Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_017359492.1 BA79_RS13175 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000691145.1:WP_017359492.1 Length = 494 Score = 409 bits (1051), Expect = e-118 Identities = 214/477 (44%), Positives = 300/477 (62%), Gaps = 5/477 (1%) Query: 21 RAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAP 80 + +ING++ + +TF +P G L V AD + AV+ A+ F+ G W ++ Sbjct: 21 KLYINGQFVTSHDNKTFSTPNPATGETLIDVYEAGAADIDEAVKAAKKAFH-GPWRSMSA 79 Query: 81 AKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYD 140 A+R + + ADL+ ++ EELA LETLD GKPI ++++ DIP A + + + A K+ Sbjct: 80 AERARLMFKLADLMEEHQEELAQLETLDNGKPINETTNADIPLAIEHMRYYAGWTTKMTG 139 Query: 141 EVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTA 200 + P EPVGVVG I+PWNFPLLMA WK+G ALATG ++VLKP+E++PL+A Sbjct: 140 QTLPVSQGYFNYTRHEPVGVVGQIIPWNFPLLMAMWKMGAALATGCTIVLKPAEQTPLSA 199 Query: 201 IRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESN 260 + +A+L +AG P GV+N++PG+G T G+AL H DV+ L FTGST + K +M A +S Sbjct: 200 LYLAELVDKAGFPEGVINIVPGFGETAGEALTDHPDVNKLAFTGSTSVGKLIMEKAAKS- 258 Query: 261 MKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFLP 320 +KR+ LE GGKSPNI+ DA DL+ A A + + FNQG+VC AGSR+ V RS D+ + Sbjct: 259 IKRVTLELGGKSPNIILPDA-DLKKAIPGALNGVMFNQGQVCCAGSRVFVHRSQYDEVVD 317 Query: 321 MVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEETGG 380 + + K G L T +G LV +Q VL YIE G +GA + GG E G Sbjct: 318 QMAKYATSLKQGAGLHHDTQIGPLVSKEQHERVLGYIEKGKSEGATAVVGGDCPYE--AG 375 Query: 381 TYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSDISK 440 +V PT+F V + M IA+EEIFGPVLS I +D+ +E V AN + YGLAAG+WT ++ Sbjct: 376 YFVSPTVFRDVEDEMTIAKEEIFGPVLSAIPYDSIDEVVERANQSDYGLAAGLWTENLKH 435 Query: 441 AHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKATWIKL 497 AH A + AG++WVN Y+ D +PFGG+KQSG GR+ +AL YTE+K+ WI L Sbjct: 436 AHDIAARLEAGTIWVNCYNVFDAASPFGGYKQSGLGREMGSYALNNYTEVKSVWINL 492 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: 650 Number of extensions: 19 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: 494 Length adjustment: 34 Effective length of query: 463 Effective length of database: 460 Effective search space: 212980 Effective search space used: 212980 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