Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_011428645.1 RHE_RS28190 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000092045.1:WP_011428645.1 Length = 487 Score = 332 bits (851), Expect = 2e-95 Identities = 193/476 (40%), Positives = 268/476 (56%), Gaps = 6/476 (1%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 FI G A + + P DG+ A D A ++AVE AR + W P + Sbjct: 17 FIGGRLVPAEA--VIDMHRPSDGKAYAGCPLADAALVDQAVETAREALDRSNWGGGRPRE 74 Query: 83 RKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDEV 142 R L R+ADL+ E LA LE L +P+G + DI A+ I + AE DK ++ Sbjct: 75 RTKALQRWADLIEAEAETLARLEALSSTRPVGHLVAGDIAVTAEQIRFFAEFADKEGGDL 134 Query: 143 APTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAIR 202 PT LG++ EP GVVGAI PWNFPL MA WKLGPALA GN+VVLKPSE +P + + Sbjct: 135 VPTDDANLGMIMTEPYGVVGAITPWNFPLSMAGWKLGPALAAGNAVVLKPSEMTPFSTLY 194 Query: 203 IAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESNMK 262 +A+L++ AG+PAG++NV+ G G G A+ H + + FTGST +M + +K Sbjct: 195 LAELSVRAGLPAGLVNVVLGDGPITGTAITGHPGISKVSFTGSTAAGAAIMTNIARTGVK 254 Query: 263 RIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFLPMV 322 + LE GGKSP +VFADA DL AA A A++I N G+ C GSRL+VE + D + + Sbjct: 255 PMTLELGGKSPQLVFADA-DLDLAAGAIAASILSNAGQACICGSRLIVEAKVADALVAAL 313 Query: 323 VEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEETGGTY 382 V L +PG + T ++ +Q+ + I A GA+ L GG R E G + Sbjct: 314 VARLAAVRPGPTWEETTDYSPVISERQIARMDGIIRAAIDGGAECLTGGGRLDRE--GYF 371 Query: 383 VEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSDISKAH 442 PT+ GVT EEIFGPVL++ F+ EEA+++A+ YGLAAG++T D+S+A Sbjct: 372 YAPTLISGVTATSPAVLEEIFGPVLTIQTFEDEEEALSLADHPSYGLAAGLFTRDLSRAI 431 Query: 443 KTARAVRAGSVWVNQYD-GGDMTAPFGGFKQSGNGRDKSLHALEKYTELKATWIKL 497 + R ++AG+VWVN+Y D P GG+KQSG G+D A + K+ I L Sbjct: 432 RLTRRLQAGTVWVNRYGRSRDHILPTGGYKQSGIGKDLGREAYHANRKSKSVLISL 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: 641 Number of extensions: 24 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: 487 Length adjustment: 34 Effective length of query: 463 Effective length of database: 453 Effective search space: 209739 Effective search space used: 209739 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