Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_017549143.1 C792_RS0108995 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000330705.1:WP_017549143.1 Length = 501 Score = 348 bits (892), Expect = e-100 Identities = 197/473 (41%), Positives = 283/473 (59%), Gaps = 7/473 (1%) Query: 23 FINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAK 82 FINGE ++ G T + ++P G +AKVA DA RAV AR F + W ++ PA Sbjct: 18 FINGEKVESSDGGTNDIINPATGEVIAKVAMATGEDAERAVMAARDAFENSKW-KIYPAS 76 Query: 83 RKAKLI-RFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDE 141 ++AK++ R A ++R+ +EL LE L+ GK I ++ I A + + A A+ + Sbjct: 77 KRAKILNRIASIMRERFKELVELEVLNSGKSINAATG-QINQAVEDFEYYAGAVCNHGGQ 135 Query: 142 VAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSPLTAI 201 P +EPVGV IVPWN+PL+MA WK+ PALA G +VVLKP+ +PLTA+ Sbjct: 136 TNDVPGQFHNYTEKEPVGVCAQIVPWNYPLMMAAWKVAPALAAGCTVVLKPASLTPLTAL 195 Query: 202 RIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAGESNM 261 + ++ EAG+P GV+N+LPG G VG L H +VD + FTGST K +M A + + Sbjct: 196 ILGEICQEAGVPDGVINILPGSGSRVGDYLVEHPEVDKVAFTGSTDTGKDIMSKASRT-L 254 Query: 262 KRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDKFLPM 321 KR+ LE GGKSP ++F DA +L+ A ++ I N G+ C A SR+ VE I DKF+ Sbjct: 255 KRLTLELGGKSPALIFGDA-ELENAVASSVYGIYNNTGQSCDARSRIYVEDRIYDKFVEQ 313 Query: 322 VVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEE--TG 379 VE K K G+P+ +T +G+L+D Q+ +V +YIE ++GA + GG R E G Sbjct: 314 FVEKTKQMKMGDPMSKETHMGSLIDKSQLESVEAYIETARQEGATIAYGGNRLSIEGYEG 373 Query: 380 GTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSDIS 439 G ++EPTI VT M + ++EIFGPV+ + F +EAV++AN+T YGLA+ I+T D Sbjct: 374 GFWLEPTIITDVTEDMTVVRDEIFGPVVVISRFSDEKEAVSLANNTIYGLASSIYTEDTR 433 Query: 440 KAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKA 492 KA + A +RAG V +N PFGG+KQSG GR+ S L+ Y+E K+ Sbjct: 434 KAKRVADKIRAGIVMINCPFSAFPGTPFGGYKQSGFGRELSAETLDLYSETKS 486 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: 607 Number of extensions: 26 Number of successful extensions: 6 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: 501 Length adjustment: 34 Effective length of query: 463 Effective length of database: 467 Effective search space: 216221 Effective search space used: 216221 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