Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_022669887.1 G415_RS0101870 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000420385.1:WP_022669887.1 Length = 474 Score = 260 bits (665), Expect = 6e-74 Identities = 161/485 (33%), Positives = 258/485 (53%), Gaps = 20/485 (4%) Query: 19 EGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQL 78 E + +I GE+ + +T + + G +AKV D ++AV+ A F + ++ Sbjct: 3 EFKTYIGGEWVS--TNKTIDVIDKYSGEVIAKVPKADKKLVDKAVDAAAEAFEE--FKKM 58 Query: 79 APAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKV 138 +R L + ADL+++ +E+A + GK S ++ + + +E ++ Sbjct: 59 PAYQRSEILEKAADLIKERSDEIAETICREAGKAWKYSVG-EVNRGFETFKFASEEAKRI 117 Query: 139 YDEVAPTPHD-----QLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPS 193 + E P ++G R P+GV+GAI P+NFPL + K+ PA+A+GN++VLKP+ Sbjct: 118 HGETVPMDASAGGVGRVGYYIRVPMGVLGAITPFNFPLNLVAHKVAPAIASGNTIVLKPA 177 Query: 194 EKSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLM 253 +P+TA+ +A++ EAG+P GV NV+ G G VG++L + V + FTGS K+ +L Sbjct: 178 SSTPITALILAEILEEAGLPKGVFNVVIGPGGEVGESLVTNDKVRKITFTGSAKVGHRLT 237 Query: 254 VYAGESNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERS 313 AG +KRI LE G S I+ DA +A SA A N G+VC + R+ V + Sbjct: 238 QIAG---IKRITLELGNNSATIIEKDADIDKAIPRCVDSAFA-NSGQVCISLQRIYVHKD 293 Query: 314 IKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKR 373 I D+F EA K K GNP++ T +G ++D + +I+ GA+L+ GGKR Sbjct: 294 IADEFTEKFAEATKKLKVGNPVEKDTDLGPMIDENEAKRAEEWIKEAVNMGAELVVGGKR 353 Query: 374 TLEETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGI 433 G ++PT+ T MR+ E+F P++S++ +DT E+A+ ND+ YGL AGI Sbjct: 354 E-----GRVLQPTVLRNTTKDMRVMCMEVFAPIVSIVEYDTFEDAIQHVNDSDYGLQAGI 408 Query: 434 WTSDISKAHKTARAVRAGSVWVNQYDGGDMT-APFGGFKQSGNGRDKSLHALEKYTELKA 492 +T+DI K H + G V +N + P+GG K SG GR+ A+E+ T +K Sbjct: 409 YTNDIRKIHYAIDNLDVGGVMINDTSIFRVDHMPYGGNKMSGIGREGVRFAIEEMTNIKM 468 Query: 493 TWIKL 497 I L Sbjct: 469 VMINL 473 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: 584 Number of extensions: 32 Number of successful extensions: 4 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: 474 Length adjustment: 34 Effective length of query: 463 Effective length of database: 440 Effective search space: 203720 Effective search space used: 203720 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