Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_110805439.1 C8J30_RS08590 betaine-aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_003217355.1:WP_110805439.1 Length = 483 Score = 346 bits (888), Expect = e-100 Identities = 192/477 (40%), Positives = 283/477 (59%), Gaps = 8/477 (1%) Query: 19 EGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQL 78 E F+NG + + +G E + P G +A + A A+ A+A + W+ L Sbjct: 6 EASHFVNGNWVEDAAGAEIEVIFPGTGEVIAILHEATPAVIEEALAGAQAAQRA--WAAL 63 Query: 79 APAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKV 138 P +R L R ADL+R ELALLETLD GKPI ++S D P A ++ + A + Sbjct: 64 KPVERARILRRAADLIRARRAELALLETLDTGKPIQETSVADWPSGADSLEYFAGLAPTL 123 Query: 139 YDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPL 198 E P D REP+GV I WN+P +ACWK PAL+TGN+++ KPSE +PL Sbjct: 124 TGETIPLGGD-FAYTIREPLGVCVGIGAWNYPSQIACWKAAPALSTGNAMIFKPSEITPL 182 Query: 199 TAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGE 258 A+++A + +EAG+PAGV NV+ G G VG LA V + TGS ++ AG Sbjct: 183 GALQLAAIFVEAGMPAGVFNVVQGRG-AVGGRLATDSRVAKVSLTGSVPTGAKVYAAAG- 240 Query: 259 SNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKF 318 + MK + +E GGKSP IVF DA DL++A AA ++ G++C+ G+R+ V ++IK++F Sbjct: 241 AGMKHVTMELGGKSPLIVFEDA-DLESAIGAAMLGNFYSSGQICSNGTRVFVHKAIKERF 299 Query: 319 LPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEET 378 L + E K G+PLD T G LV Q VL YI +GA+L+ GG E Sbjct: 300 LTRLAERTAAIKAGDPLDETTQFGPLVSAAQHAKVLGYIATAKSEGARLVCGGAAGAE-- 357 Query: 379 GGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSDI 438 G +V+PT+F VT++M IA+EE+FGPV++V+ F+T +E +A AN T +GLAAG++T+D+ Sbjct: 358 GALFVQPTVFADVTDSMTIAREEVFGPVMAVLDFETEDEVIARANGTDFGLAAGVFTADL 417 Query: 439 SKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKATWI 495 ++ H+ ++AG+ W+N Y+ + PFG K SG GR+ S A+E YT++KA ++ Sbjct: 418 ARGHRVIAQLQAGTTWINAYNLTPVEMPFGAVKSSGVGRENSKAAIEHYTQVKAVYV 474 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: 627 Number of extensions: 30 Number of successful extensions: 5 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: 483 Length adjustment: 34 Effective length of query: 463 Effective length of database: 449 Effective search space: 207887 Effective search space used: 207887 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