Align lactaldehyde dehydrogenase (EC 1.2.1.22); 2,5-dioxovalerate dehydrogenase (EC 1.2.1.26) (characterized)
to candidate Pf1N1B4_1109 2-ketoglutaric semialdehyde dehydrogenase (EC 1.2.1.26)
Query= BRENDA::Q97UA1 (478 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_1109 Length = 481 Score = 353 bits (905), Expect = e-102 Identities = 194/476 (40%), Positives = 279/476 (58%), Gaps = 10/476 (2%) Query: 9 DKWIKG---SGEEY-LDINPADKDHVLAKIRLYTKDDVKEAINKAVAKFDEWSRTPAPKR 64 D +I G SG +Y +INP++ + V AI+ A A F WS + R Sbjct: 8 DNYINGEWVSGADYSANINPSELTDTIGDYAKADLAQVHAAIDAARAAFPAWSTSGIQAR 67 Query: 65 GSILLKAGELMEQEAQEFALLMTLEEGKTLKDSMFEVTRSYNLLKFYGALAFKISGKTLP 124 L K G + +E L+ EEGKTL +++ EVTR+ N+ KF+ ++SG LP Sbjct: 68 HDSLDKVGTEILARREELGTLLAREEGKTLPEAIGEVTRAGNIFKFFAGECLRLSGDYLP 127 Query: 125 SADPNTRIFTVKEPLGVVALITPWNFPLSIPVWKLAPALAAGNTAVIKPATKTPLMVAKL 184 S P + +E LGVV LITPWNFP++IP WK+APALA GN V+KPA P L Sbjct: 128 SVRPGVNVEVTREALGVVGLITPWNFPIAIPAWKIAPALAYGNCVVLKPADLVPGCAWAL 187 Query: 185 VEVLSKAGLPEGVVNLVVGKGSEVGDTIVSDDNIAAVSFTGSTEVGKRIYKLVGNKNRMT 244 E++S+AG P GV NLV+G G VGD +V + +SFTGS VG++I V +R Sbjct: 188 AEIISRAGFPAGVFNLVMGSGRVVGDALVQSPKVDGISFTGSVGVGRQI--AVSCVSRQA 245 Query: 245 RIQLELGGKNALYVDKSADLTLAAELAVRGGFGLTGQSCTATSRLIINKDVYTQFKQRLL 304 ++QLE+GGKN + ADL A EL+V+ F TGQ CTA+SR I+ ++ +F + + Sbjct: 246 KVQLEMGGKNPQIILDDADLKQAVELSVQSAFYSTGQRCTASSRFIVTAGIHDKFVEAMA 305 Query: 305 ERVKKWRVGPGTE-DVDMGPVVDEGQFKKDLEYIEYGKNVGAKLIYGGNII--PGKGYFL 361 ER+K +VG + D+GPVV + Q ++DL+YI+ G++ GA+L+ GG ++ +GYFL Sbjct: 306 ERMKSIKVGHALKTGTDIGPVVSQAQLEQDLKYIDIGQSEGARLVSGGGLVACDTEGYFL 365 Query: 362 EPTIFEGVTSDMRLFKEEIFGPVLSVTEAKDLDEAIRLVNAVDYGHTAGIVASDIKAINE 421 PT+F T+ MR+ +EEIFGPV ++ D + A+ + N ++G +AGI + +K N Sbjct: 366 APTLFADSTAAMRISREEIFGPVANIVRVADYEAALAMANDTEFGLSAGIATTSLKYANH 425 Query: 422 FVSRVEAGVIKVNKPTVGLELQAPFGGFKNSGATTWKEMGEDALEFYLKEKTVYEG 477 F +AG++ VN PT G++ PFGG K S + +E G A EFY KT Y G Sbjct: 426 FKRHSQAGMVMVNLPTAGVDYHVPFGGRKGSSYGS-REQGRYAQEFYTVVKTSYIG 480 Lambda K H 0.316 0.135 0.389 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: 553 Number of extensions: 16 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: 478 Length of database: 481 Length adjustment: 34 Effective length of query: 444 Effective length of database: 447 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 (21.6 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