Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate WP_054255254.1 BN2503_RS03555 CoA-acylating methylmalonate-semialdehyde dehydrogenase
Query= BRENDA::Q9K9B2 (515 letters) >NCBI__GCF_001298675.1:WP_054255254.1 Length = 505 Score = 203 bits (516), Expect = 1e-56 Identities = 146/486 (30%), Positives = 234/486 (48%), Gaps = 21/486 (4%) Query: 40 IINGERVTTEDKIQS-WNPARKDQLVGSVSKANQDLAEKAIQSADEAFQTWRNVNPEERA 98 +I+G+ V ++ Q +NPA Q V+ A+Q E AI SA+ AF WRN P +RA Sbjct: 14 LIDGQLVADTERTQPVFNPAT-GQSTTRVALASQATVEAAIASAEAAFPAWRNTPPLKRA 72 Query: 99 NILVKAAAIIRRRKHEFSAWLVHEAGKPWKEADADTAEAIDFLEY--YARQMIELNRGKE 156 ++ K ++ + +A + E GK +A + I+ +EY YA ++++ + Sbjct: 73 RVMSKLKVLLEENADKIAALITAEHGKVLADAHGELQRGIENVEYASYAPELLKGEHSRN 132 Query: 157 ILSRPGEQNRYFYTPMGVTVTISPWNFALAIMVGTAVAPIVTGNTVVLKPASTTPVVAAK 216 + P + + +GVT I+P+NF + + + GNT VLKP+ P A Sbjct: 133 V--GPSIDSWSEFQALGVTAGITPFNFPAMVPLWMWPMAVACGNTFVLKPSERDPTSALF 190 Query: 217 FVEVLEDAGLPKGVINYVPGSGAEVGDYLVDHPKTSLITFTGSKDVGVRLYERAAVVRPG 276 ++ +AGLP GV+N V G V D L+ P+ ++F GS + +Y G Sbjct: 191 IAQLALEAGLPPGVLNVVNGDKLAV-DTLLQDPRVKAVSFVGSTPIAEYIYAE------G 243 Query: 277 QNHLKRVIVEMGGKDTVVVDRDADLDLAAESILVSAFGFSGQKCSAGSRAVIHKD-VYDE 335 H KRV G K+ V+ DAD+D A +++ +A+G G++C A V D V D Sbjct: 244 CKHGKRVQALGGAKNHAVLMPDADVDNAVSALMGAAYGSCGERCMAIPLLVAVGDAVGDA 303 Query: 336 VLEKTVALAKNLTVGDPTNRDNYMGPVIDEKAFEKIMSYIEIGKKEG-RLMTGGEG---- 390 V+ + VG T+ N MGP++ + FEK+ +Y++ G EG L+ G G Sbjct: 304 VIAGLKTEIAKMKVGPGTDNSNDMGPLVTKPHFEKVKAYVDSGVAEGASLVVDGRGVQVA 363 Query: 391 DSSTGFFIQPTIIADLDPEAVIMQEEIFGPVVAFSKANDFDHALEIANNTEYGLTGAVIT 450 G+F+ + + P I QEEIFGPV+ + A+++ N+ EYG + T Sbjct: 364 GHEEGYFLGACLFDHVKPGMKIYQEEIFGPVLGVVRVKTLQEAMQLINDHEYGNGTCIFT 423 Query: 451 RNRAHIEQAKREFHVGNLYFNRNCTGAIVGYHPFGGFKMS-GTDSKAGGPDYLALHMQAK 509 R+ VG + N V YH FGG+K S D A GPD + + + K Sbjct: 424 RDGEAARYFTDHIQVGMVGVNVPLP-VPVAYHSFGGWKRSLFGDLHAYGPDAVRFYTKRK 482 Query: 510 TVSEMY 515 T+++ + Sbjct: 483 TITQRW 488 Lambda K H 0.316 0.134 0.388 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: 569 Number of extensions: 35 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: 515 Length of database: 505 Length adjustment: 34 Effective length of query: 481 Effective length of database: 471 Effective search space: 226551 Effective search space used: 226551 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 (21.6 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