Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_023432018.1 N177_RS09120 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000496075.1:WP_023432018.1 Length = 492 Score = 328 bits (842), Expect = 2e-94 Identities = 192/485 (39%), Positives = 279/485 (57%), Gaps = 14/485 (2%) Query: 19 EGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQL 78 E + I GE+T E + ++P A + AD RA+E A T+ S VW + Sbjct: 4 EYQMLIGGEWTGGSGSERLDSVNPYTQEVWATLPQAGDADVARAIEIAHDTYVS-VWRGV 62 Query: 79 APAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKV 138 R L R ADL+ +N +LA ++T D GK I ++ S + AA+ + A DK+ Sbjct: 63 NGRDRALMLNRLADLVEQNGPDLARIDTTDNGKVIRETGS-QMKFAARNYRYFAGLADKL 121 Query: 139 YDEVAPTPH-DQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSP 197 P + + L EP+GV I WN PL + KL PALA GN+VV+KPSE + Sbjct: 122 QGNTIPLDNGEMLDYTIVEPLGVAVLITAWNSPLPLLANKLAPALAAGNTVVIKPSEHAS 181 Query: 198 LTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAG 257 ++ + +L EAG P GV+N++ G G +G AL H V + FTG A++++ A Sbjct: 182 ISTLAFGRLIAEAGFPDGVVNIVTGDGR-IGPALTTHKRVKKISFTGGLPTARRILEAAA 240 Query: 258 ESNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDK 317 + + E GGKSPNI+F DA DL+AA A + I G+ C AGSRLLV+ SI D+ Sbjct: 241 R-RLVPVTTELGGKSPNIIFEDA-DLKAAVNGAVAGIFGASGQTCIAGSRLLVQSSIYDE 298 Query: 318 FLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEE 377 V+E ++G + GNPLDP T +G + + Q + +LS I +GAKL GG++ Sbjct: 299 VCDRVLEKVRGIRLGNPLDPATEMGPVANRAQFDRILSLIAQAENEGAKLALGGRQA--- 355 Query: 378 TG-----GTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAG 432 TG G ++EPT+ V ++ IA++E+FGPVL ++ F+ +AV IAND+ YGLAAG Sbjct: 356 TGPGLERGFFIEPTVLKDVEPSLTIARDEVFGPVLCILRFEDEADAVRIANDSDYGLAAG 415 Query: 433 IWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKA 492 +WT+D+ +AH+ AR + AG VWVN Y + APFGG K SG+GR++S H L +YT++K Sbjct: 416 VWTNDVRRAHRMAREIEAGLVWVNTYRASYVGAPFGGTKLSGHGRERSWHTLMEYTQVKN 475 Query: 493 TWIKL 497 + L Sbjct: 476 VMLDL 480 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: 701 Number of extensions: 37 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: 492 Length adjustment: 34 Effective length of query: 463 Effective length of database: 458 Effective search space: 212054 Effective search space used: 212054 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