Align 2-ketoglutaric semialdehyde dehydrogenase (EC 1.2.1.26) (characterized)
to candidate AZOBR_RS29185 AZOBR_RS29185 aldehyde dehydrogenase
Query= reanno::pseudo1_N1B4:Pf1N1B4_1109 (481 letters) >FitnessBrowser__azobra:AZOBR_RS29185 Length = 478 Score = 501 bits (1291), Expect = e-146 Identities = 259/471 (54%), Positives = 327/471 (69%), Gaps = 4/471 (0%) Query: 9 NYINGEWVSGADYSANINPSELTDTIGDYAKADLAQVHAAIDAARAAFPAWSTSGIQARH 68 N+I G V G AN NP+ + IG YA A + Q A+ AA AA P W+ S Q R Sbjct: 6 NWIAGRLVDGVRMEANRNPARPGEVIGHYAWASVEQAEEALGAAHAALPGWAASNPQTRS 65 Query: 69 DSLDKVGTEILARREELGTLLAREEGKTLPEAIGEVTRAGNIFKFFAGECLRLSGDYLPS 128 D L +VG E+ AR EELG LL REEGKTL E IGEV R+ IF + AGE LR G+ LP Sbjct: 66 DVLRRVGDELNARAEELGALLTREEGKTLREGIGEVRRSAQIFHYAAGEPLRQGGEALPG 125 Query: 129 VRPGVNVEVTREALGVVGLITPWNFPIAIPAWKIAPALAYGNCVVLKPADLVPGCAWALA 188 +R G V+RE +GVV LITPWNFP+A+PAWK A ALA+GN VVLKP+++ P CAW LA Sbjct: 126 LRDGTTAMVSREPVGVVVLITPWNFPMAVPAWKTAYALAFGNTVVLKPSEVTPACAWELA 185 Query: 189 EIISRAGFPAGVFNLVMGSGRVVGDALVQSPKVDGISFTGSVGVGRQIAVSCVSRQAKVQ 248 +I+ RAG PAG FNLV+G GR +G ALV D +SFTGS GVGR I V+R +VQ Sbjct: 186 DILHRAGLPAGAFNLVVGDGRTLGPALVDG--ADAVSFTGSPGVGRAILERSVARMTRVQ 243 Query: 249 LEMGGKNPQIILDDADLKQAVELSVQSAFYSTGQRCTASSRFIVTAGIHDKFVEAMAERM 308 LE+GGKNP ++ DDADL+ AV++++Q AF+STGQRCTA+SR IV +HD FVE + R+ Sbjct: 244 LELGGKNPLVVHDDADLELAVDIALQGAFHSTGQRCTATSRIIVDRRVHDAFVERLVTRI 303 Query: 309 KSIKVGHALKTGTDIGPVVSQAQLEQDLKYIDIGQSEGARLVSGGGLVACDTEGYFLAPT 368 +++VG + TD+GPVVS+AQL +DL I +SEGA L GGG + D +GYFL PT Sbjct: 304 AALRVGDPMDAATDMGPVVSEAQLAKDLHCIADARSEGAELAFGGGRM--DGDGYFLEPT 361 Query: 369 LFADSTAAMRISREEIFGPVANIVRVADYEAALAMANDTEFGLSAGIATTSLKYANHFKR 428 LF + AMRI+R+E+FGPVA ++ + A+A+AND++ LS+GI T L A F+R Sbjct: 362 LFVGTDNAMRINRDEVFGPVACVIPADGLDHAIAIANDSDHALSSGIVTRGLASAETFRR 421 Query: 429 HSQAGMVMVNLPTAGVDYHVPFGGRKGSSYGSREQGRYAQEFYTVVKTSYI 479 S+AG+VMVN PTAG+DYHVPFGGR S YG REQG A EF+T KT+YI Sbjct: 422 RSRAGLVMVNAPTAGIDYHVPFGGRGPSGYGGREQGSAAVEFFTEGKTAYI 472 Lambda K H 0.318 0.134 0.391 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: 604 Number of extensions: 19 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: 481 Length of database: 478 Length adjustment: 34 Effective length of query: 447 Effective length of database: 444 Effective search space: 198468 Effective search space used: 198468 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: 51 (24.3 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