Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate WP_110206341.1 DNK54_RS07665 aldehyde dehydrogenase family protein
Query= BRENDA::Q72IB9 (516 letters) >NCBI__GCF_003194585.1:WP_110206341.1 Length = 498 Score = 243 bits (621), Expect = 9e-69 Identities = 171/471 (36%), Positives = 241/471 (51%), Gaps = 31/471 (6%) Query: 38 YPLYIGGEWVD-TKERMVSLNPSAPSEVVGTTAKAGKAEAEAALEAAWKAF-KTWKDWPQ 95 Y L++ GE+VD ++NP A EV+ A+A A+ +AA+ AA +A+ + W P Sbjct: 37 YGLFVNGEFVDGAGASFKTINP-ATEEVLAEIAEANAADVDAAVRAARRAYARVWSKMPG 95 Query: 96 EDRSRLLLKAAALMRRRKRELEATLVYEVGKNWVEA-SADVAEAIDFIEYYARAALRYRY 154 ++R++ L + A +++ R REL + GK EA DV A YYA A + Y Sbjct: 96 KERAKYLFRIARILQERARELAVLESIDNGKPIKEARDVDVPVAAAHFFYYAGWADKLEY 155 Query: 155 PAVEVVPYPGEDNESFYVPLGAGVVIAPWNFPVAIFTGMIMGPVAVGNTVIAKPAEDAVV 214 PG + LG + PWNFP+ + I +A GNTV+ KPAE + Sbjct: 156 AL------PGNAHSGVR-SLGVAAQVIPWNFPLLMLAWKIAPALAAGNTVVLKPAETTPL 208 Query: 215 VGAKVFEIFHEAGFPPGVVNFLPGVGEEVGAYLVEHPRTRFINFTGSLEVGLKIYEAAGR 274 EI +A P GVVN + G G+ G LV H + FTGS EVG +A R Sbjct: 209 TALLFAEICQQADLPAGVVNIVTGAGD-TGQALVGHADVDKVAFTGSTEVG----KAIAR 263 Query: 275 LAPGQTWFKRAYVETGGKDAIIVDETADFDLAAEGVVVSAYGFQGQKCSAASRLILTQGA 334 G KR +E GGK A IV + A D A EG+V + QG C A SRL++ + Sbjct: 264 TVAGTD--KRVTLELGGKAANIVFDDAPLDQAIEGIVSGIFFNQGHVCCAGSRLLVQESV 321 Query: 335 YEPVLERVLKRAERLSVG-PAEENPDLGPVVSAEQERKVLSYIEIGKNEGQLVLGGKR-- 391 + VLER+ R L VG P ++N D+G + SAEQ ++ IG+ E + G+R Sbjct: 322 ADEVLERLKSRMGTLRVGDPLDKNTDIGAINSAEQLARIRELSAIGEQE----VAGERWS 377 Query: 392 ----LEGEGYFIAPTVFTEVPPKARIAQEEIFGPVLSVIRVKDFAEALEVANDTPYGLTG 447 L G++ PT+FT V RIA+EEIFGPVLSV+ + AEA+E AN+TPYGL+ Sbjct: 378 PPCELPERGFWFPPTIFTGVTQAHRIAREEIFGPVLSVLTFRTPAEAVEKANNTPYGLSA 437 Query: 448 GVYSRKREHLEWARREFHVGNLYFNRKITGALVGVQPFGGFKLSGTNAKTG 498 GV++ K + W + G ++ N PFGG+K SG + G Sbjct: 438 GVWTEKGSRILWMADQLRAGVVWAN--TFNKFDPTSPFGGYKESGYGREGG 486 Lambda K H 0.319 0.137 0.403 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: 572 Number of extensions: 33 Number of successful extensions: 7 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: 516 Length of database: 498 Length adjustment: 34 Effective length of query: 482 Effective length of database: 464 Effective search space: 223648 Effective search space used: 223648 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