Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_083875613.1 J416_RS14675 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000359605.1:WP_083875613.1 Length = 492 Score = 206 bits (523), Expect = 2e-57 Identities = 150/485 (30%), Positives = 246/485 (50%), Gaps = 28/485 (5%) Query: 18 IEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADAN-RAVENARATFNSGVWS 76 IE A INGE + E +P + A + + +A++ A TF + W Sbjct: 6 IEIHAMINGETYKTEENKPRE--NPTHPDEIVGYAPVNTKEETIQAIDAAHETFKT--WR 61 Query: 77 QLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAID 136 + ++R ++ + L++ LA L + + GKP+ D+ +I W A D Sbjct: 62 RSEISERVERMRNAIEKLKEETPNLAELLSREHGKPLYDAEG----EVTISIMWMEYACD 117 Query: 137 KVYDEVAPTPHDQLG---LVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPS 193 V D + D L+ R+ +GVV AI PWN+P+ ++ K+ PAL TGN++VLKPS Sbjct: 118 NVEDVLKDQVEDHDNGRTLIARDAIGVVSAISPWNYPISLSTIKIAPALLTGNTMVLKPS 177 Query: 194 EKSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLM 253 +PL + ++ I PAGVLN++ G VG L + V + FTG T+ AK +M Sbjct: 178 PMAPLAVSKCTEM-IANEFPAGVLNMVHGEA-DVGVELTSNPKVAKIAFTGGTETAKSIM 235 Query: 254 VYAGESNMKRIWLEAGGKSPNIVF--ADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVE 311 A ++ +K++ LE GG I+ D D +A S G++C R+ V Sbjct: 236 KSAADT-IKQMTLELGGNDAAIILDDFDVHDEEAMRRLVISNF-LTAGQICMIAKRIYVA 293 Query: 312 RSIKDKFLPMVVEALKGW-KPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAG 370 +SI ++F+ +EA W + G+P + T+G + + Q+ V S I+ + GA+++ Sbjct: 294 KSIYEEFVEKYIEAANKWIRVGDPFGDEVTIGPVNNKNQIEHVQSLIDDAKEKGAEVIKL 353 Query: 371 GK----RTLEETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTP 426 G+ EE G Y++P++ G + I Q+E FGP + ++ F+ E A+ +AND+ Sbjct: 354 GEILDSDLFEE--GYYMQPSVVLGASQDDPIVQKEQFGPTVPILPFEDDEHALQLANDSI 411 Query: 427 YGLAAGIWTSDISKAHKTARAVRAGSVWVN--QYDGGDMTAPFGGFKQSGNGRDKSLHAL 484 YGL + +W + + A + A+ ++AG+ +N G D+ PFGG KQSG GR+ L Sbjct: 412 YGLTSSVWGEE-THALEIAKRIQAGTTMINTAAVQGLDVRFPFGGVKQSGIGREYGKEGL 470 Query: 485 EKYTE 489 YTE Sbjct: 471 LAYTE 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: 537 Number of extensions: 31 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: 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