Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_019620489.1 G329_RS0103095 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000381785.1:WP_019620489.1 Length = 494 Score = 588 bits (1515), Expect = e-172 Identities = 281/491 (57%), Positives = 371/491 (75%), Gaps = 1/491 (0%) Query: 7 ADWEQRAQQLKIEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENA 66 ++W+ +++ L A+ING + AVSG+TF C++P + LA VASCD AD + AV NA Sbjct: 5 SEWQTQSKNLSFHNNAYINGGFQAAVSGDTFPCINPATEKLLADVASCDQADVDIAVANA 64 Query: 67 RATFNSGVWSQLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQ 126 R F SGVWS++ P +RK + ++A+L+ ++ +E ALL+TLDMGK I + +ID+P A Sbjct: 65 REVFKSGVWSEIPPRERKKAMQKWANLIEQHQDEFALLDTLDMGKSISEMVNIDVPDAID 124 Query: 127 AIHWTAEAIDKVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGN 186 I WTAE+IDK+Y E+APT D L ++ +PVGVVGAI PWN+PLLM WK+ PALA GN Sbjct: 125 CIRWTAESIDKIYGEIAPTGDDTLAMIHHQPVGVVGAITPWNYPLLMVSWKIAPALAAGN 184 Query: 187 SVVLKPSEKSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGST 246 SV+LKPSEKSPL+A+R+A+LA+EAGIPAGV NVLPG+GHT GKALALHMDV+ L FTGST Sbjct: 185 SVILKPSEKSPLSALRLAELAVEAGIPAGVFNVLPGFGHTAGKALALHMDVNVLAFTGST 244 Query: 247 KIAKQLMVYAGESNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGS 306 ++A LM YAGESNMKR+WLEAGGKSPN+VFADA D++AAA A+A+AI NQGEVC A S Sbjct: 245 RVAGMLMGYAGESNMKRVWLEAGGKSPNLVFADA-DIKAAAAASAAAIFCNQGEVCIACS 303 Query: 307 RLLVERSIKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAK 366 RL V++SIK++F+ +VEA ++PG+PLDP TT+G +VD Q+ V YI + ++G + Sbjct: 304 RLYVDKSIKEEFVAALVEAAASFQPGDPLDPATTMGPMVDGTQLAIVERYIRSAEEEGGQ 363 Query: 367 LLAGGKRTLEETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTP 426 ++ GG +E G + +PTI DG N M +EEIFGPVL+V F+T EEA+A+AND+ Sbjct: 364 VIMGGVPEYQEGKGFFAKPTIVDGAHNGMTFVKEEIFGPVLAVCEFETEEEAIALANDSV 423 Query: 427 YGLAAGIWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEK 486 YGL A +WT ++S+AH+ +R V +G VWVN + GD T PFGG K SGNGRDKSLHALEK Sbjct: 424 YGLGAAVWTQNLSRAHRVSRKVESGMVWVNTWGEGDSTVPFGGVKASGNGRDKSLHALEK 483 Query: 487 YTELKATWIKL 497 YT++K I+L Sbjct: 484 YTDIKNVLIRL 494 Lambda K H 0.316 0.132 0.390 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: 705 Number of extensions: 18 Number of successful extensions: 2 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: 497 Length of database: 494 Length adjustment: 34 Effective length of query: 463 Effective length of database: 460 Effective search space: 212980 Effective search space used: 212980 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 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