Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_012468985.1 GLOV_RS04485 aldehyde dehydrogenase family protein
Query= BRENDA::P42412 (487 letters) >NCBI__GCF_000020385.1:WP_012468985.1 Length = 483 Score = 231 bits (589), Expect = 4e-65 Identities = 150/474 (31%), Positives = 236/474 (49%), Gaps = 13/474 (2%) Query: 10 YINGEWVESKTDQYEDVVNPATKEVLCQVPISTKEDIDYAAQTAAEAFKTWSKVAVPRRA 69 YING W +S + D NP T E+L V +++D A AA+AF W+ VA ++ Sbjct: 8 YINGTWQDSADGSWFDDFNPYTGEILTTVANGSQQDALLAVNAAADAFPDWAAVAPSQKR 67 Query: 70 RILFNFQQLLSQHKEELAHLITIENGKNTKEALGEVGRGIENVEFAAGAPSLMMGDSLAS 129 + LL + K+EL L+ E G A + G + A + G L S Sbjct: 68 LLFLKAADLLEKRKDELIDLLARETGAARPFAAYQAAAGPNYLREAGSQAHRVTGTILPS 127 Query: 130 IATDVEAANYRYPIGVVGGIAPFNFPMMVPCWMFPMAIALGNTFILKPSERTPLLTEKLV 189 T V R+P+GVV GI+P+N P+++ A+A GNT +LKPSE +P+ L+ Sbjct: 128 ETTKVSMV-MRHPVGVVAGISPWNCPVVLSLRAVCFAMAYGNTVVLKPSEESPVSGGILL 186 Query: 190 -ELFEKAGLPKGVFNVV---YGAHDVVNGI-LEHPEIKAISFVGSKPVGEYVYKKGSENL 244 ELFE+AG PKGVFN+V YG V + ++ +K ISF GS VG + +K +L Sbjct: 187 AELFEEAGFPKGVFNIVTHGYGRSSEVGDLFIQDRRVKRISFTGSTRVGRELAEKCGRHL 246 Query: 245 KRVQSLTGAKNHTIVLNDANLEDTVTNIVGAAFGSAGERCMACAVVTVEEGIADEFMAKL 304 KR+ G + IVLNDA+++ V + F G+ CM + +E+ +A EF A+ Sbjct: 247 KRIALELGGNDPLIVLNDADMDHAVNAAIFGRFLHQGQVCMNAKRLIIEKTVAQEFTARF 306 Query: 305 QEKVADIKIGNGLDDGVFLGPVIREDNKKRTLSYIEKGLEEGARLVCDGRENVSDDGYFV 364 + + +K+GN LD +GP+I + + + + EGA L+C G N G Sbjct: 307 VARTSALKVGNPLDAATVIGPLINHKQYETLEGQVNRAVAEGAELLCGGYGN----GLCY 362 Query: 365 GPTIFDNVTTEMTIWKDEIFAPVLSVIRVKNLKEAIEIANKSEFANGACLFTSNSNAIRY 424 PT+ NV +M+I+ +E F PV +I ++ +A+ +AN S + A + T+N Sbjct: 363 HPTVLGNVREDMSIFHEETFGPVAPIIVAEDADDALRLANSSAYGLSAGILTNNMQQGLA 422 Query: 425 FRENIDAGMLGINLGVPAPMAFFPFSGWKSSFFGTLHANGKDSVDFYTRKKVVT 478 I++G +N P G +S +G G +++ +T ++ VT Sbjct: 423 LARRIESGACHVNDSPLYGETHAPLGGVNNSGWGKF---GIEAMHEFTEQQWVT 473 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: 515 Number of extensions: 25 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: 487 Length of database: 483 Length adjustment: 34 Effective length of query: 453 Effective length of database: 449 Effective search space: 203397 Effective search space used: 203397 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 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