Align phenylacetaldehyde dehydrogenase (EC 1.2.1.39) (characterized)
to candidate GFF2064 HP15_2020 succinate-semialdehyde dehydrogenase I
Query= BRENDA::Q5P171 (474 letters) >FitnessBrowser__Marino:GFF2064 Length = 489 Score = 308 bits (788), Expect = 3e-88 Identities = 187/470 (39%), Positives = 257/470 (54%), Gaps = 11/470 (2%) Query: 8 INGKPVRA--GSTFDVVNPATGEVFARVQAGDASHVDQAVAAARAAFPGWSRTPDAERKR 65 ING+ + A G TF V +PA GE A V D + A+ AA AA+P W TP ER Sbjct: 17 INGQWITAKSGKTFAVNDPANGEQLATVPDMDDTDARAAIEAASAAWPAWRSTPAKERAN 76 Query: 66 LMHALGAALEAHMPELMELVTKEAGKPLGGLNG-VGSGMEVGGAIAWTHVTADLELPVEV 124 ++ L A+ +L L+T E GKPL G VG G I W A + Sbjct: 77 ILRKWFNLLMANQEDLARLMTAEQGKPLAESRGEVGYGASF---IEWFAEEAKRAYGDVI 133 Query: 125 IQDNDDARIEVHRKPLGVVGSITPWNWPLMIAIWHVIPALRAGNTVVIKPSGMTPTATIR 184 D RI V ++P+GVV +ITPWN+P+ + V PAL AG VV+KP+ TP + + Sbjct: 134 PGHGKDKRIVVIKQPVGVVAAITPWNFPIAMITRKVAPALAAGCPVVVKPAEDTPLSALA 193 Query: 185 FVELAN-AILPPGVLNIVTGES----GVGSAIAKHPDINKIVFTGSTPTGKNIMQNAAGN 239 LA A +P G++NI+T VGS + +P + K+ FTGSTP GK +M+ A+ Sbjct: 194 ITALAEEAGVPAGLINIITCSKPNAVSVGSELTGNPIVRKVSFTGSTPVGKLLMRQASDT 253 Query: 240 LKRLTLELGGNDAGIVLPDVDPKAIAPKLFGVGFHNNGQTCACLKRLYVHDSIYEKVCAE 299 +K+++LELGGN IV D D A L + N GQTC C R+YV +Y+ + Sbjct: 254 VKKVSLELGGNAPFIVFDDADLDAAVAGLMASKYRNTGQTCVCANRVYVQAGVYDAFAEK 313 Query: 300 LARIAKETVVGDGLVEGTELGPVQNKAQLDFVQELVEDARAHGARILSGGKARSGGGFFF 359 L + VVG GL T+ GP+ N A L V+ +EDA + GA++ GG+A S GG FF Sbjct: 314 LKAAVSKMVVGPGLEGETQQGPLINDAALAKVKRHIEDATSKGAKVALGGRAHSLGGTFF 373 Query: 360 EPTVIADAKDGMRVVDEEQFGPVLPVIRYSDIEEVIARANNNENGLGGSIWSKDHAKAAE 419 EPT++ A M + EE FGPV P+ ++ +E IA AN++E GL +S++ + Sbjct: 374 EPTILTHATQEMLIAREETFGPVAPLFKFETDDEAIAMANDSEFGLSAYFYSRNIHRVWR 433 Query: 420 LALRLECGTAWVNEHGAVQPDAPFGGVKQSGLGVEFGRYGLEEYTSIQTL 469 +A LE G VNE APFGGVK+SGLG E YGL+EY ++ L Sbjct: 434 VAEELESGMIGVNEGIISTEVAPFGGVKESGLGREGSHYGLDEYMELKYL 483 Lambda K H 0.317 0.136 0.405 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: 646 Number of extensions: 30 Number of successful extensions: 3 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: 489 Length adjustment: 34 Effective length of query: 440 Effective length of database: 455 Effective search space: 200200 Effective search space used: 200200 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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