Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_011319687.1 AVA_RS14900 L-glutamate gamma-semialdehyde dehydrogenase
Query= BRENDA::P42412 (487 letters) >NCBI__GCF_000204075.1:WP_011319687.1 Length = 993 Score = 246 bits (629), Expect = 2e-69 Identities = 172/480 (35%), Positives = 249/480 (51%), Gaps = 22/480 (4%) Query: 11 INGEWVESKTDQYEDVVNPAT-KEVLCQVPISTKEDIDYAAQTAAEAFKTWSKVAVPRRA 69 INGE+V+ T + D VNP+ EV+ +V + + E + A Q A AF W + V RA Sbjct: 509 INGEYVQ--TAEVIDSVNPSNFGEVIGKVGLISVEQAEQAMQAAKAAFPGWRRTPVKERA 566 Query: 70 RILFNFQQLLSQHKEELAHLITIENGKNTKEALGEVGRGIENVEFAAGAPSLMMGDSLAS 129 IL LL + + EL+ I +E GK KEA EV I+ + A M Sbjct: 567 AILRRAGDLLEERRAELSAWIVLEVGKPVKEADAEVSEAIDFCRYYADE----MERLYQG 622 Query: 130 IATDVEAANYRY---PIGVVGGIAPFNFPMMVPCWMFPMAIALGNTFILKPSERTPLLTE 186 I DV RY P G+V I+P+NFP+ + C M A+ GN +LKP+E + ++T Sbjct: 623 INYDVAGETNRYIYQPRGIVVVISPWNFPLAIACGMTVAALVTGNCTLLKPAETSSVITA 682 Query: 187 KLVELFEKAGLPKGVFNVVYGAHDVVNGIL-EHPEIKAISFVGSKPVGEYVY------KK 239 KL E+ +AG+PKGVF V G V L HP+ I+F GS+ VG +Y K Sbjct: 683 KLTEILLEAGIPKGVFQYVPGKGSQVGAYLVSHPDTHLIAFTGSQEVGCRIYAEAATLKP 742 Query: 240 GSENLKRVQSLTGAKNHTIVLNDANLEDTVTNIVGAAFGSAGERCMACAVVTVEEGIADE 299 ++KRV + G KN IV A+L+ V +V +AFG +G++C AC+ V V E I D Sbjct: 743 QQRHMKRVIAEMGGKNAIIVDESADLDQAVIGVVQSAFGYSGQKCSACSRVIVVEAIYDA 802 Query: 300 FMAKLQEKVADIKIGNGLDDGVFLGPVIREDNKKRTLSYIEKGLEEGARLVCDGRENVSD 359 F+ +L E + IG +GPVI + + R YIEKG E + + + Sbjct: 803 FIHRLVEATKSLNIGEAELPSTQVGPVIDANARDRIREYIEKGKAESQVAL---ELSAPN 859 Query: 360 DGYFVGPTIFDNVTTEMTIWKDEIFAPVLSVIRVKNLKEAIEIANKSEFANGACLFTSNS 419 GYFVGP IF V TI + EIF PVL+VI+ K+ +A+ IAN +++A L++ Sbjct: 860 HGYFVGPVIFGEVPPHGTIAQQEIFGPVLAVIKAKDFAQALAIANDTDYALTGGLYSRTP 919 Query: 420 NAIRYFRENIDAGMLGINLGVP-APMAFFPFSGWKSSFFGTLHANGKDSVDFYTRKKVVT 478 + I+ +E + G L IN + A +A PF G+K S G+ A G D + + + +T Sbjct: 920 SHIQQAQEEFEVGNLYINRNITGAIVARQPFGGFKLSGVGS-KAGGPDYLLQFLEPRTIT 978 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: 907 Number of extensions: 42 Number of successful extensions: 6 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: 993 Length adjustment: 39 Effective length of query: 448 Effective length of database: 954 Effective search space: 427392 Effective search space used: 427392 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: 54 (25.4 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