Align Methylmalonate-semialdehyde dehydrogenase (EC 1.2.1.27) (characterized)
to candidate WP_015933116.1 MNOD_RS32090 aldehyde dehydrogenase
Query= reanno::pseudo3_N2E3:AO353_05990 (507 letters) >NCBI__GCF_000022085.1:WP_015933116.1 Length = 495 Score = 241 bits (615), Expect = 4e-68 Identities = 163/482 (33%), Positives = 245/482 (50%), Gaps = 23/482 (4%) Query: 17 LIDGQWVESQTTEWHDIVNPATQQVLAKVPFATPAEVDAAISAAHRAFQT--WKLTPIGA 74 ++DG+ S T W NP T + A+VP P + +AAI+AAHRAF W A Sbjct: 10 VVDGRSCASTTGRWLSSTNPYTGEDWAEVPACGPDDAEAAIAAAHRAFTQGPWASMTPTA 69 Query: 75 RMRIMLKLQALIREHSKRIAVVLSAEQGKTIADAEGDIFRGLEVVEHACSIGSLQMGEFA 134 R +++ +L LI ++R+A + + GK A+ G + + E G L A Sbjct: 70 RGKLLRRLGDLIARDAERLAAIEVRDNGKLFAEMAGQL---RYIPEWFWYFGGL-----A 121 Query: 135 ENVAGGVD--------TYTLRQPIGVCAGITPFNFPAMIPLWMFPMAIACGNTFVLKPSE 186 + + GGV TYT R+P+GV ITP+N P M+ W A+A GNT V+KPSE Sbjct: 122 DKIEGGVVPCDKPDLFTYTKREPLGVVVAITPWNSPLMLLTWKLAPALAAGNTVVVKPSE 181 Query: 187 QDPMSTMLLVELAIEAGIPAGVLNVVHG-GKDVVDALCTHKDIKAVSFVGSTAVGTHVYD 245 ST+ L+EL EAG P GV+N V G G +V L H + V+F G A G VY Sbjct: 182 FTSCSTLALMELVREAGFPDGVINTVTGYGAEVGPTLVGHPLVAKVAFTGGDATGAAVYA 241 Query: 246 LAGKHGKRVQSMMGAKNHAVVLPDANREQALNALVGAGFGAAGQRCMATS-VVVLVGAAK 304 A K K V +G K+ +V DA + A+ + F A+GQ C+A S ++V + Sbjct: 242 GAAKGIKHVTLELGGKSPNIVFADAKLDDAVKGAISGIFAASGQTCIAGSRLLVQRSVCE 301 Query: 305 QWLPDLKALAQKLKVNAGSEPGTDVGPVISKRAKARILDLIESGIKEGAKLELDGRDITV 364 + + A A K ++ E T VGP+ ++ + ++LD I+ +EGA+ L G + Sbjct: 302 EVSRRVVAFAAKARLGDPMERTTQVGPITTEPQRRKVLDYIDIARQEGARCLLGGGTPSA 361 Query: 365 PGYEKGNFVGPTLFSGVTTDMQIYTQEIFGPVLVVLEVDTLDQAIALVNANPFGNGTGLF 424 P +G FV PT+F VT M+I +E+FGPVL ++ D ++A+ + N +P+G G++ Sbjct: 362 PELARGWFVEPTIFGEVTNAMRIACEEVFGPVLSIIPFDDDEEAVTIANDSPYGLAAGVW 421 Query: 425 TQSGAAARKFQNEIDVGQVGINIPIPVPVPFFSFTGSRGSKLGDLGPYGKQVVQFYTQTK 484 T A + + + G V +N V V F G + S +G G + Y QTK Sbjct: 422 TTDMRRAIRMSDRLRAGTVWVNTYRAVSV-LMPFGGYKRSGIG--RENGLSAIDEYLQTK 478 Query: 485 TV 486 +V Sbjct: 479 SV 480 Lambda K H 0.319 0.135 0.396 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: 603 Number of extensions: 27 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: 507 Length of database: 495 Length adjustment: 34 Effective length of query: 473 Effective length of database: 461 Effective search space: 218053 Effective search space used: 218053 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 (21.7 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