLCDSGTRYQSKLFNREWLATKNLLPDE 325


Lambda     K      H
   0.316    0.134    0.399 

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: 409
Number of extensions: 17
Number of successful extensions: 4
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: 524
Length of database: 326
Length adjustment: 31
Effective length of query: 493
Effective length of database: 295
Effective search space:   145435
Effective search space used:   145435
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 (21.6 bits)
S2: 50 (23.9 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