Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_068110307.1 I601_RS12775 gamma-aminobutyraldehyde dehydrogenase
Query= reanno::WCS417:GFF2142 (499 letters) >NCBI__GCF_001653335.1:WP_068110307.1 Length = 479 Score = 220 bits (560), Expect = 1e-61 Identities = 158/484 (32%), Positives = 251/484 (51%), Gaps = 20/484 (4%) Query: 3 TTIEHYINDQRV-SRDDRYQDVFNPATGEKTGRVALASRQTVSEAVAAAQAAFAGWA-DT 60 TT ++ IN + V S DV +P TGE + + + V A AAA AAF GW + Sbjct: 4 TTFQNVINGRLVDSASGATYDVIDPTTGEVYAQAPASGAEDVDRAYAAADAAFEGWGWGS 63 Query: 61 PPIRRARVLFEYLHLLRERKDDLARIIVAEHGKVF--TDAQGEVDRGIDILEFACGIPNL 118 P RAR L + +R +++ + + GK T A+ E+ D F G L Sbjct: 64 TPQDRARALLRIADAIEDRVEEINAVECRDTGKPLGLTMAE-EMPYASDHFRFFAGAARL 122 Query: 119 LKGEHSDQVSRGMDNWTMRQPLGVVAGVTPFNFPVMVPMWMYPIAIAAGNTFILKPSPTD 178 L+G + + +W R+P+GVV VTP+N+P+++ +W A+AAGNT +LKPS T Sbjct: 123 LEGRSAGEYMAEHTSWVRREPIGVVGQVTPWNYPLLMMIWKIAPALAAGNTVVLKPSDTT 182 Query: 179 PSASLFMAELLREAGLPKGVFNVVQGDKESVDALIEHPDVKAVSFVGSTPIAQYIYETGA 238 P++S +A++ +E LP GV NVV GD+++ AL+ HP + V+ GS + T A Sbjct: 183 PASSTLLAQICQEF-LPPGVLNVVCGDRDTGRALVAHPTPQMVAITGSVRAGMEVAGTAA 241 Query: 239 RNGKRVQGLGGAKNHMVVMPDADIEKTVDALMGAAYGSAGERCMAISVAVLVGDVGDKVI 298 + K+V G K ++V DADI K + + GA +AG+ C A + ++ V D+ + Sbjct: 242 ADVKKVHLELGGKAPVIVFDDADIAKAAEGIAGAGLFNAGQDCTAATRVLVAPGVHDEFV 301 Query: 299 AALTERAKHLRITDGRDLK-AEMGPIVSRAALERISGYIEQGVQAGAQLLLDGRDYVPTE 357 AAL E A+ + T D++ GP+ + LE +SG +++ + A++ G T Sbjct: 302 AALAEAARGMP-TGRPDVEGVYYGPLNNAHQLEHVSGMVDR-LPDHARIDTGG-----TR 354 Query: 358 PGLENGFWLGATLFDHVTEEMSIYREEIFGPVLACVRVNDFAEAIKLVNAHEFGNGVSCF 417 G G++ T+ + ++ + EIFGPV+ R D AEA++ N ++G S + Sbjct: 355 QG-SAGYFYEPTVLSGLRQDDEQVQTEIFGPVMTVQRFTDEAEALRWANDVQYGLASSVW 413 Query: 418 TRDGNIAREFARRIEVGMVGINVPISVPMAWHGFGGWKKSLFG-DMHAYGTEGVRFYTKQ 476 T D A +RR++ G V IN I ++ GG+K S +G D+ YG E YT+ Sbjct: 414 TSDHARAMRVSRRLDFGAVWINTHIPF-VSEMPHGGFKHSGYGKDLSMYGLED---YTRI 469 Query: 477 KSIM 480 K +M Sbjct: 470 KHVM 473 Lambda K H 0.320 0.136 0.407 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: 578 Number of extensions: 21 Number of successful extensions: 3 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: 499 Length of database: 479 Length adjustment: 34 Effective length of query: 465 Effective length of database: 445 Effective search space: 206925 Effective search space used: 206925 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 (21.8 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