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 WP_090272725.1 BLU11_RS07285 NADP-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::A0A081YAY7 (498 letters) >NCBI__GCF_900105005.1:WP_090272725.1 Length = 480 Score = 227 bits (579), Expect = 6e-64 Identities = 139/443 (31%), Positives = 232/443 (52%), Gaps = 7/443 (1%) Query: 17 GRTADVFNPSTGEAVRKVPLADRETMQQAIDAAKAAFPAWRNTPPAKRAQVLFRFKQLLE 76 G T +++NP+TGE + VP+ ++ +QAIDAAK A P W +R+ L + +L+ Sbjct: 23 GNTQNIYNPATGELLGCVPVMRQQEARQAIDAAKRALPGWSFLTAKERSAKLRSWFELIL 82 Query: 77 ANEERIVKLISEEHGKTIEDAAGELKRGIENVEYATAAPEILKGEYSRNVGPNIDAWSDF 136 +++E + +L++ E GK + +A GE++ VE+ + + G+ N Sbjct: 83 SHQEELARLMTLEQGKPLHEARGEIQYAASFVEWFAEEGKRIYGDIIPAPQSNQRLLVLK 142 Query: 137 QPIGVVAGITPFNFPAMVPLWMYPLAIACGNTFILKPSERDPSSTLLIAELFHEAGLPKG 196 QP+GVVA ITP+NFPA + A+A G T +LKP+ + P S L +A+L +AG+P G Sbjct: 143 QPVGVVAAITPWNFPAAMITRKAAPALAAGCTLVLKPAPQTPFSALALAKLADQAGIPAG 202 Query: 197 VLNVVHGDKGAVDA-LIEAPEVKALSFVGSTPIAEYIYSEGTKRGKRVQALGGAKNHAVL 255 V NV+ GD + L P V+ L+F GST I + S+ K+V G ++ Sbjct: 203 VFNVITGDAVEIGGELTGNPTVRKLTFTGSTNIGRLLMSQCAHDVKKVSLELGGNAPFIV 262 Query: 256 MPDADLDNAVSALMGAAYGSCGERCMAISVAVCVGDQIADALVQKLVPQIKGLKIGAGTS 315 DADLD AV+ + A Y + G+ C+ + + V D + D +KL + ++G G Sbjct: 263 FEDADLDKAVAGALVAKYRNNGQTCVCTN-RIYVHDGVYDEFAEKLKQAVSAFQVGNGLD 321 Query: 316 CGLDMGPLVTGAARDKVTGYIDTGVAQGAELVVDGRGYKVAGHENGFFLGGTLFDRVTPE 375 + +GPL+ A DK+ +I+ V +GA++++ G+ + + G F T+ V + Sbjct: 322 TDITVGPLIDQVAMDKIRSHIEDAVTKGAKVLLGGKPHAL----GGTFFEPTILTDVPKD 377 Query: 376 MTIYKEEIFGPVLCIVRVNSLEEAMQLINDHEYGNGTCIFTRDGEAARLFCDEIEVGMVG 435 + +EE FGP+ + R ++ +E ++ ND EYG +T++ + +E GMVG Sbjct: 378 ALVAREETFGPLAPLFRFSNDDEVVRYANDTEYGLAAYFYTQNMNRIFRVAEALEYGMVG 437 Query: 436 VNVPLPVPVAYHSFGGWKRSLFG 458 +N + FGG K S G Sbjct: 438 INTG-AISNEMAPFGGMKSSGLG 459 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: 602 Number of extensions: 36 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: 480 Length adjustment: 34 Effective length of query: 464 Effective length of database: 446 Effective search space: 206944 Effective search space used: 206944 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 Sep 24 2021. 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