Align phenylacetaldehyde dehydrogenase (EC 1.2.1.39) (characterized)
to candidate WP_035239838.1 Q366_RS13505 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::V4GH04 (496 letters) >NCBI__GCF_000745975.1:WP_035239838.1 Length = 484 Score = 313 bits (801), Expect = 1e-89 Identities = 182/478 (38%), Positives = 266/478 (55%), Gaps = 12/478 (2%) Query: 19 IGGQWVSAQSGKTLNVYNPATGDILTEVPDGDVEDVNAAVESAAATLRSDTWRRMPPSAR 78 I +WV+A SGKT++V NPATG IL VP ++ A+ +A +L D WR R Sbjct: 16 IQDEWVAADSGKTVDVTNPATGQILGTVPFCGADETQRAINAANESL--DAWRSKTAGER 73 Query: 79 ERILLRLADLLEVHGDELARLETLNNGKLLIYSKLMEVGASAQWLRYMAGWATKLTGSTL 138 IL + DLL + ++LA + T GK L S+ E+ +A + + A A ++ G + Sbjct: 74 SAILRKWYDLLMENQEDLAVIMTAEQGKPLAESR-GEIAYAAAFFEWFAEEAKRVYGDVI 132 Query: 139 DLSLPLPPEVRS-RASTQRVPVGVVAAIIPWNFPLLMAVWKIAPALACGNTVVLKPAEET 197 P V S R + PVGVVAAI PWNFP M K ALA G T+VLKPA T Sbjct: 133 ------PQTVASQRLVVIKQPVGVVAAITPWNFPSAMITRKAGAALAAGCTMVLKPATAT 186 Query: 198 PLTALRLAELAMEAGLPAGALNVVTGRGETAGDALVRHPKVAKVAFTGSTEVGRIIGSAC 257 P +AL +A+L +AG+P G NVVTG G L +P V K+ FTGST+VG+ + C Sbjct: 187 PFSALAIAKLGQQAGVPKGVFNVVTGSSSAIGGELTANPIVRKLTFTGSTQVGKKLMRDC 246 Query: 258 GRSLKAVSLELGGKSPVIVLADCDPQEAAEGAAAAIFFNHGQVCTAGSRLYVHESIYEDV 317 ++K +S+ELGG +P IV D D A EGA A + N GQ C +R+YV +Y++ Sbjct: 247 AGTMKRLSMELGGNAPFIVFDDADIDAAVEGAMACKYRNSGQTCVCANRMYVQAGVYDEF 306 Query: 318 IQRLAVIGESIVVGSGLEQGVHMGPMVSKKHHENVLRHIRNGIEDGADLICGGTEAPCAQ 377 ++L + + VG+G + GV GP++ E V HI++ ++ G ++ GGT + Sbjct: 307 CRKLTAAVQELKVGNGFDDGVQQGPLIDMAAVETVESHIKDAVDKGGKVLAGGTRHALGR 366 Query: 378 GFFVKPTIFANREKKDIRLLSQEVFGPVLVATPFSDIAEVVNEANRSVYGLGASIWTNDL 437 FF PTI A+ D+R+ +E FGP+ F EVV +AN + +GL A +T D+ Sbjct: 367 TFFA-PTIIAD-VTDDMRVAREETFGPLAPVFKFDTEEEVVRKANDTEFGLAAYFYTRDM 424 Query: 438 SAALRINDELEAGTVWVNTHNMVDPNLPFGGFKDSGVGREHGAAAIEHYTTTRSLVIA 495 + + RI ++LE G V +N+ + +P PFGG K+SG GRE ++ Y + + +A Sbjct: 425 ARSWRIGEKLEYGLVGINSGIISNPVAPFGGVKESGNGREGSKYGLDDYLEIKYMCMA 482 Lambda K H 0.317 0.134 0.395 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: 598 Number of extensions: 27 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: 496 Length of database: 484 Length adjustment: 34 Effective length of query: 462 Effective length of database: 450 Effective search space: 207900 Effective search space used: 207900 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 (21.7 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