Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_052668356.1 NITAL_RS21380 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000969705.1:WP_052668356.1 Length = 495 Score = 367 bits (941), Expect = e-106 Identities = 205/467 (43%), Positives = 285/467 (61%), Gaps = 19/467 (4%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 FI GE+ D G +F +SP LA+VA D +RAV+ AR F + WS+L A+ Sbjct: 38 FIGGEFVDPADGGSFATISPSTEEHLAEVALGTATDVDRAVKAARKAFRT--WSKLPGAE 95 Query: 83 RKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKV-YDE 141 R L R A LL++ E A+LE++D GKPI +S +D+P AA + A DK+ + Sbjct: 96 RGKYLYRLARLLQERAREFAVLESIDNGKPIRESRDVDVPTAAAHLFHHAGWADKLDWAG 155 Query: 142 VAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAI 201 + P P P+GV G ++PWNFPLLM WK+ PALA GN+VVLKP+E +PLTA+ Sbjct: 156 LGPAPR---------PLGVAGQVIPWNFPLLMLAWKVAPALACGNTVVLKPAETTPLTAL 206 Query: 202 RIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLM-VYAGESN 260 A+L +A +P GV+N++ G G T G A+ H DVD + FTGST++ K + AG Sbjct: 207 LFAELCQQADLPPGVINIVTGAGET-GAAVVGHDDVDKVAFTGSTEVGKAIQRALAGTG- 264 Query: 261 MKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFLP 320 KR+ LE GGK+ NIVF DAP + A E + I FNQG VC AGSRLLV+ S+ D + Sbjct: 265 -KRLTLELGGKAANIVFDDAP-IDQAVEGIVAGIFFNQGHVCCAGSRLLVQESVHDLVVD 322 Query: 321 MVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEETGG 380 + + L+ + G+PLD T +GA+ +Q+ + + +EAG +G + G Sbjct: 323 KLQQRLETLRLGDPLDKNTDIGAINSAEQLERITTLVEAGEAEGGTRWESPCEL--PSSG 380 Query: 381 TYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSDISK 440 + +PT+F G+ + R+AQEEIFGPVLSV+ F T +EAVA AN+TPYGL+AG+WT S+ Sbjct: 381 FWFKPTVFTGIGQSSRVAQEEIFGPVLSVLTFRTPDEAVAKANNTPYGLSAGVWTEKGSR 440 Query: 441 AHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKY 487 A +RAG VW N ++ D T+PFGG+K+SG GR+ H L Y Sbjct: 441 ILWMADRLRAGVVWANTFNRFDPTSPFGGYKESGFGREGGRHGLASY 487 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: 45 Number of successful extensions: 7 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: 495 Length adjustment: 34 Effective length of query: 463 Effective length of database: 461 Effective search space: 213443 Effective search space used: 213443 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 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