Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_068114121.1 I601_RS01130 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_001653335.1:WP_068114121.1 Length = 481 Score = 350 bits (898), Expect = e-101 Identities = 202/469 (43%), Positives = 280/469 (59%), Gaps = 20/469 (4%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 F+NGE+ D G F+ ++P LA+VA + AD + AV+ AR ++ VW + + Sbjct: 23 FVNGEFVDG-HGTPFKTVNPATEEVLAEVAEANDADVDAAVKAARRAYDK-VWGPMPGRE 80 Query: 83 RKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDEV 142 R L R A +L++ E+++LET+D GKPI +S +D+P AA + A DK+ Sbjct: 81 RAKYLYRIARILQERAREISVLETIDNGKPIKESRDVDVPTAAAFFFYYAGWADKL---- 136 Query: 143 APTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAIR 202 H G P+GV G ++PWNFPLLM WK+ PALA GN+VVLKP+E +PLTA+ Sbjct: 137 ---EHSGYGST---PLGVAGQVIPWNFPLLMLAWKIAPALACGNTVVLKPAETTPLTALL 190 Query: 203 IAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLM-VYAGESNM 261 A++ +A +P GV+N++ G G T G+ L H DVD + FTGST + K + AG S Sbjct: 191 FAEICQQADLPPGVVNIITGAGAT-GETLVGHPDVDKVAFTGSTGVGKAIARTVAGSS-- 247 Query: 262 KRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFLPM 321 K++ LE GGK+ NIVF DAP + A E + I FNQG VC AGSRLLV+ SI D+ L Sbjct: 248 KKVTLELGGKAANIVFDDAP-IDQAIEGIVNGIFFNQGHVCCAGSRLLVQESIADEVLTR 306 Query: 322 VVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLE---ET 378 + + + G+PLD T VGA+ Q+ + + G + G+ + E + Sbjct: 307 LKRRMSTLRLGDPLDKNTDVGAINSAAQLARIHELSDIGEAEVGTGDGAGRWSPECELPS 366 Query: 379 GGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSDI 438 G + PTIF GV+ A RIA+EEIFGPVLSV+ F T EAV AN+TPYGL+AG+WT Sbjct: 367 TGFWFPPTIFTGVSQAHRIAREEIFGPVLSVLTFRTPSEAVEKANNTPYGLSAGVWTDKG 426 Query: 439 SKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKY 487 S+ A +RAG VW N ++ D T+PFGG+K+SG GR+ H L Y Sbjct: 427 SRILDIAGRLRAGVVWANTFNKFDPTSPFGGYKESGYGREGGRHGLAAY 475 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: 662 Number of extensions: 40 Number of successful extensions: 6 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: 481 Length adjustment: 34 Effective length of query: 463 Effective length of database: 447 Effective search space: 206961 Effective search space used: 206961 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