Align Alpha-ketoglutaric semialdehyde dehydrogenase; alphaKGSA dehydrogenase; 2,5-dioxovalerate dehydrogenase; EC 1.2.1.26 (characterized)
to candidate WP_038806127.1 HK29_RS05075 NADP-dependent glyceraldehyde-3-phosphate dehydrogenase
Query= SwissProt::P42236 (488 letters) >NCBI__GCF_000382825.1:WP_038806127.1 Length = 474 Score = 288 bits (738), Expect = 2e-82 Identities = 166/461 (36%), Positives = 260/461 (56%), Gaps = 18/461 (3%) Query: 10 YLNFINGEWVKSQSGDMVKVENPADVNDIVGYVQNSTAEDVERAVTAANEAKTAWRKLTG 69 Y N +NG W S+ + + +P + + +G V + +V+ A+ AA A AWR L Sbjct: 4 YQNLVNGNWKSSEKE--ITIYSPIN-QEKLGTVPAMSQAEVDEAMKAARAALPAWRDLAP 60 Query: 70 AERGQYLYKTADIMEQRLEEIAACATREMGKTLPEAKGETARGIAILRYYAGEGMRKTGD 129 ER YL+KTADI+E+ E+I +E+ K + A GE R ++R+ A EG+R TG Sbjct: 61 VERAAYLHKTADILERDKEKIGTILAKEVAKGIKAAIGEVVRTADLIRFAAEEGLRITGQ 120 Query: 130 VIP-----STDKDALMFTTRVPLGVVGVISPWNFPVAIPIWKMAPALVYGNTVVIKPATE 184 + + K+ L R P+GVV I+P+N+PV + K+APAL+ GN V+ KP T+ Sbjct: 121 AMEGGGFEAASKNKLAVVRREPVGVVLAIAPFNYPVNLSGSKIAPALIAGNVVMFKPPTQ 180 Query: 185 TAVTCAKIIACFEEAGLPAGVINLVTGPGSVVGQGLAEHDGVNAVTFTGSNQVGKIIGQA 244 +++ + F+EAG+PAGV N +TG GS +G + EH VN + FTGS +G+ IG+ Sbjct: 181 GSISGLLLAKAFDEAGIPAGVFNTITGRGSEIGDYIIEHKEVNFINFTGSTPIGERIGRL 240 Query: 245 ALARGAKYQLEMGGKNPVIVADDADLEAAAEAVITGAFRSTGQKCTATSRVIVQSGIYER 304 A R LE+GGK+ IV +DADLE AA+ ++ GAF +GQ+CTA RV+V + +R Sbjct: 241 AGMR--PIMLELGGKDAAIVLEDADLEHAAKQIVGGAFSYSGQRCTAIKRVLVVESVADR 298 Query: 305 FKEKLLQRTKDITIGDSLKEDVWMGPIASKNQLDNCLSYIEKGKQEGASLLIGGEKLENG 364 E L +T+GD ++ + P+ D I+ +++GA L + Sbjct: 299 LAELLQAEVAKLTVGDPF-DNADITPVVDNASADFIWGLIQDAQEKGAKAL-------SP 350 Query: 365 KYQNGYYVQPAIFDNVTSEMTIAQEEIFGPVIALIKVDSIEEALNIANDVKFGLSASIFT 424 + G + P +FD VT +M +A EE+FGPV+ +I+V EA+ IAN+ +FGL +S+FT Sbjct: 351 IKREGNLIWPGLFDYVTRDMKLAWEELFGPVLPIIRVADANEAVAIANESEFGLQSSVFT 410 Query: 425 ENIGRMLSFIDEIDAGLVRINAESAGVELQAPFGGMKQSSS 465 + + ++++ G V IN ++ PF G+K S + Sbjct: 411 NDFKKAFEIAEKLEVGTVHINNKTQRGPDNFPFLGVKGSGA 451 Lambda K H 0.315 0.132 0.374 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: 547 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: 488 Length of database: 474 Length adjustment: 34 Effective length of query: 454 Effective length of database: 440 Effective search space: 199760 Effective search space used: 199760 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 (21.5 bits) S2: 51 (24.3 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