Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_034274777.1 AMYHA_RS23925 gamma-aminobutyraldehyde dehydrogenase
Query= metacyc::MONOMER-15203 (503 letters) >NCBI__GCF_000504245.1:WP_034274777.1 Length = 479 Score = 244 bits (623), Expect = 5e-69 Identities = 163/490 (33%), Positives = 245/490 (50%), Gaps = 27/490 (5%) Query: 3 IKRIEHYINGHKTNGVADSHQEVTNPATGQVTGQVALASQADVDSAVAAAQAAFP-AWSD 61 ++R++++ING + E+ +PATG V + L+S DVD+A AA AF W D Sbjct: 5 VRRLKNFINGAYVDAADGRTSEIVDPATGHVVAEAPLSSADDVDTAFRAAADAFENGWRD 64 Query: 62 TPPIRRARVMFKFLELLNAHKDELAEAITREHGKVFTDAQGE-VARGIDIVEFACGIPQL 120 P R + KF + + DEL A GK + E + + +D + F G + Sbjct: 65 ATPGERQIALNKFADAVEDRADELVAAEVANCGKPAQMTKDEEIFQVLDALRFFAGASRN 124 Query: 121 LKGDYTEQVSTGIDNWTTRQPLGVVAGITPFNFPVMVPMWMFPLAIAAGNSFVLKPSPLD 180 L+G + G +W R+P+G V ITP+N+P+ + W A+AAGNS VLKPS Sbjct: 125 LEGKAAGEYMAGHTSWVRREPIGPVGQITPWNYPMAMAAWKIGPALAAGNSVVLKPSDTT 184 Query: 181 PSASLMMADLLKQAGLPDGVFNVVQGDKDSVEALIDHPDVKALSFVGSTPIANLIYERGA 240 P ++L++A++ + LP GVFNVV GD+D+ AL+DHP + +S GST I E GA Sbjct: 185 PMSTLLLAEIAAEF-LPAGVFNVVTGDRDTGRALVDHPTPRLISLTGSTRAGKEIAEAGA 243 Query: 241 RSGKRIQALGGAKNHMVVMPDANLDKAVDALIGAAYGSAGERCMAISVAVLVGDVADKIV 300 + KR+ G K +VV DA+++ A + + GA Y +AG+ C A + + + D + Sbjct: 244 KDLKRLHLELGGKAPVVVFDDADIEAAAEGIAGAGYFNAGQDCTAATRVLAAPGIHDDLA 303 Query: 301 PRLAERARDLKIKNGLELDAEMGPIVTSQAHQRITGYIEKG-----VAEGAEMVVDGRDF 355 LAE+AR DA+ GP+ R++G+I++ + G E V D F Sbjct: 304 AALAEQARKTVTAGPDNADADYGPLNNPNQLARVSGFIDRAPDHAKILAGGERVGDTGYF 363 Query: 356 DSSVTGEGCADGFWMGGTLFDHVTPEMTIYREEIFGPVLACVRVPDVATAIQLINDHEFG 415 + G G D +T +E+FGPV+ R D TA+ N E+G Sbjct: 364 YAPTVVAGLRQG--------DELT------TDEVFGPVVTVQRFDDEDTAVNWANSVEYG 409 Query: 416 NGVSCFTESGSVAREFGRRIQVGMVGINVPIPVPMAWHGFGGWKRSMFG-DTHAYGEEGV 474 S +T + A RR+ G V IN IP+ +A GG+K S +G D AY E Sbjct: 410 LASSVWTRDHARALRVSRRLDFGCVWINTHIPL-IAEMPHGGFKHSGYGKDLSAYSFEE- 467 Query: 475 RFYTKQKSIM 484 YT+ K +M Sbjct: 468 --YTRVKHVM 475 Lambda K H 0.319 0.136 0.406 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: 600 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: 503 Length of database: 479 Length adjustment: 34 Effective length of query: 469 Effective length of database: 445 Effective search space: 208705 Effective search space used: 208705 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