Align phenylacetaldehyde dehydrogenase (EC 1.2.1.39) (characterized)
to candidate WP_067907935.1 AQZ52_RS07360 aldehyde dehydrogenase family protein
Query= BRENDA::Q5P171 (474 letters) >NCBI__GCF_001519075.1:WP_067907935.1 Length = 474 Score = 435 bits (1118), Expect = e-126 Identities = 217/473 (45%), Positives = 311/473 (65%), Gaps = 6/473 (1%) Query: 2 QVFDMIINGKPVRAGSTFDVVNPATGEVFARVQAGDASHVDQAVAAARAAFPGWSRTPDA 61 +++ +I+G+ V DV+NPA +V +V A A +D+AVAAAR AF WS+TP Sbjct: 3 KLYPNLIDGELVTTAKALDVLNPANEQVIGQVPACGAEELDRAVAAARRAFKTWSKTPVD 62 Query: 62 ERKRLMHALGAALEAHMPELMELVTKEAGKPLGGLNGVGSGMEVGGAIAWTHVTADLELP 121 +R+ ++ A+ AA++A+ EL L+T E GKP + E+GG A + + L L Sbjct: 63 DRRAVIRAMAAAIDANFDELFRLLTAEQGKP-----HQQAQFEIGGCSAMMNAQSTLTLE 117 Query: 122 VEVIQDNDDARIEVHRKPLGVVGSITPWNWPLMIAIWHVIPALRAGNTVVIKPSGMTPTA 181 + +D+D+ R P+GVVG I PWN+P+++A+ + PA+ +G T+V+KPS TP Sbjct: 118 ETINEDSDERLSRTRRVPVGVVGGIVPWNFPVLMAVQKIAPAILSGCTIVLKPSPFTPLT 177 Query: 182 TIRFVELANAILPPGVLNIVTGESGVGSAIAKHPDINKIVFTGSTPTGKNIMQNAAGNLK 241 T+RF EL I+P GV+NI+TGE +G I HPDI+KI FTGST TGK IM+ A+ +LK Sbjct: 178 TLRFAELIKDIVPAGVVNIITGEDALGPMITAHPDIDKITFTGSTATGKKIMEGASKDLK 237 Query: 242 RLTLELGGNDAGIVLPDVDPKAIAPKLFGVGFHNNGQTCACLKRLYVHDSIYEKVCAELA 301 R+TLELGGNDA IVLPD D +A +LF F N GQ C KR+Y+H+ IY+++ A +A Sbjct: 238 RITLELGGNDASIVLPDADVAKVAEQLFWSSFTNAGQICVAAKRIYIHEDIYDELSAAIA 297 Query: 302 RIAKETVVGDGLVEGTELGPVQNKAQLDFVQELVEDARAHGARILSGGKA-RSGGGFFFE 360 AK VGDG +GT +GP+QNK Q D V EL+EDA+ +G + L GG SG G++ Sbjct: 298 EYAKNVKVGDGSEQGTGVGPIQNKKQFDRVCELIEDAKTNGYKFLVGGDVDPSGSGYYVP 357 Query: 361 PTVIADAKDGMRVVDEEQFGPVLPVIRYSDIEEVIARANNNENGLGGSIWSKDHAKAAEL 420 T++ + + R+V EEQFGPV+P++++S +EVIARANN+E GL G++W+KD + ++ Sbjct: 358 ITILDNPPEDARIVAEEQFGPVMPLMKFSSDDEVIARANNSEYGLAGAVWTKDTERGVKI 417 Query: 421 ALRLECGTAWVNEHGAVQPDAPFGGVKQSGLGVEFGRYGLEEYTSIQTLKIMK 473 A +LE GT W+NE + P APFGG KQSG G E+G GL+E+T Q + + K Sbjct: 418 AEQLETGTVWINEFLHLSPFAPFGGHKQSGFGAEYGIEGLKEFTYSQVITVKK 470 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: 641 Number of extensions: 35 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: 474 Length adjustment: 33 Effective length of query: 441 Effective length of database: 441 Effective search space: 194481 Effective search space used: 194481 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: 51 (24.3 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