Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate WP_028312975.1 H566_RS0120955 aldehyde dehydrogenase
Query= BRENDA::Q9K9B2 (515 letters) >NCBI__GCF_000482785.1:WP_028312975.1 Length = 479 Score = 246 bits (629), Expect = 1e-69 Identities = 163/482 (33%), Positives = 251/482 (52%), Gaps = 23/482 (4%) Query: 36 EYPLIINGERVT--TEDKIQSWNPARKDQLVGSVSKANQDLAEKAIQSADEAFQTWRNVN 93 +Y +NGE V+ +E I+ NPA L+ + + + + A+ +A +A + W + Sbjct: 4 KYSNYVNGEFVSPASEATIEVRNPA-DHALIALIPDSAPSVVDDAVAAARQAQRGWEKLP 62 Query: 94 PEERANILVKAAAIIRRRKHEFSAWLVHEAGK--PWKEADAD-TAEAIDFLEYYARQMIE 150 +RA L K +A +R ++ + + E GK P + D TA+ ID++ +AR++ Sbjct: 63 AIQRAGYLRKISAKLREQRDRLAEVITREQGKVLPLARIEVDFTADYIDYMAEWARRI-- 120 Query: 151 LNRGKEILS-RPGEQNRYFYTPMGVTVTISPWNFALAIMVGTAVAPIVTGNTVVLKPAST 209 G+ I S RP E P+GVT I PWNF ++ +VTGNT+V+KP+ Sbjct: 121 --EGEVIPSDRPNETIFLLRKPIGVTAGILPWNFPFFLIARKMAPALVTGNTIVVKPSEE 178 Query: 210 TPVVAAKFVEVLEDAGLPKGVINYVPGSGAEVGDYLVDHPKTSLITFTGSKDVGVRLYER 269 TPV A +F +++ + LP GV N V G GA G L HP L++FTGS G + + Sbjct: 179 TPVNAFEFAKLVAETDLPPGVFNLVSGRGATTGAALTGHPDVGLVSFTGSVATGQAIMKA 238 Query: 270 AAVVRPGQNHLKRVIVEMGGKDTVVVDRDADLDLAAESILVSAFGFSGQKCSAGSRAVIH 329 AA +L RV +E+GGK +V ADLDLAA+SI+ S +GQ C+ R + Sbjct: 239 AAA------NLTRVNLELGGKAPAIVLASADLDLAAKSIVASRTINTGQVCNCAERVYVQ 292 Query: 330 KDVYDEVLEKTVALAKNLTVGDPTNRDNY-MGPVIDEKAFEKIMSYIEIGKKEGR--LMT 386 + V + +K V L GDP D MGP++++ +K+ + +E + EG L+ Sbjct: 293 ESVAEAFADKVVKLMAATRYGDPLREDGLDMGPLVNQVGLDKVAAMVERARGEGAQVLLG 352 Query: 387 GGEGDSSTGFFIQPTIIADLDPEAVIMQEEIFGPVVAFSKANDFDHALEIANNTEYGLTG 446 G D GF +PT+IA + IM++EIFGPV+ D D A+ +AN+ EYGLT Sbjct: 353 GKVADLGAGFHYEPTVIAGCRADMEIMRKEIFGPVLPLQTVADLDEAITLANDCEYGLTS 412 Query: 447 AVITRNRAHIEQAKREFHVGNLYFNRNCTGAIVGYHPFGGFK--MSGTDSKAGGPDYLAL 504 ++ T++ +A RE G Y NR A+ G+H G K + G D + G +Y Sbjct: 413 SIFTQDIDAAFKACRELSFGETYVNREHFEAMQGFHA-GRRKSGIGGADGRHGLLEYTET 471 Query: 505 HM 506 H+ Sbjct: 472 HV 473 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: 533 Number of extensions: 22 Number of successful extensions: 4 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: 479 Length adjustment: 34 Effective length of query: 481 Effective length of database: 445 Effective search space: 214045 Effective search space used: 214045 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 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