Align 4-trimethylammoniobutyraldehyde dehydrogenase (EC 1.2.1.47) (characterized)
to candidate WP_085640679.1 MGEO_RS17260 betaine-aldehyde dehydrogenase
Query= BRENDA::P49189 (494 letters) >NCBI__GCF_002115805.1:WP_085640679.1 Length = 485 Score = 479 bits (1232), Expect = e-139 Identities = 251/480 (52%), Positives = 326/480 (67%), Gaps = 11/480 (2%) Query: 17 GARVEPADASGTE-KAFEPATGRVIATFTCSGEKEVNLAVQNAKAAFKIWSQKSGMERCR 75 GA VE D +GT PATG IAT + V+ A+ A A K W+ SG ER R Sbjct: 15 GAYVE--DTTGTPIPVIYPATGEQIATVYAATPAIVDKALAAAHRAQKAWAAMSGTERGR 72 Query: 76 ILLEAARIIREREDEIATMECINNGKSIFEA-RLDIDISWQCLEYYAGLAASMAGEHIQL 134 IL AA ++RER +++ +E + GK E +D LEY+ GLA S+ GEHIQL Sbjct: 73 ILRRAADMMRERNHDLSVLETYDTGKPYQETIAVDATSGADALEYFGGLAGSLTGEHIQL 132 Query: 135 PGGSFGYTRREPLGVCVGIGAWNYPFQIASWKSAPALACGNAMVFKPSPFTPVSALLLAE 194 G + YTRREPLGVCVGIGAWNYP QIA WK APALACGNAMVFKPS TP+ AL +AE Sbjct: 133 -GEDWVYTRREPLGVCVGIGAWNYPTQIACWKGAPALACGNAMVFKPSETTPLCALKVAE 191 Query: 195 IYSEAGVPPGLFNVVQGGAATGQFLCQHPDVAKVSFTGSVPTGMKIMEMSAKGIKPVTLE 254 I EAG+P G++NVVQG G L P VAKVS TGSVPTG K+ +A+ +K VT+E Sbjct: 192 ILHEAGLPAGIYNVVQGLGEVGASLVTDPRVAKVSLTGSVPTGKKVYAAAAEQMKHVTME 251 Query: 255 LGGKSPLIIFSDCDMNNAVKGALMANFLTQGQVCCNGTRVFVQKEILDKFTEEVVKQTQR 314 LGGKSPL+IF D D+ NAV GA++ NF + GQVC NGTRVFVQK I + F + + ++ Sbjct: 252 LGGKSPLLIFDDADLENAVGGAILGNFYSSGQVCSNGTRVFVQKGIKEAFLKRLTERLST 311 Query: 315 IKIGDPLLEDTRMGPLINRPHLERVLGFVKVAKEQGAKVLCGGDIYVPEDPKLKDGYYMR 374 +GDPL E T GP+++ ++ VL +++ + +GA+++ GG +DG+Y++ Sbjct: 312 AVVGDPLDEATNFGPMVSEKQMKIVLDYIEKGENEGARLVAGG------RRLNRDGFYLQ 365 Query: 375 PCVLTNCRDDMTCVKEEIFGPVMSILSFDTEAEVLERANDTTFGLAAGVFTRDIQRAHRV 434 P V + +DDM +EEIFGPVM++L F+TE E + RAN T FGL+AGVFTRD+ RAHRV Sbjct: 366 PTVFADVKDDMIIAREEIFGPVMAVLDFETEEEAITRANSTEFGLSAGVFTRDLSRAHRV 425 Query: 435 VAELQAGTCFINNYNVSPVELPFGGYKKSGFGRENGRVTIEYYSQLKTVCVEMGDVESAF 494 +A+L+AG+CFIN+YN +PVE PFGG K SG GREN + I +YS++K+V V MGDVE+ F Sbjct: 426 IAQLEAGSCFINSYNDAPVEAPFGGTKMSGVGRENSKAAINHYSEMKSVYVRMGDVEAPF 485 Lambda K H 0.320 0.137 0.411 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: 668 Number of extensions: 30 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: 494 Length of database: 485 Length adjustment: 34 Effective length of query: 460 Effective length of database: 451 Effective search space: 207460 Effective search space used: 207460 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 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