Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_073948994.1 RH94_RS20650 aldehyde dehydrogenase family protein
Query= BRENDA::C0P9J6 (505 letters) >NCBI__GCF_001906585.1:WP_073948994.1 Length = 462 Score = 336 bits (861), Expect = 1e-96 Identities = 202/482 (41%), Positives = 275/482 (57%), Gaps = 34/482 (7%) Query: 12 LFVDGEWRPPAQGRRLPVVNPTTEAHIGEIPAGTAEDVDAAVAAARAALKRNRGRDWARA 71 +++DG WRP A + VVNP E I +PAGTAEDVDAAV AARAAL WA Sbjct: 7 MYIDGAWRPAAGRDAIEVVNPADEQVIATVPAGTAEDVDAAVRAARAALP-----GWAAT 61 Query: 72 PGAVRAKYLRAIAAKVIERKPELAKLEALDCGKP--YDEA--AWDMDDVAGCFEYFADQA 127 P A RA L A+ ++ RK E+A+ + G P + +A A VAG + A Sbjct: 62 PPAERAARLTALRDVLVARKDEIAETVTAELGSPLAFSQAVHAGVPIAVAGSYADLAATY 121 Query: 128 EALDKRQNSPVSLPMETFKCHLRREPIGVVGLITPWNYPLLMATWKIAPALAAGCTAVLK 187 +K NS V EP+GVVG ITPWNYPL K APALAAGCT VLK Sbjct: 122 AFEEKVGNSTV-----------HHEPVGVVGAITPWNYPLHQIVAKAAPALAAGCTIVLK 170 Query: 188 PSELASVTCLELADICKEVGLPSGVLNIVTGLGPDAGAPLSAHPDVDKVAFTGSFETGKK 247 P+E +T A+ E G+P+GVLN+VTGLGP AG L+ HPDVD V+FTGS G++ Sbjct: 171 PAEDTPLTAQLFAEAAHEAGIPAGVLNLVTGLGPVAGQALAEHPDVDLVSFTGSTAVGRR 230 Query: 248 IMASAAPMVKPVTLELGGKSPIVVFDDVDIDKAVEWTLFGCFWTNGQICSATSRLLIHTK 307 I A+A VK V LELGGKS V+ D+ +AV + +GQ CSA +R+L+H Sbjct: 231 IGATAGAAVKRVALELGGKSANVILPSADLARAVNVGVANVMSNSGQTCSAWTRMLVH-- 288 Query: 308 IAKKFNERMVAWAKNIKVSDPLEEGCRLGPVVSEGQYEKIKKFISNAKSQGATILTGGVR 367 +++E A + + + G R+GPVV+ Q +++ +I ++GA ++ GG Sbjct: 289 -RDQYDE-----AVELAATAAAKYGDRIGPVVNAKQRARVRGYIEKGIAEGARLVAGGPE 342 Query: 368 PAHLEKGFFIEPTIITDITTSMEIWREEVFGPVLCVKEFSTEDEAIELANDTQYGLAGAV 427 A EKG+F+ PT+ D+T M + +EE+FGPVL + + ED+A+ +AN T YGLAGAV Sbjct: 343 -APCEKGYFVSPTVFADVTPDMTVAQEEIFGPVLSILRYDDEDDALRIANGTVYGLAGAV 401 Query: 428 ISGDRERCQRLSEEIDAGCIWVNCSQ--PCFCQAPWGGNKRSGFGRELGEGGIDNYLSVK 485 + D + +D G + +N + P AP+GG K+SG GRELG G+ YL K Sbjct: 402 WAADETEAVAFARRMDTGQVDINGGRFNPL---APFGGYKQSGVGRELGAHGLTEYLQTK 458 Query: 486 QV 487 + Sbjct: 459 SL 460 Lambda K H 0.318 0.135 0.422 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: 617 Number of extensions: 24 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: 505 Length of database: 462 Length adjustment: 34 Effective length of query: 471 Effective length of database: 428 Effective search space: 201588 Effective search space used: 201588 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