Align malonate-semialdehyde dehydrogenase (EC 1.2.1.15); malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18); methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate SMa0260 SMa0260 GabD3 succinate-semialdehyde dehdyrogenase
Query= BRENDA::A0A081YAY7 (498 letters) >FitnessBrowser__Smeli:SMa0260 Length = 487 Score = 231 bits (589), Expect = 4e-65 Identities = 156/453 (34%), Positives = 231/453 (50%), Gaps = 10/453 (2%) Query: 8 IGGELIADTGRTADVFNPSTGEAVRKVPLADRETMQQAIDAAKAAFPAWRNTPPAKRAQV 67 IGG+ + +G T V +PSTG + +V A E Q+A+DAA AA WR TP +R+++ Sbjct: 22 IGGKWQSGSGIT--VLDPSTGNLLAEVADASIEDAQRAVDAADAAAAGWRATPARQRSEI 79 Query: 68 LFRFKQLLEANEERIVKLISEEHGKTIEDAAGELKRGIENVEYATAAPEILKGEYSRNVG 127 L R+ QL+ + E + LI+ E+GK + DA GE+ E + + GE+ Sbjct: 80 LRRWYQLMTQHAEELATLIALENGKALADARGEVAYAAEFFRWYAEEATRIPGEFRHTPS 139 Query: 128 PNIDAWSDFQPIGVVAGITPFNFPAMVPLWMYPLAIACGNTFILKPSERDPSSTLLIAEL 187 + + D +PIG+ ITP+NFPA + A+A G T ILKP+ P + +A L Sbjct: 140 GSHNILVDHEPIGIAVLITPWNFPAAMATRKIGPALAAGCTVILKPASETPLTAYAMARL 199 Query: 188 FHEAGLPKGVLNVV--HGDKGAVDALIEAPEVKALSFVGSTPIAEYIYSEGTKRGKRVQA 245 EAG+P GV+NV+ G +A++ P V+ LSF GST + + +E K Sbjct: 200 GEEAGVPPGVVNVLTTSNPGGITNAMLADPRVRKLSFTGSTGVGRVLLAEAAKSVVSCSM 259 Query: 246 LGGAKNHAVLMPDADLDNAVSALMGAAYGSCGERCMAISVAVCVGDQIADALVQKLVPQI 305 G ++ DADL+ A+ M A + GE C A + V I DA V L ++ Sbjct: 260 ELGGNAPFIVFDDADLEVALDGAMIAKMRNAGEACTAAN-RFYVQAGIHDAFVAGLTARM 318 Query: 306 KGLKIGAGTSCGLDMGPLVTGAARDKVTGYIDTGVAQGAELVVDGRGYKVAGHENGFFLG 365 K LK+G G GP++T A K+ + +A GA G+ ENG+F Sbjct: 319 KSLKLGPGYDPETQCGPMITQNAVRKIDRLVSEALAAGARATTGGKPLT----ENGYFYP 374 Query: 366 GTLFDRVTPEMTIYKEEIFGPVLCIVRVNSLEEAMQLINDHEYGNGTCIFTRDGEAARLF 425 T+ + V +I +EEIFGPV + + S +EA++L N+ EYG I++RD + A Sbjct: 375 PTVLENVPVNASIAREEIFGPVAPVYKFESDDEAIRLANNTEYGLAAYIYSRDLKRAMKV 434 Query: 426 CDEIEVGMVGVNVPLPVPVAYHSFGGWKRSLFG 458 IE GM+G+N L A FGG K+S G Sbjct: 435 GKRIETGMLGINRGLMSDPA-APFGGVKQSGLG 466 Lambda K H 0.319 0.137 0.411 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: 606 Number of extensions: 26 Number of successful extensions: 5 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: 498 Length of database: 487 Length adjustment: 34 Effective length of query: 464 Effective length of database: 453 Effective search space: 210192 Effective search space used: 210192 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: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 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:
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