Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_245638142.1 HTA01S_RS19005 aldehyde dehydrogenase family protein
Query= BRENDA::Q8BH00 (487 letters) >NCBI__GCF_001592305.1:WP_245638142.1 Length = 487 Score = 340 bits (873), Expect = 5e-98 Identities = 195/488 (39%), Positives = 277/488 (56%), Gaps = 13/488 (2%) Query: 5 RELLMLENFIGGKFLPCNS--YIDSYDPSTGEVYCKVPNSGKEEIEAAVEAAREAFPA-- 60 + ++ L NFI G++ S + P+TG + V S ++++ AV AAR+A Sbjct: 4 KTVVTLHNFINGQYQGARSGATFEKLAPATGGLCATVSTSDADDVDTAVAAARQALRQGP 63 Query: 61 WSSRSPQERSLVLNRLADVLEQSLEELAQAESKDQGKTLTLARTMDIPRSVLNFRFFAS- 119 W++ QER L+RLAD+LE + +++QG+ MD+P SV R+FA Sbjct: 64 WATMPGQERGRCLSRLADLLEANAPAFVATLAEEQGRPAFDMTVMDLPMSVDTLRYFAGW 123 Query: 120 SNLHHVSECTQMSHLG--CMHYTVRTPVGIAGLISPWNLPLYLLTWKIAPAIAAGNTVIA 177 ++ +G +HYT PVG+A LI PWN PL + WK+APA+AAG TV+ Sbjct: 124 ADKLEGRTVPTAGFMGRQMLHYTRLEPVGVAALIVPWNAPLMIAVWKLAPALAAGCTVVI 183 Query: 178 KPSEMTSVTAWMFCKLLDKAGVPPGVINIVFGTGPRVGEALVSHPEVPLISFTGSQPTAE 237 K SE V +L+ +AG PPGV+NIV G G G AL +HP+V ISFTGS Sbjct: 184 KTSEDAPVAVGQLGRLVAEAGFPPGVVNIVHGMGAEAGAALTAHPDVSKISFTGSTGVGR 243 Query: 238 RITQLSAPHCKKLSLELGGKNPAIIFEDANLEECIPATVRSSFANQGEICLCTSRIFVQR 297 I + +A K+++LELGGK I+ +DANL+E IP F NQG+ C SRI V R Sbjct: 244 IIAREAAASFKRVTLELGGKAAQILLQDANLDEAIPGVAMGLFVNQGQTCAAGSRILVHR 303 Query: 298 SIYSEFLKRFVEATRKWKVGVPSDPSANMGALISKAHLEKVRSYVLKAQTEGARILCGEG 357 S+ + + A ++G A MGALIS H E+V++ + A ++GAR L G G Sbjct: 304 SLLPQVEQALAAAAESVRLGGAQVEGAQMGALISARHRERVQACIDTAISQGARRLSGAG 363 Query: 358 VDQLSLPLRNQAGYFMLPTVITDIKDESRCMTEEIFGPVTCVVPFDSEEEVITRANSVRY 417 + LP G+FM PTV TD+ + EE+FGPV ++PFD+E E I AN RY Sbjct: 364 GE---LPAE---GFFMRPTVFTDVTPGMQIAQEEVFGPVGAIIPFDTEAEAIALANDSRY 417 Query: 418 GLAATVWSKDVGRIHRVAKKLQSGLVWTNCWLIRELNLPFGGMKSSGIGREGAKDSYDFF 477 GL+A+VW++DV HRVA +L+ G V NCW + LP+GG K SGIGR+ ++ + D + Sbjct: 418 GLSASVWTRDVSAAHRVAAQLEVGAVAINCWSPLDARLPWGGTKDSGIGRDLSRKALDAY 477 Query: 478 TEIKTITI 485 E K I++ Sbjct: 478 LEEKVISL 485 Lambda K H 0.319 0.134 0.404 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: 519 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: 487 Length of database: 487 Length adjustment: 34 Effective length of query: 453 Effective length of database: 453 Effective search space: 205209 Effective search space used: 205209 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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