GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metC in Frankia alni ACN14a

Align Cystathionine beta-lyase; CBL; Beta-cystathionase; Cysteine lyase; Cysteine-S-conjugate beta-lyase; EC 4.4.1.13 (characterized)
to candidate WP_011607176.1 FRAAL_RS35345 succinyldiaminopimelate transaminase

Query= SwissProt::Q5SHW0
         (354 letters)



>NCBI__GCF_000058485.1:WP_011607176.1
          Length = 592

 Score = 67.4 bits (163), Expect = 9e-16
 Identities = 104/354 (29%), Positives = 137/354 (38%), Gaps = 51/354 (14%)

Query: 14  TYPEDVLPLWVAD-MDFPPAEAIQQALAERARGFLGYPPREGDRELRELILEALGLEAEL 72
           T+P  ++ L V   +D  PA  +QQALA  A    GYP   G  +LRE     L     +
Sbjct: 20  THPYGLVDLSVGTPVDSTPA-VVQQALAGAADA-PGYPLTVGTPDLREAAAGWLARRLGV 77

Query: 73  AFMPGVVV---GLYAAVAAFTA-----PGQGVLTQVPIYPPFLAAIRDQRRTVLANPLRE 124
              PG V+   G    VA         PG  V    P YP +       R   +  P   
Sbjct: 78  LVDPGAVLPVLGTKELVAQLPGQLGLEPGDRVWVPTPAYPTYEVGALLARCEPVVGP--- 134

Query: 125 TPEGYRLDLAGLERLAFATRLLLFCHPHNPTGRVFGEEELAALAQIARRHDLIVVSDELH 184
                          A    L+    P NPTGRV   +E+ A+   AR   +IV SDE +
Sbjct: 135 ---------------ADGVTLVWLNSPANPTGRVLTVDEMRAVVTWARERGVIVASDECY 179

Query: 185 APLTYE-KP----HVPLARFLPERTLTLVGPGKTYNLAGLPIGAVLGPKPLVE---AVKR 236
             L +E +P    H  +     E  L +    K  NLAG   G V G   LVE    V++
Sbjct: 180 IELGWEARPVSVLHPDVCGGSHEGLLAVHSLSKRSNLAGYRAGFVTGDPQLVEGLTGVRK 239

Query: 237 HLPHVFPNVLAMAAWKAALKEGGPWLKATLEQLR-ANRDRV--AAWAKARGLGHHPPEGT 293
           H   + P  +A AA  AA  +    +    ++ R ANR  V  AA A A     H   G 
Sbjct: 240 HAGFMMPTPVA-AAMAAAYADD---IHVADQRARYANRRAVLAAALAVAGFTIDHSEAGL 295

Query: 294 YLAWIQTPFPKAAAYFLERARVALNPGESFGRGYDTYVRL-------NFATYPE 340
           YL   +     A    L    V + PG  +G G   +VR+         AT PE
Sbjct: 296 YLWATRGEDAWATVDALAGVGVLVAPGTFYGEGGRHHVRVALTAPDSQVATVPE 349


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: 861
Number of extensions: 59
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: 354
Length of database: 592
Length adjustment: 33
Effective length of query: 321
Effective length of database: 559
Effective search space:   179439
Effective search space used:   179439
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: 51 (24.3 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