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 7025489 Shewana3_2643 methionine gamma-lyase (RefSeq)
Query= SwissProt::O31632 (390 letters) >lcl|FitnessBrowser__ANA3:7025489 Shewana3_2643 methionine gamma-lyase (RefSeq) Length = 397 Score = 317 bits (813), Expect = 3e-91 Identities = 171/394 (43%), Positives = 238/394 (60%), Gaps = 11/394 (2%) Query: 2 SKHNWTLETQLVHNPFKTDGGTGAVSVPIQHASTFHQSSFEEFG--------AYDYSRSG 53 S W TQ +H + + G + P+ +TF S ++ G Y Y+R G Sbjct: 5 SSKQWKAATQAIHAGHEREA-FGTLVTPLYQTATFVFESAQQGGERFAGNEPGYIYTRLG 63 Query: 54 TPTRTALEETIAALEGGTRGFAFSSGMAAISTAFLL-LSQGDHVLVTEDVYGGTFRMVTE 112 PT LE +A LEG A +SGM A+S A L L GDH++ + VYG TF ++T Sbjct: 64 NPTVAELERKMAILEGAEAAAATASGMGAVSAALLANLQMGDHLVASNAVYGCTFALMTS 123 Query: 113 VLTRFGIEHTFVDMTDRNEVARSIKPNTKVIYMETPSNPTLGITDIKAVVQLAKENGCLT 172 RFGIE T VD TD + R+IKPNT+VI+ ETP NP L + D+K + +AK + ++ Sbjct: 124 QFARFGIEVTLVDFTDLAAIERAIKPNTRVIFCETPVNPHLQVFDLKGIADIAKRHQLVS 183 Query: 173 FLDNTFMTPALQRPLDLGVDIVLHSATKFLSGHSDVLSGLAAVKDEELGKQLYKLQNAFG 232 +DNTFMTP LQ+PL G+D+V+HSATK+L+GH DV++G+ +E+L + Y++ G Sbjct: 184 IVDNTFMTPLLQQPLAFGIDLVVHSATKYLNGHGDVIAGVVCGSEEQLHRVKYEILKDIG 243 Query: 233 AVLGVQDCWLVLRGLKTLQVRLEKASQTAQRLAEFFQKHPAVKRVYYPGLADHPGAETHK 292 AV+ D WL+LRGLKTL VRL++ +AQR+AEF ++HPAV RVYYPGL H G Sbjct: 244 AVMSPHDAWLILRGLKTLDVRLQRHCDSAQRVAEFLEQHPAVTRVYYPGLKSHSGHRFIG 303 Query: 293 SQSTGAGAVLSFEL-ESKEAVKKLVENVSLPVFAVSLGAVESILSYPATMSHAAMPKEER 351 Q AG V++FEL S E V + L AVSLG ES++ +PA+M+H+ E R Sbjct: 304 GQMAKAGGVIAFELAASLEQAMAFVGYLKLFSIAVSLGDAESLIQHPASMTHSPYTPEAR 363 Query: 352 EKRGITDGLLRLSVGVEHADDLEHDFEQALKEIA 385 + GI+D LLR+S+G+E D+ D QAL +A Sbjct: 364 QAAGISDNLLRISIGLEDCGDIIEDLNQALAMLA 397 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: 389 Number of extensions: 16 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: 397 Length adjustment: 31 Effective length of query: 359 Effective length of database: 366 Effective search space: 131394 Effective search space used: 131394 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 Aug 03 2021. The underlying query database was built on Aug 03 2021.
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:
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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