Align Gamma-aminobutyraldehyde dehydrogenase; ABALDH; EC 1.2.1.19; 1-pyrroline dehydrogenase; 4-aminobutanal dehydrogenase; 5-aminopentanal dehydrogenase; EC 1.2.1.- (uncharacterized)
to candidate BWI76_RS03865 BWI76_RS03865 5-carboxymethyl-2-hydroxymuconate semialdehyde dehydrogenase
Query= curated2:A8GHZ8 (474 letters) >FitnessBrowser__Koxy:BWI76_RS03865 Length = 488 Score = 327 bits (837), Expect = 7e-94 Identities = 187/474 (39%), Positives = 272/474 (57%), Gaps = 17/474 (3%) Query: 7 INGQLVTGQGALLPVYNPATGEVVVQVAEASAEQVDQAVLAADAAFEHWGQTTPKERAEH 66 ING+ V G NPATGEV+ +VA A++V+QAV AA AF W KERA Sbjct: 8 INGKNVAGSD-YFHTTNPATGEVLAEVASGGADEVNQAVAAAKEAFPKWANLPMKERARL 66 Query: 67 LLKLADLIDSHAETFARLESINCGKPYHCVLNDELPGVADVFRFFAGASRCLSGLA--AG 124 + +L DLID + A +E+ + G P H N +P + F FFA + ++G Sbjct: 67 MRRLGDLIDQNVPEIAAMETADTGLPIHQTKNVLIPRASHNFEFFAEVCQQMNGKTYPVD 126 Query: 125 EYLAGHTSMIRRDPLGVVASIAPWNYPLMMAAWKLAPALAAGNCVVLKPSEQTPLTTFKL 184 + + +T + P+GV A ++PWN P M A WK+AP LA GN VLK SE +PLT +L Sbjct: 127 DKMLNYTLV---QPVGVCALVSPWNVPFMTATWKVAPCLALGNTAVLKMSELSPLTADRL 183 Query: 185 AELA--AGLFPPGVLNVLFGRGASVGDRLTGHNKVRMVSLTGSIATGEHIIGHTASGIKR 242 ELA AG+ P GVLNV+ G GA+ GD L H+ VR VS TG ATG +I+ + +G+K+ Sbjct: 184 GELALEAGI-PAGVLNVVQGYGATAGDALVRHHDVRAVSFTGGTATGRNIMKN--AGLKK 240 Query: 243 THMELGGKAPVLVFDDADLQQVVEGIRSFGFYNAGQDCTAACRIYAQKGIYPQLVKALGE 302 MELGGK+PVL+F+DAD+++ ++ F G+ CTA RI+ Q+ IYP+ VK E Sbjct: 241 YSMELGGKSPVLIFEDADIERALDAALFTIFSINGERCTAGSRIFIQQSIYPEFVKRFAE 300 Query: 303 AIGSLKIGPPIDASSELGPLITAQHLERVVGFVERAKALPHVQVVTGGERVNG------P 356 L++G P D ++++G LI+ QH E+V G++ + G ++ Sbjct: 301 RANRLRVGDPTDPNTQVGALISQQHWEKVSGYIRLGIEEGATLLAGGADKPTDLPAHLRN 360 Query: 357 GYYFQPTLLAGARQEDEIVQREVFGPVVTVTPFDDEAQVLAWANESDYGLASSLWTRDVG 416 G + +PT+LA + Q E+FGPV + PF DEA+ L AN+ +YGLAS +WT+DV Sbjct: 361 GNFLRPTVLADVDNRMRVAQEEIFGPVACLLPFKDEAEGLRLANDVEYGLASYIWTQDVS 420 Query: 417 RAHRLSARLQYGCTWVNTHFMLVSEMPHGGQKLSGYGKDMSMYGLEDYTAIRHV 470 + RL+ ++ G +VNT + P GG K SG G++ Y E + +++V Sbjct: 421 KVLRLARGIEAGMVFVNTQNVRDLRQPFGGVKASGTGREGGEYSFEVFAEMKNV 474 Lambda K H 0.320 0.136 0.410 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: 521 Number of extensions: 21 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: 474 Length of database: 488 Length adjustment: 34 Effective length of query: 440 Effective length of database: 454 Effective search space: 199760 Effective search space used: 199760 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 (21.8 bits) S2: 51 (24.3 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