Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_073949813.1 RH94_RS23895 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_001906585.1:WP_073949813.1 Length = 507 Score = 352 bits (902), Expect = e-101 Identities = 200/476 (42%), Positives = 278/476 (58%), Gaps = 12/476 (2%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 FI GEY G+ FE SPV+G+ +VA D RA++ A A W + + + Sbjct: 23 FIGGEYVPPARGQYFENPSPVNGQPFTEVARGTAEDVERALDAAHAAAPG--WGRTSVGE 80 Query: 83 RKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDEV 142 R L++ AD + +E LA+ E+ + GKP+ ++ + DIP A + A AI + Sbjct: 81 RAGILLKIADRMEAYLEPLAVAESWENGKPVRETLAADIPLAIDHFRYFAGAIRAQEGSL 140 Query: 143 APTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAIR 202 D + EP+GVV I+PWNFP+LMA WKL PALA GN+VVLKP+E++P +I Sbjct: 141 GEIDDDTVAYHFHEPLGVVAQIIPWNFPILMAAWKLAPALAAGNAVVLKPAEQTP-ASIH 199 Query: 203 IAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESNMK 262 I +P GV+N++ G+G GK LA V + FTG T + +M YA E N+K Sbjct: 200 YWMSLIADLLPPGVVNIVNGFGVEAGKPLASSPRVAKVAFTGETTTGRLIMQYASE-NIK 258 Query: 263 RIWLEAGGKSPNIVFADAP----DLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKF 318 + LE GGKSPNI F D D + A + A NQGEVCT SR L++R +F Sbjct: 259 PVTLELGGKSPNIFFDDVSAAHDDFRDKALEGFTMFALNQGEVCTCPSRALIQRGHYAEF 318 Query: 319 LPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEE- 377 + V + PG+PLD T +GA Q+ +LSY++ G ++GA++LAGG+R E Sbjct: 319 VQAAVARTELITPGHPLDTDTMIGAQASNDQLEKILSYLDIGRQEGARVLAGGERIEHEG 378 Query: 378 --TGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWT 435 GG YV+PTIF+G N MRI QEEIFGPV+SV +FD ++A+ IANDT YGL AG+WT Sbjct: 379 ELKGGYYVQPTIFEG-DNRMRIFQEEIFGPVVSVTSFDDFDDAIKIANDTLYGLGAGVWT 437 Query: 436 SDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELK 491 D++ A++ RA++AG VW N Y + FGG+KQSG GR+ L+ Y + K Sbjct: 438 RDMNTAYRAGRAIQAGRVWTNCYHQYPAHSAFGGYKQSGIGRETHRMMLDHYQQTK 493 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: 672 Number of extensions: 39 Number of successful extensions: 8 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: 507 Length adjustment: 34 Effective length of query: 463 Effective length of database: 473 Effective search space: 218999 Effective search space used: 218999 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