Align Alpha-ketoglutarate semialdehyde dehydrogenase; KGSADH; EC 1.2.1.26 (characterized)
to candidate WP_068105462.1 I601_RS01380 aldehyde dehydrogenase family protein
Query= SwissProt::D4GP41 (482 letters) >NCBI__GCF_001653335.1:WP_068105462.1 Length = 506 Score = 285 bits (730), Expect = 2e-81 Identities = 180/486 (37%), Positives = 246/486 (50%), Gaps = 18/486 (3%) Query: 8 YVNGEWVTSETGETTEVTNPANPSEVVAAYQHSNENDAAAAVDAAVAAEDE--WRNTPGP 65 Y++G W + G T ++ PA+ VV + E DA AAV AA +A D W +TP P Sbjct: 5 YIDGTWRDAADGATRDIHCPADGHHVVTVSE-GGEQDAVAAVVAARSAFDNGPWPHTPAP 63 Query: 66 ERGRILREAGTLLAQRKDELTEILTAEEGKARPEAAGEVQRAIDIFHYFSSKAADLGGTK 125 ER +L L KDE+ + + + GK E+ +V + +F +F+S A G Sbjct: 64 ERAALLHRLADRLEADKDEVARLESLDTGKRFVESQIDVDDIVSVFRHFASLAQGEAGRV 123 Query: 126 KGASGPNTNLYTRQEPVGVAALITPWNYPIAIPAWKLAPALAAGNTVVLKPASIAPGVVI 185 A P EP+GV LITPWNYP+ +WK+AP LAAGNT +LKP+ + P I Sbjct: 124 VDAGMPGVVSRVVHEPIGVCTLITPWNYPLLQTSWKVAPCLAAGNTFILKPSELTPSTAI 183 Query: 186 EIARALDEAGLPDGVLNVVTGPGSSVGSEFIGNEGTDLVSFTGSSQVGEMVYEQATDAGK 245 + AL +AGLPDGV N+V G G VG DLVSFTG G V A K Sbjct: 184 WLMGALSDAGLPDGVANLVLGAGDRVGPTLTEAPEVDLVSFTGGVVTGRRVMVAAAPTVK 243 Query: 246 RVQTELGGKNPTLVADSANPAEAADIVANGGFGTTGQSCTACSRAIVHEDVYDDFVAELV 305 +V ELGGKNP ++ A+ A D F +GQ C+A +R +V + V+D V ELV Sbjct: 244 KVALELGGKNPNVIFADADLDAAIDNALTAVFLDSGQVCSAGARLVVEDTVHDQVVDELV 303 Query: 306 DRAESLDVGP--GTDHEMGPQVSESELSSTLEYIDIAEAEGATLVAGGGVPEG----EAV 359 RA + +G D E GP +S + Y+ AEGATL GGG PEG + Sbjct: 304 RRAGRIRLGGPFDDDAETGPLISAAHRDKVEAYVAAGIAEGATLRVGGGRPEGAGYAAGL 363 Query: 360 ETGHFVEPTVFTDVDPDMRIAQEEVFGPVVAVIEVSDFD------EGLAVANDVDYGLSA 413 G + PT+ D DM QEE FGPV+ V + D +++AND YGL+ Sbjct: 364 AEGFYYLPTILDDCSADMSCVQEESFGPVLTVERFTGEDADAREEAAVSIANDTVYGLAG 423 Query: 414 SIVTDDHTEANRFVDEVEAGVVKVNDKTTGLELHVPFGGFKRSSSETWREQGDAGLDFYT 473 ++ T D A R + G + +ND + +GG+K+S T RE G AGL+ Y Sbjct: 424 AVWTSDAGRAERVASRLRHGTIWINDYHPYV-AQAEWGGYKQSG--TGRELGIAGLEEYR 480 Query: 474 IEKTVY 479 K ++ Sbjct: 481 ETKHIW 486 Lambda K H 0.310 0.130 0.370 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: 663 Number of extensions: 40 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: 482 Length of database: 506 Length adjustment: 34 Effective length of query: 448 Effective length of database: 472 Effective search space: 211456 Effective search space used: 211456 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (21.7 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