Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_009547631.1 CCE_RS15270 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000017845.1:WP_009547631.1 Length = 490 Score = 458 bits (1178), Expect = e-133 Identities = 239/497 (48%), Positives = 317/497 (63%), Gaps = 7/497 (1%) Query: 1 MTTLTRADWEQRAQQLKIEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADAN 60 M T TR + + + ++ IN E+ ++ SG+ FE ++P G + VA D D + Sbjct: 1 MVTATRPESKAKIGPTQL----LINNEWIESASGKRFETINPTTGEVICDVAEADATDVD 56 Query: 61 RAVENARATFNSGVWSQLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSID 120 +AV+ AR FN G W L+ ++R L + ADL+ N+EELA LETLD GKP DS + D Sbjct: 57 KAVKAARNAFNQGDWPNLSASQRGQLLYKLADLIEANIEELARLETLDNGKPYQDSLNAD 116 Query: 121 IPGAAQAIHWTAEAIDKVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGP 180 + + A DK+ + P EPVGVVG I+PWNFPLLM WKL P Sbjct: 117 LQLVIACYRYYAGWADKIQGKTIPINGPYFCYTRHEPVGVVGQIIPWNFPLLMQAWKLAP 176 Query: 181 ALATGNSVVLKPSEKSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTL 240 ALA GN+VV+K +E++PL+A R+ +L IEAG P GV+N+L GYG T G+A+A H D+D + Sbjct: 177 ALAAGNTVVMKTAEQTPLSAFRVGELIIEAGFPPGVVNLLSGYGPTAGQAIARHHDIDKV 236 Query: 241 VFTGSTKIAKQLMVYAGESNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGE 300 FTGST++ +M A ++N+KR+ LE GGKSPNIVFADA +L A E A + FNQG+ Sbjct: 237 AFTGSTEVGHLIMEAAAQTNLKRVTLELGGKSPNIVFADA-NLDQAIEGAHFGLFFNQGQ 295 Query: 301 VCTAGSRLLVERSIKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAG 360 C AGSRL VE D+F+ VE K G+P D TT G VD Q + V+ YIE+G Sbjct: 296 CCCAGSRLFVEEKCYDEFVAKSVERAKQRIVGDPFDDHTTQGPQVDKTQFDKVMEYIESG 355 Query: 361 HKDGAKLLAGGKRTLEETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVA 420 ++GAKLL GG R + G ++EPT+F V + M+IAQEEIFGPV+S+I F +E + Sbjct: 356 QREGAKLLCGGGRVGDR--GYFIEPTVFADVQDDMKIAQEEIFGPVMSIIKFKDMDEVIQ 413 Query: 421 IANDTPYGLAAGIWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKS 480 ANDT YGLAA +WT DISK H A A+RAG+VWVN YD D APFGGFKQSG GR+ Sbjct: 414 RANDTMYGLAAAVWTQDISKGHAIANALRAGTVWVNCYDVFDAAAPFGGFKQSGMGRELG 473 Query: 481 LHALEKYTELKATWIKL 497 + L++YTE+K +KL Sbjct: 474 EYGLQQYTEIKTVTVKL 490 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: 626 Number of extensions: 16 Number of successful extensions: 3 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: 490 Length adjustment: 34 Effective length of query: 463 Effective length of database: 456 Effective search space: 211128 Effective search space used: 211128 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