GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metC in Phaeobacter inhibens BS107

Align Cystathionine beta-lyase MetC; CBL; Beta-cystathionase MetC; Cysteine lyase MetC; Cysteine-S-conjugate beta-lyase MetC; EC 4.4.1.13 (characterized)
to candidate GFF1560 PGA1_c15810 pyridoxal phosphate-dependent enzyme, cysteine / methionine metabolism

Query= SwissProt::O31632
         (390 letters)



>FitnessBrowser__Phaeo:GFF1560
          Length = 385

 Score =  231 bits (589), Expect = 3e-65
 Identities = 136/338 (40%), Positives = 185/338 (54%), Gaps = 3/338 (0%)

Query: 47  YDYSRSGTPTRTALEETIAALEGGTRGFAFSSGMAAISTAFL-LLSQGDHVLVTEDVYGG 105
           Y YSR G P    + + + A+EG   G    SGMAA+S   L LL  GDHV+    +YG 
Sbjct: 43  YTYSREGHPNADVVAKRLDAMEGMPGGVVTGSGMAAVSAVLLGLLKTGDHVIGGNQLYGR 102

Query: 106 TFRMVTEVLTRFGIEHTFVDMTDRNEVARSIKPNTKVIYMETPSNPTLGITDIKAVVQLA 165
           + R++ E L R GIE T  +  D   V  +I+P T +I +E  SNPTL + DI  + QL 
Sbjct: 103 SMRLMAEDLPRLGIETTLANPGDVAAVKAAIRPETTMILVEAVSNPTLAVADIDGLAQLC 162

Query: 166 KENGCLTFLDNTFMTPALQRPLDLGVDIVLHSATKFLSGHSDVLSGLAAVKDEELGKQLY 225
           K+   L  +DNTF TP   +P D G DIV+HS TK L+GHSDV+ G    KD E+  +L 
Sbjct: 163 KDRDILLVVDNTFTTPRGFQPFDHGADIVIHSITKLLAGHSDVMLGYVVAKDPEINTRLS 222

Query: 226 KLQNAFGAVLGVQDCWLVLRGLKTLQVRLEKASQTAQRLAEFFQKHPAVKRVYYPGLADH 285
                 G      DCWL  RG+ + ++R E+A  TA  LA+     P VKRV YP   DH
Sbjct: 223 VYVVTTGMTPSPFDCWLAERGMLSFELRFERAQATAVTLADHLAGLPGVKRVIYPTRKDH 282

Query: 286 PGAETHKSQSTGAGA-VLSFELE-SKEAVKKLVENVSLPVFAVSLGAVESILSYPATMSH 343
           P  E   +   G G  ++SFELE  + A            FA +LG V + LS+PA+ SH
Sbjct: 283 PDHERAMALLDGKGCNMVSFELEGGRAAANAFTRGADGLNFAPTLGDVGTTLSHPASSSH 342

Query: 344 AAMPKEEREKRGITDGLLRLSVGVEHADDLEHDFEQAL 381
            A+  E+R K G+++G  R+SVG+E  + L   F +A+
Sbjct: 343 RALSTEDRAKLGLSEGFFRISVGLEDPETLCAVFTEAV 380


Lambda     K      H
   0.317    0.132    0.374 

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: 406
Number of extensions: 21
Number of successful extensions: 3
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: 390
Length of database: 385
Length adjustment: 30
Effective length of query: 360
Effective length of database: 355
Effective search space:   127800
Effective search space used:   127800
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 (21.7 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