GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Echinicola vietnamensis KMM 6221, DSM 17526

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate Echvi_2283 Echvi_2283 Cystathionine beta-lyases/cystathionine gamma-synthases

Query= metacyc::HP_RS00540-MONOMER
         (380 letters)



>FitnessBrowser__Cola:Echvi_2283
          Length = 391

 Score =  276 bits (705), Expect = 9e-79
 Identities = 150/367 (40%), Positives = 219/367 (59%), Gaps = 11/367 (2%)

Query: 22  SVPIYQTSTYRQDAIGRHK--------GYEYSRSGNPTRFALEELIADLEGGVKGFAFAS 73
           S PIY TS++  D+    +        G  YSR  NP    L E +  +EG   G A AS
Sbjct: 24  SAPIYMTSSFTFDSAEEARQMFAEEIPGNIYSRYANPNSSDLIEKVCAVEGTEDGIATAS 83

Query: 74  GLAGIH-AVFSLLQSGDHVLLGDDVYGGTFRLFNQVLVKNGLSCTIIDTSDISQIKKAIK 132
           G+A +  ++ SLL+ GDH+L    ++G T +L  +V  K G++ T  D SDI    K +K
Sbjct: 84  GMAAMFGSMASLLEQGDHILASRSLFGSTHQLLTRVFPKWGITSTYGDISDIENWDKLVK 143

Query: 133 PNTKALYLETPSNPLLKITDLAQCASVAKDHGLLTIVDNTFATPYYQNPLLLGADIVAHS 192
           PNTK L++ETPSNP L++ DL      AK H L+ +VDN FATPY Q P   GADIVAHS
Sbjct: 144 PNTKMLFIETPSNPGLEVIDLEWIGKFAKAHNLILVVDNCFATPYLQQPAKWGADIVAHS 203

Query: 193 GTKYLGGHSDVVAGLVTTNNEALAQEIAFFQNAIGGVLGPQDSWLLQRGIKTLGLRMEAH 252
            TKY+ G   V+ GL+    E L +E+ FF    G  + P ++W+L R ++TL +RME H
Sbjct: 204 ATKYIDGQGRVLGGLILGKQE-LIKEVQFFTRHTGPSISPFNAWILSRSMETLAIRMERH 262

Query: 253 QKNALCVAEFLEKHPKVERVYYPGLPTHPNYELAKKQMRGFSGMLSFTLKNDSE-AVAFV 311
             NAL VA + + + ++E V YP L +HP ++LAKKQM+   G+++ TLK   E A  F+
Sbjct: 263 CANALAVASYFQDNKELEFVKYPFLKSHPQHDLAKKQMKHGGGIVTLTLKGGIERAQRFI 322

Query: 312 ESLKLFILGESLGGVESLVGIPAFMTHACIPKTQREAAGIRDGLVRLSVGIEHEQDLLED 371
           + L++  +  +LG   S++  PA  TH+ + + +R+  GI  GL+RLS G+EH  D++ D
Sbjct: 323 DELQMITVTANLGDTRSIITHPASTTHSKLTEEERQRVGILPGLIRLSAGLEHHDDIIAD 382

Query: 372 LEQAFAK 378
           +E+A  +
Sbjct: 383 IERALER 389


Lambda     K      H
   0.319    0.137    0.394 

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: 385
Number of extensions: 22
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: 380
Length of database: 391
Length adjustment: 30
Effective length of query: 350
Effective length of database: 361
Effective search space:   126350
Effective search space used:   126350
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 (21.7 bits)
S2: 50 (23.9 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