Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_023434135.1 N177_RS19425 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P42412 (487 letters) >NCBI__GCF_000496075.1:WP_023434135.1 Length = 489 Score = 249 bits (635), Expect = 2e-70 Identities = 150/459 (32%), Positives = 241/459 (52%), Gaps = 8/459 (1%) Query: 2 AEIRKLKNYINGEWVESKTDQYEDVVNPATKEVLCQVPISTKEDIDYAAQTAAEAFKTWS 61 A + K + Y+NG WV V NPAT E L VP + A + A +AFK W+ Sbjct: 13 ASLLKSQCYVNGRWVGEGEIA---VTNPATGETLASVPRFGGAEAREAIEAAEKAFKPWA 69 Query: 62 KVAVPRRARILFNFQQLLSQHKEELAHLITIENGKNTKEALGEVGRGIENVEFAAGAPSL 121 K R++IL + +L+ ++KE+LA ++T E GK E+ GE+ VEF A Sbjct: 70 KKTAKERSKILRRWYELMMENKEDLAFIMTSEQGKPLTESRGEIDYAANFVEFFAEEAKR 129 Query: 122 MMGDSLASIATDVEAANYRYPIGVVGGIAPFNFPMMVPCWMFPMAIALGNTFILKPSERT 181 + GD++ S D + PIGV I P+NFP + A+A G T ++KP+ T Sbjct: 130 IYGDTIPSHKADARIVVGKQPIGVTCAITPWNFPAAMITRKAGPALAAGCTMVVKPATET 189 Query: 182 PLLTEKLVELFEKAGLPKGVFNVVYGAHDVVNG-ILEHPEIKAISFVGSKPVGEYVYKKG 240 PL L EL +AG+P+GVF+V+ G + + +P +K I+F GS VG+ + ++ Sbjct: 190 PLTALALAELAHRAGIPEGVFSVITGKSSEIGAEMTSNPIVKLITFTGSTEVGKKLMEQS 249 Query: 241 SENLKRVQSLTGAKNHTIVLNDANLEDTVTNIVGAAFGSAGERCMACAVVTVEEGIADEF 300 + +K+V G +V +DA+L+ V + + F + G+ C+ + V+ G+ + F Sbjct: 250 ASTVKKVALELGGNAPFLVFDDADLDAAVQGAIASKFRNMGQTCVCANRIYVQSGVYEAF 309 Query: 301 MAKLQEKVADIKIGNGLDDGVFLGPVIREDNKKRTLSYIEKGLEEGARLVCDGRENVSDD 360 KL E V +K+G+G + V GP+I ED K+ +I +GA++V G+ SD Sbjct: 310 AGKLAEAVKKLKVGDGAQEDVQQGPLINEDAVKKVEEHISDATSKGAKVVLGGKR--SDL 367 Query: 361 GY-FVGPTIFDNVTTEMTIWKDEIFAPVLSVIRVKNLKEAIEIANKSEFANGACLFTSNS 419 G+ F PT+ +VT EM + ++E F PV + R + +EAIE+AN ++F + ++ + Sbjct: 368 GHSFFQPTVLTDVTPEMVVTREETFGPVAPLFRFETEEEAIELANATQFGLASYFYSRDI 427 Query: 420 NAIRYFRENIDAGMLGINLGVPAPMAFFPFSGWKSSFFG 458 E ++ G++GIN G+ PF G K S G Sbjct: 428 GRCWRVAEALEYGIVGINEGL-ISTEVAPFGGVKESGIG 465 Lambda K H 0.318 0.136 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: 580 Number of extensions: 23 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: 487 Length of database: 489 Length adjustment: 34 Effective length of query: 453 Effective length of database: 455 Effective search space: 206115 Effective search space used: 206115 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 (21.7 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