Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_010440535.1 G7G_RS0108790 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000192475.1:WP_010440535.1 Length = 498 Score = 456 bits (1172), Expect = e-132 Identities = 232/498 (46%), Positives = 323/498 (64%), Gaps = 10/498 (2%) Query: 1 MTTLTRADWEQRAQQLKIEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADAN 60 M+ LT+ ++E A + AFI+G Y A+SG+ FE ++P G L +A+C + D + Sbjct: 1 MSLLTKDEYESIAAHQDLPTGAFIDGGYRPAISGQVFETVNPATGALLTSIAACGVEDVD 60 Query: 61 RAVENARATFNSGVWSQLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSID 120 AVE AR F+ G WS++ P+ RK LIR L+ +N ELA++E++D GK I D ++D Sbjct: 61 FAVEKAREAFDDGRWSKMHPSDRKDVLIRLCKLITRNARELAVMESIDSGKTIYDCETVD 120 Query: 121 IPGAAQAIHWTAEAIDKVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGP 180 +P + W AEAIDK+YD+V+P D + +V REP+GVVG ++PWNFPLLM WK+GP Sbjct: 121 VPETIHCLKWHAEAIDKIYDQVSPASDDHIAMVVREPIGVVGLVLPWNFPLLMLAWKIGP 180 Query: 181 ALATGNSVVLKPSEKSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTL 240 ALA G SVV+KP+ ++ LTA+++A+LA EAG+P GVLNV+PG G VG+ + HMD+D + Sbjct: 181 ALAAGCSVVVKPATETSLTALKVAELASEAGLPRGVLNVVPGGGAEVGEPIGRHMDIDMV 240 Query: 241 VFTGSTKIAKQLMVYAGESNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGE 300 FTGST K+ + Y+ ESN K + LE GGK+P IV DA +L A + +N GE Sbjct: 241 SFTGSTVTGKKFLSYSAESNAKEVVLEMGGKNPAIVMDDAENLDRVAAHVVNGAFWNMGE 300 Query: 301 VCTAGSRLLVERSIKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAG 360 C+A SRL+V + +K + L + K W G PLDP+T +GALV N V Y+E Sbjct: 301 NCSASSRLIVHKDVKAELLERIAHHAKHWNVGEPLDPETRMGALVSEGHYNKVCGYLE-- 358 Query: 361 HKDGAKLLAGGKRTLEETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVA 420 +L GGK E G +VE T+ + N +A+EEIFGPVLSVI +EA++ Sbjct: 359 --QAENVLIGGK---AEKG--FVEATVVEVPGNDATLAREEIFGPVLSVIEVSGFDEAIS 411 Query: 421 IANDTPYGLAAGIWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSG-NGRDK 479 IANDT YGL A I+ ++ +A + ARA+RAG+V VN + GD+T PFGG+KQSG GRD Sbjct: 412 IANDTEYGLCASIFMANAKRAIRGARAIRAGTVTVNSFGEGDITTPFGGYKQSGFGGRDN 471 Query: 480 SLHALEKYTELKATWIKL 497 S+HA ++YT+LK WI L Sbjct: 472 SVHAHDQYTQLKTIWIDL 489 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: 647 Number of extensions: 23 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: 497 Length of database: 498 Length adjustment: 34 Effective length of query: 463 Effective length of database: 464 Effective search space: 214832 Effective search space used: 214832 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