GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metC in Halococcus hamelinensis 100A6

Align Cystathionine beta-lyase; CBL; Beta-cystathionase; Cysteine lyase; Cysteine-S-conjugate beta-lyase; EC 4.4.1.13 (characterized)
to candidate WP_007691658.1 C447_RS05410 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= SwissProt::Q5SHW0
         (354 letters)



>NCBI__GCF_000336675.1:WP_007691658.1
          Length = 379

 Score =  142 bits (357), Expect = 2e-38
 Identities = 110/357 (30%), Positives = 169/357 (47%), Gaps = 22/357 (6%)

Query: 17  EDVLPLWVADMDFP-PAEAIQQALAERARGFLGYPPREGDRELRELILEALGLEAELAFM 75
           +DV+ L V + DF  P  A + A+    RG   Y    G RELRE I      E +L + 
Sbjct: 26  DDVISLGVGEPDFTAPWSAREAAIDSLERGKTSYTANRGMRELREAIAGRAATEYDLDYD 85

Query: 76  P--------GVVVGLYAAVAAFTAPGQGVLTQVPIYPPFLAAIRDQRRTVLANPLRETPE 127
           P        G    + AA  AF  PG  V    P Y  ++  +       L  P RE  E
Sbjct: 86  PDEEILVTAGASEAIDAAFRAFCDPGDTVAVAQPSYVSYVPGVVFAGGEPLPVPTREADE 145

Query: 128 GYRLDLAGL-ERLAFATRLLLFCHPHNPTGRVFGEEELAALAQIARRHDLIVVSDELHAP 186
            +RL    L E  A     L++C+P+NPTG    EE L  +A  AR HDL V++DE++A 
Sbjct: 146 -FRLTAEVLREAGAEEAEALVYCYPNNPTGATMREEHLEPVAAFAREHDLTVLADEIYAD 204

Query: 187 LTYEKPHVPLARF--LPERTLTLVGPGKTYNLAGLPIGAVLGPKPLVEAVKRHLPHVFPN 244
           LTY+  H  +A    + ERT+   G  K Y + GL +G  L P   ++A+ R   H +  
Sbjct: 205 LTYDGDHTSIATLPGMRERTVVFNGFSKAYAMTGLRLGYALAPPEAIQAMNR--IHQYGM 262

Query: 245 VLAMAAWKAALKEGGPWLKATLEQLRANRDRVAAWAKAR----GLGHHPPEGTYLAWIQT 300
           + A    + A  +        ++++RA  DR   +  +R    G+      G +  + ++
Sbjct: 263 LSAPTTAQYAALDALEHCSDDVQEMRAQYDRRRRFVLSRFAEMGIECFEATGAFYVFPES 322

Query: 301 PFPKAAAY---FLERARVALNPGESFGRGYDTYVRLNFATYPEVLEEALRRLDGALK 354
           P+  A A+    LE   VA+ PG+ FG G + ++R+++AT    L EA+ R++  L+
Sbjct: 323 PWEDAEAFAEALLEECGVAMVPGDVFGAGGEGHLRVSYATGLNELREAMDRIEAFLE 379


Lambda     K      H
   0.322    0.140    0.433 

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: 343
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: 354
Length of database: 379
Length adjustment: 30
Effective length of query: 324
Effective length of database: 349
Effective search space:   113076
Effective search space used:   113076
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 (21.9 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